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Tenofovir alafenamide

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  • ¥109 - 2730
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  • A138397
  • 2026年05月21日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 英文名

      Isopropyl ((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(phenoxy)phosphoryl)-L-alaninate

    • 供应商

      上海安毕达生物科技有限公司

    • CAS号

      379270-37-8

    • 规格

      50μL/1mL/5mg/10mg/25mg/50mg/100mg

    规格:50μL产品价格:¥109.0
    规格:1mL产品价格:¥440.0
    规格:5mg产品价格:¥420.0
    规格:10mg产品价格:¥630.0
    规格:25mg产品价格:¥1295.0
    规格:50mg产品价格:¥2030.0
    规格:100mg产品价格:¥2730.0
    Tenofovir alafenamide 是替诺福韦的前体化合物,通过抑制逆转录酶活性,常用于 HIV 和乙型肝炎病毒感染机制的研究。

    Reverse transcription and integration are the defining features of the Retroviridae; the common name "retrovirus" derives from the fact that these viruses use a virally encoded enzyme, reverse transcriptase (RT), to convert their RNA genomes into DNA3. GS-7340 (Tenofovir alafenamide) is an investigational oral prodrug of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor. Tenofovir alafenamide (GS-7340) hemifumarate is an amidate prodrug of Tenofovir with good oral bioavailability and increases plasma stability compared to Tenofovir disoproxil fumarate (TDF)4. GS-7340 antiviral activities are similar across all cell types, ranging from 5 to 7 nM. The antiviral activity of TAF (Tenofovir alafenamide) is evaluated against a panel of HIV-1 and HIV-2 isolates, including HIV-1 group M subtypes A to G, as well as group N and O isolates. Overall, for the 29 primary HIV-1 isolates tested in PBMCs, TAF EC50s range from 0.1 to 12 nM, with a mean EC50 of 3.5 nM compared to a mean EC50 of 11.8 nM for AZT, which is used as an internal control. For the HIV-2 isolates, the mean EC50s are 1.8 nM for TAF and 6.4 nM for AZT5. GS-7340 is less nephrotoxic than its predecessor prodrug, tenofovir disoproxil fumarate (TDF). GS-7340's unique pharmacokinetic profile enables provision of lower required doses for antiviral efficacy. Lower concentrations reach renal tubules minimizing intracellular accumulation and mitochondrial damage6.

    溶解方案(细胞实验)

    DMSO 中的溶解度 : ≥ 31 mg/mL (65.06 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)|H2O 中的溶解度 : 6.67 mg/mL (14.00 mM; 超声助溶)|* "≥" means soluble, but saturation unknown.

    溶解方案(动物实验)

    "方案 一": "请依序添加每种溶剂:10% DMSO 40% PEG300 5% Tween-80 45% SalineSolubility: ≥ 2.08 mg/mL (4.37 mM); 澄清溶液 此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液。以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL。生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。"

    "方案 二": "请依序添加每种溶剂:10% DMSO 90% (20% SBE-β-CD in Saline)Solubility: ≥ 2.08 mg/mL (4.37 mM); 澄清溶液 此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液。以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液 中,混合均匀。2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。"

    "方案 三": "请依序添加每种溶剂:10% DMSO 90% Corn OilSolubility: ≥ 2.08 mg/mL (4.37 mM); 澄清溶液 此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。"

    "方案 一": "请依序添加每种溶剂:PBSSolubility: 40 mg/mL (83.95 mM); 澄清溶液; 超声助溶"

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    图标文献和实验
    该产品被引用文献
    Lee WA, He GX, et al. Selective intracellular activation of a novel prodrug of the human immunodeficiency virus reverse transcriptase inhibitor tenofovir leads to preferential distribution and accumulation in lymphatic tissue. Antimicrob Agents Chemother. 2005 May;49(5):1898-906.

    Chapman H, Kernan M, et al. Purification of PMPA amidate prodrugs by SMB chromatography and x-ray crystallography of the diastereomerically pure GS-7340. Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):1085-90.

    Wei-Shau Hu,et al. HIV-1 reverse transcription. Cold Spring Harb Perspect Med. 2012 Oct 1;2(10):a006882.

    Babusis D, et al. Mechanism for effective lymphoid cell and tissue loading following oral administration of nucleotide prodrug GS-7340. Mol Pharm. 2013. 10(2), 459-66.

    Ruane PJ, et al. Antiviral activity, safety, and pharmacokinetics/pharmacodynamics of tenofovir alafenamide as 10-day monotherapy in HIV-1-positive adults. J Acquir Immune Defic Syndr. 2013. 63(4),449-55.

    Tessa K Novick,et al. Tenofovir alafenamide nephrotoxicity in an HIV-positive patient: A case report. Medicine (Baltimore). 2017. 96(36), e8046.

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    文献支持
    Tenofovir alafenamide
    ¥109 - 2730