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Enantiomeric characterization and structure elucidation of Otamixaban 被引量:1
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作者 Jian Shen Jiping Yang +10 位作者 Winfried Heyse Harald Schweitzer Norbert Nagel Doris Andert Chengyue Zhu Vincent Morrison gregory a.nemeth Teng-Man Chen Zhicheng Zhao Timothy A.Ayers Yong-Mi Choi 《Journal of Pharmaceutical Analysis》 SCIE CAS 2014年第3期197-204,共8页
Otamixaban is a potent (Ki=0.5 nM) fXa inhibitor currently in late-stage clinical develop-ment at Sanofi for the management of acute coronary syndrome. Being unproductive in obtaining a suitable crystal of Otamixaba... Otamixaban is a potent (Ki=0.5 nM) fXa inhibitor currently in late-stage clinical develop-ment at Sanofi for the management of acute coronary syndrome. Being unproductive in obtaining a suitable crystal of Otamixaban, the required enantiomeric characterization has been accomplished using vibrational circular dichroism (VCD) spectroscopy. Selected by a spectrum similarity index, the calculated spectra of several higher energy conformers were found to match well with the observed spectra. The characteristic IR bands of these conformers were also identified and attributed to the solvation effect. Combined with both the single crystal x-ray diffraction results for an intermediate and the proton NMR study, the absolute configuration of Otamixaban is unambiguously determined to be (R,R). 展开更多
关键词 Vibrational circular dichroism DFT IR Absolute configuration Vicinal proton-proton COUPLING scXRD
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