ChemicalBook--->CAS DataBase List--->1847461-43-1

1847461-43-1

1847461-43-1 Structure

1847461-43-1 Structure
IdentificationBack Directory
[Name]

TAK-788
[CAS]

1847461-43-1
[Synonyms]

TAK-788
AP 32788
Mobocertinib
Mobocertinib (TAK788)
AP32788, MOBOCERTINIB
Isopropyl 2-((5-acrylamido-4-((2-(dimethylamino)ethyl)(methyl)amino)-2-methoxyphenyl)amino)-4-(1-methyl-1H-indol-3-yl)pyrimidine-5-carboxylate
5-Pyrimidinecarboxylic acid, 2-[[4-[[2-(dimethylamino)ethyl]methylamino]-2-methoxy-5-[(1-oxo-2-propen-1-yl)amino]phenyl]amino]-4-(1-methyl-1H-indol-3-yl)-, 1-methylethyl ester
[Molecular Formula]

C32H39N7O4
[MDL Number]

MFCD32669806
[MOL File]

1847461-43-1.mol
[Molecular Weight]

585.71
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 10 mg/ml,DMF:PBS (pH 7.2) (1:8): 0.11 mg/ml
[form ]

A crystalline solid
Hazard InformationBack Directory
[Uses]

Mobocertinib (TAK-788,1847461-43-1) is an orally active and irreversible EGFR/HER2 inhibitor. Mobocertinib effectively inhibits oncogenic variants containing mutations that activate the EGFRex20ins, with selectivity superior to that of wild-type EGFR. Mobocertinib is FDA-approved for the treatment of patients with non-small cell lung cancer (NSCLC) who have a HER2 mutation or an EGFR mutation, including an exon 20 insertion mutation. Mobocertinib is approved by the FDA for the treatment of patients with non-small cell lung cancer (NSCLC) who have HER2 mutations or EGFR mutations, including exon 20 insertion mutations.
Spectrum DetailBack Directory
[Spectrum Detail]

TAK-788(1847461-43-1)1HNMR
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