5 results for "CDK5 Subfamily Inhibitors" in 产品
CDK5 Subfamily Inhibitors
The CDK5 subfamily of cyclin-dependent kinases includes CDK5, CDK14, CDK15, CDK16, CDK17 and CDK18. CDK16, CDK17 and CDK18 have a PCTAIRE sequence in the C-terminal helix and bind cyclin Y.
CDK5
CDK5, also known as neuronal CDC2-like kinase (NCLK), was first identified as a result of structural similarities to CDK1, however its activators are non-cyclin proteins CDK5R1 (p35) and CDK5R2 (p39). Due to the selective expression of p35 and p39, CDK5 activity is restricted to terminally ...
Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members
| Chemical Name: | N-[1-[[3-[[(2E)-4-(Dimethylamino)-1-oxo-2-buten-1-yl]amino]phenyl]sulfonyl]-4-piperidinyl]-4-[(2,4,6- trichlorobenzoyl)amino]-1H-pyrazole-3-carboxamide |
| Purity: | ≥98% |
Potent CDK14 and CDK16 inhibitor; displays reversible inhibition of CDK14
| Chemical Name: | N-(1-((3-(4-(Dimethylamino)butanamido)phenyl)sulfonyl)piperidin-4-yl)-4-(2,4,6-trichlorobenzamido)-1H-pyrazole-3-carboxamide |
| Purity: | ≥98% |
Potent and selective B-Raf, CDK16 and NEK9 inhibitor; anticancer; also targets human proteins in the SARS-CoV-2 interactome
| Chemical Name: | N-[3-[5-(2-Aminopyrimidin-4-yl)-2-tert-butyl-1,3-thiazol-4-yl]-2-fluorophenyl]-2,6-difluorobenzenesulfonamide methanesulfonate |
| Purity: | ≥98% |
Potent and selective inhibitor of CDK2, CDK5, CDK1 and CDK9
| Alternate Names: | SCH 727965 |
| Chemical Name: | (2S)-1-[3-Ethyl-7-[[(1-oxido-3-pyridinyl)methyl]amino]pyrazolo[1,5-a]pyrimidin-5-yl]-2-piperidineethanol |
| Purity: | ≥98% |
Potent and selective CDKL5 inhibitor
| Chemical Name: | N-[5-[(5-Propan-2-yl-1,3-oxazol-2-yl)methylsulfanyl]-1,3-thiazol-2-yl]piperidine-4-carboxamide trifluoroacetate |
| Purity: | ≥98% |
