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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Oxidation of N-hydroxyguanidines by cytochromes P450 and NO-synthases and formation of nitric oxide. | 2002 Aug |
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Ceramide binding to African-American hair fibre correlates with resistance to hair breakage. | 2002 Feb |
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Electrochemical and peroxidase oxidation study of N'-hydroxyguanidine derivatives as NO donors. | 2002 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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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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Discovery and clinical evaluation of 1-{N-[2-(amidinoaminooxy)ethyl]amino}carbonylmethyl-6-methyl-3-[2,2-difluoro-2-phenylethylamino]pyrazinone (RWJ-671818), a thrombin inhibitor with an oxyguanidine P1 motif. | 2010 Feb 25 |
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529357
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43089
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DB03770
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DTXSID00156915
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80668
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8767F421T7
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13115-21-4
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SUBSTANCE RECORD