ChemicalBook--->CAS DataBase List--->1048007-93-7

1048007-93-7

1048007-93-7 Structure

1048007-93-7 Structure
IdentificationBack Directory
[Name]

AB 1010 Mesylate
[CAS]

1048007-93-7
[Synonyms]

AB1010 Mesylate
AB-1010 Mesylate
Masivet Mesylate
AB 1010 Mesylate
Masitinib (Mesylate)
Masitinib mesylate (AB1010 mesylate
AB1010 MESYLATE;AB-1010 MESYLATE;AB 1010 MESYLATE
AB1010 MESYLATE; MASIVET MESYLATE; AB-1010 MESYLATE; AB 1010 MESYLATE
N-(4-methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide methanesulfonate
Benzamide,4-[(4-methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-thiazolyl]amino]phenyl]-,methanesulfonate
methanesulfonicacid,4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[(4-pyridin-3-yl-1,3-thiazol-2-yl)amino]phenyl]benzamide
[Molecular Formula]

C29H34N6O4S2
[MOL File]

1048007-93-7.mol
[Molecular Weight]

594.748
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: ≥ 30 mg/mL (50.44 mM)
[form ]

Powder
[color ]

White to yellow
[InChIKey]

TXCWBWKVIZGWEQ-UHFFFAOYSA-N
[SMILES]

CS(O)(=O)=O.C(NC1=CC=C(C)C(NC2=NC(C3=CC=CN=C3)=CS2)=C1)(=O)C1=CC=C(CN2CCN(C)CC2)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)Exclamation Mark (GHS07)
GHS08,GHS07
[Signal word ]

Warning
[Hazard statements ]

H361-H302-H351
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P312-P330-P501-P201-P202-P281-P308+P313-P405-P501
Hazard InformationBack Directory
[Uses]

Masitinib is a novel tyrosine kinases inhibitor for Kit and PDGFRα/β with IC50 of 200 nM and 540 nM/800 nM, resectively.
[Uses]

Masitinib Mesylate can be used to treat sickle cell disease.
[Synthesis]

Masitinib

790299-79-5

Methanesulfonic acid

75-75-2

AB 1010 Mesylate

1048007-93-7

Synthesis of N-(4-methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide and methanesulfonic acid as 4-[(4-methyl-1-piperazinyl)methyl]-N-(4-methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamidic acid The general procedure for the sulfonate is as follows: 4-[(4-methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-thiazolyl]amino]phenyl]benzamide (1.0 eq.) was dissolved in ethanol (4.5 v/v), and heated to 65-70°C to dissolve it completely. Under the condition of maintaining the same temperature, methanesulfonic acid (1.0 eq.) was slowly added. Upon completion of the reaction, the mixture was cooled to 25-30 °C and kept at this temperature for 6 hours to promote crystallization. The product was collected by filtration and dried in a vacuum disk dryer at 55-60°C. The yield of this step was 85-90% and the starting melting point of the product was 236°C.

[in vivo]

Masitinib inhibits tumour growth and increases the median survival time in Δ27-expressing Ba/F3 tumor models at 30 mg/kg, without cardiotoxicity or genotoxicity[1].
Masitinib (12.5 mg/kg/d, p.o.) increases overall TTP (time-to-tumor progression) compared with placebo in dogs[3].

[storage]

Store at -20°C
[References]

[1] Patent: WO2008/98949, 2008, A2. Location in patent: Page/Page column 23
Spectrum DetailBack Directory
[Spectrum Detail]

AB 1010 Mesylate(1048007-93-7)1HNMR
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