(S)-<wbr/>10-<wbr/>hydroxy-<wbr/>Camptothecin

(S)-10-hydroxy-Camptothecin

CAT N°: 14635
Price:

From 85.00 72.25

DNA topoisomerases relax supercoiled DNA during replication, transcription, recombination, repair, and chromosome condensation. The relaxation of DNA supercoiling by topoisomerase I at single-strand breaks represents a target for anticancer agents to intercalate between DNA base pairs, leading to the activation of apoptotic and cell cycle arrest pathways.{21116} (S)-10-hydroxy-Camptothecin is an inhibitor of topoisomerase I originally isolated from the Chinese tree C. acuminata. It is a member of the camptothecin family that demonstrates less toxicity than its parent compound.{23556} (S)-10-hydroxy-Camptothecin has strong anti-tumor activity against a wide range of experimental tumors including L1210 leukemia cells (IC50 = 1.15 ?M).{23556} In vitro treatment of human HepG2 cells with 5-20 ?M (S)-10-hydroxy-camptothecin results in cell cycle arrest at the G2/M phase.{23557}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (4S)-4-ethyl-4,9-dihydroxy-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • Correlated keywords
    • 104155-90-0 157405-42-0 DNA topoisomerase I anticancers cells cycles arrest antitumors alkaloid DNA-strand breaks DNA damages camptothecin Chinese tree camptotheca acuminate C. anti-tumors tumors anti anti-cancers cancers L1210 leukemia cells in vitro treatments human HepG2 arrest G2/M phases inhibits inhibitions NSCs 107124 NAC107124 NSC-107124 ChEMBL-273862 ChEMBL273862 ChEMBLs 273862 hydroxycamptothecin 10-hydroxycamptothecin C.amptotheca acuminata
  • Product Overview:
    DNA topoisomerases relax supercoiled DNA during replication, transcription, recombination, repair, and chromosome condensation. The relaxation of DNA supercoiling by topoisomerase I at single-strand breaks represents a target for anticancer agents to intercalate between DNA base pairs, leading to the activation of apoptotic and cell cycle arrest pathways.{21116} (S)-10-hydroxy-Camptothecin is an inhibitor of topoisomerase I originally isolated from the Chinese tree C. acuminata. It is a member of the camptothecin family that demonstrates less toxicity than its parent compound.{23556} (S)-10-hydroxy-Camptothecin has strong anti-tumor activity against a wide range of experimental tumors including L1210 leukemia cells (IC50 = 1.15 ?M).{23556} In vitro treatment of human HepG2 cells with 5-20 ?M (S)-10-hydroxy-camptothecin results in cell cycle arrest at the G2/M phase.{23557}

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