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 |
| R2103563 | AZD1152 (Barasertib) | AZD1152 is a pro-drug of Barasertib-hQPA, which is a highly selective Aurora B i |
| R2103564 | LYS-006 | LYS-006 is a novel leukotriene A4 hydrolase inhibitor. |
| R2103565 | Vacuolin-1 | Vacuolin-1 is a potent and cell-permeable lysosomal exocytosis inhibitor. Vacuol |
| R2103566 | Tubulin inhibitor 6(IHAP1) | Tubulin inhibitor 6 (Compound 14b) is a tubulin inhibitor and a potent inhibitor |
| R2103567 | NAO3 | |
| R2103568 | Turofexorate isopropyl (FXR-450) | Turofexorate isopropyl (FXR-450) is a potent, selective, and orally bioavailable |
| R2103569 | BCI | BCI is an allosteric inhibitor of dual specificity phosphatase (DUSP). BCI speci |
| R2103570 | Ferrostatin-1 | Ferrostatin-1, a potent and selective ferroptosis inhibitor, suppresses Erastin- |
| R2103571 | Rotigotine (N-0437; N-0923) | Rotigotine (N-0437; N-0923) is a full agonist of dopamine receptor, a partial ag |
| R2103572 | BAY 2416964 | BAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antago |
| R2103573 | Fondaparinux sodium | Fondaparinux sodium is an antithrombin-dependent factor Xa inhibitor. |
| R2103574 | laninamivir octanoate | Laninamivir Octanoate is a long acting neuraminidase inhibitor which shows super |
| R2103575 | PT2977 (MK-6482) | PT2977 (MK-6482) is an orally active and selective HIF-2α inhibitor with an IC50 |
| R2103576 | CWP232228 sodium | CWP232228 is a highly effective selective inhibitor of Wnt/ -catenin signaling p |
| R2103577 | THAL-SNS-032 | THAL-SNS-032 is a selective CDK9 degrader PROTAC consisting of a CDK-binding SNS |
| R2103578 | DT2216 | DT2216 is a potent and selective BCL-XL degrader based on PROTAC technology. SIA |
| R2103579 | JTZ-951;Enarodustat | Enarodustat is a potent and orally active factor prolyl hydroxylase inhibitor, w |
| R2103580 | CBR-5884 | CBR-5884 is an active, selective inhibitor of phosphoglycerate dehydrogenase (PH |
| R2103581 | Homo-PROTAC cereblon degrader 1 (compound 15a) | Homo-PROTAC cereblon degrader 1 (compound 15a) is a highly potent and efficient |
| R2103582 | RU-301 | RU-301 is a pan-TAM receptor inhibitor, exerts pan-TAM inhibitory activity by bi |
| R2103583 | Desmorpholinyl Navitoclax-NH-Me | Desmorpholinyl Navitoclax-NH-Me is a Bcl-xL inhibitor. Desmorpholinyl Navitoclax |
| R2103584 | TVB-3664 | TVB-3664 is an orally available, reversible, potent, selective and highly bioava |
| R2103585 | VTP50469 | VTP50469 is a potent, highly selective and orally active Menin-MLL interaction i |
| R2103586 | G1T28;Trilaciclib | Trilaciclib is a potential first-in-class short-acting CDK4/6 inhibitor in devel |
| R2103587 | Trilaciclib hydrochloride (G1T28 hydrochloride) | Trilaciclib hydrochloride (G1T28 hydrochloride) is a CDK4/6 inhibitor with IC50s |
