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Cat. No. | Product Name | Target | Signaling Pathways |
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T76172 |
Neuraminidase
|
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Neuraminidase(Exo-α-sialidase)为一种常用于生化研究的外唾液酸酶,能够在唾液酸(N-acetylneuraminic)与临近糖残基间切断α-酮甙键(α-ketosidic)。该酶源自黏膜病原体,作为一种调整宿主感染反应的毒力因子。 | |||
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。 | |||
T62346 | Neuraminidase-IN-7 | ||
Neuraminidase-IN-7 (compound 4b) 是一种噻吩衍生物,是一种神经氨酸酶 (neuraminidase) 的有效抑制剂 (IC50: 0.03 μM)。Neuraminidase-IN-7 对 A/chicken/Hubei/327/2004 (H5N1-DW) 表现出显著的抗病毒作用 (EC50: 1.59 μM)。Neuraminidase-IN-7 具有潜力进行流感的研究。 | |||
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。 | |||
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。 | |||
T78675 | Neuraminidase-IN-13 | Influenza Virus | Microbiology/Virology |
Neuraminidase-IN-13 (Compound 10) 为神经氨酸酶抑制剂,展现抗病毒功效及低细胞毒性。该化合物显著抑制Vero细胞中NDV感染,其作用机制为阻断病毒颗粒从受感染细胞的释放。 | |||
T74766 | Neuraminidase-IN-12 | ||
NDV-IN-1 是一种具有高神经氨酸酶抑制活性的抗病毒剂。 NDV-IN-1 对新城疫病毒 (NDV) 具有体外抑制活性。NDV-IN-1 通过阻止病毒颗粒从感染细胞中释放出来,显著抑制 Vero 细胞的 NDV 感染。 | |||
T60939 |
Neuraminidase-IN-6
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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。 | |||
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
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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)。 | |||
T63754 | Neuraminidase-IN-9 | ||
Neuraminidase-IN-9 (Compound 6l) 是流感病毒神经氨酸酶 (influenzaneuraminidase) 的有效抑制剂,能够作用于 H5N1 (IC50: 0.12 μM)、H5N2 (IC50: 0.049 μM) 和 H5N6 (IC50: 0.16 μM)。 | |||
T62345 | Neuraminidase-IN-4 | ||
Neuraminidase-IN-4 (Compound 4b) 是一种 neuraminidase 的有效抑制剂 (EC50: 1.59 μM)。神经氨酸酶(NA)是治疗流感的重要靶点。Neuraminidase-IN-4 对 A/chicken/Hubei/327/2004 (H5N1-DW) 表现出显著的抗病毒作用。 | |||
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)。 | |||
T61394 |
Neuraminidase-IN-5
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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。 | |||
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。 | |||
T5186 |
Oseltamivir acid
GS 4071,oseltamivir carboxylate,奥斯他伟酸,Ro 64-0802 |
Influenza Virus; Drug Metabolite | Metabolism; Microbiology/Virology |
Oseltamivir acid (GS 4071) 是Oseltamivir phosphate 的活性代谢产物,是一种有效的流感病毒神经氨酸酶抑制剂和 GS4071 的前药。 | |||
T21339 |
Peramivir
RWJ 270201,BCX1812,BCX 1812,帕拉米韦,RWJ270201 |
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Peramivir, a neuraminidase inhibitor, acts as a transition-state analogue inhibitor of influenza neuraminidase and thereby preventing new viruses from emerging from infected cells. It is used as an antiviral drug for the treatment of influenza. | |||
T2522 |
Peramivir Trihydrate
RWJ-270201,帕拉米韦三水合物,S-021812,BCX-1812,RWJ 270201 trihydrate,BCX 1812 trihydrate |
Influenza Virus | Microbiology/Virology |
Peramivir Trihydrate (RWJ-270201) 是一种高效、选择性和口服有效的流感病毒神经氨酸酶(NA)抑制剂,对 9 个亚型 NA 抑制作用的IC50值为 0.9-4.3 nM。它是一种环戊烷衍生物,具有抗甲型和乙型流感病毒的活性。 | |||
T2529 |
Zanamivir
扎那米韦,GG167 |
Influenza Virus; Antibiotic | Microbiology/Virology |
Zanamivir (GG167) 是神经氨酸酶抑制剂,对于流感病毒 A 和B 的IC50值分别为0.95 nM 和2.7 nM。 | |||
T21486 |
X-NeuNAc
X-Neu5Ac,5-Bromo-4-chloro-3-indolyl-alpha-D-N-acetylneuraminic acid sodium salt |
Others | Others |
X-NeuNAc (5-Bromo-4-chloro-3-indolyl-alpha-D-N-acetylneuraminic acid sodium salt) 是细菌表达系统中神经氨酸酶活性的一种新的显色测定底物。 | |||
T15707 |
Laninamivir
(4S,5R,6R)-5-乙酰氨基-4-胍基-6-((1R,2R)-2,3-二羟基-1-甲氧基丙基)-5,6-二氢-4H-吡喃-2-甲酸,R 125489 |
Influenza Virus | Microbiology/Virology |
Laninamivir (R 125489) 是一种流感神经氨酸酶抑制剂,对流感病毒 H12N5 NA (N5),pH1N1 N1 NA (p09N1) 和 A/RI/5+/1957 H2N2 N2 (p57N2) 的 IC50值分别为 0.90 nM、1.83 nM 和 3.12 nM。 | |||
T27797 |
Laninamivir Octanoate Monohydrate
CS8958,CS-8958,CS 8958,Inavir |
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Laninamivir Octanoate Monohydrate is a neuraminidase inhibitor. | |||
T28209 |
NSC65847
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NSC65847 is a novel dual inhibitor of viral and Streptococcus pneumoniae neuraminidase. | |||
T38120 |
4-MUNANA
4-Methylumbelliferyl-N-acetyl-α-D-Neuraminic Acid sodium salt |
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4-MUNANA(4-Methylumbelliferyl-N-acetyl-α-D-Neuraminic Acid sodium salt) 是用于神经氨酸酶 (neuraminidase) 活性测定的荧光底物,是神经氨酸酶底物类似物。 | |||
T68964 | Neuraminin | ||
Neuraminin inhibits viral but not bacterial neuraminidase. | |||
T2529L |
Zanamivir hydrate
D01937,J1.917.534K |
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Zanamivir hydrate is neuraminidase inhibitors. It is used worldwide for the treatment and prophylaxis of influenza caused by influenza A and B viruses. | |||
T40140 |
Zanamivir-Cholesterol Conjugate
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Zanamivir-cholesterol conjugate is an extended-duration neuraminidase inhibitor highly effective against drug-resistant influenza strains. | |||
T37510 |
Oseltamivir-acetate
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Oseltamivir-acetate, an impurity of Oseltamivir, is a recommended neuraminidase inhibitor for both the treatment and prophylaxis of influenza A and B[1][2]. | |||
T61557 |
Influenza A virus-IN-4
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Influenza A virus-IN-4 (compound 23b), a derivative of Oseltamivir, is a highly effective neuraminidase inhibitor. It exerts potent inhibitory effects on influenza viruses [1]. | |||
T25618 |
Laninamivir trifluoroacetate
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Laninamivir trifluoroacetate 是一种抗病毒化合物,用于治疗和预防甲型流感病毒和乙型流感病毒。它是一种通过鼻吸入给药的长效神经氨酸酶抑制物。 | |||
T62197 |
Influenza virus-IN-4
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Influenza virus-IN-4 (compound 11e) 是一种流感病毒神经氨酸酶的有效抑制剂,能够作用于 H5N1 (IC50: 3.4 μM)、H5N2 (IC50: 0.094 μM)、H5N6 (IC50: 0.79 μM)、H5N8 (IC50: 0.077 μM)。Influenza virus-IN-4 能够抑制 NA(神经氨酸酶),并具有低细胞毒性(CC50>200 μM)。Influenza virus-IN-4 在1500 mg/kg 时,对小鼠没有明显的毒性。 | |||
T60663 |
Oseltamivir acid methyl ester
|
Others | Others |
Oseltamivir acid methyl ester 是Oseltamivir acid 的前体形式,可通过羧酸酯酶1 (CES1) 转化为Oseltamivir acid。Oseltamivir acid 是神经氨酸酶抑制剂和抗病毒剂。 | |||
T73347 |
BCX-1898
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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。 | |||
T76415L |
Asp-Asp-Asp-Asp-Asp-Asp TFA
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Asp-Asp-Asp-Asp-Asp-Asp TFA,一种以聚天冬氨酸形式出现的化合物,与流感病毒神经氨酸酶的催化位点和抗原位点具有特异性关联,此关联取决于特定氨基酸的数量。 | |||
T76415 |
Asp-Asp-Asp-Asp-Asp-Asp
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Asp-Asp-Asp-Asp-Asp-Asp是一种聚天冬氨酸,其特性关键在于流感病毒神经氨酸酶的催化位点及抗原位点的特异性与特殊氨基酸数量的相关性。 | |||
T62837 |
Influenza virus-IN-3
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Influenza virus-IN-3 (compound 9) 是一种选择性流感病毒的有效抑制剂,能够作用于 H5N1 (IC50: 0.88 μM)、H5N2 (IC50: 0.10 μM)、H5N6 (IC50: 5.5 μM)、H5N8 (IC50: 0.51 μM)。Influenza virus-IN-3 具有抗病毒和 NA (神经氨酸酶) 抑制作用,且细胞毒性低 (CC50>200 μM)。 | |||
T38118 |
Zanamivir-13C,15N2
Zanamivir-13C,15N2 |
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Zanamivir-13C,15N2is intended for use as an internal standard for the quantification of zanamivir by GC- or LC-MS. Zanamivir is a sialic acid analog that inhibits neuraminidase release of newly replicated influenza virus particles.1It has been shown to selectively inhibit the growth of influenza A and B viruses in plaque reduction assays with IC50values ranging from 5 to 14 nM and to directly inhibit influenza A and B virus neuraminidases with IC50values ranging from 0.6 to 7.9 nMin vitro. Intra... | |||
T70207 |
Pimodivir tosylate
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Pimodivir, also known as VX-787, JNJ-872, is a novel inhibitor of influenza virus replication that blocks the PB2 cap-snatching activity of the influenza viral polymerase complex. VX-787 binds the cap-binding domain of the PB2 subunit with a KD (dissociation constant) of 24 nM as determined by isothermal titration calorimetry (ITC). The cell-based EC50 (the concentration of compound that ensures 50% cell viability of an uninfected control) for VX-787 is 1.6 nM in a cytopathic effect (CPE) assay... | |||
T37295 |
Ganglioside GM1 Asialo Mixture
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Ganglioside GM1 asialo is a component of cellular lipid rafts and can be formed by the cleavage of the sialic acid residue from ganglioside GM1 by neuraminidase. Ganglioside GM1 asialo is a glycolipid receptor for P. aeruginosa flagellin and stimulates defensive responses in host cells, including extracellular ATP release, calcium mobilization, and ERK1/2 phosphorylation when stimulated by flagellin and an anti-ganglioside GM1 asialo antibody. The percentage of ganglioside GM1 asialo-positive na... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TL0005 |
3,5-O-Dicaffeoylquinic acid
Isochlorogenic Acid A,(-)-3,5-二咖啡酰奎宁酸,(-)-3,5-Dicaffeoyl quinic acid,3,5-Dicaffeoylquinic Acid |
Others | Others |
3,5-O-Dicaffeoylquinic acid (Isochlorogenic Acid A) 能够改善由三甲基锡诱导的学习和记忆缺陷。 | |||
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。 | |||
T72732 |
Massarilactone H
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Massarilactone H 是一种聚酮化合物,是神经氨酸酶抑制剂,IC50值为 8.18 µM。 | |||
T81020 |
Tenaxin I
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Tenaxin I,一种从黄芩提取物中鉴定出的成分,具有神经氨酸酶抑制活性。 | |||
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. | |||
TN3995 |
Erythrabyssin II
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Antifection | Microbiology/Virology |
Erythrabyssin II actives against several strains of Staphylococcus and Streptococcus with an MIC range of 0.78-1.56 microg/ml. It inhibits bacterial neuraminidase in a dose-dependent manner with significant inhibition (IC(50)=0.09-3.25 μM). | |||
TN4392 |
Koaburaside
|
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. | |||
TN4108 |
Ganoderic acid Z
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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.... |