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Details

Stereochemistry ACHIRAL
Molecular Formula C28H30N6OS.CH4O3S
Molecular Weight 594.748
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MASITINIB MESYLATE

SMILES

CS(O)(=O)=O.CN1CCN(CC2=CC=C(C=C2)C(=O)NC3=CC=C(C)C(NC4=NC(=CS4)C5=CN=CC=C5)=C3)CC1

InChI

InChIKey=TXCWBWKVIZGWEQ-UHFFFAOYSA-N
InChI=1S/C28H30N6OS.CH4O3S/c1-20-5-10-24(16-25(20)31-28-32-26(19-36-28)23-4-3-11-29-17-23)30-27(35)22-8-6-21(7-9-22)18-34-14-12-33(2)13-15-34;1-5(2,3)4/h3-11,16-17,19H,12-15,18H2,1-2H3,(H,30,35)(H,31,32);1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula C28H30N6OS
Molecular Weight 498.642
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Masitinib is a new orally administered tyrosine kinase inhibitor that targets mast cells and macrophages, important cells for immunity, through inhibiting a limited number of kinases. Based on its unique mechanism of action, masitinib can be developed in a large number of conditions in oncology, in inflammatory diseases, and in certain diseases of the central nervous system. In oncology due to its immunotherapy effect, masitinib can have an effect on survival, alone or in combination with chemotherapy. Through its activity on mast cells and consequently the inhibition of the activation of the inflammatory process, masitinib can have an effect on the symptoms associated with some inflammatory and central nervous system diseases and the degeneration of these diseases. AB Science is developing masitinib in multiple sclerosis and alzheimer's disease. Masitinib targets kinases, including c-Kit, PDGFR, and Lyn. It is used in the treatment of mast cell tumors in animals, specifically dogs. Since its introduction in November 2008 it has been distributed under the commercial name Masivet. It has been available in Europe since the second part of 2009. In the USA it is distributed under the name Kinavet.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Masivet

Approved Use

Treatment of non-resectable dog mast cell tumours (Grade 2 or 3) with confirmed mutated c-kit tyrosine kinase receptor.

Launch Date

2008
PubMed

PubMed

TitleDatePubMed
Pharmacokinetics of masitinib in cats.
2009 Dec
Masitinib (AB1010), a potent and selective tyrosine kinase inhibitor targeting KIT.
2009 Sep 30
[New drugs for small animals in 2009].
2010
Churg and Strauss vasculitis in the course of masitinib treatment: a first report.
2010 Aug
Masitinib for the treatment of systemic and cutaneous mastocytosis with handicap: a phase 2a study.
2010 Dec
Masitinib combined with standard gemcitabine chemotherapy: in vitro and in vivo studies in human pancreatic tumour cell lines and ectopic mouse model.
2010 Mar 4
Evaluation of 12- and 24-month survival rates after treatment with masitinib in dogs with nonresectable mast cell tumors.
2010 Nov
Comprehensive analysis of kinase inhibitor selectivity.
2011 Oct 30
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery.
2013 Apr 15
Patents

Sample Use Guides

6 mg/kg/day
Route of Administration: Oral
In Ba/F3 cells expressing human wild-type Kit, Masitinib inhibits SCF (stem cell factor)-induced cell proliferation with an IC50 of 150 nM, while the IC50 for inhibition of IL-3-stimulated proliferation is at approximately >10 µM. In Ba/F3 cells expressing PDGFRα, Masitinib inhibits PDGF-BB-stimulated proliferation and PDGFRα tyrosine phosphorylation with IC50 of 300 nM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:20:56 GMT 2023
Edited
by admin
on Fri Dec 15 17:20:56 GMT 2023
Record UNII
ZK89EG3A18
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MASITINIB MESYLATE
Common Name English
4-((4-METHYLPIPERAZIN-1-YL)METHYL)-N-(4-METHYL-3-((4-PYRIDIN-3-YL-1,3-THIAZOL-2-YL)AMINO)PHENYL)BENZAMIDE METHANESULPHONATE
Systematic Name English
MASITINIB MESILATE
WHO-DD  
Common Name English
4-((4-METHYLPIPERAZIN-1-YL)METHYL)-N-(4-METHYL-3-((4-PYRIDIN-3-YL-1,3-THIAZOL-2-YL)AMINO)PHENYL)BENZAMIDE METHANESULFONATE
Systematic Name English
Masitinib mesilate [WHO-DD]
Common Name English
BENZAMIDE, 4-((4-METHYL-1-PIPERAZINYL)METHYL)-N-(4-METHYL-3-((4-(3-PYRIDINYL)-2-THIAZOLYL)AMINO)PHENYL)-, METHANESULFONATE (1:1)
Systematic Name English
AB-1010
Code English
BENZAMIDE, 4-((4-METHYL-1-PIPERAZINYL)METHYL)-N-(4-METHYL-3-((4-(3-PYRIDINYL)-2-THIAZOLYL)AMINO)PHENYL)-, METHANESULPHONATE (1:1)
Systematic Name English
MASIVIERA
Brand Name English
MASITINIB METHANESULFONATE [MI]
Common Name English
AB1010
Code English
MASIVET
Brand Name English
MASITINIB MESYLATE [EMA EPAR VETERINARY]
Common Name English
MASICAN
Brand Name English
MASITINIB MESYLATE [GREEN BOOK]
Common Name English
Classification Tree Code System Code
EMA ASSESSMENT REPORTS MASICAN (REFUSED: GASTROINTESTINAL STROMAL TUMORS)
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
FDA ORPHAN DRUG 490815
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
EMA ASSESSMENT REPORTS MASIVIERA (REFUSED: PANCREATIC NEOPLASMS)
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
NCI_THESAURUS C1967
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
EU-Orphan Drug EU/3/16/1722
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
FDA ORPHAN DRUG 469415
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
NCI_THESAURUS C129825
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
Code System Code Type Description
EVMPD
SUB32266
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
FDA UNII
ZK89EG3A18
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
CHEBI
63450
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
SMS_ID
100000151886
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
EVMPD
SUB126308
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID70146747
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
NCI_THESAURUS
C79831
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
MERCK INDEX
m7092
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY Merck Index
EMA VETERINARY ASSESSMENT REPORTS
MASIVET [AUTHORIZED]
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY DOGS
PUBCHEM
25024769
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
CAS
1048007-93-7
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
DRUG BANK
DBSALT001689
Created by admin on Fri Dec 15 17:20:56 GMT 2023 , Edited by admin on Fri Dec 15 17:20:56 GMT 2023
PRIMARY
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ACTIVE MOIETY