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ChemicalBook--->CAS DataBase List--->119577-28-5

119577-28-5

119577-28-5 Structure

119577-28-5 Structure
IdentificationBack Directory
[Name]

7-ETHYL-10-HYDROXYCAMPTOTHECIN,98%
[CAS]

119577-28-5
[Synonyms]

Camptothecin Impurity 7
12-Ethyl-9-hydroxycamptothecin
7-Ethyl-10-hydroxycamptothecin
4,7-Diethyl-10-hydroxycamptothecin
7-ETHYL-10-HYDROXYCAMPTOTHECIN,98%
7-Ethyl-10-hydroxycamptothecin 119577-28-5 For Human Health
(S)-4,7-Diethyl-4,10-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-3,14(4H,12H)-dione
1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4,7-diethyl-4,10-dihydroxy-, (S)- (9CI)
(S)?-4,?7-Diethyl-?4,?10-?dihydroxy-1H-?pyrano[3',?4':6,?7]?indolizino[1,?2-?b]?quinoline-?3,?14(4H,?12H)?-?dione
[Molecular Formula]

C22H20N2O5
[MDL Number]

MFCD06762720
[MOL File]

119577-28-5.mol
[Molecular Weight]

392.4
Chemical PropertiesBack Directory
[Boiling point ]

813.7±65.0 °C(Predicted)
[density ]

1.51±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

9.08±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

12-Ethyl-9-hydroxycamptothecin is a derivative of Camptothecin. Camptothecin (CPT), a kind of alkaloid, is a DNA topoisomerase I (Topo I) inhibitor with an IC50 of 679 nM[1].
[References]

[1] Luzzio MJ, et al. Synthesis and antitumor activity of novel water soluble derivatives of camptothecin as specific inhibitors of topoisomerase I. J Med Chem. 1995;38(3):395-401. DOI:10.1021/jm00003a001
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