G-744|G 744;G744

Cas No.:	1346669-54-2
Chemical Name:	2-(2-(hydroxymethyl)-3-(1-methyl-6-oxo-5-(pyrimidin-4-ylamino)-1,6-dihydropyridin-3-yl)phenyl)-6,6-dimethyl-3,4,6,7-tetrahydro-2H-cyclopenta[4,5]thieno[2,3-c]pyridin-1(5H)-one
Synonyms:	G 744;G744
SMILES:	C(=O)1N(C2=CC=CC(C3C=C(NC4C=CN=CN=4)C(=O)N(C)C=3)=C2CO)CCC2C3CC(C)(C)CC=3SC1=2
Formula:	C₂₉H₂₉N₅O₃S
M.Wt:	527.643
Purity:	>98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Description:

G-744 is a highly potent, selective inhibitor of BTK with biochemical Ki of 1.28 nM; demonstrates >1,000-fold selectivity against a panel 285 kinase (exception with EphA7 and Fgr, 400-800 fold); prevents BCR-mediated CD86 induction (EC50=64 nM), also inhibits BCR-stimulated B-cell proliferation in human B-cells (EC50=22 nM), abrogates production of TNFα in human monocytes (EC50=33 nM); demonstrates efficacy in the developing CIA model in rats.

Cat. No.	Product name	Field of application
DC47719	BTK inhibitor 19	BTK inhibitor 19 is a highly selective, covalent BTK inhibitor (IC50 = 2.7 nM).
DC46928	TL-895	TL-895 is a potent, orally active, ATP-competitive, and highly selective irreversible BTK inhibitor with an IC50 and a Ki of 1.5 nM and 11.9 nM, respectively. TL-895 is used be for JAKi-relapsed/refractory myelofibrosis, acute myeloid leukemia, COVID-19 and cancer research.
DC46051	Zanubrutinib D5	Zanubrutinib D5 (BGB-3111 D5) is deuterium labeled Zanubrutinib. Zanubrutinib is a selective Bruton tyrosine kinase (Btk) inhibitor.
DC45785	Elsubrutinib	Elsubrutinib (ABBV-105) is an orally active, potent, selective and irreversible Bruton's tyrosine kinase (BTK) inhibitor。The IC50 of Elsubrutinib for BTK catalytic domain is 0.18 μM. Elsubrutinib can be used for the research of inflammatory disease.
DC44005	BTK inhibitor 17	BTK inhibitor 17 is a potent and orally active irreversible BTK inhibitor with an IC50 of 2.1 nM. BTK inhibitor 17 can be used for rheumatoid arthritis research.
DC42422	IBT6A hydrochloride	IBT6A hydrochloride is an impurity of Ibrutinib. IBT6A can be used in synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a selective, irreversible Btk with an IC50 of 0.5 nM.
DC42421	IBT6A	IBT6A is an impurity of Ibrutinib. IBT6A can be used in synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a selective, irreversible Btk with an IC50 of 0.5 nM.
DC41149	Ibrutinib deacryloylpiperidine	Ibrutinib deacryloylpiperidine (IBT4A) is an impurity of Ibrutinib. Ibrutinib is a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM.
DC41102	Acalabrutinib D4	Acalabrutinib D4 (ACP-196 D4) is a deuterium labeled Acalabrutinib. Acalabrutinib (ACP-196) is an orally active, irreversible, and highly selective second-generation BTK inhibitor.
DC11776	G-744	G-744 is a highly potent, selective inhibitor of BTK with biochemical Ki of 1.28 nM.