4846
133
3
35
105
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; |
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。 |
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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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... |
Cat. No. | Product Name | Target | Signaling Pathways |
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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
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JNJ-61393215 is a novel selective orexin-1 receptor (OX1R) antagonist. | |||
T69673 |
Deucrictibant
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Deucrictibant is a bradykinin receptor antagonist. | |||
TMIH-0314 |
Lurasidone-d8 HCl
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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
|
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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
|
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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
|
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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
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Metoprolol-d6 是 Metoprolol 的氘代化合物。Metoprolol 的 CAS 号为 51384-51-1。 | |||
TMID-0125 |
Canrenone-d4
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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
|
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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
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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
|
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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
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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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