RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
| Cat.No. | Product name | Product Description |
| R2101057 | CGS-15943 | CGS15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor |
| R2101058 | NSC177223 | API-1 (NSC 177223) is a potent inhibitor of Akt that induces GSK3-dependent, β-T |
| R2101059 | ML162 | ML162 is a small-molecule probe that selectively kills cells induced to express |
| R2101060 | GSK-843 | GSK-843 (GSK'843) is a potent inhibitor of receptor-interacting protein kinase 3 |
| R2101061 | Imidazenil | Imidazenil is a GABA-A modulator that blocks the sedative effects without loweri |
| R2101062 | FIT-039 | FIT-039 is a potent, selective CDK9 inhibitor with IC50 of 5.8 uM for CKD9/cycli |
| R2101063 | SR8278 | SR8278 is a competitive synthetic antagonist of nuclear heme receptor REV-ERB. S |
| R2101064 | VPC23019 | VPC 23019 is a competitive antagonist at the S1P1 and S1P3 receptors (pKi= 7.86 |
| R2101065 | HS-1793 | HS-1793 is a stable resveratrol analog that protects cardiac against mitochondri |
| R2101066 | Mycro3 | Mycro 3 is a potent and selective inhibitor of c-Myc in whole cell assays. |
| R2101067 | RBC10 | RBC10 is an inhibitor of Ral binding to RALBP1 (the effector). |
| R2101068 | PD089828 | |
| R2101069 | CRANAD-28 | |
| R2101070 | BPU-11 | BPU-11 is a HCN4 CLP ligand. It acts by modulating channel function and complete |
| R2101071 | CE3F4 | CE3F4 is a selective antagonist of exchange protein directly activated by cAMP ( |
| R2101072 | NIBR-0213 | A potent, selective, orally active S1P1 antagonist with IC50 of 2.5 nM Ca2+ mobi |
| R2101073 | BDP5290 | BDP5290 is a potent inhibitor of both ROCK and MRCK(IC50s of 5 nM, 50 nM, 10 nM |
| R2101074 | PH-064 | PH-064 is a heterotrimeric G-protein complex inhibitor. |
| R2101075 | ry785;Kv2-IN-A1 | Kv2-IN-A1 is a Kv2.1 and Kv2.2 inhibitor. |
| R2101076 | DD1 | DD1 is a proteasome inhibitor that induces human myeloid tumor-selective apoptos |
| R2101077 | AEM1 | AEM1 is an inhibitor of deregulated NRF2 transcriptional activity in cancer. |
| R2101078 | SAR405 R enantiomer | SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibi |
| R2101079 | (S)-3,4-DCPG | mGlu8a agonist |
| R2101080 | JCP174 | JCP174 is an inhibitor of a depalmitoylase that enhances Toxoplasma host-cell in |
| R2101081 | SGA360 | SGA360 is a selective modulator of aryl hydrocarbon (Ah) receptor that exhibits |
