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Synonym: O-Diazoacetyl-
CAS Number: 115-02-6
Empirical Formula (Hill Notation): C5H7N3O4
Molecular Weight: 173.13
Beilstein Registry Number: 1726602
EC Number: 204-061-6
MDL number: MFCD00036802
PubChem Substance ID: 24890830![]()
| Related Categories | Amino Acid Derivatives, Antibiotics, Antibiotics A to Z, Antibiotics A-F, Antibiotics by Application, |
| assay | ≥98% (TLC) |
| storage temp. | −20°C |
Used in cell culture for the selection of HGPRT revertants.
Azaserine is an antibiotic and antifungal; it may also act as a tumor inducer. It is a structural analog of glutamine and competes with glutamine in binding to enzymes involved in purine biosynthesis. Azaserine inhibits purine biosynthesis by covalently reacting with cysteine residues in the enzyme active sites, such as in formylglycinamide ribonucleotide amidotransferase and PRPP amidotransferase.1 Azaserine can induce DNA damage via the formation of carboxymethylated bases and O6-methylguanine. Secretion of exo-1,3-β-glucanase and germ-tube formation of Candida albicans were inhibited by azaserine.2
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| A4142 - Product Information Sheet (26 KB) |
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| Symbol | ![]() GHS06, GHS08 |
| Signal word | Danger |
| Hazard statements | H301-H351 |
| Precautionary statements | P281-P301 + P310 |
| Personal Protective Equipment | Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges |
| Hazard Codes | T |
| Risk Statements | 25-40 |
| Safety Statements | 53-36/37/39-45 |
| RIDADR | UN 3462 6.1/PG 3 |
| WGK Germany | 3 |
| RTECS | VT9625000 |
1. Kornberg, A., and Baker, T. DNA Replication 2ndth ed.,, (1992), 57-60, 440-442
2. Ram, S.P., et al., Exo-(1→3)-β-glucanase, autolysin and trehalase activities during yeast growth and germ-tube formation in Candida albicans. J. Gen. Microbiol. 130, 1227, (1984) Abstract![]()
Merck 14,899
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