444200
MDL-12,330A hydrochloride
Cell-permeable and irreversible inhibitor of adenylate cyclase (IC₅₀ = 250 µM).
别名:
MDL-12,330A, Hydrochloride, cis-N-(2-Phenylcyclopentyl)azacyclotridec-1-en-2-amine, HCl, RMI 12330
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关于此项目
经验公式(希尔记法):
C23H36N2 · xHCl
化学文摘社编号:
分子量:
340.55 (free base basis)
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77
产品名称
MDL-12,330A, Hydrochloride, Cell-permeable and irreversible inhibitor of adenylate cyclase (IC₅₀ = 250 µM).
质量水平
方案
≥98% (HPLC)
表单
solid
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
protect from light
颜色
white
溶解性
DMSO: 10 mg/mL
water: 3 mg/mL
ethanol: 5 mg/mL
运输
ambient
储存温度
2-8°C
InChI
1S/C23H36N2.ClH/c1-2-4-6-11-18-23(24-19-12-7-5-3-1)25-22-17-13-16-21(22)20-14-9-8-10-15-20;/h8-10,14-15,21-22H,1-7,11-13,16-19H2,(H,24,25);1H/t21-,22-;/m0./s1
InChI key
CKOPQUCSDBVAQG-VROPFNGYSA-N
相关类别
一般描述
Cell-permeable and irreversible inhibitor of adenylate cyclase (IC50 = 250 µM).
Cell-permeable irreversible inhibitor of adenylate cyclase (IC50 = 250 µM).
生化/生理作用
Cell permeable: yes
Primary Target
Adenylate cyclase
Adenylate cyclase
Product does not compete with ATP.
Reversible: no
Target IC50: 250 µM against adenylate cyclase
制备说明
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 2 months at -20°C.
其他说明
Correia-de-Sa, P., and Ribeiro, J.A. 1994. Eur. J. Pharmacol. 271, 349.
Gorczynska, E., et al. 1994. Endocrinology134, 293.
Delpiano, M.A., and Acker, H. 1991. J. Neurochem.57, 291.
Lippe, C., and Ardizzone, C. 1991. Comp. Biochem. Physiol.99, 209.
Guellaen, G., et al. 1977. Biochim. Biophys. Acta 484, 465.
Gorczynska, E., et al. 1994. Endocrinology134, 293.
Delpiano, M.A., and Acker, H. 1991. J. Neurochem.57, 291.
Lippe, C., and Ardizzone, C. 1991. Comp. Biochem. Physiol.99, 209.
Guellaen, G., et al. 1977. Biochim. Biophys. Acta 484, 465.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
免责声明
Toxicity: Standard Handling (A)
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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