Details
Stereochemistry | ACHIRAL |
Molecular Formula | CH5N3O |
Molecular Weight | 75.0699 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=N)NO
InChI
InChIKey=WFBHRSAKANVBKH-UHFFFAOYSA-N
InChI=1S/CH5N3O/c2-1(3)4-5/h5H,(H4,2,3,4)
Approval Year
PubMed
Title | Date | PubMed |
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N-hydroxyguanidines as new heme ligands: UV-visible, EPR, and resonance Raman studies of the interaction of various compounds bearing a C=NOH function with microperoxidase-8. | 2001 Aug 21 |
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Involvement of NO in the endothelium-independent relaxing effects of N(omega)-hydroxy-L-arginine and other compounds bearing a C=NOH function in the rat aorta. | 2002 Nov |
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Microperoxidase 8 catalysed nitrogen oxides formation from oxidation of N-hydroxyguanidines by hydrogen peroxide. | 2003 Jan |
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Oxidation of N-hydroxyguanidines by copper(II): model systems for elucidating the physiological chemistry of the nitric oxide biosynthetic intermediate N-hydroxyl-L-arginine. | 2003 Sep 1 |
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Synthesis and quantitative structure-activity relationship of hydrazones of N-amino-N'-hydroxyguanidine as electron acceptors for xanthine oxidase. | 2004 Jun 3 |
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Metabolism of N-hydroxyguanidines (N-hydroxydebrisoquine) in human and porcine hepatocytes: reduction and formation of glucuronides. | 2005 Oct |
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2-(2-Chloro-6-fluorophenyl)acetamides as potent thrombin inhibitors. | 2007 Nov 15 |
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Reaction of N-hydroxyguanidine with the ferrous-oxy state of a heme peroxidase cavity mutant: a model for the reactions of nitric oxide synthase. | 2010 Aug 1 |
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Dimerization of protegrin-1 in different environments. | 2010 Sep 9 |
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13115-21-4
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SUBSTANCE RECORD