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| Cat.No. | Product name | Product Description |
| R240402200 | D-(+)-2-磷酸甘油酸钠 | D-(+)-2-Phosphoglyceric Acid Sodium Hydrate |
| R240402201 | β-Secretase Inhibitor IV | β-Secretase Inhibitor IV is a potent, cell-active BACE-1 inhibitor with IC50s of |
| R240402202 | BI-2493 | BI-2493 is a structural analogue of BI-2865 and a highly selective pan-KRAS inhi |
| R240402203 | GSK 3008348 hydrochloride | GSK 3008348 hydrochloride is a small molecule integrin αvβ6 antagonist, extracte |
| R240402204 | ZK53 | ZK53 is a selective and potent activator of mitochondrial casein hydrolase prote |
| R240402205 | DSM705 | DSM705 is a pyrrole-based Dihydroorotate Dehydrogenase inhibitor. It exhibits na |
| R240402206 | AS-99 | AS-99 is a first-in-class, potent and selective ASH1L histone methyltransferase |
| R240402207 | FNDR-20123 | FNDR-20123 is a safe, first-in-class, and orally active anti-malarial HDAC inhib |
| R240402208 | 右氯谷胺 | Dexloxiglumide is a selective cholecystokinin type A (CCKA) receptor antagonist. |
| R240402209 | Emidurdar | Endovion is a pharmacological anion channel inhibitor (like chloride channel) an |
| R240402210 | α5IA | α5IA (L-822179) is a selective α5 GABAA receptor inverse agonist with neuroprote |
| R240402211 | Loreclezole | Loreclezole, an antiepileptic compound, is a selective GABAA receptor modulator |
| R240402212 | TUG-770 | TUG-770 is a potent, selective and orally active GPR40/FFA1 agonist with an EC50 |
| R240402213 | U-69593 | U-69593 is a potent and selective κ1-opioid receptor agonist. It attenuates addi |
| R240402214 | 喹乙宗； 喹噻酮； 喹乙唑酮 | Quinethazone is an orally active diuretic agent and is also a weak inhibitor of |
| R240402215 | PhiKan 083 | PhiKan 083 is a carbazole derivative, which binds to the surface cavity and stab |
| R240402216 | Mezigdomide (CC-92480) | Mezigdomide (CC-92480), a cereblon E3 ubiquitin ligase modulating agent (CELMoD) |
| R240402217 | 帕呋拉定; DB289 | Pafuramidine (DB289) is an orally active proagent of Furamidine (HY-110137A). Pa |
| R240402218 | ML-030 | ML-030 is a potent PDE4 inhibitor, with IC50 of 6.7 nM, 12.9 nM, 48.2 nM, 37.2 n |
| R240402219 | CM-579 | CM-579 is a first-in-class reversible, dual inhibitor of G9a and DNMT, with IC50 |
| R240402220 | DMNB-caged-Serine | DMNB-caged-Serine is a photocaged amino acid. It can be used as a catalytic resi |
| R240402221 | ADH-6 | ADH-6 is a tripyridylamide compound. It abrogates self-assembly of the aggregati |
| R240402222 | Abemaciclib metabolite M18 hydrochloride | Abemaciclib metabolite M18 (LSN3106729) hydrochloride, the metabolite of Abemaci |
| R240402223 | AK2292 | AK2292 |
| R240402224 | 氯离子载体IV | Chloride Ionophore IV is a thiourea type hydrogen bonding-based receptor. It is |
