4.7 Article

Design, synthesis, and biological evaluation of new-generation taxoids

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 51, Issue 11, Pages 3203-3221

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm800086e

Keywords

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Funding

  1. NCI NIH HHS [R56 CA055360, R01 CA103314-13A2, R01 CA103314-15, P01 CA028146, R01 CA077263, CA 077263, CA 103314, CA 55360, R01 CA103314, R01 CA055360, R01 CA103314-17, R01 CA083185, CA 083185, CA 73872, R01 CA103314-14, R01 CA103314-16, R37 CA055360] Funding Source: Medline
  2. NIGMS NIH HHS [T32 GM008444, GM 42798] Funding Source: Medline

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Novel second-generation taxoids with systematic modifications at the C2, C10, and C3'N positions were synthesized and their structure-activity relationships studied. A number of these taxoids exhibited exceptionally high potency against multidrug-resistant cell lines, and several taxoids exhibited virtually no difference in potency against the drug-sensitive and drug-resistant cell lines. These exceptionally potent taxoids were termed third-generation taxoids. 19 (SB-T-1214), 14g(SB-T-121303), and 14i (SB-T-1213031) exhibited excellent activity against paclitaxel-resistant ovarian cancer cell lines with mutations in beta-tubulin as well, wherein the drug resistance is mediated by the beta-tubulin mutation. These taxoids were found to possess exceptional activity in promoting tubulin assembly, forming numerous very short microtubules similar to those formed by discodermolide. Taxoids 19 and 14g also showed excellent cytotoxicity against four pancreatic cancer cell lines, expressing three to four multidrug-resistant genes. Moreover, taxoid 19 exhibited excellent in vivo efficacy against highly drug-resistant CFPAC-1 pancreatic as well as DLD-1 human colon tumor xenografts in mice.

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