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| Cat.No. | Product name | Product Description |
| R10100 | GSK2646264A | |
| R10427 | Jaceosidin | |
| R10428 | eupatilin | |
| R10437 | Darusentan | Darusentan is a selective endothelin A (ETA) receptor antago |
| R10440 | Esmolol | Esmolol is a cardioselective beta1 receptor blocker with rapid onset, |
| R10442 | Milrinone | Milrinone is a PDE3 inhibitor, and also an inotrope and vasodilator. |
| R10478 | Cefotetan | Cefotetan is a semisynthetic cephamycin antibiotic that exerts its bactericidal |
| R10498 | GTS21 dihydrochloride; DMXBA | GTS-21 dihydrochloride is a selective α7 nicotinic acetylcholine receptor agonis |
| R10499 | Polymyxin | |
| R10542 | Zearalenone (Synonyms: Mycotoxin F2; Toxin F2) | Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusar |
| R10557 | Fruquintinib; HMPL-013 | Fruquintinib (HMPL-013) is a highly potent and selective VEGFR 1/2/3 inhibitor w |
| R10562 | TP-353 | Product Name：2-Benzyloxy-3-dibenzylamino-5-fluoro-6-methyl-benzoic acid phenyl e |
| R10563 | LHW090-A7 | LHW090-A7 is a compound developed as an inhibitor of neutral endopeptidase (NEP) |
| R10587 | UNC0064-12 | |
| R10597 | Tenovin-3 | Tenovin-3 is able to increase p53 levels, determined in MCF-7 cells treated for |
| R10598 | Tenovin-6 | Tenovin-6 is an inhibitor of SIRT1 and SIRT2, slightly inhibits HDAC8, and is al |
| R10605 | Isoindigotin | Isoindigotin is used in the therapy of Y. |
| R10642 | Des(benzylpyridyl) Atazanavir | Atazanavir is a highly effective HIV-1 protease inhibitor. |
| R10650 | (R)-P7C3-Ome | P7C3 is a drug related to latrepirdine (dimebon), which has neuroprotective and |
| R10661 | KPT-330 | KPT-330 is a CRM1-selective inhibitor of nuclear export. It inhibits protein tra |
| R10682 | Z-JIB-04;NSC693627 | Z-JIB-04 is an isomer of JIB-04. |
| R10703 | STATIL | |
| R10708 | NG-52 | NG 52 (Compound 52 ) is a potent, cell-permeable, reversible, selective, and ATP |
| R10713 | Bohemine | Bohemine is a CDK inhibitor with IC50s of 4.6, 83, and 2.7 μM for Cdk |
| R10714 | WHI-P258 | WHI-P258, a quinazoline compound, binds to the active site of JAK3 with an estim |
