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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T81527 |
Pegloxenatide
PEX 168 |
||
Pegloxenatide,一种胰高血糖素样肽-1受体(GLP-1 RA)激动剂,主要用于2型糖尿病的研究。 | |||
T8310 |
MMP-9-IN-1
|
MMP | Proteases/Proteasome |
MMP-9-IN-1 是特异性的基质金属蛋白酶-9 抑制剂,选择性靶向 MMP-9 的血红素域,对其他 MMP 无影响。 | |||
T81503 | PEX5-PEX14 PPI-IN-2 | ||
PEX5-PEX14 PPI-IN-2(化合物 12)是一种抑制PEX14-PEX5蛋白质-蛋白质相互作用(PPI)的化合物,其在T. b. brucei细胞和HepG2细胞中的EC50值分别为5 µM和17 µM。该化合物适用于研究与锥虫感染有关的疾病。 | |||
T79457 |
PEX5-PEX14 PPI-IN-1
|
||
PEX5-PEX14 PPI-IN-1(Compound 8)为PEX14-PEX5 PPI 抑制剂,其通过破坏PEX5-TbPEX14 PPI的作用并表现出53 μM的Ki值。该化合物还能抑制T. b. brucei的bloodstream形式,EC50为5 μM。 | |||
T0322 |
Fipexide
|
Dopamine Receptor; AChR | GPCR/G Protein; Neuroscience |
Fipexide 是对氯苯乙酸衍生物,是哌嗪化学类的精神活性药物,作为促智药物,有用于老年痴呆的研究潜力。它可降低了纹状体腺苷酸环化酶的活性,通过多巴胺能神经传递对认知表现出积极的作用。 | |||
T11318 |
Dopexamine hydrochloride
盐酸多培沙明,FPL60278AR |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dopexamine hydrochloride (FPL60278AR) 是β2肾上腺素能受体激动剂。 | |||
T11011 |
Dexpramipexole dihydrochloride
普拉克索杂质D,KNS-760704 dihydrochloride,R-(+)-Pramipexole dihydrochloride,右旋普拉克索二盐酸盐,(R)-Pramipexole dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Dexpramipexole dihydrochloride (KNS-760704 dihydrochloride) 是一种神经保护剂,是一种弱的非麦角类多巴胺受体激动剂。 | |||
T1476 |
Pramipexole
SND 919,普拉克索 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Pramipexole (SND 919) 是能够透过血脑屏障的 D2 型多巴胺受体的选择性激动剂,对 D2 型受体、D2、D3、D4亚型受体的Ki 分别为 2.2 nM、3.9 nM、0.5 nM、1.3 nM。它可用于研究帕金森综合症和腿多动综合征。 | |||
T2115 |
Pexidartinib
PLX-3397 |
Apoptosis; c-Fms; FLT; CSF-1R; c-Kit | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Pexidartinib (PLX-3397) 是具有口服活性的选择性ATP-竞争性的集落刺激因子 1 和c-Kit 抑制剂,IC50值分别为 20 和 10 nM。它可诱导细胞凋亡,具有抗肿瘤活性。 | |||
T6951 |
Pramipexole dihydrochloride hydrate
Pramipexole 2HCl Monohydrate,普拉克索盐酸盐水合物,Mirapex,普拉克索 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Pramipexole dihydrochloride hydrate (Mirapex) 是选择性的,具有血脑屏障 (BBB) 渗透性的 D2 型多巴胺受体激动剂,对 D2 型受体、D2、D3、D4亚型受体的 Ki 分别为 2.2 nM、3.9 nM、0.5 nM、1.3 nM,可用于研究帕金森综合症和腿多动综合征。 | |||
TP1930L1 |
Spexin acetate(1370290-58-6 free base)
|
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Spexin acetate(1370290-58-6 free base) 是一种有效的甘丙肽受体 2/3 (GAL2/GAL3) 激动剂(EC50 值分别为 45.7 和 112.2 nM)。对甘丙肽受体 1 没有显着的活性。抑制脂肪细胞对长链脂肪酸的摄取并减少饮食诱导的肥胖小鼠和大鼠的食物消耗。减少金鱼的 LH 分泌。在体内表现出抗焦虑作用。 | |||
T6934 |
Pexmetinib
ARRY-614 |
Tie-2; p38 MAPK; Autophagy | Autophagy; MAPK; Tyrosine Kinase/Adaptors |
Pexmetinib (ARRY-614) 是一种口服生物可利用的双重 p38 MAPK/Tie-2 抑制剂,可研究急性骨髓性白血病。在 HEK-293 细胞系中的 IC50 为 4 nM/18 nM。 | |||
T14490 |
Talipexole dihydrochloride
Domnin,盐酸他利克索,B-HT 920 dihydrochloride |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Talipexole dihydrochloride (Domnin) 是一种多巴胺 D2 受体激动剂、α2-肾上腺素受体激动剂和 5-HT3 受体拮抗剂,有抗帕金森病活性。 | |||
T16475 |
Pexacerfont
BMS-562086 |
CRFR | GPCR/G Protein |
Pexacerfont (BMS-562086) 是一种选择性的促肾上腺皮质激素释放因子 (CRF1) 受体拮抗剂,作用于人 CRF1 受体,IC50 为 6.1±0.6 nM。 | |||
T21787L |
Azepexole hydrochloride
4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Azepexole hydrochloride (4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1)) 是一种具有麻醉作用的强效α2-肾上腺素受体激动剂。 | |||
T8653 |
DOPEXAMINE
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
DOPEXAMINE 是一种多巴胺能激动剂。 | |||
T81118 |
Spexin-2 (53-70), human,mouse,rat
NPQ 53-70 |
||
Spexin-2 (53-70), human, mouse, rat (NPQ 53-70) 是一种在哺乳动物中保守的非酰胺化Spexin-2肽段,具备生物活性。作为新型肽激素proNPQ的一个片段,它在调节心血管与肾功能方面发挥关键作用。在大鼠体内,Spexin-2能有效降低心率并促进尿流量增加。 | |||
T32187 |
Ipexidine mesylate
Guanidino propyl piperazine,UNII-CI8CT0864P |
||
Ipexidine mesylate is a bio-active chemical. | |||
T41073 |
Pexopiprant
|
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Pexopiprant, a potent oral antagonist of the prostaglandin D2 receptor 2 (DP2) with a K i value less than 100nM, is a valuable compound for asthma research. | |||
T1476L | Pramipexole dihydrochloride | Dopamine Receptor | GPCR/G Protein; Neuroscience |
Pramipexole dihydrochloride could be used to treat Parkinson disease. | |||
T77163 | Pexelizumab | ||
Pexelizumab (h5G1.1-SC)为一种针对C5补体成分的人源化单克隆抗体。该化合物可抑制凋亡(apoptosis)和白细胞浸润,常用于研究脑缺血再灌注损伤和心肌梗死。 | |||
T76002 |
Spexin TFA
|
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Spexin TFA, a potent agonist for galanin receptor 2/3 (GAL2/GAL3) with EC50 values of 45.7 and 112.2 nM respectively, shows no significant activity towards galanin receptor 1. As an endogenous peptide promoting satiety, it reduces long chain fatty acid uptake by adipocytes and lowers food consumption in diet-induced obese mice and rats. Additionally, it moderates LH secretion in goldfish and demonstrates anxiolytic effects in vivo. | |||
T83717 |
Cys-Pexiganan TFA
|
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Cys-pexiganan是一种抗微生物肽,是pexiganan的衍生物,具有N-末端的半胱氨酸。它对P. aeruginosa和S. aureus具有活性(MICs分别为64和16 µg/ml)。Cys-pexiganan与含醋酸纤维素的聚乙烯醇电纺垫结合,可以加速隔离的重钙化人类血浆的凝血。 | |||
T62788 |
Pexidartinib hydrochloride
|
||
Pexidartinib hydrochloride (PLX-3397 hydrochloride) 是一种有效的、选择性的、口服具有活力的、ATP-竞争性的集落刺激因子 1 (CSF1R 或 M-CSFR) (IC50: 20 nM) 和 c-Kit (IC50: 10 nM) 抑制剂。Pexidartinib hydrochloride 对 c-Kit 和 CSF1R 的选择性是对其他相关激酶的 10-100 倍,作用于 FLT3 (IC50: 160 nM)、KDR (VEGFR2) (IC50: 350 nM)、LCK (IC50: 860 nM)、FLT1 (VEGFR1) (IC50: 880 nM) 和 NTRK3 (TRKC) (IC50: 890 nM)。Pexidartinib hydrochloride 能够诱导细胞凋亡,表现出抗肿瘤作用。 | |||
T6934L |
Pexmetinib hydrochloride
|
||
Pexmetinib hydrochloride is a biochemical. | |||
TQ0175 |
Dexpramipexole
右旋普拉克索,R-(+)-Pramipexole,(R)-Pramipexole,KNS-760704 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Dexpramipexole (KNS-760704, R-(+)-Pramipexole) is a neuroprotective agent and weak non-ergoline dopamine agonist. | |||
T13070 |
Talipexole
B-HT 920 |
Others | Others |
Talipexole (B-HT920) is an agonist of dopamine, and is an antiparkinsonian agent. | |||
TP1930 |
Spexin
|
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Potent galanin receptor 2/3 (GAL2/GAL3) agonist (EC50 values are 45.7 and 112.2 nM, respectively). Exhibits no significant activity at galanin receptor 1. Endogenous satiety-inducing peptide; inhibits long chain fatty acid uptake by adipocytes and decreas | |||
T20845 |
Kopexil
Mexoryl SAG,Aminexil |
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Kopexil, an N-oxide, is used to treat hair loss. | |||
T22332 |
Fipexide hydrochloride
盐酸非哌西特 |
Others | Others |
Fipexide (hydrochloride) is a kind of psychoactive drug of the piperazine class. | |||
T69367 |
Azepexole
|
||
Azepexole is a selective α2-adrenoceptor agonist that exhibits greater than 300-fold selectivity for the α2-adrenoceptor over the α1-adrenoceptor. | |||
T1891 |
NSC 405020
|
MMP | Proteases/Proteasome |
NSC 405020 是一种 MT1-MMP 的非催化抑制剂,可特异地靶向 MT1-MMP 的 PEX 结构域,不会抑制 MT1-MMP 和 MMP-2的催化活性。 | |||
T37666 |
Trihydroxycholestanoic Acid
Trihydroxycoprostanic Acid |
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Trihydroxycholestanoic acid is an intermediate in the biosynthesis of cholic acid .1 Elevated plasma levels of trihydroxycholestanoic acid have been found in patients with Zellweger syndrome, a neurological disorder characterized by mutations in PEX genes which result in defects in peroxisome formation.2,3 |1. Keane, M.H., Overmars, H., Wikander, T.M., et al. Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice. Hepatology 45(4), 982-997 ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T73653 |
Pexiganan
|
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Pexiganan(MSI 78 free base),maganin 2 的合成类似物,是一种具有口服活性的广谱强效抗菌肽,主要用于研究糖尿病足溃疡等相关感染。 |