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抑制剂&激动剂
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TargetMol产品目录中 "H1N1"的结果
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TargetMol产品目录中 "

H1N1

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  • 抑制剂&激动剂
    54
    TargetMol | Inhibitors_Agonists
  • 化合物库
    1
    TargetMol | Compound_Libraries
  • 重组蛋白
    161
    TargetMol | Recombinant_Protein
  • 多肽产品
    1
    TargetMol | Peptide_Products
  • 抗体抑制剂
    1
    TargetMol | Inhibitory_Antibodies
  • 染料试剂
    1
    TargetMol | Dye_Reagents
  • 天然产物
    12
    TargetMol | Natural_Products
  • 同位素
    1
    TargetMol | Isotope_Products
  • 检测抗体
    23
    TargetMol | Antibody_Products
  • Neuraminidase-IN-1
    Novel NA Inhibitor, Compound Y-1
    T85552379438-80-7
    Neuraminidase-IN-1 (Compound Y-1) 是一种神经氨酸酶抑制剂,其IC50值为 0.21 μM,具有抗H1N1流感病毒的活性。
    • ¥ 227
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • CBS1117
    T8793959245-08-0
    CBS1117 是一种病毒进入抑制剂,对甲型流感病毒 A Puerto Rico 8 34 的 IC50为 70 nM。它干扰血凝素介导的融合过程。
    • ¥ 478
    In stock
    规格
    数量
  • ML303
    T120771638211-04-7
    ML303 是吡唑并吡啶流感病毒非结构蛋白 1 的一种拮抗剂,IC90值为 155 nM。它对流感病毒H1N1亚型的EC50值为0.7 μM。
    • ¥ 412
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Ganoderic acid TR
    灵芝酸 TR
    T11364862893-75-2
    Ganoderic acid TR 是一种从药用灵芝中分离出口来的三萜化合物,是 H5N1 和 H1N1 NAs 抑制剂,具有广谱的抗病毒活性。
    • ¥ 1960
    In stock
    规格
    数量
  • Ganoderic acid T-Q
    TN4105112430-66-7
    Ganoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs.
    • ¥ 3710
    待询
    规格
    数量
  • eckol
    T2402588798-74-7In house
    Eckol inhibits ultraviolet B-induced cell damage by a decrease in oxidative stress in human keratinocytes.This compound is unstable in powder form and other related salt forms are recommended.
    • 待询
    3-6月
    规格
    数量
  • Dendrobine
    石斛碱
    T5S17082115-91-5
    Dendrobine 是从石斛中分离的一种生物碱,对甲型流感病毒具有抗病毒活性。
    • ¥ 239
    In stock
    规格
    数量
  • U0126-EtOH
    U0126 Ethanol, U0126
    T62231173097-76-1
    U0126-EtOH (U0126 Ethanol) 是一种非 ATP 竞争性的选择性MEK1和MEK2抑制剂,IC50分别为 72 nM 和 58 nM。U0126-EtOH 可抑制自噬和线粒体自噬。
    • ¥ 167
    In stock
    规格
    数量
  • PP7
    T12526433238-84-7
    PP7 是一种PB1-PB2互作抑制剂,IC50为 8.6 μM。PB1-PB2 抑制病毒聚合酶的活性,IC50为9.5 μM。它对甲型流感病毒 A 包括 (H1N1)pdm09 (EC50=1.4 μM),A(H7N9),A(H9N2) 亚型具有抗病毒活性。
    • ¥ 780
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Influenza A virus-IN-1
    T397782250313-14-3
    Influenza A virus-IN-1, a dihydropyrrolidones derivative, is a highly effective inhibitor of various subtypes of influenza A virus (IAV) with IC 50 values ranging from 3.11 μM to 7.13 μM. It effectively suppresses IAV replication and enhances the expression of key antiviral cytokines, such as IFN-β, and the antiviral protein MxA.
    • ¥ 10600
    6-8周
    规格
    数量
  • Crystal Violet
    氯化结晶紫, 结晶紫, Methyl Violet 10B, Hexamethylpararosaniline chloride, Gentian Violet, Basic Violet 3
    T1343L548-62-9
    Crystal Violet (Hexamethylpararosaniline chloride) 是革兰氏染色染料。它对H1N1具有抗病毒作用,有显著杀菌活性。
    • ¥ 225
    In stock
    规格
    数量
  • β-Cyclodextrin
    Betadex, Beta-Cyclodextrin, beta-环糊精, Cyclomaltoheptaose, β-环糊精, NSC 269471
    T29517585-39-9
    β-Cyclodextrin (NSC 269471) 是一种环状多糖,由 α-D-吡喃型葡萄糖单元通过 α-(1,4) 糖苷键连接而成,通常用于增强药物的溶解度,可抑制流感病毒H1N1
    • ¥ 99
    In stock
    规格
    数量
  • Amitivir
    LY217896, LY 217896, 阿米替韦, LY-217896
    T26619111393-84-1
    Amitivir (LY 217896) 是一种噻二唑衍生物,对 A 和 B 型流感病毒均有效,对正粘病毒和副粘病毒具有广泛的抗病毒活性。
    • ¥ 1300
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Mbx2329
    T92311438272-42-4
    MBX2329 是一种流感病毒抑制剂,能特异性地抑制血凝素介导的病毒进入,HIV HA(H5) 的 IC90值为8.6 μM。它能够有效地抑制多种甲型流感病毒。
    • ¥ 108
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • 2-PADQZ
    2-PADQZ, 2PADQZ
    T1984960547-97-9
    DPQ is an antiviral compound. DPQ has also been shown to bind to a widened RNA major groove at the internal loop. DPQ acts against the H1N1 and H3N2 strains of influenza A as well as influenza B.
    • ¥ 10600
    2-4周
    规格
    数量
  • Antiviral agent 65
    T2033961004319-61-2
    Antiviralagent 65 (compound 9) 是靶向甲型H1N1流感病毒的抗病毒试剂,具有EC50=7 μg mL的活性。
    • 待询
    10-14周
    规格
    数量
  • Neuraminidase-IN-23
    T204312
    Neuraminidase-IN-23 (33c) 是一种高效的流感病毒神经氨酸酶neuraminidase (NA)抑制剂,其对各类流感病毒的IC50值分别为0.049 μM (H1N1)、0.26 μM (H3N2)、0.17 μM (H5N1)、0.013 μM (H5N8) 和 0.74 μM (H5N1-H274Y)。
    • 待询
    规格
    数量
  • ATV2301
    T2046653049172-60-0
    ATV2301 是一种口服有效的抗流感药物,其对 H1N1 的 EC50 为 1.88 nM,对 H3N2 的 EC50 为 4.77 nM。ATV2301 的抗流感活性源于其对聚合酶酸蛋白 (PA)、核蛋白 (NP) 以及 RNA 依赖性 RNA 聚合酶 (RdRp) 的影响。
    • 待询
    10-14周
    规格
    数量
  • M090
    M-090, M 090
    T24428
    M090 is a potent inhibitor against amantadine-resistant viruses, including the 2009 H1N1 pandemic strains and oseltamivir-resistant viruses.
    • 待询
    3-6月
    规格
    数量
  • BMS-199945
    BMS199945,BMS 199945
    T268441026926-30-6
    BMS-199945 is an Influenza H1N1 Virus inhibitor.
    • ¥ 10600
    6-8周
    规格
    数量
  • MBX2546
    MBX-2546,MBX 2546
    T27983695160-12-4
    MBX2546 is an Influenza A Virus Fusion Inhibitor. MBX2546 binds to HA and inhibits HA-mediated membrane fusion. Both binding and stabilization of HA by MBX2546 are required for the inhibition of viral infection. Mutations in MBX2546-resistant influenza A
    • ¥ 10600
    6-8周
    规格
    数量
  • RO5464466
    RO 5464466,RO-5464466
    T286041399767-47-5
    RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.
    • ¥ 10600
    6-8周
    规格
    数量
  • Methyl brevifolincarboxylate
    T36734154702-76-8
    Methyl brevifolincarboxylate (Brevifolincarboxylic acid methyl ester) is a potent influenza virus PB2 cap-binding inhibitor. Methyl brevifolincarboxylate exhibits inhibitory activity against influenza virus A Puerto Rico 8 34 (H1N1) and A Aichi 2 68 (H3N2) with IC50s of 27.16 μM and 33.41 μM. Anti-oxidant activity[1][2]. Methyl brevifolincarboxylate exhibits significant DPPH radical scavenging activity with an IC50 value of 8.9 μM. [1]. Wu QY, et al. Chromatographic fingerprint and the simultaneous determination of five bioactive components of geranium carolinianum L. water extract by high performance liquid chromatography. Int J Mol Sci. 2011;12(12):8740-8749. [2]. Fang SH, et al. Anti-oxidant and inflammatory mediator's growth inhibitory effects of compounds isolated from Phyllanthus urinaria. J Ethnopharmacol. 2008;116(2):333-340.
    • ¥ 9644
    待询
    规格
    数量
  • Colletodiol
    T3698621142-67-6
    Colletodiol is a fungal metabolite that has been found inD. grovesiiand has immunosuppressant and antiviral activities.1,2It inhibits concanavalin A- or LPS-induced proliferation of isolated mouse splenocytes (IC50s = 12 and 5 μg ml, respectively).1Colletodiol inhibits influenza A viral replication in HeLa-IAV-Luc cells.2 1.Fujimoto, H., Nagano, J., Yamaguchi, K., et al.Immunosuppressive components from an ascomycete, Diplogelasinospora grovesiChem. Pharm. Bull.46(3)423-429(1998) 2.Lai, W., Wang, S., and Ye, X.Colletodiol inhibits the replication of influenza A virus WSN H1N1 by reducing the activity of viral RNA polymeraseWei Sheng Wu Xue Bao53(12)1334-1339(2013)
    • ¥ 3437
    待询
    规格
    数量