普乐沙福
| CAS号 | 110078-46-1 | 货号 | BCP02337 |
| 中文名 | 普乐沙福 | ||
| 英文名 | Plerixafor | ||
| 中文别名 | |||
| 英文别名 | JM-3100; JM 3100; JM3100; AMD-3100; AMD 3100; AMD3100; | ||
| 分子式 | C28H54N8 | 分子量 | 502.78 |
| 生物活性 | Plerixafor inhibits CXCL12-mediated chemotaxis with a potency lightly better than its affinity for CXCR4. Plerixafor also antagonizes SDF-1/CXCL12 ligand binding with an IC50 of 651 nM. Plerixafor inhibits SDF-1 mediated GTP-binding, SDF-1 mediated calcium flux and SDF-1 stimulated chemotaxis with IC50 of 27 nM, 572 nM and 51 nM, respectively. Plerixafor does not inhibit calcium flux against cells expressing CXCR3, CCR1, CCR2b, CCR4, CCR5 or CCR7 when stimulated with their cognate ligands, nor does Plerixafor inhibit receptor binding of LTB4. Plerixafor does not, on its own, induce a calcium flux in the CCRF–CEM cells, which express multiple GPCRs including CXCR4, CCR4 and CCR7. | ||
| 上下游产品 | 155148-31-5（八盐酸普乐沙福） 155148-32-6（普乐沙福八氢溴酸盐） | ||
| 信号通路 | GPCR/G Protein | ||
| 靶 点 | CXCR | ||
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Synergetic regulation of kupffer cells, extracellular matrix and hepatic stellate cells with versatile CXCR4-inhibiting nanocomplex for magnified therapy in liver fibrosis
购于瀚香生物(Biochempartner)的普乐沙福(CAS:110078-46-1)被引用 |
|
Balancing polymer hydrophobicity for ligand presentation and siRNA delivery in dual function CXCR4 inhibiting polyplexes
购于瀚香生物(Biochempartner)的普乐沙福(CAS:110078-46-1)被引用 |
结构式
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