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10 results for "BTK" in Products

BTK Products

Bruton tyrosine kinase (Btk) is a 75 kDa cytoplasmic protein tyrosine kinase that is widely expressed in hematopoietic cells. Btk is required for B cell receptor signaling and B cell development. Defects in Btk result in X-linked agammaglobulinemia which is characterized by a severely decreased level of circulating antibodies. Like other Tec family kinases, Btk contains a Pleckstrin homology domain, a Tec homology domain, an SH3 domain, an SH2 domain, and a protein kinase domain. Association of ...

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Highly potent pan-Src/Bcr-Abl inhibitor

Alternate Names:
BMS-354825
Chemical Name:
N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamide
Purity:
≥98%
Highly potent pan-Src/Bcr-Abl inhibitor

Potent, selective BTK inhibitor

Chemical Name:
2-Cyano-N-(2,5-dibromophenyl)-3-hydroxy-2-butenamide
Purity:
≥98%
Potent, selective BTK inhibitor

Potent and selective BTK inhibitor

Chemical Name:
1-[(3R)-3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-piperidinyl]-2-propen-1-one
Purity:
≥98%
Potent and selective BTK inhibitor

Potent and selective BTK Degrader (PROTAC®)

Chemical Name:
4-(1,1-Dimethylethyl)-N-[3-[6-[[4-[[4-[6-[[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]acetyl]amino]hexyl]-1-piperazinyl]carbonyl]phenyl]amino]-4,5-dihydro-4-methyl-5-oxo-2-pyrazinyl]-2-methylphenyl]benzamide
Purity:
≥98%
Potent and selective BTK Degrader (PROTAC®)

Potent ITK inhibitor; also inhibits BTK

Chemical Name:
(R)-3-(1-(1-Acryloylpiperidin-3-yl)-4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-N-(3-methyl-4-(1-methylethyl))benzamide
Purity:
≥95%
Potent ITK inhibitor; also inhibits BTK

Potent BTK inhibitor

Chemical Name:
1-Cyclopentyl-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
Purity:
≥98%
Potent BTK inhibitor

Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk

Chemical Name:
3-[[2-[3-(4-Morpholinylmethyl)phenyl]thieno[3,2-b]pyridin-7-yl]amino]phenol dihydrochloride
Purity:
≥98%
Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk

Potent, reversible BTK inhibitor

Chemical Name:
N-[3-[4,5-Dihydro-4-methyl-6-[[4-(4-morpholinylcarbonyl)phenyl]amino]-5-oxo-2-pyrazinyl]-2-methylphenyl]-4-(1,1-dimethylethyl)benzamide
Purity:
≥97%
Potent, reversible BTK inhibitor

Potent and selective BTK Degrader (PROTAC®)

Chemical Name:
3-[[4-[1-[[1-[6-[[[(3S)-2,6-Dioxo-3-piperidinyl]amino]carbonyl]-3-pyridinyl]-4-piperidinyl]methyl]-4-piperidinyl]phenyl]amino]-5-[(3R)-3-(3-methyl-2-oxo-1-imidazolidinyl)-1-piperidinyl]-2-pyrazinecarboxamide
Purity:
≥98%
Selective BTK Degrader

Potent, reversible BTK inhibitor

Chemical Name:
N-[3-[4,5-Dihydro-4-methyl-6-[[4-(4-morpholinylcarbonyl)phenyl]amino]-5-oxo-2-pyrazinyl]-2-methylphenyl]-4-(1,1-dimethylethyl)benzamide
Purity:
≥97%
Potent, reversible BTK inhibitor
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