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| Cat.No. | Product name | Product Description |
| R2202115 | PFI-90 | PFI-90 is a selective inhibitor of histone demethylase (KDM3B) that inhibits PAX |
| R2202116 | TBAP-001 | TBAP-001 (Synthesis 13), extracted from patent WO2015075483A1, is a pan-RAF kina |
| R2202117 | Robinetin | Robinetin (3,3',4',5',7-Pentahydroxyflavone), a naturally occurring flavonoid wi |
| R2202118 | MRTX1133 | MRTX1133 is a noncovalent, potent, and selective KRAS G12D inhibitor. MRTX1133 o |
| R2202119 | HLY78 | HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the |
| R2202120 | SB-265610 | SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonis |
| R2202121 | GSK2033 | GSK2033 is a LXR antagonist with pIC50s of 7 and 7.4 for LXRα or LXRβ, respectiv |
| R2202122 | KL-11743 | KL-11743 is a potent, orally active, and glucose-competitive inhibitor of the cl |
| R2202123 | Ch55 | Ch55 is a potent synthetic retinoid. Ch55 binds to RAR-α and RAR-β receptors wit |
| R2103226 | Polyphyllin I | Polyphyllin I is a bioactive constituent extracted from Paris polyphylla, h |
| R2001291 | Coti-2 | COTI-2, an anti-cancer drug with low toxicity, is an orally available third gene |
| R2204121 | Lisavanbulin | (S)-2,6-diamino-N-(4-(2-(2-(4-((2-cyanoethyl)amino)-1,2,5-oxadiazol-3-yl)-1H-ben |
| R2204201 | MRTX-1719 | MRTX-1719 is a potent first-in-class selective inhibitor of the PRMT5/MTA&n |
| R2202125 | Remibrutinib（LOU064） | Remibrutinib, is a potent and orally active bruton tyrosine kinase (BTK) inhibit |
| R2202126 | AZD9056 hydrochloride | AZD9056 hydrochloride is a selective orally active inhibitor of P2X7 which plays |
| R2202127 | UCB-9260 | UCB-9260, an orally active compound, inhibits TNF signaling by stabilising an as |
| R2202128 | LM22A-4 | LM22A-4 is a specific agonist of tyrosine kinase receptor B, used for neurologic |
| R2202129 | BI-4464 | BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC5 |
| R2204281 | Brusatol | Brusatol (NSC 172924) is a unique inhibitor of the Nrf2 pathway t |
| R2202132 | Besifovir (LB8033) | Besifovir (LB80331), a parent drug converted by LB80380, further metabolizes to |
| R2202133 | Cichoric Acid | Cichoric Acid, a natural product, is reported to be antioxidative. |
| R2202134 | BMS-P5 hydrochloride | BMS-P5 is a specific and orally active peptidylarginine deiminase 4 (PAD4) inhib |
| R2202135 | Letrozole | Letrozole (CGS 20267) is a potent, selective, reversible and orally active non-s |
| R2202136 | Anastrozole | Anastrozole is a potent, highly selective aromatase inhibitor, which inhibits hu |
| R2202137 | Glibenclamide impurity Ⅱ | Glibenclamide (Glyburide) is an orally active ATP-sensitive K+ channel (KATP) in |
