ACP-5862 4420 InChi: InChI=1S/C31H20ClN5OS/c1-19-34-35-28-18-33-29(24-13-4-6-14-26(24)32)25-17-20(39-31(25)37(19)28)9-8-16-36-27-15-7-5-11-22(27)21-10-2-3-12-23(21)30(36)38/h2-7

InChi: InChI=1S/C31H20ClN5OS/c1-19-34-35-28-18-33-29(24-13-4-6-14-26(24)32)25-17-20(39-31(25)37(19)28)9-8-16-36-27-15-7-5-11-22(27)21-10-2-3-12-23(21)30(36)38/h2-7

With cyclin

GSK269962A completely abolished the actin stress fiber formation induced by angiotensin II in human smooth muscles

35)/t26-/m1/s1

InChi: InChI=1S/C28H32F2N2O/c29-26-12-8-24(9-13-26)28(25-10-14-27(30)15-11-25)33-22-21-32-19-17-31(18-20-32)16-4-7-23-5-2-1-3-6-23/h1-3

ACP-5862 4420 InChi: InChI=1S/C31H20ClN5OS/c1-19-34-35-28-18-33-29(24-13-4-6-14-26(24)32)25-17-20(39-31(25)37(19)28)9-8-16-36-27-15-7-5-11-22(27)21-10-2-3-12-23(21)30(36)38/h2-7ACP 5862 is a major active, circulating, pyrrolidine ring opened metabolite of Acalabrutinib with an IC50 of 5. 0 nM for Bruton tyrosine kinase (BTK). ACP5862 is a weak timedependent inactivator of CYP3A4 and CYP2C8. Acalabrutinib is an orally active, irreversible, and highly selective BTK inhibitor, with an IC50 of 3 nM and EC50 of 8 nM. Product information CAS Number: 2230757 47 6 Molecular Weight: 481. 51 Formula: C26H23N7O3 Chemical Name: 4 {8