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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T0104 | Umifenovir hydrochloride | Arbidol hydrochloride,Arbidol HCl | SARS-CoV , Influenza Virus |
Umifenovir hydrochloride (Arbidol HCl) , an broad-spectrum antiviral chemical agent, can inhibit cell invade of enveloped viruses by blocking viral fusion with host cell membrane. | |||
T9602 | Monocaprin | Anti-infection , Antibacterial | |
Monocaprin is a 1-monoglyceride of capric acid that has antimicrobial activity against enveloped viruses, certain bacteria, and the yeast Candida albicans. | |||
T32804 | LJ-001 | LJ 001,LJ001 | Antiviral , HIV Protease |
LJ-001 shows broad-spectrum activity against virtually all enveloped RNA and DNA viruses. LJ001 inhibits the infection of transmissible gastroenteritis virus (TGEV) and porcine delta coronavirus (PDCoV). | |||
T3226 | Paritaprevir | ABT-450,Veruprevir | HCV Protease |
Paritaprevir (ABT-450) is an orally bioavailable, synthetic acylsulfonamide inhibitor of the hepatitis C virus (HCV) protease complex comprised of non-structural protein 3 and 4A (NS3/NS4A), with potential activity again... | |||
T27590 | IHVR-11029 | IHVR 11029 | |
IHVR-11029 is a potent inhibitor of ER α-glucosidase. IHVR-11029 is active against multiple hemorrhagic fever viruses and efficiently disrupts the morphogenesis of a broad spectrum of enveloped viruses. | |||
T74943L | SARS-CoV-2-IN-25 disodium | ||
SARS-CoV-2-IN-25 (Compound CP026) disodium, a potent inhibitor of SARS-CoV-2 spike pseudoparticle transduction, demonstrates significant efficacy with an IC50 value of 1.6 μM. Additionally, it effectively inhibits envelo... | |||
T7911 | Arbidol | ||
Umifenovir is a potent, orally active broad-spectrum antiviral agent with activity against a number of enveloped and non-enveloped viruses. Umifenovir both suppresses virus propagation and modulates the expression of inf... | |||
T74943 | SARS-CoV-2-IN-25 | ||
SARS-CoV-2-IN-25 (Compound CP026) is a potent inhibitor, specifically targeting the transduction of SARS-CoV-2 spike pseudoparticles, with an inhibitory concentration (IC50) of 1.6 μM. It effectively inhibits enveloped v... | |||
T73987 | Pradimicin A | ||
Pradimicin A (PRM-A) is a compound with potent antifungal capabilities, demonstrating a minimum inhibitory concentration (MIC) of 4 μg/mL against Candida rugosa. It also exhibits antiviral activity against viruses such a... | |||
T80375 | Human α-defensin 5 | Parasite | |
Human α-defensin 5 is an antiviral peptide that inhibits the infection of non-enveloped viruses such as AdV, HPV, and polyomaviruses, with an IC50 range of 0.6-1.25 μM specifically for HPV16. It functions by binding to t... |