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Merck
CN

410957

3-异丁基-1-甲基黄嘌呤

≥98% (HPLC), solid, cAMP and cGMP phosphodiesterase inhibitor, Calbiochem®

别名:

3-异丁基-1-甲基黄嘌呤

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关于此项目

经验公式(希尔记法):
C10H14N4O2
化学文摘社编号:
分子量:
222.24
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
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产品名称

3-异丁基-1-甲基黄嘌呤, A cell-permeable, non-specific inhibitor of cAMP and cGMP phosphodiesterases (IC50 = 2-50 µM).

SMILES string

[n]1(c2nc[nH]c2[c]([n]([c]1=O)C)=O)CC(C)C

InChI

1S/C10H14N4O2/c1-6(2)4-14-8-7(11-5-12-8)9(15)13(3)10(14)16/h5-6H,4H2,1-3H3,(H,11,12)

InChI key

APIXJSLKIYYUKG-UHFFFAOYSA-N

description

RTECS - ZD8500000

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

white

solubility

ethanol: 10 mg/mL
DMSO: 100 mM
methanol: 50 mg/mL

shipped in

ambient

storage temp.

−20°C

Quality Level

Biochem/physiol Actions

主要靶标
cAMP和cGMP磷酸二酯酶
产物不与ATP竞争。
可逆:否
细胞可渗透性:具有
靶标IC50:2-50 µM,靶向cAMP和cGMP磷酸二酯酶

Disclaimer

毒性:标准处理(A)

General description

cAMP和cGMP磷酸二酯酶的一种非特异性细胞可渗透抑制剂(IC50 = 2-50 µM)。还可作为一种腺苷受体拮抗剂。已报道可抑制TNFα在脂肪细胞前体细胞中的表达。
cAMP和cGMP磷酸二酯酶的细胞可渗透非特异性抑制剂(IC50 = 2-50 µM)。还可作为一种腺苷受体拮抗剂。已报道可抑制TNF-α在脂肪细胞前体细胞中的表达。

Other Notes

Hube, F., et al. 1999.Horm.代谢Res.31, 359.
Morgan, A.J., et al. 1993.生物化学。Pharmacol.45, 2373.
Scamps, F., et al. 1993.Eur. J. Pharmacol.244, 119.
Turner, N.C., et al. 1993.Br. J. Pharmacol.108, 876.
Tamura, T., et al. 1991.J. Gen.Physiol.98, 95.
Beavo, J.A., and Reifsnyder, D.H.1990.Trends Pharmacol.Sci.11, 150.
Russell, T.R.1979.Proc.Natl.Acad.Sci. USA76, 4451.

Preparation Note

可能需要加热才能完全溶解。
在乙醇或甲醇中重溶后,冷藏保存(4°C)。在DMSO中重溶后,等分并冷冻保存(-20°C)。乙醇/甲醇和DMSO储备溶液可分别在4°C或-20°C下稳定保存长达6个月。

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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