Drotaverine hydrochloride
CAS No. 985-12-6
Drotaverine hydrochloride ( —— )
产品货号. M22762 CAS No. 985-12-6
Drotaverine (hydrochloride) 是一种磷酸二酯酶 4 (PDE4) 的抑制剂,也是一种 L 型电压依赖钙通道(L-VDCC)的阻滞剂,可阻断3',5'-环腺苷单磷酸的降解。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥470 | 有现货 |
|
| 10MG | ¥710 | 有现货 |
|
| 25MG | ¥1349 | 有现货 |
|
| 50MG | ¥2474 | 有现货 |
|
| 100MG | ¥3537 | 有现货 |
|
| 500MG | ¥7911 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥520 | 有现货 |
|
生物学信息
-
产品名称Drotaverine hydrochloride
-
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Drotaverine (hydrochloride) 是一种磷酸二酯酶 4 (PDE4) 的抑制剂,也是一种 L 型电压依赖钙通道(L-VDCC)的阻滞剂,可阻断3',5'-环腺苷单磷酸的降解。
-
产品描述Drotaverine hydrochloride is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor,and is an antispasmodic drug, used to enhance cervical dilation during childbirth.?Drotaverine hydrochloride?is structurally related to papaverine?drotaverine not only relaxed the precontracted tracheal preparations but also decreased mediator-induced contraction.?These effects of drotaverine were concentration dependent, with a significantly higher potency on the KCl-induced response, than on either the histamine or methacholine induced one.?A similar result was noted for nifedipine.?The PDE inhibitor, theophylline, also relaxed the precontracted preparations but was ineffective on the mediator-induced contraction in a physiologically relevant concentration range.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Angiogenesis
-
靶点PDE
-
受体PDE4
-
研究领域——
-
适应症——
化学信息
-
CAS Number985-12-6
-
分子量433.97
-
分子式C24H32ClNO4
-
纯度>98% (HPLC)
-
溶解度In Vitro:?H2O : 100 mg/mL (230.43 mM)
-
SMILESCl.CCOc1ccc(cc1OCC)CC2=NCCc3cc(OCC)c(OCC)cc23
-
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. Patai, Zoltán, Guttman, András, Mikus E . Assessment of the Airway Smooth Muscle Relaxant Effect of Drotaverine[J]. Pharmacology, 2018:163.
产品手册
关联产品
-
Dypyridamole
双嘧达莫(Persantine)是一种磷酸二酯酶抑制剂,可阻断红细胞和血管内皮细胞对腺苷的摄取和代谢。
-
Vardenafil hydrochlo...
Vardenafil dihydrochloride 是一种具有高选择性和口服活性的磷酸二酯酶 5 (PDE5) 抑制剂,IC50 为 0.7 nM。Vardenafil dihydrochloride 对 PDE1、PDE6 的 IC50 为 180 nM,11 nM,对 PDE3、PDE4 的 IC50 >1000 nM。Vardenafil dihydrochloride 非竞争性地抑制环磷酸鸟苷 (cGMP) 水解,从而提高 cGMP 水平。
-
BIO-32546
BIO-32546 (example 12b, S-isomer) 是autotaxin (ATX) 的调节剂 (IC50: 1 nM),信息来自专利 US20170158687A1。
021-51111890
购物车()
sales@molnova.cn

