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15

抑制剂 & 化合物

4

天然产物

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Cat. No. Product Name Target Signaling Pathways
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。
T0994 Ketotifen fumarate

HC 20511 fumarate,富马酸酮替芬

PDE; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience
Ketotifen fumarate (HC 20511 fumarate) 是组胺 H1 受体和炎症介质释放的环七噻吩阻滞剂。
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.
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...
T14035 3M-011

TLR Immunology/Inflammation
3M-011, a potent dual toll-like receptor TLR7/8 agonist and cytokine inducer, serves as a powerful adjuvant to radiotherapy, eliciting significant local and systemic immune responses. Additionally, it effectively inhibits H3N2 influenza viral replication in the nasal cavity and exhibits strong antitumor activity[1][2][3].
T63981 Cap-dependent endonuclease-IN-17

Cap-dependent endonuclease-IN-17 是帽依赖性核酸内切酶 (CEN) 抑制剂。Cap-dependent endonuclease-IN-17 对流感病毒 A/Hanfang/359/95 (H3N2) 表现出抗病毒作用 (IC50: 1.29 μM)。
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。
T62216 Influenza virus-IN-5

Influenza virus-IN-5 (Compound 5f) 是一种流感病毒血球凝集素 (hemagglutinin (HA)) 抑制剂,能够作用于 A/H3N2 病毒 (EC50: 1 nM)。
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。
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。
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...
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。
T37330 Pyridindolol

Pyrindolol is a bacterial metabolite that has been found inS. alboverticillatus.1It inhibits neutral β-galactosidase by 50% under acidic, but not neutral, conditions when used at a concentration of 2 μg/ml. It is selective for β-galactosidase isolated from bovine liver over β-galactosidases isolated from human, bovine, pig, and rat tissues and sialidases isolated fromC. perfringens,Streptomyces, and the H3N2 strain of influenza virus (IC50s = >250 μg/ml for all).1,2 1.Aoyagi, T., Kumagai, M., Ha...
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

Laninamivir octanoate
Cat.No: T9124
Synonym: 辛酸拉尼米韦,CS-8958
Target: Influenza Virus
Ketotifen fumarate
Cat.No: T0994
Synonym: HC 20511 fumarate,富马酸酮替芬
Target: PDE, Histamine Receptor
2-PADQZ
Cat.No: T19849
Synonym: 2PADQZ,2-PADQZ
Target:
Aureonitol
Cat.No: T37752
Synonym:
Target:
3M-011
Cat.No: T14035
Synonym:
Target: TLR
Cap-dependent endonuclease-IN-17
Cat.No: T63981
Synonym:
Target:
Neuraminidase-IN-16
Cat.No: T74774
Synonym:
Target:
Influenza virus-IN-5
Cat.No: T62216
Synonym:
Target:
Anti-Influenza agent 3
Cat.No: T60778
Synonym:
Target:
HSP90-IN-14
Cat.No: T61904
Synonym:
Target:
LUN15104
Cat.No: T69398
Synonym:
Target:
BCX-1898
Cat.No: T73347
Synonym:
Target:
Pyridindolol
Cat.No: T37330
Synonym:
Target:
RSV/IAV-IN-3
Cat.No: T62469
Synonym:
Target:
Influenza A virus-IN-1
Cat.No: T39778
Synonym:
Target:
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。
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。
TN1245 3-Deoxysappanchalcone

Others; Akt; mTOR Cytoskeletal Signaling; Others; PI3K/Akt/mTOR signaling
3-Deoxysappanchalcone is an effective HO-1 inducer at the translational level.

天然产物

2-Desoxy-4-epi-pulchellin
Cat.No: TN2755
Synonym:
Target: Anti-infection
Methyl brevifolincarboxylate
Cat.No: T36734
Synonym:
Target:
Dendrobine
Cat.No: T5S1708
Synonym:
Target: Others, Influenza Virus
3-Deoxysappanchalcone
Cat.No: TN1245
Synonym:
Target: Others, Akt, mTOR
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