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S80810

Miltefosine

源葉(MedMol) 98%
  • 英文名:
  • Miltefosine
  • 別名:
  • 米替福星;hexadecyl 2-(trimethylammonio)ethyl phosphate
  • CAS號:
  • 58066-85-6
  • 分子式:
  • C21H46NO4P
  • 分子量:
  • 407.57
  • 核磁/質(zhì)譜:
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S80810-100mg 98% ¥43.00元 10 - - - EA 加入購物車
源葉(MedMol) S80810-500mg 98% ¥134.00元 2 - - - EA 加入購物車
源葉(MedMol) S80810-1g 98% ¥224.00元 4 - - - EA 加入購物車
源葉(MedMol) S80810-5g 98% ¥850.00元 4 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻(1篇)

質(zhì)檢證書(COA)

摩爾濃度計算器

相關(guān)產(chǎn)品

  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Miltefosine is a broad spectrum antimicrobial, anti-leishmanial, phospholipid agent acting by inhibiting the PI3K/Akt activity. Miltefosine is an inhibitor of CTP-phosphocholine cytidyltransferase (CCT)
  • 靶點: HIV-1
  • 體內(nèi)研究:
    Mice are randomized into groups of 5 and injected intraperitoneally 5 days a week with 50 mg/kg of either Miltefosine or Perifosine dissolved in PBS, or equivalent volume of vehicle (PBS). Both Miltefosine and Perifosine inhibit the growth rate of tumors compared with vehicle-treated mice. By day 14 after treatment, there is an approximately 50% decrease in average tumor volume in Perifosine- and Miltefosine-treated mice, compared with vehicle-treated mice (P<0.04). Tumor growth is also significantly retarded (P<0.04 for Perifosine and P≤0.055 for Miltefosine by linear mixed-effects model analysis). Immunohistochemical analyses display an overall reduction in staining for phosphorylated ribosomal S6 protein in tumor sections from Miltefosine- and Perifosine-treated mice compared with the PBS-treated mice. This reduced phosphorylation correlated with the delay in tumor progression in drug-treated animals
  • 參考文獻:
    1. Chugh P, et al. Akt inhibitors as an HIV-1 infected macrophage-specific anti-viral therapy. Retrovirology. 2008 Jan 31;5:11 2. Uberall F, et al. Hexadecylphosphocholine inhibits inositol phosphate formation and protein kinase C activity. Cancer Res. 1991 Feb 1;51(3):807-12. 3. Bhatt AP, et al. Dual inhibition of PI3K and mTOR inhibits autocrine and paracrine proliferative loops in PI3K/Akt/mTOR-addicted lymphomas. Blood. 2010 Jun 3;115(22):4455-63. 4. Eissa MM, et al. Miltefosine Lipid Nanocapsules for Single Dose Oral Treatment of Schistosomiasis Mansoni: A Preclinical Study. PLoS One. 2015 Nov 17;10(11):e0141788 5. de Freitas-Junior PR, et al. Effects of miltefosine on the proliferation, ultrastructure, and phospholipid composition of Angomonas deanei, a trypanosomatid protozoan that harbors a symbiotic bacterium. FEMS Microbiol Lett. 2012 Aug;333(2):129-37.
  • 溶解性: H2O  :  50  mg/mL  (122.68  mM;  Need  ultrasonic)    DMSO  :  5  mg/mL  (12.27  mM;  Need  ultrasonic)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.454 ml 12.268 ml 24.536 ml
    5 mM 0.491 ml 2.454 ml 4.907 ml
    10 mM 0.245 ml 1.227 ml 2.454 ml
    50 mM 0.049 ml 0.245 ml 0.491 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
  • 1. 梁德鳳,周鑫才,吳蕓菲.二甲雙胍調(diào)節(jié)PI3K/AKT通路對高糖誘導(dǎo)牙周膜成纖維細胞凋亡的影響研究[J].口腔醫(yī)學(xué)研究,2020,36(12):1103-1107.
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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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