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Home > Products
| Cat.No. | Product name | Product Description |
| R21082453 | TPRC3 Channel Inhibitor III, Pyr10 | Pyr10 is a novel selective inhibitor of TRPC3. It acts on HEK293 cells transfect |
| R21082454 | Cysteine thiol probe | Cysteine Thiol Probe is a thiol-based Probe designed to label electrophilic natu |
| R21082455 | IM156 | IM156, a metformin derivative, is a potent activator of AMPK that increases AMPK |
| R21082456 | DGY-06-116 | Dodgy 06-116 is an irreversible covalent selective Src inhibitor. |
| R21082457 | CPD3616 | Jbj-04-125-02 is a potent, selectively mutated, allosteric, and orally active EG |
| R21082458 | ULK-101 | ULK-101 is a potent and selective ULK1 inhibitor with in vitro IC50 of 8.3 nM. |
| R21082459 | DS-6051B | Taletrectinib (DS-6051B) Free Base is a new generation selective ROS1/NTRK inhib |
| R21082460 | Elenbecestat(E2609) | Elenbecestat (E2609) is a novel and highly effective β -secretase 1 (BACE-1) inh |
| R21082461 | JHU-083 | Jhu-083 selectively blocks glutaminase activity in CD11b+ cells in the brain. T |
| R21082462 | SR-4835 | SR-4835 is a highly selective dual inhibitor of CDK12 and CDK13. |
| R21082463 | ASP4132 | ASP4132 is an orally active, potent AMPK activator with an EC50 of 18 nM. ASP41 |
| R21082464 | MYCI975 | MYCi975 (NUCC-0200975) is an orally active MYC inhibitor that disrupts the MYC/M |
| R21082465 | MYCI361 | MYCi361 (NUCC-0196361) is a MYC inhibitor with a Kd of 3.2 μM. MYCi361 (NUCC-01 |
| R21082466 | GSK2837808A | GSK2837808A is A potent and selective lactate dehydrogenase A (LDHA) inhibitor w |
| R21082467 | ML-9 hydrochloride | Ml-9 is a potent and selective inhibitor of Akt kinase that inhibits myosin ligh |
| R21082468 | PRI-724 | PRI-724, an isomer or enantiomer of ICG-001, is a potent, specific inhibitor of |
| R21082469 | Picropodophyllotoxin(PPP) | Picropodophyllin (AXL1717) is a selective insulin-like growth factor-1 receptor |
| R21082470 | GCN2iB | GCN2iB is an ATP-competitive inhibitor of stress response kinase (GCN2), a serin |
| R21082471 | Fatostatin HBr | Fatostatin hydrobromide (125B11 hydrobromide) is a specific inhibitor of SREBP a |
| R21082472 | MYF-01-37 | MYF-01-37 is a novel covalent inhibitor of TEAD targeting Cys380 when incubated |
| R21082473 | Valemetostat | Valemetostat is an antitumor agent. |
| R21082474 | HS-243 | HS-243 is an inhibitor of transforming growth factor-beta kinase. HS-243 can be |
| R21082475 | LY-3381916 | Ly-3381916 is an effective, selective, transbbB IDO1 inhibitor that can bind to |
| R21082476 | CU-CPT-9a | CU-CPT9b is an antagonist of toll-like receptor 8 (TLR8; Kd = 21 nM). It inhibit |
| R21082477 | Pitstop 2 | Pitstop 2 is a small molecule inhibitor of clathrin terminal domain and inhibits |
