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| Cat.No. | Product name | Product Description |
| R21082440 | Vindesine sulfate | Vindesine sulfate is a vinca alkaloid which is a synthetic derivative of vinblas |
| R21082441 | EOAI3402143 | EOAI3402143 is a deubiquitination enzyme (DUB) inhibitor that inhibits Usp9x/Usp |
| R21082442 | KY-226 | KY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0. |
| R21082443 | TP-003 | TP003 is a potent, functional selectivity for α3 subunit-containing GABAA recept |
| R21082444 | RMS060 | Protein kinase Affinity Probe 1 is a novel Protein kinase affinity probe used fo |
| R21082445 | SRT1460 | SRT 1460 is an effective sirTUin-1 (SIRT1) agonist with an EC1.5 value of 2.9 μM |
| R21082446 | Curcumin analog C1 | TFEB Activator 1 is an orally effective, mTOR independent TFEB activator. TFEB |
| R21082447 | Probe 388-9 | |
| R21082448 | OMO-1 | Jnj-38877618 is a potent, highly selective, orally available (Met) kinase inhibi |
| R21082449 | ARQ-531 | ARQ 531 is a reversible non-covalent inhibitor of BTK, with IC50 values of 0.85 |
| R21082450 | RU320521 | RU.521 (RU320521) is a potent dsDNA inhibitor (IC50 : 700 nM), inhibition of the |
| R21082451 | SNDX-5613 | Sndx-5613 is a potent and specific menin-MLL inhibitor, binding Ki at 0.149 nM a |
| R21082452 | mitoNEET Inhibitor NL-1, Thi | Nl-1 is a mitoNEET inhibitor with anti-leukemia effects. Nl-1 inhibited the gro |
| 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 |
