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S88774

HCH6-1

源叶(MedMol) 98%
  • 英文名:
  • D-Phenylalanine, N-benzoyl-L-tryptophyl-, methyl ester
  • 别名:
  • CAS号:
  • 1435265-06-7
  • 分子式:
  • C28H27N3O4
  • 分子量:
  • 469.53168
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S88774-10mg 98% ¥164.00元 >10 - - - EA 加入购物车
源叶(MedMol) S88774-50mg 98% ¥550.00元 6 - - - EA 加入购物车
源叶(MedMol) S88774-100mg 98% ¥950.00元 6 - - - EA 加入购物车
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产品介绍

参考文献

质检证书(COA)

摩尔浓度计算器

相关产品

  • 产品描述: HCH6-1 is a potent and competitive dipeptide antagonist of Formyl peptide receptor 1 (FPR1). HCH6-1 inhibits chemotaxis, superoxide anion generation, and elastase release in human neutrophils specifically activated by fMLF (an FPR1 agonist). HCH6-1 has protective effects against acute lung injury (ALI) in vivo and can be used for the research of FPR1-involved inflammatory lung diseases
  • 靶点: IC50: Formyl peptide receptor 1 (FPR1)
  • 体内研究:
    HCH6-1 (intraperitoneal injection; 50 mg/kg; 1 h before LPS spray or 30 min after LPS spray) alone does not induce airspace inflammation. HCH6-1 pretreatment reduces inflammatory cell infiltration and distortion of pulmonary architecture in the presence of LPS. HCH6-1 posttreatment shows inhibitory effects on neutrophil accumulation and lung damage in LPS-induced ALI mice Animal Model: C57BL/6 mice (20-25 g, 7-8 weeks old) Dosage: 50 mg/kg Administration: Intraperitoneal injection; 50 mg/kg; 1 h before LPS spray or 30 min after LPS spray Result: Ameliorated ALI in LPS-induced mice.HCH6-1-mediated decreasing of neutrophil recruitment serves as a protective mechanism in ALI mice.
  • 参考文献:
    1. Yang SC, et al. Dipeptide HCH6-1 inhibits neutrophil activation and protects against acute lung injury by blocking FPR1. Free Radic Biol Med. 2017 May;106:254-269
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.13 ml 10.649 ml 21.298 ml
    5 mM 0.426 ml 2.13 ml 4.26 ml
    10 mM 0.213 ml 1.065 ml 2.13 ml
    50 mM 0.043 ml 0.213 ml 0.426 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)


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