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Plerixafor 98%

Plerixafor

源葉(MedMol)
S80094
110078-46-1
C28H54N8
502.78
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80094-5mg 98% ¥120.00元 2 - - -
源葉(MedMol) S80094-10mg 98% ¥180.00元 8 - - -
源葉(MedMol) S80094-25mg 98% ¥300.00元 5 - - -
源葉(MedMol) S80094-100mg 98% ¥800.00元 4 - - -
源葉(MedMol) S80094-1g 98% ¥2000.00元 預(yù)計交期:2-3天 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Plerixafor (AMD 3100) is a selective CXCR4 antagonist with an IC50 of 44 nM. Plerixafor, an immunostimulant and a hematopoietic stem cell (HSC) mobilizer, is an allosteric agonist of CXCR7. Plerixafor inhibits HIV-1 and HIV-2 replication with an EC50 of 1-10 nM
產(chǎn)品描述: Plerixafor (AMD 3100) is a selective CXCR4 antagonist with an IC50 of 44 nM. Plerixafor, an immunostimulant and a hematopoietic stem cell (HSC) mobilizer, is an allosteric agonist of CXCR7. Plerixafor inhibits HIV-1 and HIV-2 replication with an EC50 of 1-10 nM
靶點: 125I-CXCL12-CXCR4:44 nM (IC50);125I-CXCL12-CXCR7;HIV-1:1-10 nM (EC50);HIV-2:1-10 nM (EC50);VirusProtease;HIVProtease;CXCR
體內(nèi)研究:
Plerixafor (2 mg/kg) administration to UUO mice exacerbates renal interstitial T cell infiltration, resulting in increased production of the pro-inflammatory cytokines IL-6 and IFN-γ and decreased expression of the anti-inflammatory cytokine IL-10. Both perivascular and interstitial fibrosis are significantly reduced by the CXCR4 antagonist, Plerixafor (AMD3100) at 8 weeks. LD50, mouse, SC: 16.3 mg/kg; LD50, rat, SC: >50 mg/kg; LD50, mouse and rat, IV injection: 5.2 mg/kg.
參考文獻:
1. Yang J, et al. Continuous AMD3100 Treatment Worsens Renal Fibrosis through Regulation of Bone Marrow Derived Pro-Angiogenic Cells Homing and T-Cell-Related Inflammation. PLoS One. 2016 Feb 22;11(2):e0149926.2. Seki JT, et al. Chemical Stability of Plerixafor after Opening of Single-Use Vial. Can J Hosp Pharm. 2017 Jul-Aug;70(4):270-275. 3. Zabel BA, et al. Elucidation of CXCR7-mediated signaling events and inhibition of CXCR4-mediated tumor cell transendothelial migration by CXCR7 ligands. J Immunol. 2009 Sep 1;183(5):3204-11. 4. De Clercq E, et al. Mozobil? (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration. Antivir Chem Chemother. 2019 Jan-Dec;27:2040206619829382. 5. Mercurio L, et al. Targeting CXCR4 by a selective peptide antagonist modulates tumor microenvironment and microglia reactivity in a human glioblastoma model. J Exp Clin Cancer Res. 2016 Mar 25;35:55. 6. Chu PY, et al. CXCR4 Antagonism Attenuates the Development of Diabetic Cardiac Fibrosis. PLoS One. 2015 Jul 27;10(7):e0133616. 7. Schols D, et al. HIV co-receptor inhibitors as novel class of anti-HIV drugs. Antiviral Res. 2006 Sep;71(2-3):216-26. 8. Zheng J, et al. Toward Normalization of the Tumor Microenvironment for Cancer Therapy. Integr Cancer Ther. 2019;18:1534735419862352.
溶解性: Ethanol  :  50  mg/mL  (99.45  mM;  Need  ultrasonic)    DMF  :  1  mg/mL  (1.99  mM;  Need  ultrasonic)    H2O  :  1  mg/mL  (1.99  mM;  Need  ultrasonic)    DMSO  :  1  mg/mL  (1.99  mM;  ultrasonic  and  warming  and  heat  to  60°C)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.989 ml 9.945 ml 19.889 ml
5 mM 0.398 ml 1.989 ml 3.978 ml
10 mM 0.199 ml 0.994 ml 1.989 ml
50 mM 0.04 ml 0.199 ml 0.398 ml
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參考文獻

質(zhì)檢證書(COA)

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批號:C10000001 貨號:A800001-25g
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摩爾濃度計算器

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