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 |
Home > Products
| Cat.No. | Product name | Product Description |
| RH131564 | Z-LEED-FMK | Z-LEED-FMK is a caspase-13 and caspase-4 inhibitor. Z-LEED-FMK also inhibits cas |
| RH131565 | Z-LEVD-FMK | Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor. Z-LEVD-FMK blocks ER stress- |
| RH131566 | Z-LEHD-FMK | Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects agai |
| RH131567 | Z-LETD-FMK | Z-Leu-Glu(OMe)-Thr-DL-Asp(OMe)-fluoromethylketone |
| RH131568 | (3S)-3-[[叔丁氧羰基]氨基]-5-氟-4-氧代-戊酸甲酯 | Boc-Asp(OME)-Fluoromethyl Ketone is a broad range caspase inhibitor that inhibit |
| RH131569 | Z-VEID-FMK | Z-VEID-FMK (Z-VE(OMe)ID(OMe)-FMK) is a selective and irreversible caspase-6 |
| RH131570 | CA-074（OH） | CA-074 is a potent inhibitor of cathepsin B with a Ki of 2 to 5 nM. |
| RH131571 | PD-1-IN-17 | PD-1-IN-17 is a programmed cell death-1 (PD-1) inhibitor extracted from patent W |
| RH131572 | Z-FG-NHO-BzOMe | Z-FG-NHO-BzOME is a cysteine protease inhibitor that selectively inhibits cathep |
| RH131573 | PSB-1115 | PSB-1115 is a selective A2B Adenosine Receptor antagonist. PSB-1115 inhibits the |
| RH131574 | VK-2019 | VK-2019 is an oral active, selective EBNA1((Epstein-Barr Nuclear Antigen 1) inhi |
| RH131575 | BSJ-03-204 | BSJ-03-204 is a PROTAC connected by ligands for Cereblon and CDK. BSJ-03-204 is |
| RH131576 | SRX3177 | SRX3177 is a triple inhibitor of CDK4/6, PI3K, and BRD4, with IC50s of 33 nM (BR |
| RH131578 | PE154 | PE154 (Compound 13) is a potent fluorescent inhibitor of human acetylcholinester |
| RH131579 | IT1t dihydrochloride | IT1t dihydrochloride is a potent CXCR4 antagonist; inhibits CXCL12/CXCR4 interac |
| RH131580 | Lobeglitazone sulfate | Lobeglitazone sulfate is a new type of thiazolidinedione. Lobeglitazone sulfate |
| RH131581 | NecroX-7 | NecroX-7 is a potent free radical scavenger and a HMGB1 (high-mobility group box |
| RH131582 | EGFR-IN-99 | EGFR-IN-99 (compound 1a) is a potent EGFR and HER2 Exon 20 insertion mutant inhi |
| RH131583 | UNC8153 TFA | UNC8153 TFA is a potent and selective nuclear receptor-binding SET domain-contai |
| RH131586 | Ansornitinib(ANG-3070) | Ansornitinib is an orally active dual kinase inhibitor that inhibits platelet-de |
| RH131587 | DPBQ | DPBQ (ZINC1620467) is a p53 activator. DPBQ could activate p53 and trigger apopt |
| R11111890 | CL 316243 | CL316243 is a highly potent selective agonist of β3-adrenoceptor, with a EC50 of |
| RH131589 | Sisunatovir(RV521) | Sisunatovir (RV521), an orally available inhibitor of the RSV protein, exhibits |
| RH131590 | Sirpiglenastat (DRP-104) | Sirpiglenastat (DRP-104) is a glutamine antagonist, a prodrug of DON, with antit |
| RH131591 | glucosamine | Glucosamine (D-Glucosamine) is an amino sugar and a prominent precursor in the b |
