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Capomycin

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Capomycin
Names
IUPAC name anthracen-9-yl)-4-hydroxy-2-methyloxan-3-yl] (2E,4E)-deca-2,4-dienoate
Other names
  • Capoamycin
  • Antibiotic AC 54
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
RTECS number
  • HD3510800
InChI
  • InChI=1S/C35H38O10/c1-4-5-6-7-8-9-10-11-27(38)45-33-20(3)44-25(17-24(33)36)21-12-13-22-28(30(21)39)31(40)23-14-15-34(42)18-19(2)16-26(37)35(34,43)29(23)32(22)41/h8-16,20,24-25,33,36,39,42-43H,4-7,17-18H2,1-3H3/b9-8+,11-10+Key: MCNOFFKXBMHLAD-BNFZFUHLSA-N
SMILES
  • CCCCC/C=C/C=C/C(=O)OC1C(OC(CC1O)C2=C(C3=C(C=C2)C(=O)C4=C(C3=O)C=CC5(C4(C(=O)C=C(C5)C)O)O)O)C
Properties
Chemical formula C35H38O10
Molar mass 618.679 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Capomycin is an antitumor antibiotic with the molecular formula C35H38O10 which is produced by the bacterium Streptomyces capoamus.

References

  1. Hayakawa, Yoichi; Iwakiri, Takafumi; Imamura, Kanji; Seto, Haruo; Otake, Noboru (1985). "Studies on the isotetracenone antibiotics. I. Capoamycin, a new antitumor antibiotic". The Journal of Antibiotics. 38 (7): 957–959. doi:10.7164/antibiotics.38.957. PMID 3839783.
  2. Martins, Cristiane Soares; Souto-Maior, Ana Maria (June 2003). "Anthracycline production by Streptomyces capoamus in batch fermentation". Brazilian Archives of Biology and Technology. 46 (3): 483–488. doi:10.1590/S1516-89132003000300021. ISSN 1516-8913.
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