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Maraviroc

    99%

Maraviroc

源葉(MedMol)
S81468
376348-65-1
C29H41F2N5O
513.67
MFCD13188530
UK-427857, Celsentri;4,4-difluoro-N-((S)-3-(3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-aza-bicyclo[3.2.1]octan-8-yl)-1-phenylpropyl)cyclohexanecarboxamide
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) S81468-5mg 99% ¥125.00元 3 - - -
源葉(MedMol) S81468-10mg 99% ¥238.00元 7 - - -
源葉(MedMol) S81468-25mg 99% ¥430.00元 9 - - -
源葉(MedMol) S81468-50mg 99% ¥731.00元 6 - - -
源葉(MedMol) S81468-100mg 99% ¥1020.00元 預計交期:2-3天 - - -
源葉(MedMol) S81468-200mg 99% ¥1955.00元 預計交期: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 相關產(chǎn)品

產(chǎn)品介紹

Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV.
產(chǎn)品描述: Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV.
靶點: MIP-1α-CCR5:3.3 nM (IC50, in HEK-293 cell membrane);MIP-1β-CCR5:7.2 nM (IC50, in HEK-293 cell membrane);RANTES-CCR5:5.2 nM (IC50, in HEK-293 cell membrane);HIV-1 (Ba-L):1.1 nM (IC50, in PM-1 cells);HIVProtease;?CCR
體內(nèi)研究: Clearance values are moderate to high in both rat and dog species following i.v. administration (74 and 21 mL/min/kg, respectively). Maraviroc also has a moderate volume of distribution in both species (4.3 to 6.5 liters/kg). The half-life values of maraviroc are 0.9 h in the rat and 2.3 h in the dog. Following oral administration (2 mg/kg) to the dog, the Cmax(256 ng/mL) occurs 1.5 h. post-dose, and the bioavailability is 40%. For the rat, investigation of the concentrations obtain in the portal vein following oral administration indicated that approximately 30% of the administered dose is absorbed from the intestinal tract. In the DSS/TNBS colitis and in the transfer model, Maraviroc attenuates development of intestinal inflammation by selectively reducing the recruitment of CCR5 bearing leukocytes
參考文獻: 1. Dorr P, et al. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob Agents Chemother. 2005 Nov;49(11):472 2. Mencarelli A, et al. Highly specific blockade of CCR5 inhibits leukocyte trafficking and reduces mucosal inflammation in murine colitis. Sci Rep. 2016 Aug 5;6:30802. 3. Romero-Sánchez MC, et al. Effect of maraviroc on HIV-disease progression-related biomarkers. Antimicrob Agents Chemother. 2012 Nov;56(11):5858-64. 4. Huilin Mou, et al. NRSF and CCR5 Established Neuron-glia Communication during Acute and Chronic Stresses. Journal of Drug Metabolism & Toxicology. January 10, 2016.
溶解性: DMSO  :  50  mg/mL  (97.34  mM;  Need  ultrasonic)    Ethanol  :  6.5  mg/mL  (12.65  mM;  Need  ultrasonic)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.947 ml 9.734 ml 19.468 ml
5 mM 0.389 ml 1.947 ml 3.894 ml
10 mM 0.195 ml 0.973 ml 1.947 ml
50 mM 0.039 ml 0.195 ml 0.389 ml
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參考文獻

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摩爾濃度計算器

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