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| Cat.No. | Product name | Product Description |
| R2090922 | SR-717 | SR-717 is a non-nucleotide STING agonist with EC50s of 2.1 μM and |
| R2090923 | LY 345899;LY345899 | LY 345899 is a Folate analog and is a methylene tetrahydrofolate dehydrogen |
| R2092301 | 4',5,7-Trimethoxyflavone | 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) t |
| R2092302 | WC5-2 | CAS NO.：922722-84-7 Product Name：WC5-2 Synonyms： EINECS: Molecular Formula：C15H9 |
| R2103541 | BIA;TMBIM6 antagonist-1 | TMBIM6 antagonist-1, a potential TMBIM6 antagonist, prevents TMBIM6 binding to m |
| R2103542 | ML417 | ML417 is a selective and brain penetrant D3 dopamine receptor (D3R) agonist, wit |
| R2103543 | PRI-724 | PRI-724 is a selective inhibitor of the CBP/β-catenin interaction. |
| R2103544 | KGA-2727 | KGA-2727 is a first selective, high-affinity and orally active SGLT1 inhibitor w |
| R2103545 | URB937 | URB 937 is a potent inhibitor of fatty-acid amide hydrolase (FAAH), an intracell |
| R2103546 | GNE-8324 | GNE-8324 is a potent and selective NMDA receptor PAM. |
| R2103547 | BMS986165 | BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor |
| R2103548 | TAS-116 | TAS-116 is an oral bioavailable, ATP-competitive, highly specific HSP90α/HSP90β |
| R2103549 | SAR131675 | SAR131675 is a potent and selective VEGFR3 inhibitor with an IC50 of 23 nM. |
| R2103550 | iFSP1 | iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosi |
| R2103551 | N-[[(1,2,3,5,6,7-hexahydro-s-indacen-4-yl) amino]carbonyl]-1-(1-methylethyl)-1H-Pyrazole-3-sulfonamide | N-[[(1,2,3,5,6,7-hexahydro-s-indacen-4-yl) amino]carbonyl]-1-(1-methylethyl)-1H- |
| R2103552 | Omadacycline (PTK0796) | Omadacycline is novel, aminomethyl tetracycline antibiotic being developed for t |
| R2103554 | Relacorilant | Relacorilant is a potent, selective and orally bioavailable glucocorticoid recep |
| R2103555 | LY-3475070 | CD73 inhibitor LY3475070 targets and binds to CD73, leading to clustering of and |
| R2103556 | Taletrectinib (DS-6051b;AB-106) | Taletrectinib (DS-6051b) is a potent, orally active, and new-generation selectiv |
| R2103557 | Gusacitinib hydrochloride;ASN-002 hydrochloride | Gusacitinib (ASN-002) is an orally active and potent dual inhibitor of spleen ty |
| R2103558 | Danuglipron | PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptid |
| R2103559 | Epertinib | Epertinib (S-22611) is a potent, oral, reversible, and selective tyrosine kinase |
| R2103560 | Lefamulin acetate | Lefamulin acetate (BC-3781 acetate) is an orally active antibiotic for community |
| R2103561 | AT-001;Aldose reductase-IN-1 | Aldose reductase-IN-1 is a inhibitor of aldose reductase with IC50 of 28.9 pM. I |
| R2103562 | Antrodin A | Antrodia camphorata (A. camphorata) is a rare functional fungus in Taiwan and co |
