S-Nitroso-N-acetyl-DL-penicillamine

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

S-亚硝基-N-乙酰基-DL-青霉胺是血小板聚集的稳定抑制剂，是一氧化氮供体。 S-亚硝基-N-乙酰基-DL-青霉胺（10 mM；8 小时）在常氧条件下 6 小时后通过释放一氧化氮 (NO) 诱导约 80% 的毒性。

S-Nitroso-N-acetyl-DL-penicillamine acts as a stable inhibitor of platelet aggregation, is a nitric oxide donor and . S-Nitroso-N-acetyl-DL-penicillamine (10 mM; 8 hours) after 6 hours under normoxic conditions by releasing nitric oxide (NO)induces toxicity of about 80% . S-Nitroso-N-acetyl-DL-penicillamine has a half-time about 6 hours in in isolated rat ventricular myocytes. S-Nitroso-N-acetyl-DL-penicillamine (100 μM; 30 minutes) causes sustained decrease in the basal pHi in isolated rat ventricular myocytes.

Cell Viability Assay Cell Line:Rat liver sinusoidal endothelial cells Concentration:2 mM, 5 mM, 10 mM Incubation Time:2 hours, 4 hours, 6 hours, 8 hours Result:Exhibited cytotoxicity against cultivated endothelial cells.

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SNAP

Immunology/Inflammation

NOS

NO Synthase

Others

Anesthesia

67776-06-1

220.25

C7H12N2O4S

>98% (HPLC)

DMSO:250 mg/mL (1135.07 mM; Need ultrasonic)

CC(=O)NC(C(O)=O)C(C)(C)SN=O

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(-20℃)

With Ice Pack

≥ 2 years