| Weight | 178.575 g/mol |
|---|---|
| Formula | C5H7ClN2O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
acivicin (42228-92-2)
Score:
#1801 in Biochemistry
,
#3932 in Biology
,
#4949 in Chemistry
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- The -Glutamyl Transpeptidase Inhibitor Acivicin Preserves Glutathione Released by Astroglial Cells in Culture (Neurochemical Research, 1997)
- Effects of Acivicin and Dipyridamole on Hepatoma 3924A Cells (Cancer Research, 1983)
- A short, efficient total synthesis of () acivicin and () bromo-acivicin (Tetrahedron Letters, 1984)
- Inhibition of -Glutamyl Transpeptidase Activity by Acivicin in Vivo Protects the Kidney from Cisplatin-induced Toxicity (Cancer Research, 1994)
- Mechanism for Acivicin Inactivation of Triad Glutamine Amidotransferases (Biochemistry, 2001)
- Enhancement of the Sensitivity of Human Colon Cancer Cells to Growth Inhibition by Acivicin Achieved through Inhibition of Nucleic Acid Precursor Salvage by Dipyridamole (Cancer Research, 1984)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(ON=C1Cl)C(C(=O)O)N
-
InChIKeyQAWIHIJWNYOLBE-UHFFFAOYSA-N
- Pubchem - acivicin
- Wikipedia - acivicin
Acivicin is an analog of glutamine. It is an inhibitor of gamma-glutamyl transferase. It is a fermentation product of Streptomyces sviceus.
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