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124623-00-3

124623-00-3 Structure

124623-00-3 Structure
IdentificationBack Directory
[Name]

1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4,11-diethyl-8-fluoro-4,9-dihydroxy-, (4S)-
[CAS]

124623-00-3
[Synonyms]

1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4,11-diethyl-8-fluoro-4,9-dihydroxy-, (4S)-
[Molecular Formula]

C22H19FN2O5
[MOL File]

124623-00-3.mol
[Molecular Weight]

410.4
Chemical PropertiesBack Directory
[Boiling point ]

795.8±60.0 °C(Predicted)
[density ]

1.55±0.1 g/cm3(Predicted)
[pka]

7.87±0.40(Predicted)
Hazard InformationBack Directory
[Uses]

SN-398 is a derivative of Camptothecin (HY-158230), which is an antitumor drug. Acting by inhibiting mammalian DNA topoisomerase I (Topo I), stabilizing the Topo I-DNA complex prevents DNA rewiring to induce Topo I mediated DNA breaks. In Hela cell tests, SN-398 shows stronger antitumor activity than SN-38 (HY-13704) (IC50=1.562 μM). SN-398 can be used to study the anti-proliferation and growth inhibition of Topo I in cancer cells[1].
[References]

[1] Yoshikawa M, et al. Novel camptothecin analogues that circumvent ABCG2‐associated drug resistance in human tumor cells[J]. International journal of cancer, 2004, 110(6): 921-927. DOI:10.1002/ijc.20216
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