| Weight | 267.285 g/mol |
|---|---|
| Formula | C12H17N3O4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
AGARITINE (2757-90-6)
Score:
#3 in Mycology
,
#393 in Microbiology
,
#1230 in Biochemistry
,
#3065 in Biology
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- ISOLATION AND STRUCTURE OF AGARITINE, A GAMMA-GLUTAMYL-SUBSTITUTED ARYLHYDRAZINE DERIVATIVE FROM AGARICACEAE. (Journal of Biological Chemistry, 1964)
- STRUCTURE AND ENZYMATIC CLEAVAGE OF AGARITINE, A PHENYLHYDRAZIDE OF L-GLUTAMIC ACID ISOLATED FROM AGARICACEAE1 (Journal of the American Chemical Society, 1961)
- Tumor Induction with the N-Acetyl Derivative of 4-Hydroxymethylphenylhydrazine, a Metabolite of Agaritine of Agaricus bisporus (Cancer Research, 1978)
- Agaritine: Isolation, Degradation, and Synthesis1 (Journal of Organic Chemistry, 1962)
- Attempted tumor induction with agaritine in mice. (Anticancer Research, 1981)
- Agaritine and Its Derivatives Are Potential Inhibitors against HIV Proteases (Medicinal Chemistry, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1CO)NNC(=O)CCC(C(=O)O)N
-
InChIKeySRSPQXBFDCGXIZ-UHFFFAOYSA-N
- Pubchem - AGARITINE
- Wikipedia - Agaritine
Agaritine (AGT) is an aromatic, antiviral, hydrazine-derivative mycotoxin and IARC Group 3 carcinogen that occurs in mushroom species of the genus Agaricus.
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