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Home > Products
| Cat.No. | Product name | Product Description |
| R10255 | LY2874455; dovitinib | LY2874455 is a pan-FGFR inhibitor with IC50 of 2.8 nM, 2.6 nM, 6.4 nM, and 6 nM |
| R10256 | Blu9931 | BLU9931 is a potent, highly selective, and irreversible fibroblast growth factor |
| R10258 | Sofosbuvir;PSI-7977; GS7977 | Sofosbuvir (PSI-7977, GS-7977) is a HCV NS5B polymerase inhibitor for the treatm |
| R10259 | AG490 | AG-490 (Tyrphostin B42) is an inhibitor of EGFR with IC50 of 0.1 μM in cell-free |
| R10260 | Sotagliflozin; LP802034; LX4211 | LX-4211 is a potent dual SGLT2/1 inhibitor; Antidiabetic agents. |
| R10261 | CDC0032 Intermediate | CAS NO.：1282514-63-9Product Name：Synonyms：EINEC:Molecular Formula：Molecular Weig |
| R10262 | LY294002 | LY294002 is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of |
| R10264 | RO3280 | RO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with |
| R10266 | GlyH101;GlyH-101 | GlyH-101 is a cell-permeable glycinyl hydrazone compound that blocks CFTR with K |
| R10268 | KN-93;KN93 | KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), |
| R10269 | FG-2216 (Synonyms: IOX3; YM311) | FG-2216 is a potent HIF-prolyl hydroxylase inhibitor with IC50 of 3.9 uM for PDH |
| R10270 | GSK2801 | GSK2801 is a selective bromodomains BAZ2A/B inhibitor with KD of 257 nM and 136 |
| R10271 | BI 2536;BI2536 | BI 2536 is a dual PLK1 and BRD4 inhibitor with IC50s of 0.83 and 25 nM, respecti |
| R10272 | Lersivirine(UK-453061) | Lersivirine(UK-453061) is a next-generation non-nucleoside reverse transcriptase |
| R10273 | G007-LK | G007-LK is a potent and selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 |
| R10274 | Piperlongumine | Piperlongumine, a natural alkaloid from Piper longum L., increases the level of |
| R10275 | Omarigliptin; MK3102 Intermediate1 | Omarigliptin(MK-3102) is a potent, selective and long-acting DPP-4 inhibitor wit |
| R10276 | Omarigliptin; MK3102 Intermediate2 | Omarigliptin(MK-3102) is a potent, selective and long-acting DPP-4 inhibitor wit |
| R10277 | AZD9291Intermediate3 | Osimertinib (AZD9291) is an oral, irreversible, and mutant-selective EGFR inhibi |
| R10278 | AZD9291Intermediate4 | Osimertinib (AZD9291) is an oral, irreversible, and mutant-selective EGFR inhibi |
| R10279 | AZD9291Intermediate5 | Osimertinib (AZD9291) is an oral, irreversible, and mutant-selective EGFR inhibi |
| R10280 | CAL101 Intermediate1 | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM |
| R10281 | CAL101 Intermediate2 | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM |
| R10282 | CAL101 Intermediate3 | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM |
| R10283 | Nintedanib esylate; BIBF1120 esylate | Nintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for VEGFR1/2/3, |
