Ombrabulin | |
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(2S)-2-Amino-3-hydroxy-N-[2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl]propanamide |
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Other names
AVE-8062; AVE-8062A; AC7700; CS-39-L-Ser.HCl |
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Identifiers | |
CAS number | 181816-48-8 , 253426-24-3 (HCl) |
PubChem | 6918405, 6918404 (HCl) |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C21H26N2O6 |
Molar mass | 402.44 g mol−1 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Ombrabulin is an experimental drug candidate discovered by Ajinomoto and under development by Sanofi-Aventis.[1] It is currently in Phase III clinical trials for the treatment of advanced-stage soft-tissue sarcoma.[1]
Ombrabulin was granted orphan drug status by the European Medicines Agency in April 2011.[2]
Ombrabulin is a combretastatin A-4 derivative that exerts its antitumor effect by disrupting the formation of blood vessels needed for tumor growth.[3][4]