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Search Results for " h1n1 "

31

抑制剂 & 化合物

10

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T8793	CBS1117	Influenza Virus	Microbiology/Virology
	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。
T8555	Neuraminidase-IN-1 Novel NA Inhibitor,Compound Y-1	Others; Influenza Virus	Microbiology/Virology; Others
	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。
T12077	ML303	Influenza Virus	Microbiology/Virology
	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。
T9231	Mbx2329	Antiviral	Immunology/Inflammation
	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。
T12526	PP7	Influenza Virus	Microbiology/Virology
	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。
T1343L	Crystal Violet Methyl Violet 10B,Hexamethylpararosaniline chloride,氯化结晶紫,Basic Violet 3,结晶紫,Gentian Violet	DNA; Influenza Virus; Antibacterial	DNA Damage/DNA Repair; Microbiology/Virology
	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。
T26619	Amitivir LY217896,LY 217896,阿米替韦,LY-217896	Others; Influenza Virus	Microbiology/Virology; Others
	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。
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。
T74774	Neuraminidase-IN-16
	Neuraminidase-IN-16 (Compound 43b) 是一种有效的神经氨酸酶 (neuraminidase) 抑制剂，对 H5N1、H5N8、H1N1、H3N2、H5N1–H274Y 和 H1N1–H274Y 的神经氨酸酶抑制作用的 IC50分别为 0.031、0.15、0.25、0.60、0.63 和 10.08 μM。
T26844	BMS-199945 BMS199945,BMS 199945
	BMS-199945 is an Influenza H1N1 Virus inhibitor.
T28604	RO5464466 RO 5464466,RO-5464466
	RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.
T24428	M090 M 090,M-090
	M090 is a potent inhibitor against amantadine-resistant viruses, including the 2009 H1N1 pandemic strains and oseltamivir-resistant viruses.
T74294	Cap-dependent endonuclease-IN-12
	Cap-dependent endonuclease-IN-12 (EXP-35) 为一种高效的 Cap 依赖性核酸内切酶(CEN)抑制剂，展现出对H1N1的抑制活性，同时具备低细胞毒性特性。
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。
T37752	Aureonitol
	Aureonitol is a fungal metabolite that has been found inChaetomiumand has antiviral activity.1It inhibits replication of the influenza A subtype H3N2 with an EC50value of 30 nM at a multiplicity of infection (MOI) of 0.01. It also inhibits replication of laboratory-adapted and clinical isolates of H3N2 (EC50s = 100 and 312 nM, respectively), as well as clinical isolates of the influenza A subtype H1N1 (EC50= 417 nM). Aureonitol inhibits hemagglutination activity of H3N2 and H1N1. 1.Sacramento, C...
T19849	2-PADQZ 2PADQZ,2-PADQZ
	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.
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)。
T63175	Neuraminidase-IN-3
	Neuraminidase-IN-3 (compound 23d) 是一种流感神经氨酸酶 (NA) 的有效抑制剂，能够作用于 H1N1 (IC50: 0.73 nM)、H5N1 (IC50: 0.26 nM) 和 H5N8 NAs (IC50: 0.63 nM)。
T37466	CAY10766
	CAY10766 is an antiviral compound.1It inhibits entry of influenza virus-like particles pseudotyped with hemagglutinin A (HA) from H5N1 influenza A virus into A549 cells (EC50= 0.24 μM). CAY10766 (1 μM) reduces H1N1 and H5N1 influenza A viral titers in infected MDCK cells. It also exhibits synergy with oseltamivir carboxylate in MDCK cells infected with the influenza A reporter PR8-NS1-Gluc virus.
T64274	Neuraminidase-IN-11
	Neuraminidase-IN-11 (15e) 是一种选择性的、有效的神经氨酸酶 (NA) 抑制剂，能够作用于 H1N1 病毒的神经氨酸酶 (IC50: 4.7 nM)、H5N1 病毒的神经氨酸酶 (IC50: 8.46 nM) 和 H5N8 病毒的神经氨酸酶 (IC50: 1.5 nM)。
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。
T73347	BCX-1898
	BCX-1898 是一种环戊烷衍生物，是口服有效的，选择性的流感病毒神经氨酸酶 (influenza virus neuraminidase) 抑制剂。BCX-1898 具有抗病毒活性，对 MDCK 细胞中的甲型流感病毒 (H1N1、H3N2、H5N1) 和乙型流感病毒复制的 EC50值为 <0.01-21 μM。BCX-1898 显示出对小鼠流感模型的保护作用。
T69398	LUN15104
	LUN15104 is a novel hemagglutinin (HA) protein inhibitor, inhibiting entry and replication of diverse influenza viruses via the HA protein, showing potent antiviral activity against diverse H1N1, H5N1, and H3N2 influenza viruses encoding HA proteins from both groups 1 and 2. This product has no formal name. For the convenience of scientific communication, we named it by combining its InChi Key (3 letters from the first letter of each section) with the last 5 digit of its CAS#) according to MedKo...
T27983	MBX2546 MBX-2546,MBX 2546
	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/
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。
T62812	RdRP-IN-4
	RdRP-IN-4 (compound 11q) 是一种芳基苯甲酰肼类似物，是一种口服具有活力的甲型流感病毒 RNA 依赖性 RNA 聚合酶 (RdRp) 抑制剂，能够直接结合 RdRp 的 PB1 亚基。RdRP-IN-4 可有效抑制 H5N1 禽流感病毒株，在 MDCK 细胞的 EC50=18 nM。RdRP-IN-4 对 H1N1 (A/PR/8/34) Flu A 株和 Flu B 株 (B/Lee/1940) 具有抑制作用，其 EC50 值分别为 53 nM 和 20 nM。RdRP-IN-4 以剂量依赖性方式显著抑制病毒核蛋白 (NP) 的表达水平。RdRP-IN-4 在受感染的小鼠中具有明显的抗病毒作用。
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。
T81292	Retrocyclin-3
	Retrocyclin-3是一种具有抗HIV（人类免疫缺陷病毒）、H1N1（甲型流感）以及HSV（单纯疱疹病毒）活性的抗菌肽。
T36986	Colletodiol
	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...
T62469	RSV/IAV-IN-3
	RSV/IAV-IN-3 (compound 14'i) 是一种双重的呼吸道合胞病毒 (RSV) (EC50: 2.92 μM) 和甲型流感病毒 (IAV) (EC50: 1.90 μM) 的双重抑制剂。RSV/IAV-IN-3 对 H1N1 和 H3N2 表现出抗病毒作用，在 MDCK 细胞中的 EC50值分别为 3.25 μM 和 1.50 μM。RSV/IAV-IN-3 能够剂量依赖性地明显抑制荧光素酶的活性 (EC50: 3.89 μM)。RSV/IAV-IN-3 可以抑制 IAV 感染和 RdRp 活性，在进入后阶段抑制 IAV 和 RSV 复制。
T39778	Influenza A virus-IN-1
	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.

化合物

Cat.No: T8793

Target: Influenza Virus

Neuraminidase-IN-1

Cat.No: T8555

Synonym: Novel NA Inhibitor,Compound Y-1

Target: Others, Influenza Virus

Cat.No: T12077

Target: Influenza Virus

Cat.No: T9231

Target: Antiviral

Cat.No: T12526

Target: Influenza Virus

Cat.No: T1343L

Synonym: Methyl Violet 10B,Hexamethylpararosaniline chloride,氯化结晶紫,Basic Violet 3,结晶紫,Gentian Violet

Target: DNA, Influenza Virus, Antibacterial

Cat.No: T26619

Synonym: LY217896,LY 217896,阿米替韦,LY-217896

Target: Others, Influenza Virus

Anti-IAV agent 1

Cat.No: T72717

Neuraminidase-IN-16

Cat.No: T74774

Cat.No: T26844

Synonym: BMS199945,BMS 199945

Cat.No: T28604

Synonym: RO 5464466,RO-5464466

Cat.No: T24428

Synonym: M 090,M-090

Cap-dependent endonuclease-IN-12

Cat.No: T74294

Cat.No: T77009

Cat.No: T37752

Cat.No: T19849

Synonym: 2PADQZ,2-PADQZ

Neuraminidase-IN-10

Cat.No: T63233

Neuraminidase-IN-3

Cat.No: T63175

Cat.No: T37466

Neuraminidase-IN-11

Cat.No: T64274

Cat.No: T61904

Cat.No: T73347

Cat.No: T69398

Cat.No: T27983

Synonym: MBX-2546,MBX 2546

Anti-Influenza agent 3

Cat.No: T60778

Cat.No: T62812

Antiviral agent 35

Cat.No: T79567

Target: Influenza Virus

Cat.No: T81292

Cat.No: T36986

Cat.No: T62469

Influenza A virus-IN-1

Cat.No: T39778

Cat. No.	Product Name	Target	Signaling Pathways
TN2755	2-Desoxy-4-epi-pulchellin	Anti-infection	Microbiology/Virology
	2-Desoxy-4-epi-pulchellin 是分离自 Polygonum hydropiper 的二氯甲烷可溶部分的一种化合物。
T5S0056	Coptisine chloride 盐酸黄连碱,氯化黄连碱,Q-100696,NSC-119754	Indoleamine 2,3-Dioxygenase (IDO); Influenza Virus; Antibacterial	Metabolism; Microbiology/Virology
	Coptisine chloride (NSC-119754) 是从黄连中分离到的一种生物碱，是一种非竞争性 IDO 抑制剂，Ki 值为 5.8 μM，IC50值为 6.3 μM。它是一种 H1N1 神经氨酸酶抑制剂，可用于甲型流感病毒感染，IC50为 104.6 μg/mL。
T2951	β-Cyclodextrin Betadex,Beta-Cyclodextrin,β-环糊精,beta-环糊精,Cyclomaltoheptaose,NSC 269471	Others; Influenza Virus	Microbiology/Virology; Others
	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。
T11364	Ganoderic acid TR	Others	Others
	Ganoderic acid TR is a broad-spectrum inhibitor against influenza neuraminidases (NAs), particularly H1N1 and H5N1 neuraminidases. The IC50 values of 4.6 and 10.9 μM, respectively.
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.
TN4105	Ganoderic acid T-Q	Others	Others
	Ganoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs.
T73465	Goitrin L-5-Vinyl-2-thiooxazolidone,(S)-Goitrin,(S)-Goitrin ; L-5-Vinyl-2-thiooxazolidone
	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。
T75534	Maniwamycin E
	Maniwamycin E，一种耐热链霉菌培养提取物中分离得到的马尼瓦霉素衍生物，展示了对SARS-CoV-2和H1N1流感病毒的抗病毒活性。
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...
T5S1708	Dendrobine	Others; Influenza Virus	Microbiology/Virology; Others
	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。

天然产物

2-Desoxy-4-epi-pulchellin

Cat.No: TN2755

Target: Anti-infection

Coptisine chloride

Cat.No: T5S0056

Synonym: 盐酸黄连碱,氯化黄连碱,Q-100696,NSC-119754

Target: Indoleamine 2,3-Dioxygenase (IDO), Influenza Virus, Antibacterial

β-Cyclodextrin

Cat.No: T2951

Synonym: Betadex,Beta-Cyclodextrin,β-环糊精,beta-环糊精,Cyclomaltoheptaose,NSC 269471

Target: Others, Influenza Virus

Ganoderic acid TR

Cat.No: T11364

Target: Others

Cat.No: TN2311

Synonym: 五脂素 A1

Target: Antifection

Ganoderic acid T-Q

Cat.No: TN4105

Target: Others

Cat.No: T73465

Synonym: L-5-Vinyl-2-thiooxazolidone,(S)-Goitrin,(S)-Goitrin ; L-5-Vinyl-2-thiooxazolidone

Cat.No: T75534

Methyl brevifolincarboxylate

Cat.No: T36734

Cat.No: T5S1708

Target: Others, Influenza Virus

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