Acalabrutinib
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File:Acalabrutinib.svg | |
Systematic (IUPAC) name | |
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4-{8-Amino-3-[(2S)-1-(2-butynoyl)-2-pyrrolidinyl]imidazo[1,5-a]pyrazin-1-yl}-N-(2-pyridinyl)benzamide
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Identifiers | |
CAS Number | 1420477-60-6 |
ChemSpider | 36764951 |
Chemical data | |
Formula | C26H23N7O2 |
Molecular mass | 465.507 g/mol |
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Acalabrutinib (rINN,[1] ACP-196) is an experimental anti-cancer drug and a 2nd generation BTK inhibitor[2] developed by Acerta Pharma.[3]
It is designed to be more selective (fewer side-effects) than ibrutinib.[2]
As of 2015[update] it is in late stage clinical trials for relapsed chronic lymphocytic leukemia. Interim results are encouraging : 95% overall response rate.[2][4]
It is also in another 20 clinical trials (alone and in combination) for various cancers.[4][5]
References
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- ↑ 2.0 2.1 2.2 Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ 4.0 4.1 Acerta Pharma Announces Study Published in New England Journal of Medicine Demonstrates Acalabrutinib (ACP-196) Shows Marked Activity in Relapsed Chronic Lymphocytic Leukemia
- ↑ 21 studies found for: ACP-196
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