Reparixin L-lysine salt

作者: 莫小枫 | 来源:发表于2017-11-30 14:44 被阅读0次

    "目录号: HY-15252

    GPCR/G ProteinImmunology/Inflammation-

    Reparixin L-lysine salt 是一种有效的 CXCL8 受体CXCR1/2变构抑制剂,微弱抑制CXCR2- 调节的细胞迁移 (IC50=100 nM),但强抑制CXCR1- 调节的细胞趋化 (IC50=1 nM)。

    CXCR

    相关产品

    Plerixafor octahydrochloride-Reparixin-SCH 527123-Danirixin-SCH 546738-AMD 3465 hexahydrobromide-AMG 487-SB225002-AMD-070 hydrochloride-SCH 563705-NBI-74330-MSX-122-LY2510924-WZ811-IT1t dihydrochloride-

    生物活性

    Description

    Reparixin L-lysine salt is a potent and specific allosteric inhibitor of both CXCL8 receptorsCXCR1/2, it inhibits weaklyCXCR2-mediated cell migration (IC50=100 nM), whereas it strongly blocksCXCR1-mediated chemotaxis (IC50=1 nM).

    IC50& Target

    IC50: 5.6/80 nM (CXCR1wt/CXCR1Ile43Val, in L1.2 cell)[1]

    In Vitro

    Reparixin is a potent functional inhibitor of CXCL8-induced biological activities on human PMNs with a marked selectivity (around 400-fold) for CXCR1, as shown in specific experiments on CXCR1/L1.2 and CXCR2/L1.2 transfected cells and on human PMNs. The efficacy of Reparixin is significantly lower in L1.2 cells expressing Ile43Val CXCR1 mutant (IC50values of 5.6 nM and 80 nM for CXCR1 wt and CXCR1 Ile43Val, respectively)[1]. Reparixin is a non-competitive allosteric inhibitor of IL-8 receptors with a 400-fold higher efficacy in inhibiting CXCR1 activity than CXCR2[2].

    In Vivo

    The pharmacokinetics and metabolism of Reparixin are investigated in rats and dogs after intravenous administration of [14C]-Reparixin L-lysine salt. Plasma protein binding of Reparixin is >99% in the laboratory animals and humans up to 50 μg/mL, but lower at higher concentrations. Although radioactivity is rapidly distributed into rat tissues, Vssis low (about 0.15 L/kg) in both rat and dog. Nevertheless, Reparixin is more rapidly eliminated in rats (t1/2~0.5 h) than in dogs (t1/2~10 h)[3].

    Clinical Trial

    NCT01220856

    Dompé Farmaceutici S.p.A

    Pancreatic Islet Transplantation in Type 1 Diabetes Mellitus

    July 2010

    Phase 2

    NCT02001974

    Dompé Farmaceutici S.p.A-PRA Health Sciences

    Metastatic Breast Cancer

    January 2012

    Phase 1

    NCT01861054

    Dompé Farmaceutici S.p.A

    Breast Cancer

    February 2013

    Phase 2

    NCT03031470

    Dompé Farmaceutici S.p.A

    Ischemia-reperfusion Injury in Liver Transplant-Early Allograft Dysfunction

    March 2015

    Phase 2

    NCT02370238

    Dompé Farmaceutici S.p.A-PRA Health Sciences

    Metastatic Breast Cancer

    June 2015

    Phase 2

    NCT00248040

    Dompé Farmaceutici S.p.A

    Ischemia-Reperfusion Injury-Kidney Diseases

    October 2005

    Phase 2

    NCT01967888

    Dompé Farmaceutici S.p.A

    Pancreatectomy for Chronic Pancreatitis

    February 2014

    Phase 2-Phase 3

    NCT01817959

    Dompé Farmaceutici S.p.A

    Islet Transplantation in Diabetes Mellitus Type 1,

    October 2012

    Phase 3

    NCT00224406

    Dompé Farmaceutici S.p.A

    Ischemia-Reperfusion Injury-Lung Transplantation

    May 2005

    Phase 2

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    References

    [1].Moriconi A, et al. Design of noncompetitive interleukin-8 inhibitors acting on CXCR1 and CXCR2. J Med Chem. 2007 Aug 23;50(17):3984-4002.

    [2].Bertini R, et al. Receptor binding mode and pharmacological characterization of a potent and selective dual CXCR1/CXCR2non-competitive allosteric inhibitor. Br J Pharmacol. 2012 Jan;165(2):436-54.

    [3].Midgley I, et al. Species differences in the pharmacokinetics and metabolism of reparixin in rat and dog. Xenobiotica. 2006 May;36(5):419-40.

    [4].Catrina, Anca, et al. METHODS AND COMPOUNDS FOR THE TREATMENT OF BONE LOSS AND/OR PAIN. US 20170105971 A1.

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