1791-26-0 Purity
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Specification
The molecular formula of bortezomib is C19H25BN4O4.
Some synonyms for bortezomib are Velcade, PS-341, and Bortezomib (PS-341).
The molecular weight of bortezomib is 384.2 g/mol.
Bortezomib has a role as an antineoplastic agent, a proteasome inhibitor, a protease inhibitor, and an antiprotozoal drug.
Bortezomib was first synthesized in 1995.
The mechanism of action of bortezomib is as a Proteasome Inhibitor.
Bortezomib became the first anticancer proteasome inhibitor approved by the FDA in May 2003.
Phase I, II, III, and IV clinical trials are ongoing to investigate the therapeutic efficacy of bortezomib in leukemia, myasthenia gravis, systemic lupus erythematosus, rheumatoid arthritis, and solid tumors.
The IUPAC name of bortezomib is [(1R)-3-methyl-1-[[(2S)-3-phenyl-2-(pyrazine-2-carbonylamino)propanoyl]amino]butyl]boronic acid.
The InChIKey of bortezomib is GXJABQQUPOEUTA-RDJZCZTQSA-N.
Reference: [1] Journal of Pharmaceutical Sciences, 2000, vol. 89, # 6, p. 758 - 765
Reference: [1] Journal of Pharmaceutical Sciences, 2000, vol. 89, # 6, p. 758 - 765
* For details of the synthesis route, please refer to the original source to ensure accuracy.