Sigma

Azaserine

A4142 -

≥98% (TLC)

DOWNLOAD MSDS (PDF)

Synonym: O-Diazoacetyl-L-serine

  • 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

Description

Application

Used in cell culture for the selection of HGPRT revertants.

Biochem/physiol Actions

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

Price and Availability

Customers Also Purchased

powder, BioReagent, suitable for cell culture


Documents

Certificate of Analysis

Certificate of Origin

A4142 - Product Information Sheet (26 KB)
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Safety Information

SymbolGHS06GHS08  GHS06, GHS08
Signal wordDanger
Hazard statementsH301-H351
Precautionary statementsP281-P301 + P310
Personal Protective EquipmentEyeshields, 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 CodesT
Risk Statements25-40
Safety Statements53-36/37/39-45
RIDADRUN 3462 6.1/PG 3
WGK Germany3
RTECSVT9625000
Technical information & documentation associated with this product is available in the Safety & Documentation tab.

References

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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