
Pyr10
CAS No. 1315323-00-2
Pyr10 ( —— )
产品货号. M22464 CAS No. 1315323-00-2
Pyr10 是一种吡唑衍生物,也是一种选择性 TRP 阳离子 3 抑制剂。 Pyr10 能够区分受体操作的 TRPC3 和天然基质相互作用分子 1 (STIM1)/Orai1 通道。 Pyr10 抑制卡巴胆碱刺激的 TRPC3 转染 HEK293 细胞中的 Ca2+ 流入(IC50:0.72 μM)(BRL-2H3 细胞中钙池操纵的 Ca2+ 进入的 IC50 为 13.08 μM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥437 | 有现货 |
![]() ![]() |
10MG | ¥721 | 有现货 |
![]() ![]() |
50MG | ¥2803 | 有现货 |
![]() ![]() |
100MG | 获取报价 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Pyr10
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Pyr10 是一种吡唑衍生物,也是一种选择性 TRP 阳离子 3 抑制剂。 Pyr10 能够区分受体操作的 TRPC3 和天然基质相互作用分子 1 (STIM1)/Orai1 通道。 Pyr10 抑制卡巴胆碱刺激的 TRPC3 转染 HEK293 细胞中的 Ca2+ 流入(IC50:0.72 μM)(BRL-2H3 细胞中钙池操纵的 Ca2+ 进入的 IC50 为 13.08 μM)。
-
产品描述Pyr10 is a pyrazole derivative and a selective TRP cation 3 inhibitor. Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels. Pyr10 inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells (IC50: 0.72 μM) (IC50 of 13.08 μM for store-operated Ca2+ entry in BRL-2H3 cells) . The novel pyrazole Pyr10 displayed substantial selectivity for TRPC3-mediated responses (18-fold) and the selective block of TRPC3 channels by Pyr10 barely affected mast cell activation.Pyr10 blunted ventricular CF activation and MF in l-NAME hypertensive mice.?Finally, TRPC3 was present in human ventricular CFs and upregulated in MF, whereas pharmacological modulation of TRPC3-NFATc3 decreased proliferation and collagen secretion.?TRPC3-NFATc3 signaling is modulated by P.E. and critically regulates ventricular CF phenotype and MF.?These findings strongly argue for P.E., through TRPC3 targeting, as potential and interesting therapeutics for MF management.
-
体外实验Pyr10 has the ability to discriminate between the classical Orai-mediated, highly Ca2+ selective signalling pathway and the phospholipase C-dependent Ca2+ entry-mediated by TRPC channels, specifically by TRPC3. Pyr10 (3 μM) completely eliminates TRPC3 currents as well as Ca2+ entry while exerting modest effects on Orai-mediated responses. The selective block of TRPC3 channels by Pyr10 barely affected mast cell activation.
-
体内实验Genetic deletion (TRPC3-/-) and pharmacological channel blockade with Pyr10 blunts ventricular cardiac fibroblast activation and myocardial fibrosis in N(ω)-nitro-l-arginine methyl ester (l-NAME) hypertensive mice.
-
同义词——
-
通路Membrane Transporter/Ion Channel
-
靶点TRP/TRPV Channel
-
受体TRPC3
-
研究领域——
-
适应症——
化学信息
-
CAS Number1315323-00-2
-
分子量449.37
-
分子式C18H13F6N3O2S
-
纯度>98% (HPLC)
-
溶解度DMSO:95 mg/mL (211.4 mM; Need ultrasonic)
-
SMILESCc1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)-n1nc(cc1C(F)(F)F)C(F)(F)F
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Schleifer H, et al. Novel pyrazole compounds for pharmacological discrimination between receptor-operated and store-operated Ca(2+) entry pathways. Br J Pharmacol. 2012 Dec;167(8):1712-1722.
产品手册




关联产品
-
TRPM8 antagonist 2
TRPM8 Antagonist 2 是一种有效的选择性 TRPM8 拮抗剂,IC50 为 0.2 nM,用于神经病理性疼痛综合征的研究。
-
TC-I 2014
TC-I 2014 hydrochloride 是一种口服有效的、强效的、苯并咪唑类的、 TRPM8 的拮抗剂,其对犬类、人和大鼠通道的IC50 值分别为 0.8 nM, 3.0 nM 和 4.4 nM。在疼痛动物模型中具有抗痛觉超敏作用。
-
AMG-517
AMG 517 是一种有效的选择性 TRPV1 拮抗剂,拮抗 TRPV1 的辣椒素、质子和热激活,IC50 分别为 0.76 nM、0.62 nM 和 1.3 nM。