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| Cat.No. | Product name | Product Description |
| R2123612 | HM-30181 mesylate monohydrate | Encequidar mesylate (HM30181 mesylate; HM30181A mesylate) is a competitive and p |
| R2123613 | Napabucasin analogue | Napabucasin is a STAT3 inhibitor which blocks stem cell activity in cancer cells |
| R2123614 | SP-146;SP-96 | SP-96 is a highly potent, selective and non-ATP-competitive Aurora B (IC50=0.316 |
| R2123615 | GSK2894512;Bennvitimod | Tapinarof (WBI-1001) is a natural aryl hydrocarbon receptor (AhR) agonist with a |
| R2123616 | GSK046 | GSK046 (iBET-BD2) is a potent, selective and orally active BD2 bromodomain inhib |
| R2123617 | ARRY-614;Pexmetinib | Pexmetinib is a potent Tie-2 and p38 MAPK dual inhibitor, with IC50s of 1 nM, 35 |
| R2123618 | LACS-13909 | IACS-13909 (BBP-398) is a potent and specific allosteric SHP2 inhibitor suppress |
| R2123619 | Lanraplenib;GS-9876 | Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor (IC5 |
| R2123620 | CB-103 | CB-103 is a first-in-class orally active notch signaling pathway inhibitor extra |
| R2121751 | EST73502;EST 73502;EST-73502 | EST73502 is a Dual μ-Opioid Receptor Agonist and σ1 Receptor Antagonist Clinical |
| R2121752 | Ciliobrevin D | Ciliobrevin D is a cell-permeable, reversible and specific inhibitor of AAA+ ATP |
| R2121781 | WM-2474;WM2474 | CAS NO.：2414591-05-0 Product Name：WM-2474;WM2474 Molecular Formula：C17H13FN4O3S |
| R2121782 | SCH-442416;SCH442416 | SCH-442416 is a selective antagonist of adenosine A2A receptor. SCH-442416 bind |
| R2121783 | LIN28 inhibitor LI71 | LIN28 inhibitor LI71 is a potent and cell-permeable LIN28 inhibitor, w |
| R2122060 | Finerenone;BAY 94-8862;BAY948862 | Finerenone (BAY 94-8862) is a third-generation, selective, and orally available |
| R2122301 | NIK SMI1 | NIK SMI1 is a potent, selective NF-κB inducing kinase (NIK) inhibitor, which inh |
| R2123501 | ZAP-180013 | ZAP-180013 is a zeta-chain-associated protein kinase 70 (ZAP-70) inhibitor with |
| R2123502 | AMG 487 | AMG 487 is an orally active and selective antagonist of CXC chemokine receptor 3 |
| R2123503 | Tegoprazan | Tegoprazan is a potassium competitive acid blocker, an effective, orally active, |
| R2123504 | CH6953755 | CH6953755 is a potent, orally active and selective YES1 kinase (a member of the |
| R2101002 | Nicardipine (YC-93 free base) | Nicardipine (YC-93 free base) is a calcium channel blocker with an IC50 of 1 μM |
| R2101003 | Nicardipine (YC-93 hydrochloride) | Nicardipine hydrochloride (YC-93) is a calcium channel blocker with an IC50 of 1 |
| R2101004 | 24-Norursodeoxycholic acid | 24-norursodeoxycholic acid (norUDCA) is a side chain-shortened C23 homologue of |
| R2101005 | MALAT1-IN-1 (compounds 5) | MALAT1-IN-1 modulated Malat1 downstream genes in a dose-dependent manner without |
| R2101006 | CRANAD-2 | CRANAD-2 is a curcumin-derivatized near-infrared (NIR) probe that meets all the |
