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. 2013 Sep;41(9):1651–1661. doi: 10.1124/dmd.113.051094

TABLE 3.

Vinorelbine and its CYP3A4 metabolites based on liquid chromatography–MS/MS and NMR data

ID M+H+ MS/MS Product Ions Proposed Metabolite Structure
Vinorelbine 779 719,701,510,469,457,323,122 graphic file with name dmd.113.051094fx1.jpg
M1 795 735,702,646,526,469,457,339,202,138,122 graphic file with name dmd.113.051094fx2.jpg
M2 777 717,686,580,419,321,311 graphic file with name dmd.113.051094fx3.jpg
M3 795 735,717,674,642,510.485,379,323,291,122 graphic file with name dmd.113.051094fx4.jpg
M4 811 526,508,485,473,397,345,323,202 graphic file with name dmd.113.051094fx5.jpg
M5 781 610,455,443,138,122 graphic file with name dmd.113.051094fx6.jpg
M6 795 777,717,633,526,457,403,202,122,108 graphic file with name dmd.113.051094fx7.jpg
M7 763 704,672,566,535,455,423,321 graphic file with name dmd.113.051094fx8.jpg
M8 777 718,717,658,657,467,389 graphic file with name dmd.113.051094fx9.jpg