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首页-小分子抑制剂&激动剂-Metabolic Enzyme/Protease-Phosphodiesterase (PDE)-YM976
YM976

Chemical Structure : YM976

CAS No.: 191219-80-4

YM976 (YM-976)

货号: PC-22040Not For Human Use, Lab Use Only.

YM976 is a potent, selective phosphodiesterase type 4 (PDE4) inhibitor with IC50 of 2.2 nM against PDE4 purified from human peripheral leukocytes.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

YM976 is a potent, selective phosphodiesterase type 4 (PDE4) inhibitor with IC50 of 2.2 nM against PDE4 purified from human peripheral leukocytes.
YM976 has no effects on the other PDE isozymes, PDE1, -2, -3, and -5.
YM976 potentiates prostaglandin E(2)-induced cAMP accumulation in a human mononuclear cell line, U937, and YM976 inhibits TNF-alpha production from human peripheral blood mononuclear cells stimulated by lipopolysaccharide.
YM976 inhibits the cell infiltration into the pleural cavity with oral ED(30) values of 9.1 mg/kg in rat carrageenan-induced pleurisy models.
YM976 dose dependently reduces carrageenan-induced leukocyte infiltration at the doses of 1, 3, and 10 mg/kg, p.o.

物理化学性质&存储条件

分子量 313.79
分子式 C17H16ClN3O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-(3-Chlorophenyl)-1,7-diethylpyrido[2,3-d]pyrimidin-2(1H)-one

参考文献

1. Aoki M, et al. J Pharmacol Exp Ther. 2000 Oct;295(1):255-60.

2. Aoki M, et al. J Pharmacol Exp Ther. 2000 Dec;295(3):1149-55.

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