Semisynthesis of C-ring modified triptolide analogues and their cytotoxic activities

The semisynthesis and SAR study of C-ring modified cytotoxic triptolide analogues were reported. Several C-ring modified analogues of a potent antileukemic diterpene, triptolide ( 1), were synthesized and their structure–activity relationships were studied.

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2006-04, Vol.16 (7), p.1947-1949
Hauptverfasser: Aoyagi, Yutaka, Hitotsuyanagi, Yukio, Hasuda, Tomoyo, Fukaya, Haruhiko, Takeya, Koichi, Aiyama, Ritsuo, Matsuzaki, Takeshi, Hashimoto, Shusuke
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container_end_page 1949
container_issue 7
container_start_page 1947
container_title Bioorganic & medicinal chemistry letters
container_volume 16
creator Aoyagi, Yutaka
Hitotsuyanagi, Yukio
Hasuda, Tomoyo
Fukaya, Haruhiko
Takeya, Koichi
Aiyama, Ritsuo
Matsuzaki, Takeshi
Hashimoto, Shusuke
description The semisynthesis and SAR study of C-ring modified cytotoxic triptolide analogues were reported. Several C-ring modified analogues of a potent antileukemic diterpene, triptolide ( 1), were synthesized and their structure–activity relationships were studied.
doi_str_mv 10.1016/j.bmcl.2005.12.098
format Article
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identifier ISSN: 0960-894X
ispartof Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1947-1949
issn 0960-894X
1464-3405
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Antineoplastic agents
Antitumor
Biological and medical sciences
C-ring
Cell Line, Tumor
Diterpenes - chemical synthesis
Diterpenes - chemistry
Diterpenes - pharmacology
Drug Screening Assays, Antitumor
Epoxy Compounds
General aspects
Humans
Medical sciences
Miscellaneous
Models, Molecular
Pharmacology. Drug treatments
Phenanthrenes - chemical synthesis
Phenanthrenes - chemistry
Phenanthrenes - pharmacology
Semisynthesis
Structure-Activity Relationship
Structure–activity relationships
Triptolide analogues
title Semisynthesis of C-ring modified triptolide analogues and their cytotoxic activities
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