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Search Results for " beta-nm "

Targets Recommended: PI4K

32

抑制剂 & 化合物

2

天然产物

4

重组蛋白

2

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T16967	T-00127_HEV1	PI4K	PI3K/Akt/mTOR signaling
	T-00127_HEV1 是有效的phosphatidylinositol 4-kinase III beta 抑制剂，IC50为 60 nM。
T18993	Fluorescein di-beta-D-galactopyranoside FDG,Fluorescein di(β-D-galactopyranoside)	Others	Others
	Fluorescein di-beta-D-galactopyranoside (FDG) 是通过流式细胞术检测动植物中β-半乳糖苷酶的荧光底物，λex=485 nm，λem=535 nm。
T17260	WWL70	Lipase; MAGL	Metabolism
	WWL70 是选择性 α/β 水解酶结构域 6 抑制剂，其IC50=70 nM。
T2098	A 77-01 A77-01	ALK; TGF-beta/Smad	Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors
	A 77-01 是 TGF-βI 型受体家族 ALK5抑制剂(IC50:25 nM)。
T16530	BF738735	Antiviral; PI4K	Immunology/Inflammation; PI3K/Akt/mTOR signaling
	BF738735 是有效的磷脂酰肌醇 4-激酶 IIIβ 抑制剂，IC50为 5.7 nM。
T1671	Mirabegron YM178,米拉贝隆	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Mirabegron (YM178) 是选择性的肾上腺素受体激动剂，EC50=22.4 nM。
T13253	Umibecestat CNP520	BACE	Neuroscience
	Umibecestat 是一种β-位点淀粉样前体蛋白裂解酶-1 (BACE-1) 抑制剂，对人 BACE-1 和小鼠 BACE-1 的 IC50 分别为 11 nM 和 10 nM，可用于阿尔茨海默病的研究。
T0154	Nebivolol hydrochloride R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824	Apoptosis; Adrenergic Receptor	Apoptosis; GPCR/G Protein; Neuroscience
	Nebivolol hydrochloride (R 065824 hydrochloride) 是一种β1-肾上腺素受体选择性抑制剂，IC50为0.8 nM。
T22694	CRANAD 2	Others	Others
	CRANAD 2 是一种特异性近红外 (NIR) 荧光探针，可用于检测 Aβ 斑块。它可透过血脑屏障，且对 Aβ 聚集体有高亲和性，其 Kd=38 nM。
T0277	Metaproterenol hemisulfate Orciprenaline sulfate,Metaproterenol Sulfate,硫酸奥西那林	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Metaproterenol hemisulfate (Orciprenaline sulfate) 是一种 β2-肾上腺素能受体 (β2AR) 激动剂(IC50=68 nM)，是一种直接作用的拟交感神经药，具有抗炎活性。
T1800	GW788388 GW 788388	ALK; TGF-beta/Smad	Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors
	GW788388 是一种 ALK5抑制剂(IC50:18 nM)。它也抑制 TGF-β II 型受体和激活素 II 型受体的活性，但对 BMP II 型受体无影响。
T1527	Gliclazide 格列齐特,S1702,SE1702	Potassium Channel	Membrane transporter/Ion channel
	Gliclazide (SE1702) 是一种有效的全细胞的 β 细胞 ATP 敏感型钾流阻断剂，IC50为 184 nM，用作降糖药。
T6870	L-685458 L-685,458	Apoptosis; Gamma-secretase	Apoptosis; Neuroscience; Proteases/Proteasome; Stem Cells
	L-685458 (L-685,458) 是一种过渡状态模拟 γ-分泌酶抑制剂，抑制淀粉样 β-蛋白前体 γ-分泌酶活性，选择性高于其他检测的天冬氨酸蛋白酶 50-100 倍。它抑制 γ-分泌酶介导的 APP-C99 和 Notch-100 的裂解，可研究阿尔茨海默病和癌症。
T2265	Bimiralisib 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine,PQR309,PI3K-IN-2	Others; PI3K; S6 Kinase; mTOR	MAPK; Others; PI3K/Akt/mTOR signaling
	Bimiralisib (PI3K-IN-2) 是一种有效的，可渗透脑的 mTOR/PI3K 抑制剂，是一种 mTORC1和 mTORC2抑制剂。它能够抑制 PI3Kα,PI3Kδ,PI3Kβ,PI3Kγ和 mTOR，IC50分别为 33 nM，451 nM，661 nM，708 nM 和 89 nM。
T6496	Vactosertib TEW-7197,EW-7197	ALK; TGF-beta/Smad	Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors
	Vactosertib (EW-7197) 是有效的、具有 ATP 竞争性的、具有口服活性的激活素受体样激酶 5 (ALK5) 抑制剂(IC50:12.9 nM)。它还以纳摩尔浓度抑制 ALK2 和 ALK4 (IC50为 17.3 nM)，表现出强大的抗转移活性和抗癌作用。
T22245	Arformoterol Tartrate (R,R)-Formoterol tartrate,酒石酸福莫特罗	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Arformoterol Tartrate ((R,R)-Formoterol tartrate) 是一种长效 β2-肾上腺素能受体 (β2-AR) 激动剂，Kd=2.9 nM。它是一种 Formoterol 的 (R,R)-对映异构体，可用于慢性阻塞性肺疾病 (COPD) 的研究。
T6604	Nepicastat hydrochloride Nepicastat HCl,内匹司他盐酸盐,RS-25560-197 hydrochloride,SYN-117 hydrochloride,Nepicastat (SYN-117) HCl	Hydroxylase	Metabolism
	Nepicastat hydrochloride (RS-25560-197 hydrochloride) 是一种选择性的，有效的，口服活性的多巴胺 β 羟化酶(dopamine-beta-hydroxylase)抑制剂，对牛和人多巴胺 β 羟化酶的IC50分别为IC50=8.5 nM 和IC50=9 nM。Nepicastat HCl 可以穿过血脑屏障。
T1349	5-Fluorouridine	Others; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others
	5-Fluorouridine 是一种 5-fluorouracil 的代谢物，具有抗癌作用。它对 L1210 细胞的生长具有细胞毒性作用，其作用的 IC50值为 2 nM。它能抑制人结肠癌细胞 rRNA 的合成。
T4978	Sarpogrelate hydrochloride 盐酸沙格雷酯,MCI-9042	5-HT Receptor	GPCR/G Protein; Neuroscience
	Sarpogrelate hydrochloride (MCI-9042) 是一种选择性5-HT2R 拮抗剂，可用于研究与血栓形成有关的血管疾病，对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi 值分别为 8.52、6.57 和 7.43。
T0866	Propafenone Rythmol,普罗帕酮,Propafenonum	Potassium Channel; MRP; Sodium Channel	Immunology/Inflammation; Membrane transporter/Ion channel
	Propafenone (Propafenonum) 是钠通道阻滞剂，它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ，具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡，从而抑制食管癌增殖。
T63013	Ruboxistaurin	Others	Others
	Ruboxistaurin (LY333531) 是一种选择性的、口服具有活力的 PKC beta 抑制剂，其 Ki 值为 2 nM。Ruboxistaurin 以 ATP 依赖性的方式竞争性抑制 PKC beta I (IC50: 4.7 nM)。Ruboxistaurin 能够作用于 PKC beta II (IC50: 5.9 nM)。
T12467	PI4KIII beta inhibitor 3	PI3K	PI3K/Akt/mTOR signaling
	PI4KIII beta inhibitor 3 is a novel and high effective inhibitor of PI4KIIIβ (IC50 of 5.7 nM).
T24380	L-796568 free base	Others	Others
	L-796568 free base is a β3 adrenergic receptor agonist potentially for the treatment of obesity. L-796568 is a potent full beta(3) agonist (EC50: 3.6 nM). It has 600-fold selectivity over the human beta(1) and beta(2) receptors.
T29034	U75302 U 75302,U-75302	Others	Others
	U75302 is an antagonist of thymosin beta-4 (TB4) receptor with a Ki value of 159 nM on guinea pig lung membranes.
T10014	(1α,1'S,4β)-Lanabecestat (1α,1'S,4β)-AZD3293	Others	Others
	(1α,1'S,4β)-Lanabecestat is a Beta site APP Cleaving Enzymel (BACE1) inhibitor, and has IC50s of 2.2 nM (TR-FRET assay) and 0.28 nM (sAPPp release assay), respectively.
T27786	L-796568 dihydrochloride L 796568,L-796568,L796568	Others	Others
	L-796568, is a β3 adrenergic receptor agonist. L-796568 is a potent full beta(3) agonist (EC(50) = 3.6 nM, 94% activation) with >600-fold selectivity over the human beta(1) and beta(2) receptors, which also displays good oral bioavailability in several
T11243	Ethyl tosylcarbamate	Others	Others
	Gliclazide is a whole-cell beta-cell ATP-sensitive potassium currents blocker with an IC50 of 184 nM. Ethyl tosylcarbamate is an intermediate in the synthesis of Gliclazide (G409877).
T60633	Nepicastat	Others	Others
	Nepicastat (SYN117) 是一种选择性的，有效的，口服的多巴胺 β 羟化酶抑制剂，可穿过血脑屏障(BBB)。Nepicastat (SYN117) 对牛和人多巴胺 β 羟化酶产生浓度依赖性抑制作用，IC50值分别为8.5 nM 和 9 nM。
T31828	AZD4694 Flutafuranol,AZD 4694,NAV-4694,AZD-4694,NAV 4694,NAV4694	Others	Others
	Flutafuranol, also known as AZD 4694 and NAV4694, is a bio-active chemical. AZD4694 shows high affinity for beta-amyloid fibrils in vitro (K(d) = 2.3 +/- 0.3 nM). The fluorine-18 labeled AZD4694 may have potential for PET-visualization of cerebral beta-am
T72261	Metallo-β-lactamase-IN-9	Others	Others
	Metallo-β-lactamase-IN-9 (Compound 23) 是一种高效的泛金属-β-内酰胺酶 (MBL) 抑制剂，其对 NDM-1、VIM-1 和 IMP-1 的抑制活性表现在 IC50 值上，分别为 35 nM、269 nM 和 369 nM。
T74786	BIBD-124	Others	Others
	BIBD-124 通过与淀粉样蛋白 (Aβ) 斑块结合，展现出优异的亲和力，其 IC50 值达到了 9.51 nM。作为一种放射性示踪剂，[18F]BIBD-124 能够针对 Aβ 斑块进行高效的标记。
T36296	BIO5192 hydrate	Others	Others
	BIO5192 hydrate is a selective and potent integrin α4β1 (VLA-4) inhibitor (Kd<10 pM). BIO5192 hydrate selectively binds to α4β1 (IC50=1.8 nM) over a range of other integrins. BIO5192 hydrate results in a 30-fold increase in mobilization of murine hematopoietic stem and progenitors (HSPCs) over basal levels[1][2]. The combination of BIO5192 hydrate (1 mg/kg; i.v.) and Plerixafor (5 mg/kg; s.c.) exert an additive effect on progenitor mobilization[1].BIO5192 hydrate (30 mg/kg; s.c; bid; during days...

化合物

Cat.No: T16967

Target: PI4K

Fluorescein di-beta-D-galactopyranoside

Cat.No: T18993

Synonym: FDG,Fluorescein di(β-D-galactopyranoside)

Target: Others

Cat.No: T17260

Target: Lipase, MAGL

Cat.No: T2098

Synonym: A77-01

Target: ALK, TGF-beta/Smad

Cat.No: T16530

Target: Antiviral, PI4K

Cat.No: T1671

Synonym: YM178,米拉贝隆

Target: Adrenergic Receptor

Cat.No: T13253

Synonym: CNP520

Target: BACE

Nebivolol hydrochloride

Cat.No: T0154

Synonym: R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824

Target: Apoptosis, Adrenergic Receptor

Cat.No: T22694

Target: Others

Metaproterenol hemisulfate

Cat.No: T0277

Synonym: Orciprenaline sulfate,Metaproterenol Sulfate,硫酸奥西那林

Target: Adrenergic Receptor

Cat.No: T1800

Synonym: GW 788388

Target: ALK, TGF-beta/Smad

Cat.No: T1527

Synonym: 格列齐特,S1702,SE1702

Target: Potassium Channel

Cat.No: T6870

Synonym: L-685,458

Target: Apoptosis, Gamma-secretase

Cat.No: T2265

Synonym: 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine,PQR309,PI3K-IN-2

Target: Others, PI3K, S6 Kinase, mTOR

Cat.No: T6496

Synonym: TEW-7197,EW-7197

Target: ALK, TGF-beta/Smad

Arformoterol Tartrate

Cat.No: T22245

Synonym: (R,R)-Formoterol tartrate,酒石酸福莫特罗

Target: Adrenergic Receptor

Nepicastat hydrochloride

Cat.No: T6604

Synonym: Nepicastat HCl,内匹司他盐酸盐,RS-25560-197 hydrochloride,SYN-117 hydrochloride,Nepicastat (SYN-117) HCl

Target: Hydroxylase

5-Fluorouridine

Cat.No: T1349

Target: Others, DNA/RNA Synthesis

Sarpogrelate hydrochloride

Cat.No: T4978

Synonym: 盐酸沙格雷酯,MCI-9042

Target: 5-HT Receptor

Cat.No: T0866

Synonym: Rythmol,普罗帕酮,Propafenonum

Target: Potassium Channel, MRP, Sodium Channel

Cat.No: T63013

Target: Others

PI4KIII beta inhibitor 3

Cat.No: T12467

Target: PI3K

L-796568 free base

Cat.No: T24380

Target: Others

Cat.No: T29034

Synonym: U 75302,U-75302

Target: Others

(1α,1'S,4β)-Lanabecestat

Cat.No: T10014

Synonym: (1α,1'S,4β)-AZD3293

Target: Others

L-796568 dihydrochloride

Cat.No: T27786

Synonym: L 796568,L-796568,L796568

Target: Others

Ethyl tosylcarbamate

Cat.No: T11243

Target: Others

Cat.No: T60633

Target: Others

Cat.No: T31828

Synonym: Flutafuranol,AZD 4694,NAV-4694,AZD-4694,NAV 4694,NAV4694

Target: Others

Metallo-β-lactamase-IN-9

Cat.No: T72261

Target: Others

Cat.No: T74786

Target: Others

BIO5192 hydrate

Cat.No: T36296

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T4721	β-Nicotinamide mononucleotide NMN,β-NM,β烟酰胺单核苷酸,烟酰胺单核苷酸	Others; Endogenous Metabolite	Metabolism; Others
	β-nicotinamide mononucleotide 是烟酰胺磷酸核糖转移酶 (NAMPT) 反应的产物。β-nicotinamide mononucleotide的作用包括其在细胞生化功能、心脏保护、糖尿病、肥胖相关并发症和阿尔茨海默病中的作用。
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。

天然产物

β-Nicotinamide mononucleotide

Cat.No: T4721

Synonym: NMN,β-NM,β烟酰胺单核苷酸,烟酰胺单核苷酸

Target: Others, Endogenous Metabolite

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

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-03037	Alpha-cobratoxin Protein, Naja kaouthia, Recombinant (GST & His & Myc) Alpha-CT,Alpha-Ctx,Alpha-EPTX-Nk2a,Long neurotoxin 1,Alpha-C...	Naja kaouthia	E. coli
	Monomer: binds with high affinity to muscular (alpha-1-beta-1-gamma-delta/CHRNA1-CHRNB1-CHRNG-CHRND) nAChR (tested on Torpedo californica, Kd=0.2-4.5 nM) and neuronal alpha-7/CHRNA7 nicotinic acetylcholine receptors (Kd=13-105 nM). Also inhibits GABA(A) channels. Heteropentamer targets studied are composed of alpha-1-beta-3-gamma-2 (GABRA1-GABRB3-GABRG2) subunits (IC(50)=236 nM), alpha-1-beta-2-gamma-2 (GABRA1-GABRB2-GABRG2) subunits (IC(50)=469 nM), alpha-2-beta-2-gamma-2 (GABRA2-GABRB2-GABRG2)...
TMPH-02408	SPI Protein, Lentinula edodes, Recombinant (His) Serine protease inhibitor	Lentinula edodes	E. coli
	Serine protease inhibitor. Active against beta-trypsin and alpha-chymotrypsin with dissociation constants of 0.35 nM and 40 nM respectively. Inhibits factor XIa, but not other enzymes involved in coagulation and fibrinolysis. Does not inhibit subtilisin, lysyl endopeptidase, arginyl endopeptidase or papain.
TMPH-00031	Aerolysin Protein, Aeromonas sobria, Recombinant (His & Myc) Hemolysin	Aeromonas sobria	E. coli
	Secreted, cytolytic toxin that forms pores in host membranes after proteolytic removal of a C-terminal propeptide, leading to destruction of the membrane permeability barrier and cell death. The pores are formed by transmembrane beta-strands and are approximately 3 nm in diameter.
TMPY-01660	SULT1E1 Protein, Human, Recombinant (His) ST1E1,EST,sulfotransferase family 1E member 1,EST-1,STE,MGC3...	Human	E. coli
	Estrogen sulfotransferase, also known as Sulfotransferase, estrogen-preferring, Sulfotransferase 1E1, SULT1E1 and ST1E1, is a cytoplasm enzyme that belongs to the sulfotransferase 1 family. Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. SULT1E1 may control the level of the estrogen receptor by sulfurylating free estradio...

重组蛋白

Alpha-cobratoxin Protein, Naja kaouthia, Recombinant (GST & His & Myc)

Cat.No: TMPH-03037

Species: Naja kaouthia

Expression System: E. coli

SPI Protein, Lentinula edodes, Recombinant (His)

Cat.No: TMPH-02408

Species: Lentinula edodes

Expression System: E. coli

Aerolysin Protein, Aeromonas sobria, Recombinant (His & Myc)

Cat.No: TMPH-00031

Species: Aeromonas sobria

Expression System: E. coli

SULT1E1 Protein, Human, Recombinant (His)

Cat.No: TMPY-01660

Species: Human

Expression System: E. coli

Cat. No.	Product Name	Target	Signaling Pathways
TMIH-0253	Gliclazide-d7
	Gliclazide-d7 是 Gliclazide 的氘代化合物。Gliclazide 的 CAS 号为 21187-98-4。Gliclazide 是一种有效的全细胞的 β 细胞 ATP 敏感型钾流阻断剂，IC50为 184 nM，用作降糖药。
TMIJ-0272	Sarpogrelate-d3 HCl
	Sarpogrelate-d3 HCl 是 Sarpogrelate HCl 的氘代化合物。Sarpogrelate HCl 的 CAS 号为 135159-51-2。Sarpogrelate hydrochloride 是一种选择性5-HT2R拮抗剂，可用于研究与血栓形成有关的血管疾病，对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi值分别为 8.52、6.57 和 7.43。

同位素标记化合物

Cat.No: TMIH-0253

Sarpogrelate-d3 HCl

Cat.No: TMIJ-0272

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