| Literature DB >> 15801825 |
Takashi Tsukamoto1, Pavel Majer, Dilrukshi Vitharana, Chiyou Ni, Bunda Hin, Xi-Chun M Lu, Ajit G Thomas, Krystyna M Wozniak, David C Calvin, Ying Wu, Barbara S Slusher, David Scarpetti, George W Bonneville.
Abstract
Two representative glutamate carboxypeptidase II (GCP II) inhibitors, 2-(hydroxypentafluorophenylmethyl-phosphinoylmethyl)pentanedioic acid 2 and 2-(3-mercaptopropyl)pentanedioic acid 3, were synthesized in high optical purities (>97%ee). The two enantiomers of 2 were prepared from previously reported chiral intermediates, (R)- and (S)-2-(hydroxyphosphinoylmethyl)pentanedioic acid benzyl esters 8. The synthesis of (R)- and (S)-3 involves the hydrolysis of (R)- and (S)-3-(2-oxo-tetrahydro-thiopyran-3-yl)propionic acids, (R)- and (S)-11, the corresponding optically pure thiolactones delivered by chiral chromatographic separation of the racemic 11. GCP II inhibitory assay revealed that (S)-2 is 40-fold more potent than (R)-2. In contrast, both enantiomers of 3 inhibited GCP II with nearly equal potency. The efficacy observed in subsequent animal studies with these enantiomers correlated well with the inhibitory potency in a GCP II assay.Entities:
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Year: 2005 PMID: 15801825 DOI: 10.1021/jm049258g
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446