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Home > Products
| Cat.No. | Product name | Product Description |
| R2101146 | SAR-020106 | SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an I |
| R2101147 | A-893 | A-893 is a cell-active inhibitor of Methyltransferase SMYD2, with an IC50 of 2.8 |
| R2101148 | Mirogabalin besylate | Mirogabalin besylate is a selective and orally available ligand for the α2δ subu |
| R2101149 | Px-104 | (-)-PX20606 trans isomer is an agonist of FXR (EC50s: 18 and 29 nM for FXR in FR |
| R2101150 | RUC-4 | RUC-4 (RUC4;RUC 4) is a potent, selective, non-RGD-mimetic αIIbβ3 integrin recep |
| R2101151 | GDC-0077 | GDC-0077 (RG6114) is a potent, orally available, and selective inhibitor of PI3K |
| R2101152 | CYC065;CDK259 | CYC065 is an orally available, second-generation ATP-competitive inhibitor of CD |
| R2101153 | LX-2761 | LX2761 is a chemically stable and effective inhibitor against sodium-dependent g |
| R2101154 | Baloxavir | Baloxavir is a first-in-class cap-dependent endonuclease inhibitor of the influe |
| R2101155 | ARS-1323 | ARS-1323 (the racemate of ARS-1620) is a mutant K-ras G12C inhibitor extracted f |
| R2101156 | CDDO-2-P-Im | CDDO-3P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can |
| R2101157 | R-268712 | R-268712 is an effective and selective inhibitor of ALK5 IC50: 2.5 nM). |
| R2101158 | BAZ2-ICR | BAZ2-ICR is an epigenetic chemical probe and it also is a potent, selective, cel |
| R2101159 | QC6352 | QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM). |
| R2101160 | T-26c | T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibi |
| R2101161 | CDDO-2-P-Im | CDDO-2P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can |
| R2101162 | TP 235 | CDDO-Im is an activator of Nrf2 and PPAR (Kis: 232/344 nM for PPARα/PPARγ). |
| R2101163 | BAY 299 | BAY-299 is a very potent inhibitor. For BRPF2 bromodomains (BD), TAF1 BD2, TAF1L |
| R2101164 | BMS-955176;GSK3532795 | GSK3532795 is a potent, orally active, second-generation HIV-1 maturation inhib |
| R2101165 | Quarfloxin | Quarfloxin is a fluoroquinolone derivative with antineoplastic activity with IC5 |
| R2101166 | BI-3802 | BI-3802 is a highly effective BCL6 depressant, which can inhibit the BTB domain |
| R2101167 | GSK-484 | GSK484 is a potent PAD-4 inhibitor (Protein-arginine deiminase type-4). GSK484 p |
| R2101168 | BAY-850 | BAY-850 is a potent and isoform selective ATPase family AAA domain-containing pr |
| R2101169 | SB-204990 | SB 204990 is an effective and specific ATP citrate lyase enzyme inhibitor. |
| R2101170 | Quarfloxin | Quarfloxin (CX 3543) 是一种具有抗肿瘤活性的氟喹诺酮类衍生物，其靶向抑制RNA pol I的活性，在神经母细胞瘤中的IC50 值在纳摩尔级别 |
