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plevitrexed An orally bioavailable, small molecule, non-polyglutamatable, antifolate quinazoline derivative thymidine synthetase inhibitor with potential antineoplastic activity. Plevitrexed is transported into the cell via the physiological reduced folate carrier (RFC) system. Intracellularly, this agent selectively binds to the folate binding site of thymidylate synthase and inhibits thymidine synthesis, which may result in DNA synthesis inhibition and apoptosis. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus)
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Code names: | ![](https://webarchive.library.unt.edu/eot2008/20081005091000im_/http://www.nci.nih.gov/images/spacer.gif) | BGC 9331 ZD9331 | | ![](https://webarchive.library.unt.edu/eot2008/20081005091000im_/http://www.nci.nih.gov/images/spacer.gif) | Chemical structure name: | ![](https://webarchive.library.unt.edu/eot2008/20081005091000im_/http://www.nci.nih.gov/images/spacer.gif) | (2S)-2-[[4-[[(2,7-dimethyl-4-oxo-1,4-dihydroquinazolin-6-yl)methy](prop-2-ynyl)amino]-2-fluorobenzoyl]amino]-4-(1H-tetrazol-5-yl)butanoic acid | | ![](https://webarchive.library.unt.edu/eot2008/20081005091000im_/http://www.nci.nih.gov/images/spacer.gif) |
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