S-Nitroso-N-acetyl-DL-penicillamine

Research use only, not for human use.

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 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.

——

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

——

(-20℃)

With Ice Pack

≥ 2 years