Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 20641 | KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) | 2082765-42-0 | ≧98.0% | _2082765-42-0.png) |
| KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) is a small molecule inhibitor of protein | ||||
| 20493 | KDM5-C49 | 1596348-16-1 | 98% Min. |  |
| KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49 | ||||
| 20472 | KSQ-4279 | 2446480-97-1 | 98% Min. |  |
| KSQ-4279 is a USP1 and PARP inhibitor. KSQ-4279 showed anti-proliferative effects in | ||||
| L20334 | KY19382 | 2226664-93-1 | 98% Min. |  |
| KY19382 is an orally active dual inhibitor of CXXC5-DVL and GSK3β | ||||
| 20277 | KPI-10 | 888032-58-4 | 98% Min. |  |
| KPI-10 is a new compound currently being studied for its efficacy in the treatment of | ||||
| 21246 | KUN56321 | 1771756-32-1 | 98% Min. |  |
| KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f | ||||
| 20122101 | KO-947 | 1695533-89-1 | 98% Min. |  |
| KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94 | ||||
| 2061304 | KY-226 | 98% Min. |  | |
| KY-226 is a protein tyrosine phosphatase 1B (PTP1B) inhibitor that protects neurons f | ||||
| 193203 | Kinesore | 363571-83-9 | >98% |  |
| Kinesore is an activator of the function of kinesin-1 in controlling microtubule dyna | ||||
| 19362 | KH7 | 330676-02-3 | >98% |  |
| KH7 is a novel Inhibitor of Soluble Adenylyl Cyclase (Sac). | ||||
| 192152 | KINK-1 | 600734-06-3 | >98% |  |
| KINK-1 is an inhibitor of IKKß, blocking NF-kappaB activation. | ||||
| 191281 | KHS101 HCl | 1784282-12-7 | >98% |  |
| KHS101 HCl is an inhibitor of transforming acidic coiled-coil protein 3 (TACC3). It a | ||||
| 19123 | KU59403 | 845932-30-1 | >98% |  |
| KU59403 is a potent and selective ATM (Ataxia telangiectasia mutated) inhibitor with | ||||
| 1810294 | KC01 | 1646795-59-6 | >98% |  |
| KC01 is a covalent inhibitor of ABHD16A. ABHD16A is a phosphatidylserine (PS) lipase | ||||
| 1810226 | KG-501 | 18228-17-6 | >98% |  |
| KG-501 is a cAMP response element-binding protein (CREB) inhibitor. | ||||
| 187124 | KYP-2047 | 796874-99-2 | >98% |  |
| KYP-2047 is a very potent, selective inhibitor of Prolyl oligopeptidase (POP), also k | ||||
| 3291806 | KGP-94 | 1131456-28-4 | >98% |  |
| KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L. | ||||
| 184121 | KIN-1148 | 1428729-56-9 | >98% |  |
| KIN-1148 is a IRF3 agonist. KIN1148 induced dose-dependent IRF3 nuclear translocation | ||||
| 184217 | KKL-10 | 952849-76-2 | >98% |  |
| KKL-10 is an antimicrobial agent. KKL-10 exhibited exceptional antimicrobial activity | ||||
| 1710132 | KI-696 | 1799974-70-1 | >98% |  |
| KI-696 represents an excellent LMW tool to study the KEAP1-NRF2 interaction in vivo. | ||||
| 20178211 | KAF-156 | 1261113-96-5 | 98% |  |
| KAF-156. aslo known as GNF-156, is an antimalarials potentially for treatment of Mala | ||||
| 17031301 | KM11060 | 774549-97-2 | 98% |  |
| KM11060 is a mutated F508del cystic fibrosis transmembrane conductance regulator (CFT | ||||
| 17031014 | KRIBB11 | 342639-96-7 | 98% | |
| KRIBB11 abolishes the heat shock-induced luciferase activity with an IC50 of 1.2 M. I | ||||
| 17022703 | Ki8751 | 228559-41-9 | 98% |  |
| Ki8751 is a potent, selective inhibitor of VEGFR-2 tyrosine kinase (IC50 = 0.9 nM). D | ||||
| 16123029 | KN-93 phosphate | 1188890-41-6 | 98% |  |
| KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2 | ||||
| 16123028 | K-7174 | 191089-59-5 | 98% |  |
| K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel | ||||
| 16122827 | KC7F2 | 927822-86-4 | 98% |  |
| KC7F2 is a potent HIF-1 pathway inhibitor with potential anticancer activity. KC7F2 i | ||||
| 16122826 | KB-R7943 mesylate | 182004-65-5 | 98% |  |
| KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang | ||||
| 16122824 | K-858 | 72926-24-0 | 98% |  |
| K-858 is a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell d | ||||
| 16122711 | Kenpaullone | 142273-20-9 | 98% |  |
| Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al | ||||