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Search Results for " antagonist "
Targets Recommended: Estrogen/progestogen Receptor

4846

抑制剂 & 化合物

133

天然产物

3

化合物库

35

重组蛋白

105

同位素标记化合物

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Cat. No. Product Name
L7200 钙通道分子库

140 compounds
140 种钙通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选;
L7110 抗高血压化合物库

678 compounds
678 种高血压相关的小分子,用于高通量和高内涵筛选;
L9830 抗帕金森病化合物库

857 compounds
857 种帕金森病相关的化合物集合,可用于高通量和高内涵筛选;

化合物库

钙通道分子库
Cat.No: L7200
Compounds: 140
抗高血压化合物库
Cat.No: L7110
Compounds: 678
抗帕金森病化合物库
Cat.No: L9830
Compounds: 857
Cat. No. Product Name Target Signaling Pathways
T11230 ERRα antagonist-1

ERR+/- antagonist-1,ERRa antagonist-1

Estrogen/progestogen Receptor Endocrinology/Hormones
ERRα antagonist-1 (ERR+/- antagonist-1) 是一种选择性的,高亲和力的雌激素相关受体α (ERRα) 拮抗剂。ERRα antagonist-1 抑制 ERRα 与增殖物激活的受体γ共激活因子 1α (PGC-1α) 和 PGC-1β 的相互作用,IC50 值分别为 170 nM 和 180 nM。ERRα antagonist-1 不抑制 ERRβ 或 ERRγ 与 PGC-1α 和 PGC-1β 共激活剂的相互作用,也不抑制 ERα 或 ERβ 与 PGC-1α 或 SRC-1 的相互作用。
T39078 CXCR7 antagonist-1

CXCR7 antagonist-1

CXCR Autophagy; GPCR/G Protein; Immunology/Inflammation
CXCR7 antagonist-1 是 SDF-1 趋化因子或 I-TAC 与趋化因子受体 CXCR7 结合的特异性拮抗剂。 CXCR7 antagonist-1 可防止肿瘤细胞增殖和肿瘤形成,可用于炎症性疾病的研究。
T37793 A2B receptor antagonist 2

A2B receptor antagonist 2

Adenosine Receptor GPCR/G Protein; Neuroscience
A2B receptor antagonist 2 是腺苷受体 A2B 的拮抗剂(rA1 的 Ki = 2.30 μM,rA2A 的 Ki = 6.8 μM,hA2B 的 3.44 μM)。
T10031 EP1-antagonist-1

EP1-antanoist-1,EP1 antagonist 1

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
EP1-antagonist-1 (EP1 antagonist 1) 是 EP1 的拮抗剂,pKi 和 pIC50 分别为 7.54 和 8.5。
T15785 LPA1 receptor antagonist 1

LPA1 R antagonist 1

LPA Receptor GPCR/G Protein
LPA1 receptor antagonist 1(LPA1 R antagonist 1) 是一种具有选择性和高效性的溶血磷脂酸 (LPA1) 受体拮抗剂( IC50 : 25 nM),可用于研究特发性肺纤维化。
T37792 A2A receptor antagonist 1

CPI-444 analog,A2A receptor antagonist 1

Adenosine Receptor GPCR/G Protein; Neuroscience
A2A receptor antagonist 1 (CPI-444 analog)是腺苷 A2A 和 A1受体的拮抗剂,Ki 值分别为4和264 nM。
T10250 ADRA1D receptor antagonist 1 HCl

ADRA1D receptor antagonist 1 HCl(1191908-24-3 free base)

Adrenergic Receptor GPCR/G Protein; Neuroscience
ADRA1D receptor antagonist 1 HCl 是一种具有口服活性、高效性和选择性的 α1D 肾上腺素受体拮抗剂(Ki:1.6 nM),具有潜在的抗增殖活性。
T13216 TSHR antagonist S37

TSH Receptor GPCR/G Protein
TSHR antagonist S37 是促甲状腺激素受体 (TSHR) 的选择性和竞争性拮抗剂。
T9709 TRPM8 antagonist 3

TRP/TRPV Channel Membrane transporter/Ion channel
TRPM8 antagonist 3 是 TRPM8 的阻断剂 (IC50 = 11 nM)。
T10712 CCR2 antagonist 3

AZD-2927,AZD2927

CCR Immunology/Inflammation; Microbiology/Virology
CCR2 antagonist 3 (AZD-2927) 是 CCR2的拮抗剂。
T5698 TRPM8 antagonist 2

TRP/TRPV Channel Membrane transporter/Ion channel
TRPM8 antagonist 2 是有效的 RPM8选择性 T 拮抗剂,IC50值为 0.2 nM,在神经性疼痛综合症中有研究价值。
T9983 CCR8 antagonist 1

LUN04765

CCR Immunology/Inflammation; Microbiology/Virology
CCR8 antagonist 1 是 C-C Motif 趋化因子受体 8 (CCR8) 的拮抗剂,Ki 值为 1.6 nM。
T10708 CCR1 antagonist 6

CCR Immunology/Inflammation; Microbiology/Virology
CCR1 antagonist 6是一种 CCR1 拮抗剂(IC50 :3 nM)。
TP1935L1 RAGE antagonist peptide acetate

Beta Amyloid Neuroscience
RAGE antagonist peptide acetate 是一种高级的糖基化终产物 (RAGE) 拮抗剂。 它具有抗肿瘤和抗炎活性。 它可防止 RAGE 与其几个重要的配体结合,包括 HMGB-1、S100P 和 S100A4。
T5622 BAY-218

AHR antagonist 1

AhR; Aryl Hydrocarbon Receptor Immunology/Inflammation; Metabolism
BAY-218 (AHR antagonist 1) 是一种芳基烃受体(AHR)拮抗剂,在人细胞系中的IC50值为 39.9 nM。
T10084 CRTh2 antagonist 1

GPR Endocrinology/Hormones; GPCR/G Protein
CRTh2 antagonist 1 是 CRTh2 拮抗剂,IC50 值为 89 nM。
T10156 CCR3 antagonist 1

CCR Immunology/Inflammation; Microbiology/Virology
CCR3 antagonist 1是一种有效的 CCR3拮抗药,用于炎症和免疫疾病的研究。
T8848 GPR34 receptor antagonist 2

Tyrosine, N-[(2E)-3-(4'-chloro[1,1'-biphenyl]-4-yl)-1-oxo-2-propen-1-yl]-O-(phenylmethyl)-,gpr34-receptor-antagonist-2

Others Others
GPR34 receptor antagonist 2 (Tyrosine, N-[(2E)-3-(4'-chloro[1,1'-biphenyl]-4-yl)-1-oxo-2-propen-1-yl]-O-(phenylmethyl)-) 是一种GPR34受体拮抗剂,可用于研究免疫疾病、炎性疾病。
T5829 H4 Receptor antagonist 1

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
H4 Receptor antagonist 1 是选择性组胺 H4受体反向激动剂,其IC50值为19 nM。
T11966 MCHR1 antagonist 2

HER; Melanin-concentrating Hormone Receptor (MCHR) Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors
MCHR1 antagonist 2 是有效的黑色素聚集激素受体 1 拮抗剂,IC50为 65 nM。它也抑制hERG,在IMR-32 细胞中的IC50为 4.0 nM。
T10169 5-HT4 antagonist 1

5-HT Receptor GPCR/G Protein; Neuroscience
5-HT4 antagonist 1 是 5-HT4 的拮抗剂 (pKi = 9.6)。
T13435 TR antagonist 1

Thyroid hormone receptor(THR) Endocrinology/Hormones
TR antagonist 1 是一种高效甲状腺激素受体(TR)拮抗剂(对 TRα 和 TRβ 的 IC50 分别为 36 和 22 nM),可用于研究内分泌异常引起的疾病。
T37429 TRPV3 antagonist 74a

TRPV3 74a

TRP/TRPV Channel Membrane transporter/Ion channel
TRPV3 antagonist 74a (TRPV3 74a) 是一种特异性 TRPV3 拮抗剂,可用于研究神经系统相关疾病。
T10359 AR antagonist 1

Androgen Receptor; Ligand for E3 Ligase; Ligands for Target Protein for PROTAC Endocrinology/Hormones; PROTAC
AR antagonist 1 是 AR 拮抗剂,能够与 E3 连接酶配体结合,与 VHL 蛋白结合亲和力较弱,用于 PROTACARD-266 合成。
T14881 CB1 antagonist 2

AM4113

Cannabinoid Receptor GPCR/G Protein
CB1 antagonist 2 (AM4113) 是一种 caimabinoid 1 拮抗剂,在体内抑制 CB1 的IC50值为 25.5 nM。
T12320 ORL1 antagonist 1

Opioid Receptor Endocrinology/Hormones; GPCR/G Protein; Neuroscience
ORL1 antagonist 1是阿片样受体1 (ORL1) 拮抗剂, IC50 值为 61 nM。
T10889 CRTh2 antagonist 2

GPR Endocrinology/Hormones; GPCR/G Protein
CRTh2 antagonist 2 是一种有效的选择性 CRTH2 抑制剂,对 CRTH2 的 IC50 值为 ≤10 nM。CRTh2 antagonist 2 可用于雄激素性脱发的研究。
T10058 A2B receptor antagonist 1

Adenosine Receptor GPCR/G Protein; Neuroscience
A2B receptor antagonist 1 是一个有效的 A2B 腺苷受体 (A2B adenosine receptor) 拮抗剂。
T12910 Sigma-1 receptor antagonist 1

Sigma receptor GPCR/G Protein
Sigma-1 receptor antagonist 1 是一种有效、特异性的 sigma-1 受体拮抗剂。 Sigma-1 receptor antagonist 1 具有抗神经性疼痛活性,可用于治疗神经性疼痛研究。
T11211 EP4 receptor antagonist 1

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
EP4 receptor antagonist 1 是一种有效的特异性前列腺素 EP4受体拮抗剂,对人和小鼠 EP4受体的 IC50分别为6.1 nM 和16.2 nM。 EP4 receptor antagonist 1 可用于癌症免疫治疗的研究。
T10269 AHR antagonist 2

Aryl Hydrocarbon Receptor Immunology/Inflammation
AHR antagonist 2 是芳基烃受体的拮抗剂。 人 AHR 和小鼠 AHR 的 IC50 分别为 0.885 和 2.03 nM。
T13453 CGRP antagonist 1

CGRP Receptor GPCR/G Protein; Neuroscience
CGRP antagonist 1是高效 CGRP 受体拮抗剂,Ki 值分别为 35nM,IC50 值为 57 nM。CGRP antagonist 1可用于研究心血管疾病和神经血管疾病。
T5522 NMDAR antagonist 1

Others; iGluR Membrane transporter/Ion channel; Neuroscience; Others
NMDAR antagonist 1 是一种 NR2B 选择性的、口服具有活力的 NMDAR 拮抗剂。
T12911 Sigma-1 receptor antagonist 2

Sigma receptor GPCR/G Protein
Sigma-1 receptor antagonist 2 是有效的sigma 1受体选择性拮抗剂,与 σ1 和 σ2 受体结合的Ki 分别为 3.88 和 1288 nM。
T39762 AHR antagonist 5 free base

Aryl Hydrocarbon Receptor Immunology/Inflammation
AHR antagonist 5 free base 是一种具有口服活性的 AHR 拮抗剂,在人和啮齿动物细胞系中的 IC50 约为 35-150 nM。
T11635 IL-17A antagonist 1

IL Receptor Immunology/Inflammation
IL-17A antagonist 1 是一种 IL-17A 拮抗剂,可用于研究和白介素相关的炎症和免疫疾病。
T10162 5-HT3 antagonist 3

5-HT Receptor GPCR/G Protein; Neuroscience
5-HT3 antagonist 3 是一种高亲和力的 5-HT3 受体拮抗剂。5-HT3 antagonist 3 结合到大鼠脑皮质膜中的 5-HT3 受体,Ki 为 0.25 nM。
T10248 Adenosine antagonist-1

Adenosine Receptor GPCR/G Protein; Neuroscience
Adenosine antagonist-1 可作为一种腺苷 A3 受体 (AA3R) 拮抗剂。
T12912 Sigma-1 receptor antagonist 3

Sigma receptor; HER Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Sigma-1 receptor antagonist 3 是 Sigma-1受体选择性拮抗剂,Ki 为 1.14 nM。它抑制 hERG,IC50为 1.54μM。它在神经性疼痛方面有研究的价值。
T12597 5-HT2 antagonist 1

5-HT Receptor GPCR/G Protein; Neuroscience
5-HT2 antagonist 1 是一种有效的 5-HT2 receptor 拮抗剂,同时对 α1 adrenoceptor 有微弱地抑制作用。
T9244 σ1 Receptor antagonist-1

Sigma receptor GPCR/G Protein
σ1 Receptor antagonist-1 是高选择性的 sigma 1受体拮抗剂,pKi 为10.28。它抑制细胞生长,在 G0/G1 期阻滞细胞周期并诱导 MCF-7/ADR 细胞凋亡。
T11851 Lin28-let-7a antagonist 1

Others Others
Lin28-let-7a antagonist 1 对 Lin28A-let-7a-1 相互作用的 IC50 为 4.03 μM,对 Lin28-let-7a 相互作用有明显的拮抗作用。
T13114 CCR2 antagonist 4

Teijin compound 1

CCR Immunology/Inflammation; Microbiology/Virology
CCR2 antagonist 4 (Teijin compound 1) 是高效的、特异性的CCR2拮抗剂,对 CCR2b 的IC50为 180 nM,抑制 MCP-1 诱导的趋化作用的 IC50为 24 nM。
T9846 5-HT3 antagonist 5

Others Others
5-HT3 antagonist 5 是喹喔啉 -2- 甲酰胺化合物,是一种5-HT3受体拮抗剂。5-HT3 antagonist 5 对5-HT3激动剂和2-甲基-5-HT 也具有拮抗作用,并在小鼠中表现出抗抑郁作用。
T38622 Bcl-xL antagonist 2

BCL Apoptosis
Bcl-xL antagonist 2 是一种有效的选择性 Bcl-xL 拮抗剂,IC50 为 91 nM,Ki 为 65 nM。 Bcl-xL antagonist 2 可诱导癌细胞凋亡,可用于慢性淋巴细胞白血病和非霍奇金淋巴瘤的研究。
T9723 GluR6 antagonist-1

Src Angiogenesis; Tyrosine Kinase/Adaptors
GluR6 antagonist-1 抑制酪氨酸激酶 p56lck SH2 结构域的 pY 结合位点。
T11560 hGPR91 antagonist 1

(S)-2-(4-(1,8-萘啶-2-基)苯基)-N-(1-(4'-氟-3'-(三氟甲基)-[1,1'-联苯]-4-基)乙基)乙酰胺

GHSR GPCR/G Protein
HGPR91 antagonist 1 是小分子hGPR91选择性拮抗剂(IC50:7 μM)。
T60145 CCR6 antagonist 1

CCR Immunology/Inflammation; Microbiology/Virology
CCR6 antagonist 1 是一种 CCR6 拮抗剂,可抑制 CCL20/CCR6 信号通路。 CCR6 antagonist 1 可用于自身免疫介导的炎症性疾病的研究,如炎症性肠病 (IBDs)。
T27682 CCR2 antagonist 5

JNJ-41443532,JNJ-41443532 Free Base,JNJ 41443532,JNJ41443532

CCR Immunology/Inflammation; Microbiology/Virology
CCR2 antagonist 5 (JNJ-41443532) 是一种具有选择性和口服活性的 hCCR2 抑制剂,具有良好的结合亲和力 (IC50=37 nM) 和有效的功能拮抗作用 (chemotaxis IC50=30 nM)。JNJ-41443532 对 mCCR2 结合的 Ki 为 9.6 µM, 可用于研究炎症性疾病和糖尿病。
T15387 GLP-1R Antagonist 1

Glucagon Receptor GPCR/G Protein
GLP-1R Antagonist 1 (compound 5d) 是口服有效的、能透过中枢神经系统的,胰高血糖素样肽 1 受体 (GLP-1R) 的非竞争性抑制,其 IC50 值为 650 nM。

化合物

ERRα antagonist-1
Cat.No: T11230
Synonym: ERR+/- antagonist-1,ERRa antagonist-1
Target: Estrogen/progestogen Receptor
CXCR7 antagonist-1
Cat.No: T39078
Synonym: CXCR7 antagonist-1
Target: CXCR
A2B receptor antagonist 2
Cat.No: T37793
Synonym: A2B receptor antagonist 2
Target: Adenosine Receptor
EP1-antagonist-1
Cat.No: T10031
Synonym: EP1-antanoist-1,EP1 antagonist 1
Target: Prostaglandin Receptor
LPA1 receptor antagonist 1
Cat.No: T15785
Synonym: LPA1 R antagonist 1
Target: LPA Receptor
A2A receptor antagonist 1
Cat.No: T37792
Synonym: CPI-444 analog,A2A receptor antagonist 1
Target: Adenosine Receptor
ADRA1D receptor antagonist 1 HCl
Cat.No: T10250
Synonym: ADRA1D receptor antagonist 1 HCl(1191908-24-3 free base)
Target: Adrenergic Receptor
TSHR antagonist S37
Cat.No: T13216
Synonym:
Target: TSH Receptor
TRPM8 antagonist 3
Cat.No: T9709
Synonym:
Target: TRP/TRPV Channel
CCR2 antagonist 3
Cat.No: T10712
Synonym: AZD-2927,AZD2927
Target: CCR
TRPM8 antagonist 2
Cat.No: T5698
Synonym:
Target: TRP/TRPV Channel
CCR8 antagonist 1
Cat.No: T9983
Synonym: LUN04765
Target: CCR
CCR1 antagonist 6
Cat.No: T10708
Synonym:
Target: CCR
RAGE antagonist peptide acetate
Cat.No: TP1935L1
Synonym:
Target: Beta Amyloid
BAY-218
Cat.No: T5622
Synonym: AHR antagonist 1
Target: AhR, Aryl Hydrocarbon Receptor
CRTh2 antagonist 1
Cat.No: T10084
Synonym:
Target: GPR
CCR3 antagonist 1
Cat.No: T10156
Synonym:
Target: CCR
GPR34 receptor antagonist 2
Cat.No: T8848
Synonym: Tyrosine, N-[(2E)-3-(4'-chloro[1,1'-biphenyl]-4-yl)-1-oxo-2-propen-1-yl]-O-(phenylmethyl)-,gpr34-receptor-antagonist-2
Target: Others
H4 Receptor antagonist 1
Cat.No: T5829
Synonym:
Target: Histamine Receptor
MCHR1 antagonist 2
Cat.No: T11966
Synonym:
Target: HER, Melanin-concentrating Hormone Receptor (MCHR)
5-HT4 antagonist 1
Cat.No: T10169
Synonym:
Target: 5-HT Receptor
TR antagonist 1
Cat.No: T13435
Synonym:
Target: Thyroid hormone receptor(THR)
TRPV3 antagonist 74a
Cat.No: T37429
Synonym: TRPV3 74a
Target: TRP/TRPV Channel
AR antagonist 1
Cat.No: T10359
Synonym:
Target: Androgen Receptor, Ligand for E3 Ligase, Ligands for Target Protein for PROTAC
CB1 antagonist 2
Cat.No: T14881
Synonym: AM4113
Target: Cannabinoid Receptor
ORL1 antagonist 1
Cat.No: T12320
Synonym:
Target: Opioid Receptor
CRTh2 antagonist 2
Cat.No: T10889
Synonym:
Target: GPR
A2B receptor antagonist 1
Cat.No: T10058
Synonym:
Target: Adenosine Receptor
Sigma-1 receptor antagonist 1
Cat.No: T12910
Synonym:
Target: Sigma receptor
EP4 receptor antagonist 1
Cat.No: T11211
Synonym:
Target: Prostaglandin Receptor
AHR antagonist 2
Cat.No: T10269
Synonym:
Target: Aryl Hydrocarbon Receptor
CGRP antagonist 1
Cat.No: T13453
Synonym:
Target: CGRP Receptor
NMDAR antagonist 1
Cat.No: T5522
Synonym:
Target: Others, iGluR
Sigma-1 receptor antagonist 2
Cat.No: T12911
Synonym:
Target: Sigma receptor
AHR antagonist 5 free base
Cat.No: T39762
Synonym:
Target: Aryl Hydrocarbon Receptor
IL-17A antagonist 1
Cat.No: T11635
Synonym:
Target: IL Receptor
5-HT3 antagonist 3
Cat.No: T10162
Synonym:
Target: 5-HT Receptor
Adenosine antagonist-1
Cat.No: T10248
Synonym:
Target: Adenosine Receptor
Sigma-1 receptor antagonist 3
Cat.No: T12912
Synonym:
Target: Sigma receptor, HER
5-HT2 antagonist 1
Cat.No: T12597
Synonym:
Target: 5-HT Receptor
σ1 Receptor antagonist-1
Cat.No: T9244
Synonym:
Target: Sigma receptor
Lin28-let-7a antagonist 1
Cat.No: T11851
Synonym:
Target: Others
CCR2 antagonist 4
Cat.No: T13114
Synonym: Teijin compound 1
Target: CCR
5-HT3 antagonist 5
Cat.No: T9846
Synonym:
Target: Others
Bcl-xL antagonist 2
Cat.No: T38622
Synonym:
Target: BCL
GluR6 antagonist-1
Cat.No: T9723
Synonym:
Target: Src
hGPR91 antagonist 1
Cat.No: T11560
Synonym: (S)-2-(4-(1,8-萘啶-2-基)苯基)-N-(1-(4'-氟-3'-(三氟甲基)-[1,1'-联苯]-4-基)乙基)乙酰胺
Target: GHSR
CCR6 antagonist 1
Cat.No: T60145
Synonym:
Target: CCR
CCR2 antagonist 5
Cat.No: T27682
Synonym: JNJ-41443532,JNJ-41443532 Free Base,JNJ 41443532,JNJ41443532
Target: CCR
GLP-1R Antagonist 1
Cat.No: T15387
Synonym:
Target: Glucagon Receptor
Cat. No. Product Name Target Signaling Pathways
T21615 Guanidinoethyl sulfonate

脒基牛磺酸,Taurocyamine

Chloride channel Membrane transporter/Ion channel
Guanidinoethyl sulfonate (Taurocyamine) 它是一种牛磺酸的结构类似物,也是牛磺酸转运的竞争性拮抗剂。它能够诱导怀孕大鼠排泄含有大量牛磺酸的尿液,导致组织中牛磺酸含量降低,从而容易产生牛磺酸缺乏的胎鼠。
T8268 6,2'-Dihydroxyflavone

6,2-二羟基黄酮,6,2'-二羟基黄酮

GABA Receptor Membrane transporter/Ion channel; Neuroscience
6,2'-Dihydroxyflavone 是一种新型GABAA 受体拮抗剂。
T21499 Dimebolin

Latrepirdine,Dimebon,Dimebone

5-HT Receptor GPCR/G Protein; Neuroscience
Dimebolin (Latrepirdine) 是一种 5-HT6 拮抗剂。
T3917 Protopanaxatriol

20(R)-APPT,20(R)-Protopanaxatriol,原人参三醇,(20R)-Protopanaxatriol

PPAR DNA Damage/DNA Repair; Metabolism
Protopanaxatriol (20(R)-APPT) 是天然的人参皂苷的糖苷配基,包括 Re,Rf,Rg1,Rg2 和 Rh。
TN1519L (-)-Coclaurine hydrochloride

(-)-Coclaurine hydrochloride (486-39-5 Free base)

AChR Neuroscience
(-)-Coclaurine hydrochloride 是从 Sarcopetalum harveyanum 中分离出来的,是一种 nAChR 拮抗剂。
TQ0197 Acenocoumarol

醋硝香豆素,新抗凝

Acenocoumarol 是一种抗凝血剂,与 Vitamin K 拮抗剂的功能相似。
T19713 HHQ

2-庚基-4-喹啉酮,2-heptylquinolin-4(1H)-one

Others Others
HHQ (2-heptylquinolin-4(1H)-one) 是一种 PqsR 拮抗剂。
T3S2100 (-)-Securinine

一叶秋碱,Securinine

GABA Receptor Membrane transporter/Ion channel; Neuroscience
(-)-Securinine (Securinine) 是来自叶底珠的一种生物碱,也是 GABAA 受体拮抗剂。
TJS0341 7-Amino-4-(trifluoromethyl)coumarin

香豆素151,Coumarin 151,AFC,7-氨基-4-(三氟甲基)香豆素

5-HT Receptor GPCR/G Protein; Neuroscience
7-Amino-4-(trifluoromethyl)coumarin (Coumarin 151) 是一种荧光标记物,其激发和发射波长分别为400和500 nm,可用来灵敏的检测蛋白酶。
T7177 Capsazepine

Apoptosis; TRP/TRPV Channel Apoptosis; Membrane transporter/Ion channel
Capsazepine 是一种 TRPV1 受体的拮抗剂, IC50值为 562 nM。 它可阻断由激活 TRPV1 离子通道的辣椒素引起的热痛感,是辣椒素拮抗剂。
T2751 Ginkgolide B

BN-52021,银杏内酯B

Apoptosis; PAFR; Endogenous Metabolite Apoptosis; GPCR/G Protein; Metabolism
Ginkgolide B (BN-52021) 是一种萜类物质,是银杏叶中的重要的活性物质之一。
T21504 γ-Linolenic Acid methyl ester

Methyl gamma-linolenate,γ-亚麻酸甲酯

LTR Immunology/Inflammation
γ-Linolenic Acid methyl ester (Methyl gamma-linolenate) 是一种弱白三烯 B4 (LTB4) 受体拮抗剂。
T8304 Anisodamine Hydrobromide

6-Hydroxyhyoscyamine,氢溴酸山莨菪碱

Adrenergic Receptor; AChR GPCR/G Protein; Neuroscience
Anisodamine Hydrobromide (6-Hydroxyhyoscyamine) 是来自颠茄的一种生物碱,具有抗氧化、抗炎活性。它也是一种非亚型的选择性毒蕈碱和烟碱类胆碱受体拮抗剂。
T0525 Flopropione

夫洛丙酮,Phloropropiophenone

5-HT Receptor; Transferase GPCR/G Protein; Metabolism; Neuroscience
Flopropione (Phloropropiophenone) 是一种解痉剂,用作 5-HT1A 受体拮抗剂,也是儿茶酚-O-甲基转移酶抑制剂。
T0354 Canrenone

6,7-Dehydro-7α-desthioacetylspironolactone,SC9376,Aldadiene,坎利酮,RP-11614,SC14266

Glucocorticoid Receptor; Endogenous Metabolite Endocrinology/Hormones; Metabolism
Canrenone (SC14266) 是一种醛固酮 (aldosterone) 拮抗剂,广泛用作利尿剂。
TN1465 Cannabigerol

NOS; 5-HT Receptor; ROS GPCR/G Protein; Immunology/Inflammation; Neuroscience
Cannabigerol 是一种植物大麻素,是一种高亲和力 α2-肾上腺素能受体激动剂、中度亲和力 5-HT1A 受体拮抗剂和低亲和力 CB1/CB2受体拮抗剂。它可降低眼压,有潜力治疗青光眼。
T3668 Galangin

Norizalpinin,高良姜素,3,5,7-Trihydroxyflavone

ERK; P450; NF-κB; Autophagy Autophagy; MAPK; Metabolism; NF-κB
Galangin (Norizalpinin) 是芳烃受体的激动剂/拮抗剂,并且还显示对 CYP1A1 活性的抑制作用。
T1680 Tolazoline hydrochloride

Imidaline hydrochloride,苯甲唑啉盐酸盐,Imidaline (hydrochloride),Benzidazol hydrochloride,Tolazoline HCl,NSC35110 (hydrochloride)

Adrenergic Receptor GPCR/G Protein; Neuroscience
Tolazoline hydrochloride (NSC35110(hydrochloride)) 是一种 α 肾上腺素受体抑制剂。
T3379 Decanoic Acid

Decoic acid,CAPRIC ACID,Caprynic acid,癸酸

GluR; iGluR Membrane transporter/Ion channel; Neuroscience
Decanoic Acid (Caprynic acid) 是中链甘油三酯中的成分,是非竞争性和可透过血脑屏障的 AMPA 受体抑制剂,具有抗癫痫作用。
T0970 Racanisodamine

山莨菪碱,Anisodamine,7β-Hydroxyhyoscyamine,Raceanisodamine,消旋山莨菪碱

Adrenergic Receptor; AChR GPCR/G Protein; Neuroscience
Racanisodamine (7β-Hydroxyhyoscyamine) 是 anisodamine 的消旋体,是非选择性的毒蕈碱拮抗剂,是近视控制滴眼液的有效成分。
T5743 Gymnemagenin

Liver X Receptor Metabolism
Gymnemagenin 是一种分离自G. sylvestre 的三萜。 它具有抗病毒作用,对糖尿病和肥胖症具有潜在的研究价值。
T2S1464 Thiocolchicoside

硫秋水仙苷;噻可撒可,Thiocolchicine 2-glucoside analog,硫秋水仙苷,Coltramyl

Others; GABA Receptor Membrane transporter/Ion channel; Neuroscience; Others
Thiocolchicoside (Thiocolchicine 2-glucoside analog) 是秋水仙碱的半合成硫衍生物,是竞争性 GABAA 受体拮抗剂和甘氨酸受体拮抗剂。它是肌肉松弛剂,具有抗炎作用,可用于缓解疼痛的研究。
T20884 Hydroxyzine

Hydroxyzine free base,羟嗪

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Hydroxyzine (Hydroxyzine free base) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。
T1156 Palonosetron hydrochloride

盐酸帕洛诺司琼,RS 25259 197,Palonosetron HCl,RS 25259

5-HT Receptor GPCR/G Protein; Neuroscience
Palonosetron hydrochloride (RS 25259) 是一种 5-HT3 拮抗剂,用于预防和治疗化疗引起的恶心和呕吐。
TQ0027 Transcrocetinate disodium

Disodium trans-crocetinate,藏红花,藏红花酸二钠盐

NMDAR; iGluR Membrane transporter/Ion channel; Neuroscience
Transcrocetinate disodium (Disodium trans-crocetinate) 从藏红花中提取的一种天然产物,是高亲和力NMDA 受体拮抗剂。
T1186 Ifenprodil Tartrate

Potassium Channel; NMDAR; iGluR Membrane transporter/Ion channel; Neuroscience
Ifenprodil tartrate 是典型的非竞争性 NMDA 受体拮抗剂,抑制 GIRK (Kir3),通过基底 GIRK 活性减少内向电流,有用做脑血管舒张试剂的潜力。它对 NR1A/NR2B 受体亲和力是 NR1A/NR2A 受体的 400 倍。
T0268 Lobeline hydrochloride

盐酸洛贝林,α-Lobeline hydrochloride,L-Lobeline hydrochloride

AChR Neuroscience
Lobeline hydrochloride (α-Lobeline hydrochloride) 是一种烟碱样受体激动剂,是神经元烟碱受体α3β2和α4β2拮抗剂。
T2815 Puerarin

葛根素,Kakonein

5-HT Receptor GPCR/G Protein; Neuroscience
Puerarin (Kakonein) 是从葛根中提取的一种异黄酮,是一种5-HT2C 受体拮抗剂。
T4429 Rauwolscine hydrochloride

Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
Rauwolscine hydrochloride (Isoyohimbine hydrochloride) 是一种高选择性的 α2 adrenergic 受体拮抗剂,Ki=12 nM。
T21165 Pellitorine

AI3-19560,墙草碱,Pellitorin

TRP/TRPV Channel Membrane transporter/Ion channel
Pellitorine (Pellitorin) 是提取自 Piper nigrum 的根的一种化合物。它对 HL60 和 MCT-7 细胞系表现出显著的细胞毒活性。它可用于癌症疾病的研究。
T16535 Picrotoxinin

Chloride channel; GABA Receptor Membrane transporter/Ion channel; Neuroscience
Picrotoxinin 是一种氯离子通道阻断剂和 GABAA 的非竞争性拮抗剂,对 α1β2γ2L GABAA 的 IC50 为 1.15 μM。 Picrotoxinin 具有惊厥作用。
T7939 Fingolimod

2-氨基-2-[2-(4-辛基苯基)乙基]-1,3-丙二醇,FTY-720A,FTY-720,芬戈莫德

S1P Receptor; PAK; LPL Receptor Cytoskeletal Signaling; GPCR/G Protein
Fingolimod (FTY-720A) 是一种 1-磷酸鞘氨醇 (S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它还是pak1激活剂和免疫抑制剂。
T2898 Andrographolide

Andrographis,穿心莲内酯

SARS-CoV; Influenza Virus; NF-κB; Autophagy Autophagy; Microbiology/Virology; NF-κB
Andrographolide (Andrographis) 是 NF-κB 的不可逆拮抗剂,具有抗病毒、抗炎和抗血小板聚集活性和潜在的抗肿瘤作用。
T21581L AC 187 Acetate

AC 187 Acetate (151804-77-2 Free base)

Amylin Receptor GPCR/G Protein
AC 187 Acetate 是胰淀素受体的强效拮抗剂。AC 187 对胰淀素受体的选择性高于降钙素和 CGRP 受体。
T2825 Cyclopamine

环巴胺,11-Deoxojervine

Hedgehog/Smoothened; Endogenous Metabolite; Smo GPCR/G Protein; Metabolism; Stem Cells
Cyclopamine (11-Deoxojervine) 是Hedgehog 通路的拮抗剂,细胞实验中IC50=46 nM。它还是选择性Smo 抑制剂。
T3915 Ginsenoside Ro

人参皂苷Ro,Chikusetsusaponin 5,Polysciasaponin P3,人参皂苷 Ro,Chikusetsusaponin V

Calcium Channel; Reductase; Prostaglandin Receptor Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
Ginsenoside Ro (Chikusetsusaponin V) 能降低 TXA2产量,较弱降低 COX-1 和 TXAS 活性,具有 Ca2+拮抗剂的抗血小板作用,IC50为 155 μM。
T10822 Cirsimarin

Cirsitakaoside

Adenosine Receptor GPCR/G Protein; Neuroscience
Cirsimarin (Cirsitakaoside) 是一种从 Microtea debilis 中分离出来的黄酮类化合物。它具有很强的抗脂肪生成作用,能减少小鼠脂肪组织的沉积。Cirsimarin 对腺苷 A1 受体有拮抗作用,对磷酸二酯酶有抑制作用
TN1849 Kuwanon H

GPR; Bombesin Receptor Endocrinology/Hormones; GPCR/G Protein
Kuwanon H 是分离自桑白皮的黄酮类化合物,具有拮抗非肽类蛙皮素受体的活性。Kuwanon H 特异性抑制细胞内胃泌激素释放肽 CRP 与GRP-preferring 受体的结合,Ki 为 290 nM。
T22583 Arcaine sulfate

NMDAR Neuroscience
Arcaine sulfate 是一种多胺,是 N-甲基-d-天冬氨酸 (NMDA) 受体多胺结合位点的拮抗剂。 Arcaine 是一种胍丁胺类似物,与 ifenprodil 一起,可能有可能用于治疗癫痫疾病。
T7060 Amantadine

1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine

Others Others
Amantadine (1-Aminoadamantane) 是抗病毒药物,也是是 NMDA 型谷氨酸受体的弱拮抗剂,能促进高多巴胺的释放,并阻断多巴胺的再摄取。
T3865 beta-Eudesmol

β-桉叶醇,Beta-Selinenol,beta-桉叶醇

TRP/TRPV Channel; AChR Membrane transporter/Ion channel; Neuroscience
beta-Eudesmol (Beta-Selinenol) 是天然的含氧倍半萜烯,可激活hTRPA1,EC50值为 32.5 μM。Beta-Eudesmol 有增加食欲的功效。
T6648 Rotundine

Gindarine,L-Tetrahydropalmatine,Caseanine,罗通定,(-)-Tetrahydropalmatine

Dopamine Receptor; 5-HT Receptor GPCR/G Protein; Neuroscience
Rotundine (Gindarine) 是多巴胺D1、D2和D3受体的拮抗剂,IC50值分别为 166、1.4 和 3.3 μM。 它也是5-HT1A 的拮抗剂,IC50值为 370 nM。
T5776 pimpinellin

Apoptosis; Anti-infection Apoptosis; Microbiology/Virology
Pimpinellin 是贯众的一种成分,可通过诱导肿瘤细胞凋亡抑制肿瘤细胞的生长,可作为具有 GABA 受体活性的蛋白质的拮抗剂。
T6S0109 Sipeimine

Kashmirine,西贝母碱,Imperialine,西贝碱

Others Others
Sipeimine (Kashmirine) 是一种天然产物,从平贝母中分离得到。
TN2247 Swertisin

Adenosine Receptor GPCR/G Protein; Neuroscience
Swertisin 是从日本紫菜中分离出的 C-葡萄糖基黄酮,是腺苷 A1 受体拮抗剂,具有抗糖尿病、抗炎和抗氧化作用。
TN7129 Methyl maslinate

马斯里酸甲酯,Maslinic acid methyl ester,Crategolic acid methyl ester

Adrenergic Receptor GPCR/G Protein; Neuroscience
Methyl maslinate (Maslinic acid methyl ester) 是一种具有强心和抗心律失常特性的 β-肾上腺素受体拮抗剂。Methyl maslinate 可用于高血压研究。
T5S0273 Hypaphorine

Lenticin,Glyyunnanenine,Tryptophan Betaine,刺桐碱

Others Others
Hypaphorine (Lenticin) 是一种提取自 Pisolithus tinctorius 中的吲哚类生物碱,对啮齿动物具有有神经学影响降糖活性。
T8373 6-Diazo-5-oxo-L-nor-Leucine

DON,L-6-Diazo-5-oxonorleucine,6-重氮-5-氧代-L-正亮氨酸,Diazooxonorleucine

Influenza Virus; Glutaminase; Antibacterial; Antibiotic Microbiology/Virology; Proteases/Proteasome
6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine) 是一种谷氨酰胺拮抗剂,具有抗菌、抗病毒和抗癌作用,其Ki 值为 6 μM。它能降低肿瘤细胞的自我更新能力和转移能力 ,在体外表现出遗传毒性。
TN3695 Coniine hydrochloride

Others Others
Coniine hydrochloride 是一种聚酮化合物衍生的生物碱,对人类和动物有毒。它是一种烟碱型乙酰胆碱受体拮抗剂,可抑制神经系统。
T5S2178 Fargesin

辛夷脂素,(+/-)-Fargesin

Adrenergic Receptor GPCR/G Protein; Neuroscience
Fargesin ((+/-)-Fargesin) 是一种活性新木脂素,从木兰植物中分离得到,具有抗高血压和抗炎活性。
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天然产物

Guanidinoethyl sulfonate
Cat.No: T21615
Synonym: 脒基牛磺酸,Taurocyamine
Target: Chloride channel
6,2'-Dihydroxyflavone
Cat.No: T8268
Synonym: 6,2-二羟基黄酮,6,2'-二羟基黄酮
Target: GABA Receptor
Dimebolin
Cat.No: T21499
Synonym: Latrepirdine,Dimebon,Dimebone
Target: 5-HT Receptor
Protopanaxatriol
Cat.No: T3917
Synonym: 20(R)-APPT,20(R)-Protopanaxatriol,原人参三醇,(20R)-Protopanaxatriol
Target: PPAR
(-)-Coclaurine hydrochloride
Cat.No: TN1519L
Synonym: (-)-Coclaurine hydrochloride (486-39-5 Free base)
Target: AChR
Acenocoumarol
Cat.No: TQ0197
Synonym: 醋硝香豆素,新抗凝
Target:
HHQ
Cat.No: T19713
Synonym: 2-庚基-4-喹啉酮,2-heptylquinolin-4(1H)-one
Target: Others
(-)-Securinine
Cat.No: T3S2100
Synonym: 一叶秋碱,Securinine
Target: GABA Receptor
7-Amino-4-(trifluoromethyl)coumarin
Cat.No: TJS0341
Synonym: 香豆素151,Coumarin 151,AFC,7-氨基-4-(三氟甲基)香豆素
Target: 5-HT Receptor
Capsazepine
Cat.No: T7177
Synonym:
Target: Apoptosis, TRP/TRPV Channel
Ginkgolide B
Cat.No: T2751
Synonym: BN-52021,银杏内酯B
Target: Apoptosis, PAFR, Endogenous Metabolite
γ-Linolenic Acid methyl ester
Cat.No: T21504
Synonym: Methyl gamma-linolenate,γ-亚麻酸甲酯
Target: LTR
Anisodamine Hydrobromide
Cat.No: T8304
Synonym: 6-Hydroxyhyoscyamine,氢溴酸山莨菪碱
Target: Adrenergic Receptor, AChR
Flopropione
Cat.No: T0525
Synonym: 夫洛丙酮,Phloropropiophenone
Target: 5-HT Receptor, Transferase
Canrenone
Cat.No: T0354
Synonym: 6,7-Dehydro-7α-desthioacetylspironolactone,SC9376,Aldadiene,坎利酮,RP-11614,SC14266
Target: Glucocorticoid Receptor, Endogenous Metabolite
Cannabigerol
Cat.No: TN1465
Synonym:
Target: NOS, 5-HT Receptor, ROS
Galangin
Cat.No: T3668
Synonym: Norizalpinin,高良姜素,3,5,7-Trihydroxyflavone
Target: ERK, P450, NF-κB, Autophagy
Tolazoline hydrochloride
Cat.No: T1680
Synonym: Imidaline hydrochloride,苯甲唑啉盐酸盐,Imidaline (hydrochloride),Benzidazol hydrochloride,Tolazoline HCl,NSC35110 (hydrochloride)
Target: Adrenergic Receptor
Decanoic Acid
Cat.No: T3379
Synonym: Decoic acid,CAPRIC ACID,Caprynic acid,癸酸
Target: GluR, iGluR
Racanisodamine
Cat.No: T0970
Synonym: 山莨菪碱,Anisodamine,7β-Hydroxyhyoscyamine,Raceanisodamine,消旋山莨菪碱
Target: Adrenergic Receptor, AChR
Gymnemagenin
Cat.No: T5743
Synonym:
Target: Liver X Receptor
Thiocolchicoside
Cat.No: T2S1464
Synonym: 硫秋水仙苷;噻可撒可,Thiocolchicine 2-glucoside analog,硫秋水仙苷,Coltramyl
Target: Others, GABA Receptor
Hydroxyzine
Cat.No: T20884
Synonym: Hydroxyzine free base,羟嗪
Target: Histamine Receptor
Palonosetron hydrochloride
Cat.No: T1156
Synonym: 盐酸帕洛诺司琼,RS 25259 197,Palonosetron HCl,RS 25259
Target: 5-HT Receptor
Transcrocetinate disodium
Cat.No: TQ0027
Synonym: Disodium trans-crocetinate,藏红花,藏红花酸二钠盐
Target: NMDAR, iGluR
Ifenprodil Tartrate
Cat.No: T1186
Synonym:
Target: Potassium Channel, NMDAR, iGluR
Lobeline hydrochloride
Cat.No: T0268
Synonym: 盐酸洛贝林,α-Lobeline hydrochloride,L-Lobeline hydrochloride
Target: AChR
Puerarin
Cat.No: T2815
Synonym: 葛根素,Kakonein
Target: 5-HT Receptor
Rauwolscine hydrochloride
Cat.No: T4429
Synonym: Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride
Target: Adrenergic Receptor
Pellitorine
Cat.No: T21165
Synonym: AI3-19560,墙草碱,Pellitorin
Target: TRP/TRPV Channel
Picrotoxinin
Cat.No: T16535
Synonym:
Target: Chloride channel, GABA Receptor
Fingolimod
Cat.No: T7939
Synonym: 2-氨基-2-[2-(4-辛基苯基)乙基]-1,3-丙二醇,FTY-720A,FTY-720,芬戈莫德
Target: S1P Receptor, PAK, LPL Receptor
Andrographolide
Cat.No: T2898
Synonym: Andrographis,穿心莲内酯
Target: SARS-CoV, Influenza Virus, NF-κB, Autophagy
AC 187 Acetate
Cat.No: T21581L
Synonym: AC 187 Acetate (151804-77-2 Free base)
Target: Amylin Receptor
Cyclopamine
Cat.No: T2825
Synonym: 环巴胺,11-Deoxojervine
Target: Hedgehog/Smoothened, Endogenous Metabolite, Smo
Ginsenoside Ro
Cat.No: T3915
Synonym: 人参皂苷Ro,Chikusetsusaponin 5,Polysciasaponin P3,人参皂苷 Ro,Chikusetsusaponin V
Target: Calcium Channel, Reductase, Prostaglandin Receptor
Cirsimarin
Cat.No: T10822
Synonym: Cirsitakaoside
Target: Adenosine Receptor
Kuwanon H
Cat.No: TN1849
Synonym:
Target: GPR, Bombesin Receptor
Arcaine sulfate
Cat.No: T22583
Synonym:
Target: NMDAR
Amantadine
Cat.No: T7060
Synonym: 1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine
Target: Others
beta-Eudesmol
Cat.No: T3865
Synonym: β-桉叶醇,Beta-Selinenol,beta-桉叶醇
Target: TRP/TRPV Channel, AChR
Rotundine
Cat.No: T6648
Synonym: Gindarine,L-Tetrahydropalmatine,Caseanine,罗通定,(-)-Tetrahydropalmatine
Target: Dopamine Receptor, 5-HT Receptor
pimpinellin
Cat.No: T5776
Synonym:
Target: Apoptosis, Anti-infection
Sipeimine
Cat.No: T6S0109
Synonym: Kashmirine,西贝母碱,Imperialine,西贝碱
Target: Others
Swertisin
Cat.No: TN2247
Synonym:
Target: Adenosine Receptor
Methyl maslinate
Cat.No: TN7129
Synonym: 马斯里酸甲酯,Maslinic acid methyl ester,Crategolic acid methyl ester
Target: Adrenergic Receptor
Hypaphorine
Cat.No: T5S0273
Synonym: Lenticin,Glyyunnanenine,Tryptophan Betaine,刺桐碱
Target: Others
6-Diazo-5-oxo-L-nor-Leucine
Cat.No: T8373
Synonym: DON,L-6-Diazo-5-oxonorleucine,6-重氮-5-氧代-L-正亮氨酸,Diazooxonorleucine
Target: Influenza Virus, Glutaminase, Antibacterial, Antibiotic
Coniine hydrochloride
Cat.No: TN3695
Synonym:
Target: Others
Fargesin
Cat.No: T5S2178
Synonym: 辛夷脂素,(+/-)-Fargesin
Target: Adrenergic Receptor
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Cat. No. Product Name Species Expression System
TMPY-00484 Cerberus 1/CER1 Protein, Human, Recombinant (His)

DAND4,cerberus 1, DAN family BMP antagonist

Human Baculovirus Insect Cells
Cerberus 1/CER1 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 29.6 kDa and the accession number is AAH69371.1.
TMPY-04275 IL-36RN/IL-1F5 Protein, Mouse, Recombinant

Fil1δ,AI413231,RP23-176J12.6,Fil1delta,Il1hy1,Il-1h3,interle...

Mouse E. coli
IL-36RN/IL-1F5 Protein, Mouse, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 17 kDa and the accession number is Q9QYY1.
TMPY-00853 IL-1RA Protein, Human, Recombinant

DIRA,IL1RA,interleukin 1 receptor antagonist,ICIL-1...

Human E. coli
IL-1RA Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 17.3 kDa and the accession number is P18510-1.
TMPY-05845 IL-1RA Protein, Cynomolgus, Recombinant (His)

interleukin 1 receptor antagonist

Cynomolgus E. coli
IL-1RA Protein, Cynomolgus, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 18.63 kDa and the accession number is Q866R8.
TMPY-05837 IL-1RA Protein, Rat, Recombinant (His)

interleukin 1 receptor antagonist

Rat E. coli
IL-1RA Protein, Rat, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 19.01 kDa and the accession number is A6JSY4.
TMPY-03081 IL-1RA Protein, Rat, Recombinant (hFc)

interleukin 1 receptor antagonist

Rat HEK293 Cells
IL-1RA Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 45.8 kDa and the accession number is P25086.
TMPY-02670 NBL1 Protein, Mouse, Recombinant (His)

neuroblastoma 1, DAN family BMP antagonist,DAN,NO3,...

Mouse HEK293 Cells
NBL1 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 18.8 kDa and the accession number is Q61477.
TMPY-00771 NBL1 Protein, Human, Recombinant (hFc)

neuroblastoma 1, DAN family BMP antagonist,NO3,NB,D...

Human HEK293 Cells
NBL1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 44.4 kDa and the accession number is P41271-1.
TMPY-01039 NBL1 Protein, Human, Recombinant (His)

neuroblastoma 1, DAN family BMP antagonist,NO3,DAN,...

Human HEK293 Cells
NBL1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 19.3 kDa and the accession number is P41271-1.
TMPJ-00909 IL-1RA Protein, Mouse, Recombinant

IL-1RN,IRAP,Interleukin-1 Receptor Antagonist Prote...

Mouse E. coli
Interleukin-1 receptor antagonist protein (Il1rn), also known as IL-1ra, IRAP or IL1 inhibitor, is a member of the interleukin 1 cytokine family. This protein inhibits the activities of interleukin 1 alpha (IL1A) and interleukin 1 beta (IL1B), and modulates a variety of interleukin 1 related immune and inflammatory responses. The mouse Il1rn gene encodes a 178 amino acids (aa) protein with a 26 aa signal peptide. Mouse Il1rn protein shares 26% and 19% identity with its homologues IL-1 beta and I...
TMPY-00852 IL-1RA Protein, Human, Recombinant (hFc)

interleukin 1 receptor antagonist,MVCD4,IRAP,IL1RA,...

Human HEK293 Cells
IL-1RA Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 43.8 kDa and the accession number is P18510-1.
TMPH-03308 Gremlin-1 Protein, Rat, Recombinant (His & Myc)

Down-regulated in Mos-transformed cells protein,Gremlin-1,Cy...

Rat HEK293 Cells
Gremlin-1 Protein, Rat, Recombinant (His & Myc) is expressed in HEK293.
TMPY-00847 IL-36RN/IL-1F5 Protein, Human, Recombinant

IL1L1,IL1F5,FIL1,interleukin 36 receptor antagonist...

Human E. coli
IL-36RN/IL-1F5 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 17.1 kDa and the accession number is Q9UBH0.
TMPJ-00418 TRAIL R3/TNFRSF10C Protein, Human, Recombinant (hFc & His)

Decoy Receptor 1,Antagonist Decoy Receptor for TRAI...

Human HEK293 Cells
Tumor Necrosis Factor Receptor Superfamily Member 10C (TNFRSF10C) is a glycosyl-phosphatidylinositol-linked membrane protein which binds TRAIL with high affinity. TNFRSF10C has the TRAIL-binding extracellular cysteine-rich domains, lacks the intracellular signaling domain. As a result, binding of TRAIL to TRAIL R3 doesn’t transduce an apoptosis signal. The expression of TRAIL R3 gene has been shown to protect cells bearing TRAIL R1 and/or TRAIL R2 from TRAIL-induced apoptosis.
TMPK-00925 Noggin/NOG Protein, Mouse, Recombinant

NOG,SYM1,SYNS1,Noggin

Mouse HEK293 Cells
Noggin is an antagonist of bone morphogenetic proteins (BMP), being indispensable for certain developmental events.Noggin expression positively correlated with EGFR expression in both GC cell line models and The Cancer Genome Atlas human GC cohort. Targeting EGFR and its downstream pathways diminished cell proliferation which was promoted by Noggin. Noggin promotes the proliferation of GC cells by upregulating EGFR and enhancing a vicious circle formed by β‑catenin, EGFR, ERK and Akt. Noggin/NOG...
TMPJ-01099 IL-15RA Protein, Human, Recombinant (hFc, Human Cells)

interleukin-15 receptor subunit α,IL15RA,interleukin-15 rece...

Human HEK293 Cells
Interleukin 15 Receptor alpha (IL-15Rα) is a transmembrane glycoprotein that plays a pleiotropic role in immune development and function, including the positive maintenance of lymphocyte homeostasis. IL-15Rα chain can bind soluble IL-15 and “transpresent” cytokine to the cells, allowing them to respond to IL-15. Soluble IL-15Rα can function as a specific high-affinity IL-15 antagonist. The soluble IL-15/IL-15Rα complexes exhibit a strong agonistic activity which is mediated through membrane-boun...
TMPJ-01065 Noggin/NOG Protein, Mouse, Recombinant (His)

Nog,Noggin

Mouse HEK293 Cells
Noggin is a secreted homodimeric glycoprotein that is an antagonist of bone morphogenetic proteins (BMPs). Mouse Noggin cDNA encodes a 232 amino acid (aa) residue precursor protein with 19 aa residue putative signal peptide that is cleaved to generate the 213 aa residue mature protein which is secreted as a homodimeric glycoprotein. Secreted Noggin probably remains close to the cell surface due to its binding of heparin-containing proteoglycans. Noggin binds some BMPs such as BMP4 with high affi...
TMPH-01952 SPRY2 Protein, Human, Recombinant (His & Myc)

Protein sprouty homolog 2,SPRY2

Human E. coli
Antagonist of fibroblast growth factor (FGF) pathways via inhibition of FGF-mediated phosphorylation of ERK1/2. Thereby acts as an antagonist of FGF-induced retinal lens fiber differentiation, may inhibit limb bud outgrowth and may negatively modulate respiratory organogenesis. Inhibits TGFB-induced epithelial-to-mesenchymal transition in retinal lens epithelial cells. Inhibits CBL/C-CBL-mediated EGFR ubiquitination. SPRY2 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expressio...
TMPJ-00742 GCG Protein, Human, Recombinant (His)

Glicentin,GRPP,GLP-2,Glucagon-Like Peptide 1,OXM,Glucagon,GL...

Human HEK293 Cells
Glucagon is a secreted protein and belongs to the glucagon family. Glucagon can be cleved into 8 chains, playing an important role in initiating and maintaining hyperglycemic conditions in diabetes. Glucagon can regulates blood glucose by decreasing glycolysis and increasing gluconeogenesis. In addition, Glucagon is involved in initiating and maintaining hyperglycemic conditions in diabetes. Glucagon release is stimulated by hypoglycemia and inhibited by hyperglycemia, insulin, and somatostatin....
TMPK-00806 GHR/Growth Hormone R Protein, Human, Recombinant (His)

GHR/BP,GH receptor,GHBP,GHR

Human HEK293 Cells
Pegvisomant, a growth hormone receptor (GHR) antagonist, is a well-known drug that was designed to treat acromegaly. However, recent studies have indicated that the GHR is a "moonlighting" protein that may exhibit dual functions based on its localization in the plasma membrane and nucleus.
TMPJ-00119 IL-22RA2 Protein, Human, Recombinant (hFc)

Cytokine Receptor Family 2 Member 10,CRF2-10,IL-22RA2,Interl...

Human HEK293 Cells
Interleukin-22 Receptor Subunit α-2 (IL22RA2) belongs to the type II cytokine receptor family. IL22RA2 is a secreted protein and contains three fibronectin type-III domains. IL22RA2 is widely expressed in many tissues. IL22RA2 functions as an IL22 antagonist and may be important in the regulation of inflammatory response. Three alternatively spliced transcript variants encoding distinct isoforms have been described.
TMPK-00156 DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi)

Dickkopf-1,Dkk1,hDkk-1,hDkk1,Dkk-1,SK,Dickkopf-related 1

Human HEK293 Cells
Dickkopf-1 (Dkk1), the founding and best-studied member of the Dkk family, functions as an antagonist of canonical Wnt/β-catenin. Dkk1 is considered to play a broad role in a variety of biological processes. DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi) is expressed in HEK293 mammalian cells with C-hFc-Avi tag. The predicted molecular weight is 40.25 kDa and the accession number is O94907.
TMPK-00158 DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated

hDkk1,Dkk1,Dickkopf-1,Dkk-1,Dickkopf-related 1,SK,hDkk-1

Human HEK293 Cells
Dickkopf-1 (Dkk1), the founding and best-studied member of the Dkk family, functions as an antagonist of canonical Wnt/β-catenin. Dkk1 is considered to play a broad role in a variety of biological processes. DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-hFc-Avi tag. The predicted molecular weight is 40.25 kDa and the accession number is O94907.
TMPK-00155 DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi)

hDkk-1,Dickkopf-1,Dkk1,hDkk1,SK,Dkk-1,Dickkopf-related 1

Human HEK293 Cells
Dickkopf-1 (Dkk1), the founding and best-studied member of the Dkk family, functions as an antagonist of canonical Wnt/β-catenin. Dkk1 is considered to play a broad role in a variety of biological processes. DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi) is expressed in HEK293 mammalian cells with C-hFc-Avi tag. The predicted molecular weight is 38.69 kDa and the accession number is O94907.
TMPK-01152 CHRDL1 Protein, Human, Recombinant (His)

VOPT,Ventroptin,Neuralin-1,dA141H5.1,CHL,Chordin-like 1,CRDL...

Human E. coli
CHRDL1 (Chordin-like 1) is a secreted protein that acts as an antagonist of bone morphogenetic protein (BMP). BMP plays a role as an activator of BMP receptor II (BMPR II), which mediates extracellular to intracellular signal transmission and is involved in carcinogenesis and metastasis.The hypermethylation of the CHRDL1 promoter in gastric cancer, which induced low expression of CHRDL1 and decreased its secretion to the supernatant.
TMPH-01595 KMO Protein, Human, Recombinant (His)

Kynurenine 3-monooxygenase,KMO,Kynurenine 3-hydroxylase

Human E. coli
Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid, a neurotoxic NMDA receptor antagonist and potential endogenous inhibitor of NMDA receptor signaling in axonal targeting, synaptogenesis and apoptosis during brain development. Quinolinic acid may also affect NMDA receptor signaling in pancreatic beta cells, osteoblasts, myocardial cells, and the gastrointestinal tract (Probable).
TMPK-00157 DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated

hDkk-1,SK,Dkk1,Dickkopf-related 1,Dickkopf-1,Dkk-1,hDkk1

Human HEK293 Cells
Dickkopf-1 (Dkk1), the founding and best-studied member of the Dkk family, functions as an antagonist of canonical Wnt/β-catenin. Dkk1 is considered to play a broad role in a variety of biological processes. DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-hFc-Avi tag. The predicted molecular weight is 38.69 kDa and the accession number is O94907.
TMPY-01755 VWC2 Protein, Human, Recombinant (His)

PSST739,von Willebrand factor C domain containing 2,UNQ739

Human HEK293 Cells
Brorin, also known as brain-specific chordin-like protein, von Willebrand factor C domain-containing protein 2 and VWC2, is a secreted protein that contains two VWFC domains. VWC2 / Brorin is a BMP antagonist that may play a role in neural development. It promotes cell adhesion. VWC2 / Brorin is a unique member of the chordin family. It inhibited the activity of bone morphogenetic protein 2 (BMP2) and BMP6 in mouse preosteoblastic MC3T3-E1 cells. Mouse Brorin was predominantly expressed in neura...
TMPH-01597 KYAT1 Protein, Human, Recombinant (His & SUMO)

Kynurenine aminotransferase 1,KYAT1,Glutamine--phenylpyruvat...

Human E. coli
Catalyzes the irreversible transamination of the L-tryptophan metabolite L-kynurenine to form kynurenic acid (KA), an intermediate in the tryptophan catabolic pathway which is also a broad spectrum antagonist of the three ionotropic excitatory amino acid receptors among others. Also metabolizes the cysteine conjugates of certain halogenated alkenes and alkanes to form reactive metabolites. Catalyzes the beta-elimination of S-conjugates and Se-conjugates of L-(seleno)cysteine, resulting in the cl...
TMPK-00926 Noggin/NOG Protein, Mouse, Recombinant (His & Flag)

SYNS1,NOG,SYM1,Noggin

Mouse HEK293 Cells
Noggin is an antagonist of bone morphogenetic proteins (BMP), being indispensable for certain developmental events.Noggin expression positively correlated with EGFR expression in both GC cell line models and The Cancer Genome Atlas human GC cohort. Targeting EGFR and its downstream pathways diminished cell proliferation which was promoted by Noggin. Noggin promotes the proliferation of GC cells by upregulating EGFR and enhancing a vicious circle formed by β‑catenin, EGFR, ERK and Akt. Noggin/NOG...
TMPJ-00513 LTF Protein, Human, Recombinant (His)

Lactoferroxin-A,Talalactoferrin,LTF,Lactotransferrin,Lactofe...

Human HEK293 Cells
Lactotransferrin is a member of the transferrin family that transfer iron to the cells and control the level of free iron in the blood and external secretions. Lactotransferrin is a secreted protein and contains two transferrin-like domains. Lactotransferrin can be cleaved into the following four chains: Kaliocin-1, Lactoferroxin-A, Lactoferroxin-B, and Lactoferroxin-C. Lactoferroxin A, Lactoferroxin B, and Lactoferroxin C have opioid antagonist activity. Lactoferroxin A shows preference for mu-...
TMPJ-00238 Lefty-A Protein, Human, Recombinant (His)

Endometrial bleeding-associated factor,TGFB4,TGF-β-4,EBAF,LE...

Human HEK293 Cells
Left-right determination factor 2(LEFTY2) is a secreted protein which belongs to the TGF-beta family. Lefty was first identified in a screen for undifferentiated cell-specific cDNAs from the P19 mouse embryonal carcinoma cells. Its mRNA expression on the left side of the developing embryo earned the name “Lefty”. The human orthologue was initially identified as Ebaf, Endometrial bleeding associated factor. Lefty contains the six cysteine residues that are conserved among TGF-β related proteins a...
TMPY-03963 CALCB Protein, Human, Recombinant (mFc)

CGRP-II,calcitonin-related polypeptide β,calcitonin-related ...

Human HEK293 Cells
CALCB, also known as CGPR and calcitonin 2, belongs to the calcitonin family. CALCB is a calcitonin (CT) peptide which may play a role in the mediation of human inflammatory diseases. It is highly expressed in the skin, blood, and cerebrospinal fluid. CGRP immunolabeling (IL) was detected in epidermal keratinocytes at levels that were especially high and widespread in the skin of humans from locations afflicted with postherpetic neuralgia (PHN) and complex region pain syndrome type 1 (CRPS), of ...
TMPY-00186 GHRH Protein, Human, Recombinant (hFc)

GRF,INN,growth hormone releasing hormone,GHRF

Human HEK293 Cells
The role of hypothalamic growth hormone-releasing hormone (GHRH) in the release of growth hormone (GH) from the pituitary is well established. Extra-hypothalamic growth hormone-releasing hormone (GHRH) plays an important role in infertility. Growth hormone releasing hormone (GHRH) has recently been shown to increase the level of gamma-aminobutyric acid (GABA) and activate GABA receptors (GABARs) in the cerebral cortex. GABA is an inhibitory neurotransmitter that can inhibit seizures. GHRH may pl...
TMPY-03046 APCDD1 Protein, Human, Recombinant (hFc)

HYPT1,B7323,adenomatosis polyposis coli down-regulated 1,HTS...

Human HEK293 Cells
Osteosarcoma (OS) is the most common type of bone tumor in children and adults. The expression of APCDD1, a Wnt antagonist, was reduced in OS tissues and cells compared to adjacent normal tissue and osteoblast cells, respectively. Mechanistically, this was due to increased levels of methylation in the promoter region of the APCDD1 gene. Consistently, the DNA methyltransferase inhibitor 5-AZA-dC, reduced DNA methylation in the APCDD1 promoter, and restored APCDD1 expression in OS tissue and cells...

重组蛋白

Cerberus 1/CER1 Protein, Human, Recombinant (His)
Cat.No: TMPY-00484
Species: Human
Expression System: Baculovirus Insect Cells
IL-36RN/IL-1F5 Protein, Mouse, Recombinant
Cat.No: TMPY-04275
Species: Mouse
Expression System: E. coli
IL-1RA Protein, Human, Recombinant
Cat.No: TMPY-00853
Species: Human
Expression System: E. coli
IL-1RA Protein, Cynomolgus, Recombinant (His)
Cat.No: TMPY-05845
Species: Cynomolgus
Expression System: E. coli
IL-1RA Protein, Rat, Recombinant (His)
Cat.No: TMPY-05837
Species: Rat
Expression System: E. coli
IL-1RA Protein, Rat, Recombinant (hFc)
Cat.No: TMPY-03081
Species: Rat
Expression System: HEK293 Cells
NBL1 Protein, Mouse, Recombinant (His)
Cat.No: TMPY-02670
Species: Mouse
Expression System: HEK293 Cells
NBL1 Protein, Human, Recombinant (hFc)
Cat.No: TMPY-00771
Species: Human
Expression System: HEK293 Cells
NBL1 Protein, Human, Recombinant (His)
Cat.No: TMPY-01039
Species: Human
Expression System: HEK293 Cells
IL-1RA Protein, Mouse, Recombinant
Cat.No: TMPJ-00909
Species: Mouse
Expression System: E. coli
IL-1RA Protein, Human, Recombinant (hFc)
Cat.No: TMPY-00852
Species: Human
Expression System: HEK293 Cells
Gremlin-1 Protein, Rat, Recombinant (His & Myc)
Cat.No: TMPH-03308
Species: Rat
Expression System: HEK293 Cells
IL-36RN/IL-1F5 Protein, Human, Recombinant
Cat.No: TMPY-00847
Species: Human
Expression System: E. coli
TRAIL R3/TNFRSF10C Protein, Human, Recombinant (hFc & His)
Cat.No: TMPJ-00418
Species: Human
Expression System: HEK293 Cells
Noggin/NOG Protein, Mouse, Recombinant
Cat.No: TMPK-00925
Species: Mouse
Expression System: HEK293 Cells
IL-15RA Protein, Human, Recombinant (hFc, Human Cells)
Cat.No: TMPJ-01099
Species: Human
Expression System: HEK293 Cells
Noggin/NOG Protein, Mouse, Recombinant (His)
Cat.No: TMPJ-01065
Species: Mouse
Expression System: HEK293 Cells
SPRY2 Protein, Human, Recombinant (His & Myc)
Cat.No: TMPH-01952
Species: Human
Expression System: E. coli
GCG Protein, Human, Recombinant (His)
Cat.No: TMPJ-00742
Species: Human
Expression System: HEK293 Cells
GHR/Growth Hormone R Protein, Human, Recombinant (His)
Cat.No: TMPK-00806
Species: Human
Expression System: HEK293 Cells
IL-22RA2 Protein, Human, Recombinant (hFc)
Cat.No: TMPJ-00119
Species: Human
Expression System: HEK293 Cells
DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi)
Cat.No: TMPK-00156
Species: Human
Expression System: HEK293 Cells
DKK1 N terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated
Cat.No: TMPK-00158
Species: Human
Expression System: HEK293 Cells
DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi)
Cat.No: TMPK-00155
Species: Human
Expression System: HEK293 Cells
CHRDL1 Protein, Human, Recombinant (His)
Cat.No: TMPK-01152
Species: Human
Expression System: E. coli
KMO Protein, Human, Recombinant (His)
Cat.No: TMPH-01595
Species: Human
Expression System: E. coli
DKK1 C terminal Domain Protein, Human, Recombinant (hFc & Avi), Biotinylated
Cat.No: TMPK-00157
Species: Human
Expression System: HEK293 Cells
VWC2 Protein, Human, Recombinant (His)
Cat.No: TMPY-01755
Species: Human
Expression System: HEK293 Cells
KYAT1 Protein, Human, Recombinant (His & SUMO)
Cat.No: TMPH-01597
Species: Human
Expression System: E. coli
Noggin/NOG Protein, Mouse, Recombinant (His & Flag)
Cat.No: TMPK-00926
Species: Mouse
Expression System: HEK293 Cells
LTF Protein, Human, Recombinant (His)
Cat.No: TMPJ-00513
Species: Human
Expression System: HEK293 Cells
Lefty-A Protein, Human, Recombinant (His)
Cat.No: TMPJ-00238
Species: Human
Expression System: HEK293 Cells
CALCB Protein, Human, Recombinant (mFc)
Cat.No: TMPY-03963
Species: Human
Expression System: HEK293 Cells
GHRH Protein, Human, Recombinant (hFc)
Cat.No: TMPY-00186
Species: Human
Expression System: HEK293 Cells
APCDD1 Protein, Human, Recombinant (hFc)
Cat.No: TMPY-03046
Species: Human
Expression System: HEK293 Cells
Cat. No. Product Name Target Signaling Pathways
T40376 L-Phenylalanine-15N

L-苯丙氨酸 15N,(S)-2-Amino-3-phenylpropionic acid-15N,L-Phenylalanine-15N

Calcium Channel Membrane transporter/Ion channel; Metabolism
L-Phenylalanine-15N ((S)-2-Amino-3-phenylpropionic acid-15N) 是 15N 标记的 L-Phenylalanine。L-Phenylalanine 是从大肠杆菌中分离出来的一种必需氨基酸。 L-Phenylalanine 广泛用于食品香精和药物的生产。
T70332 JNJ-61393215

JNJ-61393215 is a novel selective orexin-1 receptor (OX1R) antagonist.
T69673 Deucrictibant

Deucrictibant is a bradykinin receptor antagonist.
TMIH-0314 Lurasidone-d8 HCl

Lurasidone-d8 HCl 是 Lurasidone HCl 的氘代化合物。Lurasidone HCl 的 CAS 号为 367514-88-3。Lurasidone hydrochloride 是多巴胺 D2和5-HT7的拮抗剂,IC50值分别为 1.68 和 0.495 nM,用于治疗精神分裂症和双相情感障碍。它也是5-HT1A受体的部分激动剂,IC50值为 6.75 nM。
T12442 Phenindione D5

Rectadione D5,苯茚二酮 D5

Others Others
Phenindione D5 is deuterium labeled Phenindione, which functions as a Vitamin K antagonist.
T11592 Hydroxyzine D8

Others Others
Hydroxyzine D8, a deuterium-labeled version of Hydroxyzine, acts as a histamine H1-receptor antagonist.
T11675 Irbesartan-d4

厄贝沙坦 D4,SR-47436 D4,BMS-186295 D4

Others Others
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
T11536 Haloperidol (D4')

Haloperidol D4',氟哌啶醇 (D4')

Others Others
Haloperidol D4' is deuterium-labeled haloperidol. Haloperidol is a dopamine D2 receptor antagonist.
T11869 Losartan (D4 Carboxylic Acid)

E-3174 D4,氯沙坦羧酸 D4,EXP-3174 D4

Others Others
Losartan D4 Carboxylic Acid is the deuterium labeled Losartan, which is an angiotensin II receptor antagonist.
T10181 6-beta-Naloxol D5 hydrochloride

6β-Naloxol D5 hydrochloride

Others Others
6-beta-Naloxol D5 hydrochloride is a deuterium-labeled opioid antagonist, closely related to naloxone, that serves as an effective compound in the field of chemical research.
T12631 (R)-Mirtazapine D3

(R)-6-Azamianserin D3,(R)-Org3770 D3

5-HT Receptor GPCR/G Protein; Neuroscience
(R)-Mirtazapine D3 is a deuterium labeled (R)-Mirtazapine.(R)-Mirtazapine is a antagonist of 5-HT3 receptor.
T11591 Hydroxyzine D4

羟嗪 D4

Others Others
Hydroxyzine D4 is a deuterium-labeled variation of Hydroxyzine, a chemical compound known for its anticholinergic, anxiolytic, and analgesic properties. It is classified as a heterocyclic histamine H1-receptor antagonist.
T12806 (S)-Mirtazapine D3

(S)-Org3770 D3,(S)-6-Azamianserin D3

5-HT Receptor GPCR/G Protein; Neuroscience
(S)-Mirtazapine D3 is a deuterium labeled (S)-Mirtazapine. (S)-Mirtazapine is a stereoselective antagonist of 5-HT2 receptor. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2.
T10241 Acrivastine D7

BW825C D7

Others Others
Acrivastine D7 is a deuterium labeled Acrivastine. Acrivastine is a short acting antagonist of histamine 1 receptor.
TMIJ-0172 Mifepristone-d6

Mifepristone-d6 是 Mifepristone 的氘代化合物。Mifepristone 的 CAS 号为 84371-65-3。Mifepristone 是一种黄体酮受体和糖皮质激素受体拮抗剂,在体外实验中的IC50值分别为 0.2 nM 和 2.6 nM。
T10670 Candesartan-d4

坎地沙坦 D4,CV-11974 D4

Others Others
Candesartan D4 is the deuterium labeled Candesartan. Candesartan is an antagonist of angiotensin II receptor.
T12300 Olmesartan-d4

RNH-6270 D4,奥美沙坦 D4

Others Others
Olmesartan D4 is the deuterium labeled Olmesartan. Olmesartan is an antagonist of angiotensin II receptor (AT1R) used to treat high blood pressure.
T10559 Blonanserin D8

AD-5423 D8

Others Others
Blonanserin D8 is a deuterium-labeled Blonanserin. Blonanserin (AD-5423) is a dopamine D2/5-HT2 receptor antagonist with an atypical antipsychotic effect.
T19190 Alosetron D3 Hydrochloride

GR-68755C D3

Others Others
Alosetron D3 (GR 68755 D3) Hydrochloride is a deuterium-labeled Alosetron. Alosetron is an antagonist of 5HT3-receptor.
T19233 Cetirizine D4 dihydrochloride

Cetirizine D4 dihydrochloride (1219803-84-5 free base)

Others Others
Cetirizine D4 dihydrochloride is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist.
T13432 β-Apo-13-carotenone D3

D'Orenone D3

Others Others
β-Apo-13-carotenone D3 is the deuterium labeled β-Apo-13-carotenone. β-Apo-13-carotenone is an antagonist of RXRα.
T19234 Cetirizine D8 dihydrochloride

盐酸西替利嗪 D8

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Cetirizine D8 dihydrochloride is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist.
TMIJ-0213 Naloxone-d5 HCl

Naloxone-d5 HCl 是 Naloxone HCl 的氘代化合物。Naloxone HCl 的 CAS 号为 357-08-4。Naloxone hydrochloride 是一种特异性、没有激动剂活性的opiate拮抗剂。它是 mu、delta 和 kappa 阿片受体的竞争性拮抗剂。
T11870 Losartan D4

氯沙坦 D4,DuP-753 D4

Others Others
Losartan D4, the deuterium-labeled version of Losartan, functions as an angiotensin II receptor antagonist. It inhibits the interaction between angiotensin II and AT1 receptors by competing for binding, achieving an IC50 value of 20 nM.
T11208 Enzalutamide-d3

MDV3100 D3

Others Others
Enzalutamide D3 is a deuterium labeled Enzalutamide . Enzalutamide is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells.
T13185 Topiramate D12

RWJ 17021 D12,McN 4853 D12

Others Others
Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.
T19191 Alosetron-d3

Alosetron D3,GR 68755 D3,GR 68755X D3

Others Others
Alosetron D3 (GR 68755 D3) is a deuterium-labeled Alosetron. Alosetron is an antagonist of 5HT3-receptor.
T10558 Blonanserin D5

AD-5423 D5

Others Others
Blonanserin D5 is a deuterium-labeled Blonanserin. Blonanserin (AD-5423) is a dopamine D2/5-HT2 receptor antagonist with an atypical antipsychotic effect.
T12618L Quetiapine-d4 hemifumarate

半富马酸奎硫平 D4

Others Others
Quetiapine D4 hemifumarate is the deuterium labeled Quetiapine hemifumarate. Quetiapine hemifumarate is a agonist of 5-HT receptors and a antagonist of dopamine receptor,with ntidepressant and anxiolytic.
T12210 Netupitant D6

CID-6451149 D6

Others Others
Netupitant D6 is the deuterium labeled Netupitant, which is a selective and orally active antagonist of neurokinin-1 receptor.
T10113 3-Hydroxy agomelatine D3

5-HT Receptor GPCR/G Protein; Neuroscience
3-Hydroxy agomelatine D3 is a deuterium labeled 3-Hydroxy agomelatine. 3-Hydroxy agomelatine is an Agomelatine metabolite and a 5-HT2C receptor antagonist (IC50: 3.2 μM; Ki: 1.8 μM).
TMID-0022 Spironolactone-d3

Spironolactone-d3 是 Spironolactone 的氘代化合物。Spironolactone 的 CAS 号为 52-01-7。Abbolactone 是一种可口服的醛固酮盐皮质激素受体拮抗剂,IC50值为 24 nM。它也是雄激素受体拮抗剂,促进足细胞自噬,IC50值为 77 nM。
T12618 Quetiapine-d4 fumarate

Quetiapine D4 fumarate,富马酸奎硫平 D4

Others Others
Quetiapine D4 fumarate is the deuterium labeled Quetiapine fumarate. Quetiapine fumarate is a agonist of 5-HT receptors and a antagonist of dopamine receptor,with antidepressant and anxiolytic.
T12550 Propranolol-d7 hydrochloride

Propranolol D7 hydrochloride

Others Others
Propranolol D7 hydrochloride is a deuterium labeled Propranolol hydrochloride. Propranolol hydrochloride is a nonselective antagonist of β-adrenergic receptor (βAR).
T10440 Azilsartan-d5

TAK-536 D5

Others Others
Azilsartan (TAK-536) D5 is the deuterium-labeled Azilsartan. Azilsartan is a specific antagonist of the angiotensin II type 1 receptor.
T10770 Cetirizine D8

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Cetirizine D8 is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist.
T10769 Cetirizine D4

Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Cetirizine D4 is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist.
TMIJ-0112 Aripiprazole-d8

Aripiprazole-d8 是 Aripiprazole 的氘代化合物。Aripiprazole 的 CAS 号为 129722-12-9。Aripiprazole 是血清素受体 5-HT1A 和多巴胺 D2 受体的部分激动剂,还用作突触后拮抗剂和血清素受体 5-HT2A 的拮抗剂。
T13400 Ziprasidone D8

CP-88059 D8

Others Others
Ziprasidone D8 is deuterium labeled Ziprasidone, which is a antagonist of combined 5-HT (serotonin) and dopamine receptor and exhibits potent effects of antipsychotic activity.
T12973 Solifenacin D5 hydrochloride

Others Others
Solifenacin D5 hydrochloride is a deuterium labeled Solifenacin hydrochloride. Solifenacin hydrochloride is an antagonist of muscarinic receptor(pKis of 7.6, 6.9 and 8.0 for M1, M2 and M3 receptors, respectively).
T10351 Aprocitentan D4

ACT-132577 D4

Others Others
Aprocitentan D4 (ACT-132577 D4) is a deuterium-labeled Aprocitentan. Aprocitentan is a major and pharmacologically active metabolite of Macitentan. Aprocitentan is a dual ETA/ETB antagonist (IC50s: 3.4 nM and 987 nM; pA2s: 6.7 and 5.5).
TMID-0197 Metoprolol-d6

Metoprolol-d6 是 Metoprolol 的氘代化合物。Metoprolol 的 CAS 号为 51384-51-1。
TMID-0125 Canrenone-d4

Canrenone-d4 是 Canrenone 的氘代化合物。Canrenone 的 CAS 号为 976-71-6。Canrenone 是一种醛固酮 (aldosterone) 拮抗剂,广泛用作利尿剂。
T13282 Valsartan-d9

CGP-48933 D9,缬沙坦 D9

Others Others
Valsartan D9 is a deuterium-labeled valsartan. Valsartan is an antagonist of the angiotensin II receptor and for the treatment of high blood pressure and heart failure.
T10229 Acebutolol D7

Others Others
Acebutolol D7 is a deuterium-labeled Acebutolol. Acebutolol is a selective antagonist of the β1 adrenergic receptor used in the treatment of angina pectoris, hypertension, and cardiac arrhythmias.
TMIH-0573 Thiothixene-d8 P2

Thiothixene-d8 P2 是 Thiothixene 的氘代化合物。Thiothixene 的 CAS 号为 3313-26-6。(Z)-Thiothixene 是一种血清素受体拮抗剂。
TMIH-0572 Thiothixene-d8 P1

Thiothixene-d8 P1 是 Thiothixene 的氘代化合物。Thiothixene 的 CAS 号为 3313-26-6。(Z)-Thiothixene 是一种血清素受体拮抗剂。
TMID-0124 Canrenone-d6

Canrenone-d6 是 Canrenone 的氘代化合物。Canrenone 的 CAS 号为 976-71-6。Canrenone 是一种醛固酮 (aldosterone) 拮抗剂,广泛用作利尿剂。
T11295 Flibanserin-d4

BIMT-17BS D4,BIMT-17 D4,Flibanserin D4

Others Others
Flibanserin, a compound identified as BIMT-17, acts as a complete agonist at the serotonin 5-HT1A receptor, with a binding affinity (Ki) of 1 nM, while functioning as an antagonist at the 5-HT2A receptor with a 49 nM affinity. Flibanserin D4 represents a deuterium-labeled version of Flibanserin.
TMIH-0094 Apalutamide-d7

Apalutamide-d7 是 Apalutamide 的氘代化合物。Apalutamide 的 CAS 号为 956104-40-8。Apalutamide 是一种有效、竞争性的雄激素受体 (AR) 拮抗剂(IC50:16 nM)。
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同位素标记化合物

L-Phenylalanine-15N
Cat.No: T40376
Synonym: L-苯丙氨酸 15N,(S)-2-Amino-3-phenylpropionic acid-15N,L-Phenylalanine-15N
Target: Calcium Channel
JNJ-61393215
Cat.No: T70332
Synonym:
Target:
Deucrictibant
Cat.No: T69673
Synonym:
Target:
Lurasidone-d8 HCl
Cat.No: TMIH-0314
Synonym:
Target:
Phenindione D5
Cat.No: T12442
Synonym: Rectadione D5,苯茚二酮 D5
Target: Others
Hydroxyzine D8
Cat.No: T11592
Synonym:
Target: Others
Irbesartan-d4
Cat.No: T11675
Synonym: 厄贝沙坦 D4,SR-47436 D4,BMS-186295 D4
Target: Others
Haloperidol (D4')
Cat.No: T11536
Synonym: Haloperidol D4',氟哌啶醇 (D4')
Target: Others
Losartan (D4 Carboxylic Acid)
Cat.No: T11869
Synonym: E-3174 D4,氯沙坦羧酸 D4,EXP-3174 D4
Target: Others
6-beta-Naloxol D5 hydrochloride
Cat.No: T10181
Synonym: 6β-Naloxol D5 hydrochloride
Target: Others
(R)-Mirtazapine D3
Cat.No: T12631
Synonym: (R)-6-Azamianserin D3,(R)-Org3770 D3
Target: 5-HT Receptor
Hydroxyzine D4
Cat.No: T11591
Synonym: 羟嗪 D4
Target: Others
(S)-Mirtazapine D3
Cat.No: T12806
Synonym: (S)-Org3770 D3,(S)-6-Azamianserin D3
Target: 5-HT Receptor
Acrivastine D7
Cat.No: T10241
Synonym: BW825C D7
Target: Others
Mifepristone-d6
Cat.No: TMIJ-0172
Synonym:
Target:
Candesartan-d4
Cat.No: T10670
Synonym: 坎地沙坦 D4,CV-11974 D4
Target: Others
Olmesartan-d4
Cat.No: T12300
Synonym: RNH-6270 D4,奥美沙坦 D4
Target: Others
Blonanserin D8
Cat.No: T10559
Synonym: AD-5423 D8
Target: Others
Alosetron D3 Hydrochloride
Cat.No: T19190
Synonym: GR-68755C D3
Target: Others
Cetirizine D4 dihydrochloride
Cat.No: T19233
Synonym: Cetirizine D4 dihydrochloride (1219803-84-5 free base)
Target: Others
β-Apo-13-carotenone D3
Cat.No: T13432
Synonym: D'Orenone D3
Target: Others
Cetirizine D8 dihydrochloride
Cat.No: T19234
Synonym: 盐酸西替利嗪 D8
Target: Histamine Receptor
Naloxone-d5 HCl
Cat.No: TMIJ-0213
Synonym:
Target:
Losartan D4
Cat.No: T11870
Synonym: 氯沙坦 D4,DuP-753 D4
Target: Others
Enzalutamide-d3
Cat.No: T11208
Synonym: MDV3100 D3
Target: Others
Topiramate D12
Cat.No: T13185
Synonym: RWJ 17021 D12,McN 4853 D12
Target: Others
Alosetron-d3
Cat.No: T19191
Synonym: Alosetron D3,GR 68755 D3,GR 68755X D3
Target: Others
Blonanserin D5
Cat.No: T10558
Synonym: AD-5423 D5
Target: Others
Quetiapine-d4 hemifumarate
Cat.No: T12618L
Synonym: 半富马酸奎硫平 D4
Target: Others
Netupitant D6
Cat.No: T12210
Synonym: CID-6451149 D6
Target: Others
3-Hydroxy agomelatine D3
Cat.No: T10113
Synonym:
Target: 5-HT Receptor
Spironolactone-d3
Cat.No: TMID-0022
Synonym:
Target:
Quetiapine-d4 fumarate
Cat.No: T12618
Synonym: Quetiapine D4 fumarate,富马酸奎硫平 D4
Target: Others
Propranolol-d7 hydrochloride
Cat.No: T12550
Synonym: Propranolol D7 hydrochloride
Target: Others
Azilsartan-d5
Cat.No: T10440
Synonym: TAK-536 D5
Target: Others
Cetirizine D8
Cat.No: T10770
Synonym:
Target: Histamine Receptor
Cetirizine D4
Cat.No: T10769
Synonym:
Target: Histamine Receptor
Aripiprazole-d8
Cat.No: TMIJ-0112
Synonym:
Target:
Ziprasidone D8
Cat.No: T13400
Synonym: CP-88059 D8
Target: Others
Solifenacin D5 hydrochloride
Cat.No: T12973
Synonym:
Target: Others
Aprocitentan D4
Cat.No: T10351
Synonym: ACT-132577 D4
Target: Others
Metoprolol-d6
Cat.No: TMID-0197
Synonym:
Target:
Canrenone-d4
Cat.No: TMID-0125
Synonym:
Target:
Valsartan-d9
Cat.No: T13282
Synonym: CGP-48933 D9,缬沙坦 D9
Target: Others
Acebutolol D7
Cat.No: T10229
Synonym:
Target: Others
Thiothixene-d8 P2
Cat.No: TMIH-0573
Synonym:
Target:
Thiothixene-d8 P1
Cat.No: TMIH-0572
Synonym:
Target:
Canrenone-d6
Cat.No: TMID-0124
Synonym:
Target:
Flibanserin-d4
Cat.No: T11295
Synonym: BIMT-17BS D4,BIMT-17 D4,Flibanserin D4
Target: Others
Apalutamide-d7
Cat.No: TMIH-0094
Synonym:
Target:
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