N-piperidine Ibrutinib hydrochloride

Modify Date: 2024-01-14 11:07:28

N-piperidine Ibrutinib hydrochloride Structure
N-piperidine Ibrutinib hydrochloride structure
Common Name N-piperidine Ibrutinib hydrochloride
CAS Number 2231747-18-3 Molecular Weight 422.91
Density N/A Boiling Point N/A
Molecular Formula C22H23ClN6O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of N-piperidine Ibrutinib hydrochloride


N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC50s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively[1]. N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC50 of 7.9 nM[2].

 Names

Name N-piperidine Ibrutinib hydrochloride

 N-piperidine Ibrutinib hydrochloride Biological Activity

Description N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC50s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively[1]. N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC50 of 7.9 nM[2].
Related Catalog
Target

IC50: 51.0 nM (WT BTK), 30.7 nM (C481S BTK)[1]

In Vitro N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs. SJF638, SJF678, and SJF608 are potent PROTAC BTK degraders with DC50s of 374, 162, and 8.3 nM, respectively[2].
References

[1]. Buhimschi AD, et al. Targeting the C481S Ibrutinib-Resistance Mutation in Bruton's Tyrosine Kinase Using PROTAC-Mediated Degradation. Biochemistry. 2018 Jul 3;57(26):3564-3575.

[2]. Jaime-Figueroa S, et al. Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic properties. Bioorg Med Chem Lett. 2020 Feb 1;30(3):126877.

 Chemical & Physical Properties

Molecular Formula C22H23ClN6O
Molecular Weight 422.91