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Home > Products
| Cat.No. | Product name | Product Description |
| R2053490 | Ethyl 5-bromothieno[2,3-b]pyridine-2-carboxylate | |
| R2053491 | 4-bromo-2-(bromomethyl)thieno[2,3-c]pyridine | |
| R2053492 | 4-Chloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine | |
| R2053493 | 4-Hydroxyphenylboronic acid | |
| R2053494 | 2-Hydrazinylpyrazine | |
| R2053495 | 2-Aminopyrimidine-5-boronic acid | |
| R2053496 | 2-Bromo-4-methylpyridine | |
| R2053497 | 2-(3-Chloropropoxy)-1-methoxy-4-nitrobenzene | |
| R2053498 | trans-4-(Trifluoromethyl)cyclohexanol | |
| R2053499 | (2,5-dioxopyrrolidin-1-yl) but-2-enoate | |
| R2053471 | Meplazumab | Meplazumab, also known as Mepozumab in Chinese, was developed by Chen Zhinan, an |
| R2053480 | DBPR114;BPR1K871 | BPR1K871 is a potent and selective dual FLT3/AURKA inhibitor with IC50s of 19 nM |
| R2053481 | TBAJ-587-1 | TBAJ-587, a potent anti-tuberculosis agent, inhibits M.tb strain H37Rv growth wi |
| R2053486 | ACT-1002-1237(S,S） | |
| R2053487 | ACT-1002-1237(R,S） | |
| R2080711 | BMS-1001 hydrochloride | BMS-1001 hydrochloride is an orally active human PD-L1/PD-1 immune che |
| R2053500 | CMD178 | CMD178 is a lead peptide that consistently reduced the expression of Foxp3 and S |
| R2053501 | Cyclo（RGDfK） | Cyclo(-RGDfK) is a potent and selective inhibitor of the αvβ3 integrin, with an |
| R2053502 | BK-1361（BK1361，cyclo-RLsKDK） | Bk-1361 (BK1361, cyclo-RlSKDK) is a cyclic peptide with RLsKDK (s= D-serine), wh |
| R2053503 | BQ-123 | BQ-123 is a selective endothelin A receptors (ETAR) antagonist with an IC50 valu |
| R2053504 | Ezatiostat (TER199 free base; TLK199) | Ezatiostat (TER199 free base; TLK199) is a tripeptide analog of glutathione and |
| R2053505 | Murepavadin | Murepavadin (POL7080) is a highly effective, specific pseudomonas macrocystis an |
| R2053506 | Fmoc-L-Ser((Ac)3-β-D-GlcNAc)-OH | |
| R2053507 | Fmoc-L-Thr(β-D-GlcNAc(Ac)3)-OH | |
| R2053508 | MV1 | MV1 is an antagonist of IAP (inhibitor of apoptosis protein), leads to protein k |
