| Weight | 136.154 g/mol |
|---|---|
| Formula | C7H8N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
N-Hydroxy-benzamidine (613-92-3)
benzamidoxime
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- Identification of the Missing Component in the Mitochondrial Benzamidoxime Prodrug-converting System as a Novel Molybdenum Enzyme (Journal of Biological Chemistry, 2006)
- ISOLATION AND CHARACTERIZATION OF THE PROTEIN COMPONENTS OF THE LIVER MICROSOMAL O2-INSENSITIVE NADH-BENZAMIDOXIME REDUCTASE (Journal of Biological Chemistry, 1997)
- Uranyl complexes of acetamidoxime and benzamidoxime. Preparation, characterization, and crystal structure (Inorganica Chimica Acta, 1984)
- Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid). (Drug Metabolism and Disposition, 2005)
- CHARACTERIZATION AND PARTIAL PURIFICATION OF THE RAT AND HUMAN ENZYME SYSTEMS ACTIVE IN THE REDUCTION OF N-HYDROXYMELAGATRAN AND BENZAMIDOXIME (Drug Metabolism and Disposition, 2005)
- Enzymatic Reduction of Benzamidoxime to Benzamidoxine (Archiv Der Pharmazie, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzamidoxime
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SMILESC1=CC=C(C=C1)C(=NO)N
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InChIKeyMXOQNVMDKHLYCZ-UHFFFAOYSA-N
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