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| Cat.No. | Product name | Product Description |
| R10174 | PF429242 | PF 429242 is a reversible, competitive inhibitor of sterol regulatory element-bi |
| R10177 | GSK364735 | |
| R10195 | Enasidenib; AG221 | Enasidenib is a oral potent, selective, reversible inhibitor of mutant IDH2. |
| R10197 | AZ-33 | AZ-33： 2-(4-(4-(3-(2-methylbenzo[d]thiazol-6-ylamino)-3-oxopropylamino)-4-oxobut |
| R10201 | IP145; Duvelisib; Impurity comparison | |
| R10268 | KN-93;KN93 | KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), |
| R10272 | Lersivirine(UK-453061) | Lersivirine(UK-453061) is a next-generation non-nucleoside reverse transcriptase |
| R10274 | Piperlongumine | Piperlongumine, a natural alkaloid from Piper longum L., increases the level of |
| R10287 | TR700; DA7157; Torezolid | Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infecti |
| R10288 | TR700; DA7157; Torezolid phosphate | Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infecti |
| R10321 | MS37452 | |
| R10322 | Ryuvidine | Ryuvidine is a potent inhibitor of SET domain-containing protein 8(SETD8) with a |
| R10329 | Elafibranor;GFT505;GFT-505;GFT 505 | Elafibranor is an agonist of the peroxisome proliferator-activated receptor-α an |
| R10330 | GFT505; elafibranor E | Elafibranor is a PPARα/δ agonist with EC50s of 45 and 175 nM, respectively. |
| R10336 | Felbamate; Felbatol | Felbamate (Felbatol) is an anticonvulsant drug used in the treatment of epilepsy |
| R10342 | GW 627368 | GW627368(GW627368X) is a novel, potent and selective competitive antagonist of p |
| R10345 | SW033291 | SW033291 is a small-molecule inhibitor of 15-PGDH (Ki=0.1 nM) that increases pro |
| R10347 | Tulathromycin; Draxxin; CP472295 | Tulathromycin A is a macrolide antibiotic. IC50 Value: 1 microg/ml (MIC90 for Pa |
| R10348 | BAY632521; Riociguat | Riociguat (BAY 63-2521) is a stimulator of soluble guanylate cyclase (sGC). |
| R10351 | WEHI-345 | WEHI-345 is a potent and selective inhibitor of RIPK2, with IC50 of 0.13 μM. IC5 |
| R10352 | AI-10-49 | AI-10-49 is a protein-protein interaction inhibitor that selectively binds to CB |
| R10354 | APVT | |
| R10360 | URMC099 | URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) i |
| R10361 | GW791343 dihydrochloride | GW791343 2Hcl is a P2X7 allosteric modulator; exhibits species-specific activity |
| R10375 | Zucapsaicin | CAS NO.：25775-90-0Product Name：(Z)-N-(4-Hydroxy-3-methoxybenzyl)-8-methylnon-6-e |
