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2230757-47-6

2230757-47-6 Structure

2230757-47-6 Structure
IdentificationBack Directory
[Name]

Acalabrutinib Metabolite 27
[CAS]

2230757-47-6
[Synonyms]

ACP-5862
Acalabrutinib Impurity 1
Acalabrutinib Metabolite 27
Acalabrutinib?active?metabolite?M27
Acalabrutinib Metabolite 27 (ACP-5862)
Acalabrutinib Metabolite 27 (Acalabrutinib Impurity 1)
4-(8-Amino-3-(4-(but-2-ynamido)butanoyl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide
4-[8-amino-3-[1-oxo-4-[(1-oxo-2-butyn-1-yl)amino]butyl]imidazo[1,5-a]pyrazin-1-yl]-N-2-pyridinyl-Benzamide
Benzamide, 4-[8-amino-3-[1-oxo-4-[(1-oxo-2-butyn-1-yl)amino]butyl]imidazo[1,5-a]pyrazin-1-yl]-N-2-pyridinyl-
Acalabrutinib Metabolite (M27) ACP-5862 D4Q: What is Acalabrutinib Metabolite (M27) ACP-5862 D4 Q: What is the CAS Number of Acalabrutinib Metabolite (M27) ACP-5862 D4
[Molecular Formula]

C26H23N7O3
[MDL Number]

MFCD32693908
[MOL File]

2230757-47-6.mol
[Molecular Weight]

481.51
Chemical PropertiesBack Directory
[density ]

1.34±0.1 g/cm3(Predicted)
[pka]

11.35±0.70(Predicted)
Hazard InformationBack Directory
[Uses]

4-[8-Amino-3-[1-oxo-4-[(1-oxo-2-butyn-1-yl)amino]butyl]imidazo[1,5-a]pyrazin-1-yl]-N-2-pyridinyl-benzamide is a metabolite of Acalabrutinib (A115605) which is an experimental anti-cancer drug and a selective Bruton''s tyrosine kinase (BTK) inhibitor. This kinase transmits signals from B-cell Receptor (BCR), and thus any genetic BTK mutation causes B-Cell immunodeficiency. Therefore, BTK inhibitors targeting B-cell signaling has shown great promise for the treatment of chronic lymphocytic leukemia (CLL).
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