| Weight | 272.264 g/mol |
|---|---|
| Formula | C13H12N4O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Pyrinuron (53558-25-1)
Vacor · 1-(3-pyridylmethyl)-3-(4-nitrophenyl)urea · pyriminil monohydrochloride
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- Insulinopenic Diabetes After Rodenticide (Vacor) Ingestion: A Unique Model of Acquired Diabetes in Man (Diabetes, 1980)
- The neurotoxicity of the rat poison vacor. A clinical study of 12 cases. (The New England Journal of Medicine, 1980)
- Inhibition of Mitochondrial Complex I May Account for IDDM Induced by Intoxication With the Rodenticide Vacor (Diabetes, 1996)
- Diabetes Mellitus and Neuropathy Following Vacor Ingestion in Man (JAMA Internal Medicine, 1979)
- Muscle capillary basement membrane width in patients with vacor-induced diabetes mellitus. (Journal of Clinical Investigation, 1986)
- Diabetes Mellitus and Autonomic Dysfunction After Vacor Rodenticide Ingestion (Diabetes Care, 1978)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - Vacor
- 1-(3-pyridylmethyl)-3-(4-nitrophenyl)urea
- pyriminil monohydrochloride
- pyriminyl
- pyriminil malonate (1:1)
- RH 787
- pyriminil monohydrobromide
- N-(3-pyridylmethyl)-N'-(p-nitrophenyl)urea
- pyriminil oxalate (1:1)
- pyriminil
- pyriminil tartrate (1:1)
- pyriminil monotosylate
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SMILESC1=CC(=CN=C1)CNC(=O)NC2=CC=C(C=C2)[N+](=O)[O-]
-
InChIKeyCLKZWXHKFXZIMA-UHFFFAOYSA-N
- Pubchem - Pyrinuron
- Wikipedia - pyriminil
Pyrinuron (Pyriminil, Vacor) is a chemical compound formerly used as a rodenticide. Commercial distribution was voluntarily suspended in 1979 and it is not approved by the Environmental Protection Agency for use in the United States. If it is ingested by humans in high doses, it may selectively destroy insulin-producing beta cells in the pancreas causing type 1 diabetes.
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Pyrinuron
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