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J Nat Prod ; 72(5): 876-83, 2009 May 22.
Article in English | MEDLINE | ID: mdl-20161135

ABSTRACT

A modified synthetic route to combretastatin D-2 (5) was devised in order to further evaluate its biological activity, for its conversion to phosphate prodrugs (25-28), and as a route to obtaining dihydro-combretastatin D-2 (42). A parallel first total synthesis of dihydro-combretastatin D-2 was completed, proceeding from a saturated 3-phenylpropionic ester intermediate via the Ullmann biaryl ether reaction (39-41). In contrast to the cancer cell growth inhibitory activity exhibited by combretastatin D-2, relatively minor structural modifications (41, 42) caused elimination of those properties.


Subject(s)
Antineoplastic Agents, Phytogenic/chemical synthesis , Antineoplastic Agents, Phytogenic/pharmacology , Bibenzyls/chemical synthesis , Bibenzyls/pharmacology , Lactones/chemical synthesis , Lactones/pharmacology , Phenyl Ethers/chemical synthesis , Phenyl Ethers/pharmacology , Prodrugs/chemical synthesis , Prodrugs/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Bibenzyls/chemistry , Crystallography, X-Ray , Drug Design , Drug Screening Assays, Antitumor , Lactones/chemistry , Molecular Structure , Phenyl Ethers/chemistry , Prodrugs/chemistry , Structure-Activity Relationship
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