Oxybutynin
CAS No. 5633-20-5
Oxybutynin ( —— )
产品货号. M15049 CAS No. 5633-20-5
奥昔布宁是一种抗胆碱能化合物,用于缓解泌尿和膀胱困难。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 10MG | ¥125 | 有现货 |
|
| 25MG | ¥179 | 有现货 |
|
| 50MG | ¥247 | 有现货 |
|
| 100MG | ¥339 | 有现货 |
|
| 500MG | ¥745 | 有现货 |
|
| 1G | ¥1098 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥409 | 有现货 |
|
生物学信息
-
产品名称Oxybutynin
-
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
-
产品简述奥昔布宁是一种抗胆碱能化合物,用于缓解泌尿和膀胱困难。
-
产品描述Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties.(In Vitro):Oxybutynin (0.1, 0.3, 1, 3, 10, 30, 100 μM; 200 ms) inhibits vascular Kv channels in a concentration-dependent manner independent of anticholinergic effect in coronary arterial smooth muscle cells.(In Vivo):Oxybutynin (27.2 mg/kg; p.o.; single) exhibits significant binding of mouse brain muscarinic receptors that about a 2-fold increase in Kd?values for specific [3H]N-methylscopolamine binding 0.5 and 2 h later.
-
体外实验Oxybutynin (0.1, 0.3, 1, 3, 10, 30, 100 μM; 200 ms) inhibits vascular Kv channels in a concentration-dependent manner independent of anticholinergic effect in coronary arterial smooth muscle cells. Cell Viability Assay Cell Line:Coronary arterial smooth muscle cells (from male New Zealand White rabbits)Concentration:10 μM Incubation Time:200 ms Result:Rapidly inhibited the Kv current within 2 min and reduced the Kv current by 44% at +60 Mv.Inhibited the Kv current by changing the gating properties of Kv channels.Cell Viability Assay Cell Line:Coronary arterial smooth muscle cells (from male New Zealand White rabbits) Concentration:0.1, 0.3, 1, 3, 10, 30, 100 μM Incubation Time:200 ms Result:Reduced the Kv current amplitude in a concentration-dependent manner, with an IC50 value of 11.51 μM.
-
体内实验Oxybutynin (27.2 mg/kg; p.o.; single) exhibits significant binding of mouse brain muscarinic receptors that about a 2-fold increase in Kd values for specific [3H]N-methylscopolamine binding 0.5 and 2 h later. Animal Model:Male ddY strain mice (9 to 13-week-old).Dosage:27.2 mg/kg (76.1 μmol/kg) Administration:Oral administration; single.Result:Significant increased Kd values for specific [3H]NMS binding in mouse bladder with values of 54.7% and 40.6% when at 0.5 and 2 hours, respectively.Significant increased Kd values for specific [3H]NMS binding in mouse cerebral cortex with values of 120% and 71.2% when at 0.5 and 2 hours, respectively.
-
同义词——
-
通路Endocrinology/Hormones
-
靶点AChR
-
受体mAChR
-
研究领域Neurological Disease
-
适应症——
化学信息
-
CAS Number5633-20-5
-
分子量357.49
-
分子式C22H31NO3
-
纯度>98% (HPLC)
-
溶解度Ethanol: 71 mg/mL (198.6 mM); DMSO: 71 mg/mL (198.6 mM)
-
SMILESCCN(CC)CC#CCOC(=O)C(O)(C1CCCCC1)C1=CC=CC=C1
-
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.Ito Y, et al. Eur J Pharmacol. 2009 Aug 1;615(1-3):201-6.
产品手册
关联产品
-
Trospium chloride
Trospium chloride 是具有口服活性的,特异性、竞争性的毒蕈碱胆碱能受体 (mAChRs) 拮抗剂,具有抗毒蕈碱活性。Trospium chloride 能以高亲和力结合毒蕈碱受体 M1、M2 和 M3,但不与烟碱、胆碱能受体结合。
-
Darifenacin HBr
Darifenacin 是一种选择性毒蕈碱受体拮抗剂。
-
BNC210
BNC210 是一种 α7 nAChR 负变构调节剂。 BNC210 在焦虑和抑郁动物模型中具有有效活性。
021-51111890
购物车()
sales@molnova.cn

