产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 2071607 | Pepstatin | 26305-03-3 | 98% Min. |  |
| Pepstatin inhibits the aspartic protease endothiapepsin. | ||||
| 2071540 | PF-477736 | 952021-60-2 | 98% Min. |  |
| PF-477736, also known as PF-00477736, is a potent CHK1 inhibitor with potential chemo | ||||
| 2071506 | PF-06869206 | 2227425-05-8 | 98% Min. |  |
| PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co | ||||
| 2071401 | Pimodivir ( VX-787 ) | 1629869-44-8 | 98% Min. |  |
| Pimodivir (VX-787) 是一种可口服的甲型流感病毒聚合酶抑制剂，通过 | ||||
| 2062201 | p-Aminophenol sulfate | 85278-22-4 | 98% Min. | |
| 2062020 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE | 26033-20-5 | 96% Min. |  |
| 2061707 | Preladenant | 377727-87-2 | 98% Min. |  |
| Preladenant, also known as SCH 420814, is a potent and selective antagonist at the ad | ||||
| 2061706 | Paquinimod | 248282-01-1 | 98% Min. |  |
| Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi | ||||
| 2061301 | PDM-2 | 688348-25-6 | 98% Min. |  |
| PDM-2 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon r | ||||
| 206701 | PU-WS13 | 1454619-14-7 | 98% Min. |  |
| PU-WS13 is a potent, Grp94-specific Hsp90 inhibitor of the purine scaffold class. PU- | ||||
| S-204148 | 吡啶-2,6-二甲醛 | 5431-44-7 | 98% Min. |  |
| S-204141 | 1-((1aR,6r,10bS)-1,1-二氟-1,1a,6,10b-四氢二苯并[a,e]环丙[c][7]环壬-6-基)哌嗪盐酸盐 | 312905-21-8 | 96% Min. |  |
| 193282 | PZ-2891 | 2170608-82-7 | >98% |  |
| PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂， | ||||
| 31619 | PTI-428(PTI428) | 1953130-87-4 | 98% Min. |  |
| PTI-428是一种研究性CFTR放大器，开发用于治疗CFTR基因中发生F508del | ||||
| 1932011 | PF-05085727 | 1415637-72-7 | >98% |  |
| PF-05085727是一种强效、选择性和脑穿透性磷酸二酯酶2A抑制剂。 | ||||
| 193206 | Petesicatib | 1252637-35-6 | >98% |  |
| Petesicatib是一种组织蛋白酶抑制剂的候选药物。 | ||||
| 193204 | Pyridone 6 | 457081-03-7 | >98% |  |
| 吡啶酮6，也被称为CMP 6或JAK抑制剂I，是一种pan-janus-激活的激酶抑 | ||||
| 193110 | Pretomanid | 187235-37-6 | >98% |  |
| Pretomanid，也被称为PA-824，一种生物还原药物。PA-824具有较强的体 | ||||
| 192282 | PF-4136309 | 1341224-83-6 | >98% |  |
| PF-4136309，又称INCB8761，是一种口服的人趋化因子受体2 (CCR2)拮抗剂 | ||||
| 192272 | 帕利伐米 | 31645-39-3 | >98% |  |
| 帕利伐米，又名ZIO201，是一种具有潜在抗肿瘤活性的合成芥菜化合 | ||||
| 191145 | PF-06873600 | 2185857-97-8 | >98% |  |
| PF-06873600是一种口服生物利用的细胞周期蛋白依赖性激酶(CDK)抑制 | ||||
| 191141 | PF04418948 | 1078166-57-0 | >98% |  |
| PF-04418948是一种新型高效选择性前列腺素EP2受体拮抗剂。 | ||||
| 1812253 | PF74 | 1352879-65-2 | >98% |  |
| PF-3450074，又称PF74，是一种针对HIV衣壳蛋白的HIV-1抑制剂。PF74与HI | ||||
| 1812135 | PT2385 | 1672665-49-4 | >98% |  |
| PT2385是一种口服活性小分子缺氧诱导因子(HIF)-2alpha抑制剂，具有潜 | ||||
| 1811232 | PF 1022A | 133413-70-4 | >98% |  |
| PF1022A是一种新型的驱虫药，与嗜乳激素样跨膜受体结合，对线虫 | ||||
| 1811221 | 普拉曲沙 | 146464-95-1 | >98% |  |
| 普拉曲沙是二氢叶酸还原酶(DHFR)的一种叶酸模拟抑制剂，对叶酸还 | ||||
| 1811162 | PF-05231023 | 1037589-69-7 | >98% |  |
| PF-05231023是一种长效FGF21仿生产品。PF-05231023可以减轻非人类灵长类 | ||||
| 1810254 | PA-8 | 878437-15-1 | >98% |  |
| PA-8是PAC1受体的小分子拮抗剂。 | ||||
| 1810242 | Pyronaridine Tetraphosphate | 76748-86-2 | >98% |  |
| Pyronaridine Tetraphosphate是一种抗疟药，能阻断b -血凝素的形成，抑制 | ||||
| 1810234 | PH-002 | 1311174-68-1 | >98% |  |
| PH-002是一种新型的载脂蛋白(apo) E4分子内区域相互作用的神经细胞 | ||||