%D8%A7%D8%B3-%D9%86%DB%8C%D8%AA%D8%B1%D9%88%D8%B3%D9%88-%D8%A7%D9%86-%D8%A7%D8%B3%D8%AA%DB%8C%D9%84_%D9%BE%D9%86%DB%8C%D8%B3%DB%8C%D9%84_%D8%A2%D9%85%DB%8C%D9%86S-Nitroso-N-acetylpenicillamine%D8%A7%D8%B3-%D9%86%DB%8C%D8%AA%D8%B1%D9%88%D8%B3%D9%88-%D8%A7%D9%86-%D8%A7%D8%B3%D8%AA%DB%8C%D9%84_%D9%BE%D9%86%DB%8C%D8%B3%DB%8C%D9%84_%D8%A2%D9%85%DB%8C%D9%86S-Nitroso-N-ac%C3%A9tylp%C3%A9nicillamineS-%D0%9D%D0%B8%D1%82%D1%80%D0%BE%D0%B7%D0%BE-N-%D0%B0%D1%86%D0%B5%D1%82%D0%B8%D0%BB%D0%BF%D0%B5%D0%BD%D0%B8%D1%86%D0%B8%D0%BB%D0%BB%D0%B0%D0%BC%D0%B8%D0%BDS-Nitrozo-N-acetilpenicilaminS-Nitrozo-N-acetilpenicilaminQ4048659
about
The nitric oxide donor S-nitroso-N-acetylpenicillamine (SNAP) increases free radical generation and degrades left ventricular function after myocardial ischemia-reperfusion.Long-term nitric oxide release and elevated temperature stability with S-nitroso-N-acetylpenicillamine (SNAP)-doped Elast-eon E2As polymerS-nitroso-N-acetylpenicillamine (SNAP) derivatization of peptide primary amines to create inducible nitric oxide donor biomaterials.Role of the Listeria monocytogenes 2-Cys peroxiredoxin homologue in protection against oxidative and nitrosative stress and in virulence.Wild measles virus strain: isolation and identification.Effect of nitric oxide on the cyclic guanosine monophosphate (cGMP) pathway during meiosis resumption in bovine oocytes.Formation and stability of a nitric oxide donor: S-nitroso-N-acetylpenicillamine.Hydrogen peroxide acts upstream of nitric oxide in the heat shock pathway in Arabidopsis seedlings.Effects of acute transmural pressure elevation on endothelium-dependent vasodilation in isolated rat mesenteric veins.New insights into molecular mechanism(s) underlying the presynaptic action of nitric oxide on GABA release
P921
Q35129243-7914AAD4-A3F6-49B0-8028-E6E96ACA74F7Q37060760-75294D7E-94AA-48DE-9B7E-B1B92084271DQ39107195-43B0CAD6-9394-4003-803B-4C5C5CAAD728Q44296711-8D6E1C9C-0AE9-4840-A113-FBFF7024DCBAQ45874174-B05A89A6-B2CC-46B3-A89C-D8FAD4A676FEQ46972758-1C1C47EF-6702-44D2-AE7F-08D7D5291FB3Q46982655-455D248A-F02F-44EE-BA55-25B3236D1910Q54223576-60AC022B-CF79-4AE5-9B79-71217A9D0D76Q54530040-C9B2E70C-F403-4A16-99BD-A8865007DAABQ87199703-BC73057C-B25D-4A71-A855-67349A826134
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
S-Nitroso-N-acétylpénicillamine
@fr
S-Nitrozo-N-acetilpenicilamin
@sh
S-Nitrozo-N-acetilpenicilamin
@sr
S-nitroso-N-acetyl-D-penicillamine
@en
S-Нитрозо-N-ацетилпеницилламин
@ru
اس-نیتروسو-ان-استیل پنیسیل آمین
@azb
اس-نیتروسو-ان-استیل پنیسیل آمین
@fa
type
label
S-Nitroso-N-acétylpénicillamine
@fr
S-Nitrozo-N-acetilpenicilamin
@sh
S-Nitrozo-N-acetilpenicilamin
@sr
S-nitroso-N-acetyl-D-penicillamine
@en
S-Нитрозо-N-ацетилпеницилламин
@ru
اس-نیتروسو-ان-استیل پنیسیل آمین
@azb
اس-نیتروسو-ان-استیل پنیسیل آمین
@fa
altLabel
N-Acetyl-S-nitrosopenicillamine
@en
S-Nitrosoacetylpenicillamine
@en
S-Nonap
@en
S-nitroso-N-acetylpenicillamine
@en
SNAP
@en
prefLabel
S-Nitroso-N-acétylpénicillamine
@fr
S-Nitrozo-N-acetilpenicilamin
@sh
S-Nitrozo-N-acetilpenicilamin
@sr
S-nitroso-N-acetyl-D-penicillamine
@en
S-Нитрозо-N-ацетилпеницилламин
@ru
اس-نیتروسو-ان-استیل پنیسیل آمین
@azb
اس-نیتروسو-ان-استیل پنیسیل آمین
@fa
P2868
P527
P486
P592
P6366
P646
P661
P662
P683
P1579
P2017
CC(=O)N[C@@H](C(=O)O)C(C)(C)SN=O
P2067
P231
79032-48-7
P233
CC(=O)NC(C(=O)O)C(C)(C)SN=O
P234
1S/C7H12N2O4S/c1-4(10)8-5(6(11)12)7(2,3)14-9-13/h5H,1-3H3,(H,8,10)(H,11,12)/t5-/m0/s1
P235
ZIIQCSMRQKCOCT-YFKPBYRVSA-N
P274
C₇H₁₂N₂O₄S
P3117
DTXSID80897531
P486
P592
CHEMBL73188
P6366
2779428222
P646
/m/02q16xy