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Bizelesin _Molecular_structure_CAS_129655-21-6)
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Bizelesin

Catalog No. B591700 Name Toronto Research Chemicals
CAS Number 129655-21-6 Website http://www.trc-canada.com
M. F. C43H36Cl2N8O5 Telephone +1 (416) 665-9696
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SYNONYMS

IUPAC name
1,3-bis({2-[(1S)-1-(chloromethyl)-5-hydroxy-8-methyl-1H,2H,3H,6H-pyrrolo[3,2-e]indole-3-carbonyl]-1H-indol-5-yl})urea
IUPAC Traditional name
1,3-bis({2-[(1S)-1-(chloromethyl)-5-hydroxy-8-methyl-1H,2H,6H-pyrrolo[3,2-e]indole-3-carbonyl]-1H-indol-5-yl})urea
Synonyms
NSC 615291
(8S,8'S)-6,6'-[Carbonylbis(imino-1H-indole-5,2-diylcarbonyl)]bis[8-(chloromethyl)-3,6,7,8-tetrahydro-1-methylbenzo[1,2-b:4,3-b']dipyrrol-4-ol
U 77779
N,N'-Bis[2-[[(1S)-1-(chloromethyl)-1,6-dihydro-5-hydroxy-8-methylbenzo[1,2-b:4,3-b']dipyrrol-3(2H)-yl]carbonyl]-1H-indol-5-yl]urea

DATABASE IDS

CAS Number 129655-21-6

PROPERTIES

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DETAILS

Description (English)
As members of the cyclopropylpyrroloindole family, Adozelesin and Bizelesin cause genomic DNA lesions by alkylating DNA. Adozelesin induces single-strand DNA lesions, whereas Bizelesin induces both single-strand lesions and double-strand DNA cross-links.

REFERENCES

  • Lee, C., et al.: Cancer Res., 51, 6586 (1991)
  • McHugh, M., et al.: Biochemistry, 38, 11508 (1991)
  • Liu, J., et al.: J. Biol. Chem., 275, 1391 (1991)