Alazopeptin
Title: Alazopeptin
CAS Registry Number: 1397-84-8
Additional Names: L-Alanyl-(6-diazo-5-oxo)-L-norleucyl-(6-diazo-5-oxo)-L-norleucine
Molecular Formula: C15H20N6O5
Molecular Weight: 364.36
Percent Composition: C 49.45%, H 5.53%, N 23.07%, O 21.96%
Literature References: Tumor-inhibiting antibiotic produced by Streptomyces griseoplanus from soil near Williamsburg, Iowa: De Voe et al., Antibiot. Annu. 1956-7, p 730. Peptide consisting of one mole a-alanine and two moles of a C6 diazo keto amino acid oxidizable to glutamic acid: E. L. Patterson et al., Antimicrob. Agents Chemother. 1965, 115-118. Anti-tumor activity: T. Hata et al., J. Antibiot. 26, 181 (1973). Toxicity: J. B. Thiersch, Proc. Soc. Exp. Biol. Med. 97, 888 (1958).
 
Derivative Type: Monohydrate
Properties: Crystals from dilute acetone. Poor stability. Has no definite melting point. [a]D25 +9.5° (c = 4.7 in H2O). uv max (pH 7.0 phosphate buffer): 242, 274 nm (E1%1cm 321, 549). Freely sol in water. Somewhat sol in acetic acid, formamide, DMSO, aq solns of methanol, ethanol, acetone. Practically insol in anhydr alcohols, acetone, ethyl acetate, ether. LD50 i.p. in rats: 150 mg/kg (Thiersch).
Optical Rotation: [a]D25 +9.5° (c = 4.7 in H2O)
Absorption maximum: uv max (pH 7.0 phosphate buffer): 242, 274 nm (E1%1cm 321, 549)
Toxicity data: LD50 i.p. in rats: 150 mg/kg (Thiersch)

Others monographs:
ThalicarpinePentachlorophenolSambucusGold Selenide
CasanthranolClarase®BenzylanilineViolacein
CyfluthrinLanolinTertiapinAmmonium Phosphite
TOACFenbenicillinDiaziquoneCupric Chromate(VI)
©2016 DrugLead US FDA&EMEA