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| Cat.No. | Product name | Product Description |
| R21111504 | ACBI1 | ACBI1 is a potent PROTAC degrader of BAF ATPase subunits SMARCA2& |
| R211112 | THZ1 Hydrochloride | THZ1 Hydrochloride is a selective and potent covalent CDK7 inhibitor w |
| R211201 | PF-5190457;PF5190457 | PF-5190457 (PF-05190457) is a potent and selective ghrelin receptor in |
| R211205 | Raphin1 | Raphin1 is an orally bioavailable, selective inhibitor of the regulatory phospha |
| R211206 | Dclk1-IN-1 | DCLK1-IN-1 is a selective, oral bioavailability in vivo-compatible chemical prob |
| R211207 | RWJ 50271 | RWJ 50271 is an selective and orally active inhibitor of lymphocyte functio |
| R211208 | PLpro inhibitor | PLpro inhibitor is a potent inhibitor of papain-like protease (PLpro) |
| R211209 | Raphin1 (acetate) | Raphin1 acetate is an orally bioavailable, selective inhibitor of the regulatory |
| R211178 | Presatovir;GS-5806 | Presatovir (GS-5806) is an orally bioavailable RSV fusion inhibitor wi |
| R21122001 | ML179 | ML179 is a selective liver receptor homolog 1 (LRH1, NR5A2) inverse agonist (IC5 |
| R21122002 | ML-226 | ML-226 is an inhibitor of α/β hydrolase domain-containing protein 11 (ABHD11) th |
| R21122003 | CU-CPT-8m | CU-CPT8m is a Toll-like receptor 8 (TLR8) specific small-molecule inhibitor that |
| R21122004 | NSC370284 | NSC 370284 is a small molecule that directly binds to and inhibits STAT3/5, sign |
| R21122005 | Gingerenone A | A dual inhibitor of JAK2 and S6K1 pathways, selectively kills cancer cells while |
| R21122006 | C-170 | STING-IN-2 (C-170) is a potent and covalent STING inhibitor. STING-IN-2 efficien |
| R21122007 | DPI-201-106;SDZ-201106 | DPI-201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel in |
| R21122008 | LASV inhibitor 3.3 | LASV inhibitor 3.3 (LAMP1 inhibitor 3.3) is a specific inhibitor of Lassa fever |
| R21122009 | GSK3987 | GSK3987 is a potent and specific liver X receptor (LXR) dual agonist of LXRalpha |
| R21122010 | L82-G17 | |
| R21122011 | Arimoclomol;BRX-220 | Arimoclomol (BRX-220 Free Base) is a coinducer of heat shock protein (HSP). |
| R21122012 | AGI-001;Espindolol | Espindolol is a β-adrenoceptor antagonist potentially for the treatment of cache |
| R21122013 | PDZ1i | PDZ1i (113B7) is a specific inhibitor of MDA-9/Syntenin activity, which inhibits |
| R21122014 | ARN-21934 | Arn-21934 is a novel and highly selective human topoisomerase IIα inhibitor with |
| R21122015 | SID 26681509 | SID 26681509 is a potent, reversible, competitive and selective inhibitor of hum |
| R21122016 | FFN246 | FFN246 is a novel fluorescent substrate of 5-hydroxytryptamine transporter and v |
