MLN9708
MLN9708 Basic information
- Product Name:
- MLN9708
- Synonyms:
-
- 4-(carboxymethyl)-2-((R)-1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)-6-oxo-1,3,2-dioxaborinane-4-carboxylic acid
- MLN9708
- MLN9708,MLN-9708,MLN 9708
- 4-Carboxy-2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-6-oxo-1,3,2-dioxaborinane-4-acetic acid
- 4-Carboxy-2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-6-oxo-1,3,2-dioxaborinane-4-acetic acid MLN9708
- Ixazomib Citrate
- 4-(carboxymethyl)-2-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)-6-oxo-1,3,2-dioxaborinane-4-carboxylic acid
- MLN 9708 - Ixazomib citrate
- CAS:
- 1201902-80-8
- MF:
- C20H23BCl2N2O9
- MW:
- 517.12
- Product Categories:
-
- Inhibitors
- Inhibitor
- Apis
- Mol File:
- 1201902-80-8.mol
MLN9708 Chemical Properties
- Melting point:
- >227°C (dec.)
- Density
- 1.47
- storage temp.
- Hygroscopic, -20°C Freezer, Under inert atmosphere
- solubility
- DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
- pka
- 1.92±0.20(Predicted)
- form
- Solid
- color
- White to Off-White
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29329990
MLN9708 Usage And Synthesis
Description
Ixazomib citrate is a proteasome inhibitor prodrug for the treatment of multiple myeloma in patients who have received at least one prior therapy in combination with lenalidomide and dexamethasone. The drug was developed by Takeda and reversibly inhibits the protein proteasome subunit β type-5, which is part of the 20S proteasome complex. Ixazomib citrate (XXIV) is hydrolyzed quickly in vivo to give the biologically active compound ixazomib, which presumably is the corresponding boronic acid variant of XXIV.
Uses
MLN-9708 is a novel proteasome?inhibitor.
Clinical Use
Highly selective and reversible proteasome inhibitor:
Treatment of multiple myeloma in combination with
lenalidomide and dexamethasone
Synthesis
The structure of ixazomib citrate is particularly interesting in that it is one of the relatively few marketed drugs which feature a boron atom within its structure (others of note being the oncology medication bortezomib and the antifungal drug tavaborole13). The ostensible scale synthetic approach began with reaction of commercial 2,5-dichlorobenzoyl chloride (188) with glycine in aqueous NaOH to furnish amide 189 in 97% yield as a white crystalline solid. Acid 189 was then coupled with commercially available 1,3,2-benzodioxaborolane 190 in the presence of TBTU and DIPEA in DMF at low temperature to give diamide 191, which was used without purification for the next step. Borane 191 was then deprotected with (2-methylpropyl)boronic acid in methanolic HCl to provide trimer 192 in 74% as a white solid. Finally, boroxin 192 was reacted with citric acid in EtOAc to dissociate the trimer, resulting in ixazomib citrate (XXIV) in 88% yield as a crystalline solid.
MLN9708Supplier
- Tel
- sales@boylechem.com
- Tel
- 0512-58900862 400-0707518
- sales@alabiochem.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- 025-58741518; 18013018875
- sales@vcarepharmatech.com
- Tel
- +86 (531) 88811783
- sales@trio-pharmatech.com (International market)
MLN9708(1201902-80-8)Related Product Information
- Pevonedistat
- MLN-4760
- MLN-8237
- Ixazomib Impurity 1
- Ixazomib citrate (USAN)
- Acetamide, 2-amino-N-[(1R)-1-[(3aS,4S,6S,7aR)-hexahydro-3a,5,5-trimethyl-4,6-methano-1,3,2-benzodioxaborol-2-yl]-3-methylbutyl]-
- NS-398
- Acid resistant proteinase
- CANGRELOR
- Azilsartan
- Tigecycline
- Pazopanib
- Boric acid
- Bortezomib
- (R)-1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutylboronic acid
- Oprozomib
- CEP-18770
- ABT 263