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Home > Products
| Cat.No. | Product name | Product Description |
| R21087965 | 3-chloro-4-fluoro-N-methylaniline | |
| R21087966 | 6-broMo-5-(trifluoroMethyl)pyridin-3-aMine | |
| R21087967 | 5-(1-Methylethyl)-2-pyridinamine | |
| R21087968 | 6-CHLORO-3,4-DIMETHOXYPYRIDAZINE | |
| R21087969 | 4-(5,6-Dimethoxypyridazin-3-yl)benzaldehyde | |
| R21087970 | 5-Chloro-3-(trifluoromethyl)-2(1H)-pyridinone | |
| R21087971 | 2-BROMO-5-CHLORO-3-(TRIFLUOROMETHYL)PYRIDINE | |
| R21087972 | 2,5-DICHLORO-3-(TRIFLUOROMETHYL)PYRIDINE | |
| R21087973 | 2-chloro-5-iodo-3-trifluoromethylpyridine | CAS NO.：887707-25-7Product Name：2-chloro-5-iodo-3-trifluoromethylpyridineSynonym |
| R21087974 | 2-Bromo-5-iodo-3-(trifluoromethyl)pyridine | CAS NO.：1805025-71-1Product Name：2-Bromo-5-iodo-3-(trifluoromethyl)pyridineSynon |
| R21092501 | Sulfopin(PIN1-3) | Sulfopin (PIN1-3) is a highly selective covalent inhibitor of Pin1 wit |
| R2109301 | JTE-607 dihydrochloride | Antiinfective therapy, Treatment of Septic Shock, Antiinflammatory Drugs, Cytoki |
| R2110001 | AR-C155858 | AR-C155858 is a selective monocarboxylate transporter MCT1 and MC |
| R21101501 | DZD9008 | DZD9008是一种设计合理、选择性强、不可逆的EGFR/HER2抑制剂。 |
| R21102501 | TPX0131;TPX-0131 | TPX-0131 is a potent, selective, CNS-penetrant and orally active inhibitor of&nb |
| R21111201 | BDA-366 | BDA-366 is a Small-Molecule Bcl2 BH4 Antagonist for Lung Cancer Therapy. |
| R21111202 | DL-alpha-Tocopherol | DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alph |
| R21111203 | NVS-PAK1-1 | NVS-PAK1-1 is a potent and selective allosteric PAK1 inhibitor with an IC50 of 5 |
| R21111204 | CP-609754 (OSI754) | CP-609754 (LNK-754) is a potent and reversible farnesyltransferase inhibitor wit |
| R21111205 | STK16-IN-1 | STK16-IN-1 is a STK16 kinase inhibitor with an IC50 of 295 nM. |
| R21111206 | Pexidartinib hydrochloride;PLX-3397 HCl | Pexidartinib hydrochloride (PLX-3397 hydrochloride) is a potent, orally active, |
| R21111207 | UT-155 | UT-155 is a selective and potent androgen receptor (AR) antagonist, with a Ki of |
| R21111208 | Parsaclisib | Parsaclisib (INCB050465) is a potent, selective and orally active inhibitor of P |
| R21111209 | Parsaclisib hydrochloride | Parsaclisib hydrochloride (INCB050465 hydrochloride) is a potent, selective and |
| R21111210 | AZD-0284 | AZD-0284 is a selective inverse agonist of the nuclear receptor RORγ. AZD-0284 h |
