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 |
| R2103552 | Omadacycline (PTK0796) | Omadacycline is novel, aminomethyl tetracycline antibiotic being developed for t |
| R2103554 | Relacorilant | Relacorilant is a potent, selective and orally bioavailable glucocorticoid recep |
| R2103555 | LY-3475070 | CD73 inhibitor LY3475070 targets and binds to CD73, leading to clustering of and |
| R2103556 | Taletrectinib (DS-6051b;AB-106) | Taletrectinib (DS-6051b) is a potent, orally active, and new-generation selectiv |
| R2103557 | Gusacitinib hydrochloride;ASN-002 hydrochloride | Gusacitinib (ASN-002) is an orally active and potent dual inhibitor of spleen ty |
| R2103558 | Danuglipron | PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptid |
| R2103559 | Epertinib | Epertinib (S-22611) is a potent, oral, reversible, and selective tyrosine kinase |
| R2103560 | Lefamulin acetate | Lefamulin acetate (BC-3781 acetate) is an orally active antibiotic for community |
| R2103561 | AT-001;Aldose reductase-IN-1 | Aldose reductase-IN-1 is a inhibitor of aldose reductase with IC50 of 28.9 pM. I |
| R2103562 | Antrodin A | Antrodia camphorata (A. camphorata) is a rare functional fungus in Taiwan and co |
| 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 |
