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Home > Products
| Cat.No. | Product name | Product Description |
| R10831 | Dasatinib monohydrate | Dasatinib Monohydrate is a novel, potent and multi-targeted inhibitor that targe |
| R10833 | Lesinurad;RDEA594 | Lesinurad is a selective uric acid re-absorption inhibitor (SURI) and is also a |
| R10834 | Vinpocetine | Vinpocetine is a selective inhibitor of voltage-sensitive sodium channel for the |
| R10835 | Birabresib (Synonyms: OTX-015; MK-8628) | OTX015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM |
| R10836 | MS417 | |
| R10837 | Capmatinib (INCB28060) | Capmatinib (INC280; INCB28060) is a potent, orally active, selective, and ATP co |
| R10838 | Napabucasin | Napabucasin (BBI608) is an orally available Stat3 and cancer cell stemness inhib |
| R10265 | ID8;ID-8 | ID-8 is a DYRK inhibitor, and sustains embryonic stem cell self-renewal in long- |
| R10665 | IDO-IN-7；NLG-919 analogue; GDC-0919 analogue | NLG919 is a potent IDO (indoleamine-(2,3)-dioxygenase) pathway inhibitor with Ki |
| R10161 | GW4064 | GW4064 is an agonist of farnesoid X receptor (FXR) with EC50 of 65 nM in CV1 cel |
| R10263 | Fexaramine | Fexaramine is a small molecule farnesoid X receptor (FXR) agonist with 100-fold |
| R10546 | Obeticholic acid; INT747 | Obeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist wi |
| R10169 | CP91149 | CP-91149 is a selective glycogen phosphorylase (GP) inhibitor with IC50 of 0.13 |
| R10416 | FIPI | FIPI is a derivative of halopemide which potently inhibits both PLD1 (IC50 = 25 |
| R10163 | Aprepitant (MK-0869; MK-869; L-754030) | Aprepitant is a potent and selective neurokinin-1 receptor antagonist. |
| R10222 | BIBR953; Dabigatran | Dabigatran (BIBR 953) is a potent nonpeptide thrombin inhibitor with an IC50 of |
| R10098 | HA14-1 | HA14-1 is a non-peptidic ligand of a Bcl-2 surface pocket with IC50 of ~9 μM. |
| R10267 | GW2580 | GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited |
| R10335 | PLX647 | PLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM |
| R10548 | Avanafil (Synonyms: TA1790) | Avanafil is a highly selective PDE5 inhibitor with IC50 of 5.2 nM, >121-fold |
| R10528 | LY2409881 trihydrochloride | LY2409881 is a potent and selective IKK2 inhibitor with IC50 of 30 nM, >10-fo |
| R10683 | WS6 | WS6 is a novel small molecule that promotes β cell proliferation in rodent and h |
| R10684 | β cell proliferation agonist WS3 | WS3 is a β cell proliferation inducer via modulation of Erb3 binding protein-1 ( |
| R10018 | GMX1778;CHS828 | GMX1778(CHS-828) is a potent inhibitor of NAD+ biosynthesis enzyme NAMPT with IC |
| R10338 | CIQ | CIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or |
