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S82937

MK-5172

源葉(MedMol) 99%
  • 英文名:
  • MK-5172
  • 別名:
  • MK-5172||MK5172; UNII-8YE81R1X1J; (1aR,5S,8S,10R,22aR)-5-tert-butyl-N-((1R,2S)-1-{[(cyclopropylsulfonyl)amino]carbonyl}-2-vinylcyclopropyl)-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-te
  • CAS號(hào):
  • 1350514-68-9
  • 分子式:
  • C38H50N6O9S
  • 分子量:
  • 766.9
  • 核磁/質(zhì)譜:
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購(gòu)物車...
源葉(MedMol) S82937-1mg 99% ¥204.00元 >10 - - - EA 加入購(gòu)物車
源葉(MedMol) S82937-5mg 99% ¥670.00元 >10 - - - EA 加入購(gòu)物車
源葉(MedMol) S82937-10mg 99% ¥920.00元 >10 - - - EA 加入購(gòu)物車
源葉(MedMol) S82937-25mg 99% ¥1850.00元 >10 - - - EA 加入購(gòu)物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

摩爾濃度計(jì)算器

相關(guān)產(chǎn)品

  • 提示:詳情請(qǐng)下載說(shuō)明書(shū)。
  • 產(chǎn)品描述: Grazoprevir (MK-5172) is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Kis of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), respectively. Grazoprevir inhibits SARS-CoV-2 3CLpro activity
  • 靶點(diǎn): Ki: 0.01±<0.01 nM (gt1b), 0.01±0.01 nM (gt1a), 0.08±0.02 nM (gt2a), 0.15±0.06 nM (gt2b), 0.90±0.2 nM (gt3a);HCVProtease;?SARS-CoV
  • 體內(nèi)研究:
    Grazoprevir (MK-5172) demonstrates efficacy in vivo against chronic-HCV-infected chimpanzees. When dosed to dogs, Grazoprevir (MK-5172) shows low clearance of 5 mL/min/kg and a 3 h half-life after iv dosing and has good plasma exposure (AUC=0.4 μM h) after a 1 mg/kg oral dose. Dog liver biopsy studies showed that the liver concentration of Grazoprevir after the 1 mg/kg oral dose is 1.4 μM at the 24 h time point. Similar to its behavior in rats, Grazoprevir demonstrates effective partitioning into liver tissue and maintains high liver concentration, relative to potency, 24 h after oral dosing in dogs
  • 參考文獻(xiàn):
    1. Summa V, et al. MK-5172, a selective inhibitor of hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants. Antimicrob Agents Chemother. 2012 Aug;56(8):4161-7. 2. Harper S, et al. Discovery of MK-5172, a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor. ACS Med Chem Lett. 2012 Mar 2;3(4):332-6. 3. Qi Sun, et al. Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease. Signal Transduct Target Ther. 2021 May 29;6(1):212.
  • 溶解性: Ethanol  :  66.67  mg/mL  (86.93  mM;  Need  ultrasonic)    DMSO  :  50  mg/mL  (65.20  mM;  Need  ultrasonic)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.304 ml 6.52 ml 13.04 ml
    5 mM 0.261 ml 1.304 ml 2.608 ml
    10 mM 0.13 ml 0.652 ml 1.304 ml
    50 mM 0.026 ml 0.13 ml 0.261 ml
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質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)


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