Chemical Structure : Cladoniamide A
货号: PC-27037Not For Human Use, Lab Use Only.
Cladoniamide A is a reversible broad-spectrum antiviral targets the human V-ATPase VO domain, interferes with V-ATPase-dependent acidification of the host endolysosomal network thus preventing viral entry.
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Cladoniamide A is a reversible broad-spectrum antiviral targets the human V-ATPase VO domain, interferes with V-ATPase-dependent acidification of the host endolysosomal network thus preventing viral entry.
Cladoniamide A shows single-digit nanomolar antiviral activity and a high selectivity index (SI: 10 3 -10 4 ) against human enveloped viruses [e.g., SARS-CoV-2 variants, influenza A viruses (H1N1, H5N1), respiratory syncytial virus, dengue serotypes 1-4, and Zika virus].
Cladoniamide A inhibits the V-ATPase rotary motor by occupying unique binding sites in the membrane-embedded V o motor.
| 分子量 | 437.84 | |
| 分子式 | C22H16ClN3O5 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Pérez-Vargas J, et al. Res Sq [Preprint]. 2026 Jun 3:rs.3.rs-9889115.
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