Weight | 384.245 g/mol |
---|---|
Formula | C19H25BN4O4 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 4 |
Aromatic Rings | 2 |
Rotatable Bonds | 9 |
Bortezomib (179324-69-7)
Score:
#182 in Biochemistry
,
#748 in Biology
,
#817 in Chemistry
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- A phase 2 study of Bortezomib in relapsed, refractory myeloma (The New England Journal of Medicine, 2003)
- Bortezomib or High-Dose Dexamethasone for Relapsed Multiple Myeloma (The New England Journal of Medicine, 2005)
- Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma. (The New England Journal of Medicine, 2008)
- A phase 2 study of two doses of bortezomib in relapsed or refractory myeloma (British Journal of Haematology, 2004)
- Lenalidomide, bortezomib, and dexamethasone combination therapy in patients with newly diagnosed multiple myeloma. (Blood, 2010)
- Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: a randomised, phase 3, non-inferiority study (Lancet Oncology, 2011)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESB(C(CC(C)C)NC(=O)C(CC1=CC=CC=C1)NC(=O)C2=NC=CN=C2)(O)O
-
InChIKeyGXJABQQUPOEUTA-UHFFFAOYSA-N
- Pubchem - Bortezomib
- Wikipedia - bortezomib
Bortezomib (BAN, INN and USAN; marketed as Velcade by Millennium Pharmaceuticals; Neomib by Getwell and Bortecad by Cadila Healthcare) is an anti-cancer drug and the first therapeutic proteasome inhibitor to be used in humans. Proteasomes are cellular complexes that break down proteins. In some cancers, the proteins that normally kill cancer cells are broken down too quickly.
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Synthesis
Pyrazinamide
+
Reactant
(Alkylation of primary amines)
2-Pyrazinecarbonyl chloride
+
Reactant
(Schotten-Baumann amide from acid)
benzene
+
Reactant
(Friedel-Crafts alkylation)
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