Identification | Back Directory | [Name]
Ixazomib citrate (USAN) | [CAS]
1239908-20-3 | [Synonyms]
MLN9708(b) Ixazomib citrat Esazomib citrate Lxazomib Citrate Ixazomib Impurity N Ixazomib Impurity 19 Ixazomib citrate (USAN) Ixazomib citrate(MLN9708) IXAZOMIB CITRATE;MLN 9708;MLN-9708 IXAZOMIB; MLN-9708;MLN9708;MLN 9708 Ixazomib Impurity 23 (Ixazomib Citrate) Ixazomib citrate (USAN)(For R & D only) 2,2'-(2-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)-5-oxo-1,3,2-dioxaborolane-4,4-diyl)diacetic acid 2-[(1R)-1-[[2-[(2,5-Dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-5-oxo-1,3,2-dioxaborolane-4,4-diacetic acid (R)-2,2'-(2-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)-5-oxo-1,3,2-dioxaborolane-4,4-diyl)diacetic acid 1,3,2-Dioxaborolane-4,4-diacetic acid, 2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-5-oxo- 2-[4-(carboxymethyl)-2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-5-oxo-1,3,2-dioxaborolan-4-yl]acetic acid MLN 9708 / Ixazomib citrate / 1,3,2-Dioxaborolane-4,4-diacetic acid, 2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-5-oxo- (R)-2,2'-(2-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)-5-oxo-1,3,2-dioxaborolane-4,4-diyl)diacetic acid compound with 2-hydroxypropane-1,2,3-tricarboxylic acid (1:1) | [Molecular Formula]
C20H23BCl2N2O9 | [MDL Number]
MFCD29767859 | [MOL File]
1239908-20-3.mol | [Molecular Weight]
517.12 |
Chemical Properties | Back Directory | [density ]
1.47±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO:100.0(Max Conc. mg/mL);193.38(Max Conc. mM) Ethanol:100.0(Max Conc. mg/mL);193.38(Max Conc. mM) | [form ]
Solid | [pka]
3.59±0.10(Predicted) | [color ]
White to off-white | [InChIKey]
MBOMYENWWXQSNW-AWEZNQCLSA-N | [SMILES]
O1C(=O)C(CC(O)=O)(CC(O)=O)OB1[C@@H](NC(CNC(=O)C1=CC(Cl)=CC=C1Cl)=O)CC(C)C |
Hazard Information | Back Directory | [Uses]
Ixazomib Citrate is a reversible boronic acid proteasome inhibitor. | [Definition]
ChEBI: A glycine derivative that is the amide obtained by formal condensation of the carboxy group of N-(2,5-dichlorobenzoyl)glycine with the amino group of 2,2'-{2-[(1R)-1-amino-3-methylbutyl]-5-oxo-1,3,2-dioxaborolane-4,4-diy
}diacetic acid. A prodrug for ixazomib that is used in combination therapy for treatment of multiple myeloma. |
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