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| Cat.No. | Product name | Product Description |
| R2103588 | SX682 | SX-682 is an orally bioavailable, potent allosteric inhibitor of CXCR1 and CXCR2 |
| R2103589 | Mli-2 | MLi-2 is an orally active and highly selective LRRK2 inhibitor with an IC50 of 0 |
| R2103591 | PT-2399 | PT2399 is a potent and selective HIF-2α antagonist, which directly binds to HIF- |
| R2103592 | (Rac)-PT2399 | (Rac)-PT2399 (Compound 10e), the racemate of PT2399, acts as a potent and specif |
| R2103593 | EGFR-IN-7 (compound 34) | EGFR-IN-7 (compound 34) is a selective and potent EGFR kinase inhibitor extracte |
| R2103594 | MSAB | MSAB is a potent and selective inhibitor of Wnt/β-catenin signaling. MSAB binds |
| R2103595 | Rogaratinib;BAY1163877 | Rogaratinib is a potent and selective fibroblast growth factor receptor (FGFR) i |
| R2103553 | Omadacycline hydrochloride (PTK0796 hydrochloride) | Omadacycline hydrochloride is novel, aminomethyl tetracycline antibiotic being d |
| R2103590 | MYF-01-37 | MYF-01-37 is a novel covalent inhibitor of TEAD. |
| R2103596 | PQR530 | PQR530 is a potent, ATP-competitive, orally bioavailable and brain-penetrant dua |
| R2103597 | CD38 inhibitor 1 | CD38 inhibitor 1 (compound 78c) is a potent CD38 inhibitor with IC50s of 7.3 nM |
| R2103598 | Olutasidenib | Olutasidenib (FT-2102) is a highly potent, orally active, brain penetrant and se |
| R2103599 | PRN1008 | PRN1008 is a reversible covalent, selective and oral active inhibitor of Bruton’ |
| R2103600 | Allopregnanolone | Allopregnanolone, a neurosteroid synthesized from progesterone in brain, acts as |
| R2103601 | SEP-363856 (SEP-856) hydrochloride | SEP-363856 hydrochloride（SEP-856 hydrochloride）, an orally active and CNS active |
| R2123602 | ML251 | 2-(3,4-Dichlorophenyl)-N-[4-(1,2-oxazol-3-ylsulfamoyl)phenyl]acetamide |
| R2123603 | ML267 | 4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine |
| R2123604 | methyl 4-acetamido-2-(2-bromoethoxy)-5-chlorobenzoate | methyl 4-acetamido-2-(2-bromoethoxy)-5-chlorobenzoate |
| R2123605 | Ceftolozane sulfate | 5-amino-2-(((6R,7R)-7-((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((2-carboxypropa |
| R2123606 | CU-CPT-9a | CU-CPT-9a is a specific TLR8 antagonist, with an IC50 of 0.5 nM. |
| R2123607 | ASLAN003 | ASLAN003 is an orally active and potent Dihydroorotate Dehydrogenase (DHODH) inh |
| R2123608 | MF438 | MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhi |
| R2123609 | Calpain Inhibitor IV;IN1508 | benzyl N-[1-[[1-[[4-fluoro-1-(4-hydroxyphenyl)-3-oxobutan-2-yl]amino]-4-methyl-1 |
| R2123610 | OGT-IN-2 | Ogt-in-2 is an o-GLCNAC transferase (OGT) inhibitor with IC50 of 53 M.Ogt-in-2 d |
| R2123611 | HM30181;HM30181A;Encequidar; | Encequidar (HM30181; HM30181A) is a potent and selective inhibitor of P-glycopro |
