产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 20653 | Contezolid free base | 1112968-42-9 | 98% Min. |  |
| Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i | ||||
| 20645 | CP-506 ( Synonyms: SN-36506 ) | 2227304-19-8 | 98% Min. | _2227304-19-8.png) |
| CP-506 (SN-36506) 是一种缺氧激活的 DNA 烷基化氮芥化合物前药，能够 | ||||
| 20632 | Censavudine | 634907-30-5 | 98% Min. |  |
| Censavudine, also known as OBP-601, BMS-986001 or festinavir, is a nucleoside reverse | ||||
| 20626 | CFI-402257 free base | 1610759-22-2 | 98% Min. |  |
| CFI-402257 was discontinued for commercial reason. | ||||
| 20622 | Cantharidine | 56-25-7 | 98% Min. |  |
| Cantharidine (free base) is a PP1/2A inhibitor found in Canarthis vesicatoria. It inh | ||||
| 20575 | Compound E | 209986-17-4 | 98% Min. |  |
| Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch | ||||
| 20562 | 0990CL | 511514-03-7 | 98% Min. |  |
| 0990CL is an inhibitor of heterotrimeric Gαi subunits. 0990CL showed direct interact | ||||
| 20558 | CBiPES HCl | 856702-40-4 | 98% Min. |  |
| CBiPES HCl is a selective positive allosteric modulator of the mGlu2 receptor. | ||||
| 20555 | COH1 inhibitor | 20217-22-5 | 98% Min. |  |
| COH1 is a ribonucleotide reductase (RR) inhibitor. | ||||
| 20510 | CC-92480 ( Mezigdomide ) | 2259648-80-9 | ≧98.0% |  |
| CC-92480 是一种有效的新型 CELMoD 化合物，旨在快速最大程度地降解 | ||||
| 20488 | CYM-50308 | 1345858-76-5 | 98% Min. |  |
| CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity | ||||
| 20478 | CRANAD-28 | 1623747-97-6 | 98% Min. |  |
| CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts | ||||
| 20467 | CPPHA | 693288-97-0 | 98% Min. |  |
| CPPHA is a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5 | ||||
| 20455 | Camlipixant ( BLU-5937 ) | 1621164-74-6 | ≧98.0% | _1621164-74-6.png) |
| Camlipixant 是一种在研的每日两次口服 P2X3 受体拮抗剂，用于治疗 | ||||
| 20441 | CMP3a | 647834-15-9 | 98% Min. |  |
| CMP3a is a NEK2 kinase inhibitor. CMP3a efficiently attenuated GBM growth in a mouse | ||||
| 122622 | CNS004 抑制剂 | 695205-24-4 | ≧98.0% |  |
| CNS004是一种基于谷氨酸浓度增强NMDA受体电流的新型化合物。这种 | ||||
| 20423 | 6-氯-4-羟基-[1,5]-萘啶-3-羧酸乙酯 | 127094-58-0 | 98% Min. |  |
| 20418 | 6-氯-4-(乙基氨基)-3-吡啶甲醛 | 959163-01-0 | 98% Min. | -3-Pyridinecarboxaldehyde_959163-01-0.png) |
| 20408 | 3-(氯甲基)-2-(1-异丙基-1H-吡唑-5-基)吡啶盐酸盐 | 1446321-95-4 | 98% Min. | -2-(1-isopropyl-1H-pyrazol-5-yl)pyridine_hydrochloride_1446321-95-4.png) |
| 20393 | 2-(4-chlorophenyl)-2,2-difluoroacetic acid | 475301-73-6 | 98% Min. | -2,2-difluoroacetic_acid_475301-73-6.png) |
| 20387 | 2-氯代-4'-氟苯乙酮 | 456-04-2 | 98% Min. |  |
| G20385 | 4-cyclohexyl-1,1-dimethylpiperazin-1-ium iodide | 865144-54-3 | 98% Min. |  |
| 822225 | Cadisegliatin (TTP-399) | 859525-02-3 | ≧98.0% |  |
| Cadisegliatin(TTP-399) 是一种潜在的肝脏选择性葡萄糖激酶 (GK) 激活剂 | ||||
| L20350 | CR8 hydrochloride | 1786438-30-9 | 98% Min. |  |
| CR8 is a potent and selective inhibitor of CDK. CR8 is a more potent pyridyl analogue | ||||
| L20348 | CCT020312 | 324759-76-4 | 98% Min. |  |
| CCT020312 is a potent and selective EIF2AK3 Activator. CCT020312 modulates the biolog | ||||
| L20343 | CC-671 | 1618658-88-0 | 98% Min. |  |
| CC-671 is a potent and selective dual inhibitor of TTK (Mps1) and CLK2. | ||||
| L20340 | RO495 | 1258296-60-4 | 98% Min. |  |
| RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2 | ||||
| 20328 | 3-cyclopropyl-7-methyl-6-nitro-2H-benzo[e][1,3]oxazin-4(3H)-one | 1038984-34-7 | 96% Min. | -one_1038984-34-7.png) |
| 20322 | CB-103 | 218457-67-1 | 98% Min. |  |
| CB-103 is a γ-secretase inhibitor. CB-103 inhibits Notch signaling in primary human | ||||
| 20313 | Cenerimod ( ACT-334441 ) | 1262414-04-9 | ≧98.0% |  |
| Cenerimod 是一种有效的、具有口服活性免疫调节剂，EC50 值为 2.7 nM | ||||