37
30
Cat. No. | Product Name | Target | Signaling Pathways |
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T72037 |
Anti-Influenza agent 4
|
Influenza Virus | Microbiology/Virology |
Anti-Influenza agent 4 是一种有效且具有选择性的流感病毒 抑制剂,对A/Parma 和 A/Roma 毒株具有抑制作用, EC50 分别为 62 nM 和150 nM。 | |||
T9124 |
Laninamivir octanoate
辛酸拉尼米韦,CS-8958 |
Influenza Virus | Microbiology/Virology |
Laninamivir octanoate (CS-8958) 是一种长效流感神经氨酸酶抑制剂,是Laninamivir 的前药, 具有优异的抗流感病毒活性。 | |||
T7785 |
T-1105
|
Influenza Virus | Microbiology/Virology |
T-1105 是 T-705 的结构类似物,是一种广谱病毒聚合酶抑制剂,在转化为核糖核苷三磷酸代谢物后抑制 RNA 病毒的聚合酶,有抗病毒活性。 | |||
T8333 |
Aurintricarboxylic acid
ATA,NSC-4056,NSC4056,金精三羧酸,NSC 4056 |
Apoptosis; P2X Receptor; Influenza Virus; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Aurintricarboxylic acid (NSC-4056) 是高效的αβ-亚甲基-ATP 敏感选择性P2X1Rs 和P2X3Rs 变构拮抗剂。 它是核糖核酸酶和拓扑异构酶 II 的有效抑制剂,可阻止核酸与酶结合。 | |||
T83046 | Anti-Influenza agent 5 | Influenza Virus | Microbiology/Virology |
Anti-Influenza agent 5 (Compound IIB-2)为查耳酮类衍生物,具有抑制流感病毒核输出的活性。该化合物能有效抑制对Oseltamivir具有耐药性的病毒株,主要通过阻断流感病毒核蛋白输出作用来抑制病毒复制。 | |||
T60778 | Anti-Influenza agent 3 | ||
Anti-Influenza agent 3 (compound 11h) 是有效的抗流感药物,对 MDCK 上皮细胞显示出低细胞毒性。Anti-Influenza agent 3 抑制 M2 WT 和 S31N 离子通道的传导性。Anti-Influenza agent 3 对 A/HK/68 (H3N2, M2-WT) 菌株的 EC50值为 3.29 μM,对 A/WSN/33 (H1N1, M2-S31N) 菌株的 EC50值为 2.45 μM。 | |||
T20500 |
Salcomine
NSC32965,NSC-32965,NSC 32965,双水杨酰胺乙基钴 |
Influenza Virus | Microbiology/Virology |
Salcomine (NSC-32965) 具有抗流感病毒活性。 | |||
T16914 |
SP187
UV4,MON-DNJ |
Others; Virus Protease; Influenza Virus | Microbiology/Virology; Others |
SP187 (MON-DNJ) 是一种靶向作用于宿主的亚氨基糖。它具有抗丝状病毒感染活性。SP187可用于治疗抗流感和登革热病毒。 | |||
T6642 |
Rimantadine
金刚乙胺,1-Rimantadine,盐酸左氧氟沙星 |
Influenza Virus | Microbiology/Virology |
Rimantadine (1-Rimantadine) 是一种抗流感病毒药物。 | |||
T28443 | PPQ-581 | ||
PPQ-581 is an anti-influenza agent. PPQ-581 interrupts the crucial RNP trafficking, resulting in influenza replication inhibition, preventing virus-induced cytopathic effects. | |||
T13075L | T-705RTP sodium | Others | Others |
T-705RTP sodium is a selective and GTP-competitive of influenza virus RNA polymerase(IC50 of 0.14 μM and a Ki of 1.52 μM), has potent anti-influenza virus activity. | |||
T13075 |
T-705RTP
|
Others | Others |
T-705RTP is a selective and GTP-competitive of influenza virus RNA polymerase(IC50 of 0.14 μM and a Ki of 1.52 μM), has potent anti-influenza virus activity. | |||
T40267 |
RdRP-IN-3
|
||
RdRP-IN-3, a potential anti-influenza drug candidate, functions by inhibiting the activity of RNA-dependent RNA polymerase (RdRp). | |||
T77060 | Lesofavumab | ||
Lesofavumab (MHAB5553A) 是一种人 IgG1κ 抗influenza B virus 抗体。 | |||
T74614 | PROTAC Hemagglutinin Degrader-1 | ||
PROTACHemagglutinin Degrader-1 (Compound V3) 是一种有效的 PROTAC 流感病毒血凝素 (influenza hemagglutinin(HA)) 降解剂,降解中值浓度为 1.44 μM。PROTACHemagglutinin Degrader-1 具有广谱抗流感病毒活性。 | |||
T62059 | Influenza A virus-IN-6 | ||
Influenza A virus-IN-6 (compound 16j) 是有效的选择性甲型流感病毒抑制剂(IC50= 3.88 μM, CC50= 36.64 μM)。Influenza A virus-IN-6 显示出抗 IAV 活性和较低的细胞毒性。 | |||
T62888 |
Influenza A virus-IN-7
|
||
Influenza A virus-IN-7 (compound 16r) 是一种有效的、口服具有活力的甲型流感病毒抑制剂 (IC50: 3.43 μM, CC50>100 μM)。Influenza A virus-IN-7 具有抗 IAV 作用,细胞毒性低,对病毒 RNA 的转录和复制表现出抑制作用。 | |||
T60810 | Influenza virus-IN-2 | ||
Influenza virus-IN-2 (compound 19) 具有抗甲型流感病毒活性,是有效的流感病毒抑制剂,CC50值为 150.85 μM,EC50值为 2.58 μM,。Influenza virus-IN-2 浓度依赖性的抑制 PAN 核酸内切酶,EC50为 489.39 nM。 | |||
T60697 |
Influenza virus-IN-1
|
||
Influenza virus-IN-1 (compound 14) 具有抗甲型流感病毒活性,它是甲型流感病毒的有效抑制剂,其CC50值 >200 μM,EC50值为 2.46 μM。Influenza virus-IN-1 对 PAN 核酸内切酶显示出浓度依赖性的抑制活性 (EC50 = 312.36 nM)。 | |||
T74806 | HAA-09 | ||
HAA-09是一种靶向流感PB2_cap结合域的口服抗流感剂。其对甲型流感病毒展示出高效的抗病毒活性,其EC50值达到0.03 μM。同时,HAA-09具有显著的聚合酶抑制效果,IC50值为0.06±0.004 μM。通过阻断病毒复制,HAA-09能有效抑制病毒无引起明显的细胞毒性。 | |||
T61904 | HSP90-IN-14 | ||
HSP90-IN-14 (compound 4) 是有效的Hsp90 抑制剂(Kd= 0.26μM)。在MDCK 细胞中,HSP90-IN-14 表现出抗流感病毒活性,抗 A/H3N2、A/H1N1 和 B 型流感病毒的EC50分别为 2.6、3.9 和 17 μM。 | |||
T72717 |
Anti-IAV agent 1
|
||
Anti-IAV agent 1-1a) 是一种口服抗甲型流感病毒(IAV)剂,对IAV H1N1及Oseltamivir抗性IAV H1N1的IC50值分别是0.03μM与0.06μM。 | |||
T61394 | Neuraminidase-IN-5 | ||
Neuraminidase-IN-5 (Compound 5b) 是一种有效的 neuraminidase 抑制剂,IC50为 0.02 μM。神经氨酸酶(NA)是开发抗流感药物的有希望的靶点。Neuraminidase-IN-5 是一种二氢呋喃香豆素衍生物化合物。 | |||
T61509 | Neuraminidase-IN-8 | ||
Neuraminidase-IN-8 (Compound 6d) 是一种有效的神经氨酸酶 (neuraminidase) 抑制剂,其IC50值为 0.027 μM。Neuraminidase-IN-8 具有抗流感活性。 | |||
T38952 |
Triperiden
|
||
Triperiden is a chemical compound that serves as an inhibitor of influenza virus multiplication. Specifically, it exerts its antiviral activity by targeting the haemagglutinin of fowl plague virus (FPV) and inhibiting the conformational change in the haemagglutinin at acid pH. Additionally, Triperiden is classified as an anticholinergic anti-parkinsonism drug. | |||
T60910 |
RSV-IN-4
|
||
RSV-IN-4 (Compound 2) 具有抗 RSV 活性,EC50值为11.76 μM。RSV-IN-4 是呼吸道合胞病毒 (RSV) 和甲流病毒 A (IAV) 的双重抑制剂。 | |||
T63233 | Neuraminidase-IN-10 | ||
Neuraminidase-IN-10 是神经氨酸酶 (neuraminidase) 抑制剂,表现出抗流感作用,能够作用于 H1N1 (IC50: 2.6 nM)、H5N1 (IC50: 5.1 nM) 和 H5N8 (IC50: 1.65 nM)。 | |||
T61217 |
RSV-IN-3
|
||
RSV-IN-3 (Compound 1) 是呼吸道合胞病毒 (RSV) 和流感病毒 A (IAV) 的双重抑制剂。RSV-IN-3 具有抗 RSV 活性 (EC50=32.70 μM)。 | |||
T79444 |
HA-IN-1
|
Influenza Virus | Microbiology/Virology |
HA-IN-1(compound 5g)是靶向血凝素(HA)胰蛋白酶切割位点的配体,表现出高亲和力。该化合物能够抑制HA介导的膜融合,并在体内有效降低肺部病毒滴度,展现其作为甲型流感病毒(IAV)抑制剂和抗流感药物的潜力。 | |||
T38340 |
10-Norparvulenone
|
||
10-Norparvulenone is a fungal metabolite originally isolated fromMicrosphaeropsis.1It decreases viral sialidase activity in, and increases survival of, MDCK cells infected with the mouse-adapted influenza virus A/PR/8/34 when used at a concentration of 1 μg/ml. 1.Fukami, A., Nakamura, T., Kim, Y.P., et al.A new anti-influenza virus antibiotic, 10-norparvulenone from Microsphaeropsis sp. FO-5050J. Antibiot. (Tokyo)53(10)1215-1218(2000) | |||
T60939 |
Neuraminidase-IN-6
|
||
Neuraminidase-IN-6 (Compound 5c) 是1,3,4-triazole-3-acetamide 的衍生物。Neuraminidase-IN-6 是神经氨酸酶的有效抑制剂,IC50值为 0.11 μM。神经氨酸酶 (NA) 是抗流感药物开发的理想靶点。 | |||
T77158 | Diridavumab | ||
Diridavumab为一种针对HA茎的单克隆抗体。它能稳定HA的融合前结构,阻断细胞膜与病毒膜在核内体内因pH变化引起的融合。此抗体主要用于H2流感病毒研究。 | |||
T77009 | Firivumab | ||
Firivumab (CT-P22; CT120)是一种针对人类IgG1单克隆的抗甲型流感病毒血凝素(Anti-IAV HA)抗体。该抗体能有效中和多种亚型,包括H1N1、H5N1、H6N1、H6N2、H8N4、H8N8、H9N2和H12N7。研究发现,Firivumab在小鼠模型中对H1N1病毒展现出显著的保护效果。 | |||
T7911 | Arbidol | ||
Umifenovir 是一种有效的口服活性广谱抗病毒药物,对许多包膜病毒和非包膜病毒具有活性。Umifenovir 既能抑制病毒繁殖又能调节炎性细胞因子的表达,可用作抗流感病毒剂 (anti-influenza virus),并具有抗炎活性。Umifenovir 有效抑制病毒与宿主细胞的融合。 Umifenovir 是体外有效的 SARS-CoV-2的抑制剂。 | |||
T71291 | EICAR | ||
EICAR is a drug which acts as an inhibitor of the enzyme IMP dehydrogenase. It is a nucleoside derivative which has both anti-cancer and antiviral effects, and was originally developed for the treatment of leukemia, but was unsuccessful in human clinical trials. It has broad spectrum antiviral effects with activity against vaccinia virus, Semliki forest virus, Junin virus, reovirus, influenza, measles virus and respiratory syncytial virus among others, although it is not active against SARS. T... | |||
T79567 |
Antiviral agent 35
|
Influenza Virus | Microbiology/Virology |
Antiviralagent 35 (compound 4d) 作为一种口服抗流感病毒药物,针对流感病毒复制的早期阶段有效。该化合物能够阻断流感病毒引发的ROS积聚、自噬及细胞凋亡,同时在肺部感染的小鼠模型中,抑制RIG-1通路所介导的炎症响应。Antiviralagent 35展现出低细胞毒性(CC50>800 μM,MDCK细胞)且对H1N1(A/Weiss/43)展现出显著的抗病毒活性,EC50为2.28 μM。 | |||
T35686 |
3-Acetyl Betulinaldehyde
|
||
3-Acetyl betulinaldehyde is a triterpene and derivative of the cholesterol biosynthesis inhibitor betulin that has been found inA. japonica.1It is an intermediate in the synthesis of 3-acetylbetulinic acid, as well as various lupine and germanicane triterpenes and saponins with anticancer activity.2 1.Tung, N.H., Kwon, H.-J., Kim, J.-H., et al.An anti-influenza component of the bark of Alnus japonicaArch. Pharm. Res.33(3)363-367(2010) 2.Thibeault, D., Gauthier, C., Legault, J., et al.Synthesis a... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2331 |
Eleutheroside B1
刺五加苷B1 |
Influenza Virus | Microbiology/Virology |
Eleutheroside B1是具有广谱抗人流感病毒的一种香豆素。它抑制多种趋化因子基因和流感病毒核蛋白基因的 mRNA 表达。它具有抗病毒、抗流感和抗炎活性,且细胞毒性小。 | |||
T2738 |
Dehydroandrographolide
|
NOS; Influenza Virus | Immunology/Inflammation; Microbiology/Virology |
Dehydroandrographolide 是从草药穿心莲中提取的一种天然产物。它通过使 iNOS 失活来降低 LPS 诱导的急性肺损伤中的氧化应激,有抗感染活性。 | |||
T2982 |
Xanthone
Genicide,呫吨酮,氧杂蒽酮,Xanthenone,Benzophenone oxide |
Apoptosis; Others; Influenza Virus; Antibacterial; Antifungal | Apoptosis; Microbiology/Virology; Others |
Xanthone (Xanthenone) 是一种从山竹果中分离得到的天然产物,具有抗炎,抗氧化,抗肿瘤,抗过敏,抗细菌,抗真菌和抗病毒活性。在癌变的不同阶段可控制细胞分裂和生长,凋亡,炎症和转移。 | |||
T2957 |
Arctigenin
牛蒡苷元,牛蒡子苷元,(-)-Arctigenin |
Apoptosis; MMP; Influenza Virus; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; Proteases/Proteasome |
Arctigenin ((-)-Arctigenin) 是一种存在于牛蒡中的木脂素,具有抗氧化、抗肿瘤、抗炎和抗病毒活性。它可研究代谢紊乱和中枢神经系统功能障碍。 | |||
T13229 |
Tunicamycin
|
Influenza Virus; Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Tunicamycin 是一种抗生素的混合物,通过阻断 GlcNAc 磷酸转移酶 (GPT),抑制 N-连接糖基化。Tunicamycin 具有抗肿瘤活性,还具有抗细菌、抗真菌和抗病毒活性。 | |||
T6569 |
Mimosine
Leucenine,NSC 69188,含羞草素,Leucenol,L-Mimosine |
Others | Others |
Mimosine (Leucenol) 是一种酪氨酸类似物,具有抗癌和抗炎等活性。它可通过其强大的铁结合活性作为抗氧化剂,是一种 Fe(III) 螯合剂。它作用于人类白血病细胞,通过金属离子螯合、线粒体激活和诱导活性氧产生来诱导细胞凋亡。 | |||
T5S2059 |
Glaucine
|
Calcium Channel; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; PDE | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience |
Glaucine 是从海罂粟中分离的一种生物碱,具有镇咳、抗炎和支气管扩张作用。它是具有口服活性的磷酸二酯酶 4 选择性抑制剂。它还是非选择性的 α-肾上腺素受体拮抗剂,具有抗氧化和抗病毒活性。 | |||
T26288 |
Clovamide
trans-Clovamide,N-trans-Caffeoy-L-dopa |
Apoptosis; Influenza Virus; ROS; Antibacterial | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
Clovamide (trans-Clovamide) 是一种天然存在的咖啡酰结合物,具有抗菌、抗炎、抗氧化和神经保护作用。它是一种极好的活性氧和氧自由基清除剂。 | |||
T3376 |
Cynaroside
朝蓟糖甙,Luteoloside,Luteolin 7-β-D-Glucopyranoside,Luteolin 7-O-Glucoside,Luteolin 7-O-β-D-glucoside,木犀草苷,Luteolin 7-glucoside |
Others; Influenza Virus; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Cynaroside (Luteolin 7-O-Glucoside) 是一个抗氧化类黄酮。它还是一种流感依赖 RNA 的RNA 聚合酶抑制剂,IC50为 32 nM。 | |||
TN2353 |
8-Hydroxyapigenin
Isoscutellarein |
Antioxidant; Influenza Virus | Microbiology/Virology; oxidation-reduction |
8-Hydroxyapigenin (Isoscutellarein) 是从植物黄芩中提取的黄铜类化合物,具有抗炎抗氧和抗流感病毒的活性。 | |||
TN3120 |
5-Hydroxy-7-acetoxy-8-methoxyflavone
|
Histone Demethylase; Antiviral | Chromatin/Epigenetic; Immunology/Inflammation |
5-Hydroxy-7-acetoxy-8-methoxyflavone 是一种类黄酮化合物,可以抑制脂质过氧化,可能具有抗流感病毒活性。 | |||
T75675 |
Nepasaikosaponin K
|
Antiviral | Immunology/Inflammation |
Nepasaikosaponin K 是一种从柴胡根中分离出来小分子化合物,具有抗流感和抗病毒活性,可用于研究病毒感染。 | |||
TN2166 |
Rupestonic acid
|
ERK; p38 MAPK; Influenza Virus; Nrf2 | Immunology/Inflammation; MAPK; Microbiology/Virology |
Rupestonic acid 是青蒿 Artemisia rupestris L. 中的一种化合物,Artemisia rupestris L. 是一种著名的治疗感冒的维吾尔族传统药物。 Rupestonic acid 具有抗流感病毒活性。 | |||
T0875 |
Acetylcysteine
乙酰半胱氨酸,N-Acetyl-L-cysteine,LNAC,NAC,易咳净 |
Apoptosis; TNF; Ferroptosis; Influenza Virus; Reactive Oxygen Species; ROS; Endogenous Metabolite | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Acetylcysteine (NAC) 是半胱氨酸的 N-乙酰衍生物,是一种 ROS 抑制剂和粘液溶解剂。Acetylcysteine 可诱导细胞凋亡,可用于减少粘液的厚度,还具有抗流感病毒活性。 | |||
TN1051 |
1-Caffeoylquinic acid
金银花,1-咖啡酰奎宁酸 |
NF-κB | NF-κB |
1-Caffeoylquinic acid 是一种有效的NF-κB 抑制剂,对 p105 的 RH 结构域显示高结合亲和力,Ki= 0.002 μM,结合能为 1.50 Kcal/mol。它抑制PD-1/PD-L1相互作用。它具有抗氧化应激能力。 | |||
T4S2126 |
Ginkgetin
银杏双黄酮,银杏素 |
Apoptosis; Wnt/beta-catenin; COX; STAT; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells |
Ginkgetin 是从银杏叶中分离得到的一种双黄酮,具有抗肿瘤、抗炎、神经保护、抗真菌的作用。它也是 Wnt 信号抑制剂,IC50值为 5.92 μM。 | |||
TN5005 |
Shegansu B
|
Influenza Virus | Microbiology/Virology |
Shegansu B exhibits significant in vitro anti-influenza viral activity in MDCK cells. | |||
T27380 | FR-198248 | ||
FR-198248, a new anti-influenza agent, shows antiinfluenza virus activity in Madin-Darby canine kidney (MDCK) cells in vitro. | |||
TN1066 |
Filixic acid ABA
|
Influenza Virus | Microbiology/Virology |
Filixic acid ABA exhibits inhibitory effects on neuraminidase of influenza virus H5N1 with IC50 as 29.57 ± 2.48 μM, it may have anti-influenza virus activity. | |||
TN3461 |
Asebotin
|
Influenza Virus | Microbiology/Virology |
Asebotin shows anti-influenza A virus activity, it also possesses potent antiviral activity (100% inhibition at the concentration of 1 ug /mL) against highly pathogenic avian influenza strain H5N1. Asebotin can inhibit the proliferation of murine B cells. | |||
TN1506 |
Clemastanin B
直铁线莲宁B,落叶松树脂醇苷B |
Influenza Virus | Microbiology/Virology |
Clemastanin B has antioxidant and anti-inflammatory activities, it exerts its anti-influenza activity by inhibiting the virus multiplication, prophylaxsis and blocking the virus attachment. | |||
T8521 |
Gnetin D
|
||
Gnetin D exhibits significant in vitro anti-influenza viral activity in MDCK cells, with IC(50) values from 0.67 to 11.99 ug/mL. | |||
TN2311 |
Wulignan A1
五脂素 A1 |
Antifection | Microbiology/Virology |
Wulignan A1 exhibits activity against leukemia P-388 in vitro; it also may have anti-influenza virus H1N1 and H1N1-TR (a Tamiflu drug resistant virus strain) activities. | |||
T36734 |
Methyl brevifolincarboxylate
|
||
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 simultane... | |||
TN2176 |
Sanggenol A
|
Influenza Virus; Antifection | Microbiology/Virology |
Sanggenol A 抑制甲型流感病毒和肺炎球菌神经氨酸酶,因此可作为双重作用的抗感染试剂。 | |||
TN6204 |
Santin
5,7-Dihydroxy-3,6,4'-trimethoxyflavone |
Influenza Virus | Microbiology/Virology |
Santin (5,7-Dihydroxy-3,6,4'-trimethoxyflavone) 是从桦树芽中提取的黄酮类化合物,具有抗增殖、抗流感和抗癌活性。 Santin 可用于有关抗 IAV 药物的研究。 | |||
TN4392 |
Koaburaside
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IL Receptor; TNF; Influenza Virus | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
Koaburaside exhibits antioxidant activity with an IC50 value of 9.0μM, it shows weak inhibitory activity against influenza A neuraminidase. Koaburaside may have anti-allergic inflammatory activity, it can suppress histamine release from mast cells. | |||
TN1347 |
8-Prenylkaempferol
去甲脱水淫羊藿黄素 |
p38 MAPK; NF-κB; PI3K | MAPK; NF-κB; PI3K/Akt/mTOR signaling |
8-Prenylkaempferol is an effective agent for attenuating pro-inflammatory NO induction, it may be an anti-inflammatory agent for suppressing influenza A virus-induced RANTES production acts by blocking PI3K-mediated transcriptional activation of NF-κB and | |||
T73465 |
Goitrin
L-5-Vinyl-2-thiooxazolidone,(S)-Goitrin,(S)-Goitrin ; L-5-Vinyl-2-thiooxazolidone |
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Goitrin ((S)-Goitrin) 为芥子油苷-黑芥子酶反应产物,有效抑制甲状腺过氧化物酶并阻碍碘在甲状腺的利用。此外,该化合物亦展现出对抗流感病毒(H1N1)的活性。 | |||
TN4108 | Ganoderic acid Z | Antifection | Microbiology/Virology |
The binding affinities of ganoderic acid DM and ganoderic acid Z (ÎGbind, -16.83 and-10.99 kcal mol-1) are comparable to that of current commercial drug oseltamivir (-23.62 kcal mol-1);Ganoderic acid DM is a potential source of anti-influenza ingredient, with novel binding pattern and advantage over oseltamivir, it has steric hindrance on the 150 cavity of N1 protein, and exerts activities across the H274Y and N294S mutations, is the attractive candidates of novel neuraminidase (NA) inhibitors.... |