Reparixin

目录号: A12383

CXCL8/CXCR1/2 Inhibitor

Reparixin Chemical Structure

CAS NO. 266359-83-5

Reparixin is a potent inhibitor of both CXCL8 receptors CXCR1/2, it inhibits weakly CXCR2-mediated cell migration (IC50=100 nM), whereas it strongly blocks CXCR1-mediated chemotaxis (IC50=1 nM).

库存: 现货

规格 价格 数量
5 mg
¥ 1,800.00
10 mg
¥ 3,000.00
25 mg
¥ 6,800.00
100 mg
¥ 8,800.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

Reparixin is a potent inhibitor of both CXCL8 receptors CXCR1/2, it inhibits weakly CXCR2-mediated cell migration (IC50=100 nM), whereas it strongly blocks CXCR1-mediated chemotaxis (IC50=1 nM).
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 35.29 mL 176.44 mL 352.87 mL
0.5 mM 7.06 mL 35.29 mL 70.57 mL
1 mM 3.53 mL 17.64 mL 35.29 mL
5 mM 0.71 mL 3.53 mL 7.06 mL

*The above data is based on the productmolecular weight 283.39. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A12383
MECHANISM OF ACTION Inhibitor
M. Wt 283.39
Formula C14H21NO3S
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 266359-83-5
Synonyms DF 1681Y; Repertaxin
SMILES C[C@H](C1=CC=C(C=C1)CC(C)C)C(=O)NS(=O)(=O)C

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