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Cat. No. | Product Name | Target | Signaling Pathways |
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T1406 |
Amantadine hydrochloride
盐酸金刚烷胺,1-adamantanamine HCl,1-Adamantanamine hydrochloride,Symmetrel,CI-719,Amantadine HCl,1-Adamantylamine hydrochloride |
Dopamine Receptor; Influenza Virus | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Amantadine hydrochloride (CI-719) 是一种抗病毒药物,用于预防或对症治疗甲型流感和帕金森病。它阻断质子流通过 M2 离子通道,从而阻止病毒 RNA 释放到感染细胞的细胞质中。 | |||
T50059 |
6-ethenylquinoline
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Others | Others |
6-ethenylquinoline 是一种结构独特的芳香杂环化合物,是生产其他芳香族化合物的重要中间体,并被用作合成各种药物的起始材料,包括抗真菌剂、抗寄生虫剂和抗病毒剂。它已被证明是多种参与药物代谢的酶的抑制剂,包括细胞色素P450、醛氧化酶和黄嘌呤氧化酶等。 | |||
TNU0250 |
3’-Deoxycytidine
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Nucleoside Derivatives - 3’-Deoxy nucleosides; Drugs and Inhibitors; Antiviral agent | |||
TNU0180 |
7-Deazaguanosine
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Nucleoside Derivatives - 7-Deaza-purine nucleosides; Drugs and Inhibitors; Antiviral agent, anti-HCV | |||
TNU0456 |
N6-(4-Trifluoromethylbenzyl)adenosine
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Nucleoside Derivatives - 6-Modified purine nucleosides; Drugs and Inhibitors; Antiviral agent, cytokinin nucleoside | |||
TNU0158 |
2’-C-beta-Methylguanosine
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Nucleoside Derivatives –2’-Modified nucleosides; Drugs and Inhibitors; Antiviral agent, HCV inhibitor | |||
TNU1248 | 2’,3’-Dideoxy-3’-fluoroadenosine | ||
Nucleoside Derivatives - Fluoro-modified nucleosides; 2’,3’-Dideoxy nucleosides; Drugs and Inhbitors; Antiviral agent | |||
TNU0230 | 2’-Azido-2’-deoxycytidine | ||
Nucleoside Derivatives - Azido-nucleosides, 2’-Modified nucleosides; Drugs and Inhibitors; antiviral agent, DNA synthesis inhibitor; Ribonucleotide reductase inhibitor | |||
TNU0161 |
N6-MethyladenosineN1-oxide
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Nucleoside Derivatives –6-Modified purine nucleosides;N-Methylated nucleosides; Drugs and Inhibitors; Antiviral agent | |||
TNU1302 |
3’-Azido-2’,3’-dideoxy-5-hydroxyuridine
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Nucleoside Derivatives - 5-Modified pyrimidine nucleosides; Azido-nucleosides; 2’,3’-Dideoxy nucleosides; Drugs and Inhibitors; Antiviral agent | |||
T71809 |
L-Xylulose
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L-Xylulose is an intermediate in certain metabolic pathways and is classified as a rare sugar. It shows important physiological effects such as acting as an inhibitor of α-glucosidase and decreasing blood glucose, and it can be employed to produce other significant rare sugars, such as L-ribose and L-xylose which contribute to the production of antiviral drugs. | |||
T63537 |
SARS-CoV-2 3CLpro-IN-1
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SARS-CoV-2 3CLpro-IN-1 (Compound 14c) is a highly potent inhibitor specifically designed to target and inhibit the activity of SARS-CoV-2 3CL pro, which is a cysteine-protease found in the main coronaviruses. This particular enzyme has been recognized as a highly promising target for the development of effective antiviral drugs. Therefore, SARS-CoV-2 3CLpro-IN-1 holds significant potential for advancing research and development in the field of infectious diseases [1]. | |||
T40340 |
SARS-CoV-2-IN-10
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SARS-CoV-2-IN-10 is a powerful and non-toxic inhibitor of SARS-CoV-2 3CL protease, with IC50 and EC50 values of 0.13 nM and 1.03 nM, respectively. The SARS-CoV-2 3C-like protease (3CLpro) is a critical enzyme for viral replication and serves as an ideal target for intervention. By targeting the SARS-CoV-2 3CL protease, SARS-CoV-2-IN-10 has the potential to facilitate the development of effective antiviral drugs specific to SARS-CoV-2. | |||
TNU1050 |
3-Deoxy-1,2;5,6-di-O-isopropylidene-D-glucofuranose
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3-Deoxy-1,2;5,6-di-O-isopropylidene-D-glucofuranose 是一种多糖类的低聚糖。它用于糖基化的合成,可以定制合成用作药物中的碳水化合物。它通过抑制病毒蛋白合成而对Epstein-Barr 病毒具有抗病毒活性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T7060 |
Amantadine
1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine |
Others | Others |
Amantadine (1-Aminoadamantane) 是抗病毒药物,也是是 NMDA 型谷氨酸受体的弱拮抗剂,能促进高多巴胺的释放,并阻断多巴胺的再摄取。 | |||
T36000 |
3-Hydroxyterphenyllin
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3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi... |