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7-ETHYL-10-HYDROXYCAMPTOTHECIN,98%

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7-ETHYL-10-HYDROXYCAMPTOTHECIN,98% Basic information

Product Name:
7-ETHYL-10-HYDROXYCAMPTOTHECIN,98%
Synonyms:
  • 7-ETHYL-10-HYDROXYCAMPTOTHECIN,98%
  • (S)-4,7-Diethyl-4,10-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-3,14(4H,12H)-dione
  • 4,7-Diethyl-10-hydroxycamptothecin
  • 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
  • Camptothecin Impurity 7
  • 12-Ethyl-9-hydroxycamptothecin
  • 7-Ethyl-10-hydroxycamptothecin 119577-28-5 For Human Health
CAS:
119577-28-5
MF:
C22H20N2O5
MW:
392.4
Mol File:
119577-28-5.mol
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7-ETHYL-10-HYDROXYCAMPTOTHECIN,98% Chemical Properties

Boiling point:
813.7±65.0 °C(Predicted)
Density 
1.51±0.1 g/cm3(Predicted)
pka
9.08±0.40(Predicted)
form 
Solid
color 
White to off-white
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7-ETHYL-10-HYDROXYCAMPTOTHECIN,98% Usage And Synthesis

Chemical Properties

Yellow crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from the fruit of Camptotheca acuminata.

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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