HSV
HSV inhibitors are compounds that target the Herpes Simplex Virus (HSV), which causes infections such as cold sores and genital herpes. These inhibitors can block viral entry, replication, or the assembly of new viral particles, helping to reduce the severity and duration of HSV infections. Research into HSV inhibitors is essential for developing antiviral therapies that can manage and treat both acute and latent HSV infections. At CymitQuimica, we offer a selection of HSV inhibitors to support your research in virology, antiviral therapy, and infectious disease.
Found 87 products for "HSV".
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Valomaciclovir stearate
CAS:S-Allylmercapturic Acid (N-Acetyl-S-allyl-L-cysteine) is a metabolite of S-allyl-L-cysteine present in black garlic, with potential anti-gout effects.Formula:C33H58N6O5Purity:99.48% - >99.99%Color and Shape:Blue SolidMolecular weight:618.85HSV-TK substrate
CAS:HSV-TK substrate is a substrate for HSV-TK with antitumor activity. It induces multi-log cytotoxicity in HSV-TK-expressing and bystander cells.Formula:C11H15N5O4Purity:98%Color and Shape:SolidMolecular weight:281.27Omaciclovir
CAS:Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.Formula:C10H15N5O3Purity:99.46% - 99.46%Color and Shape:SolidMolecular weight:253.26Cyclopropavir
CAS:Cyclopropavir (Filociclovir; MBX-400) is a broad-spectrum anti-herpes drug effective against CMV and HHV-6/8 (EC50: 0.7-8 μM).Formula:C11H13N5O3Purity:98%Color and Shape:SolidMolecular weight:263.25PNU-183792
CAS:PNU-183792 is a 4-oxo-1,4-dihydroquinoline that acts as an orally active inhibitor of herpesvirus polymerases (HSV polymerases). It exhibits broad-spectrum antiviral activity, with IC50 values of 0.69 μM for human cytomegalovirus (HCM), 0.37 μM for varicella-zoster virus, and 0.58 μM for herpes simplex virus (HSV) polymerase. PNU-183792 shows no activity against human α, γ, and δ polymerases but inhibits simian varicella virus (SVV), murine cytomegalovirus (MCMV), and rat cytomegalovirus (RCMV).Formula:C23H24ClN3O3Molecular weight:425.9117,17-Ethylendioxyandrost-5-en-3β-ol
CAS:17,17-Ethylendioxyandrost-5-en-3β-ol, with an EC 50 of 629 μM, acts as an inhibitor of HSV-1. This compound is applicable in research studies focusing on viral infections.Formula:C21H32O3Color and Shape:SolidMolecular weight:332.48Mer-NF5003F
CAS:Mer-NF5003F (Stachybotrydial; F 1839M) is a sesquiterpene isolated from Stachybotrys, effective in inhibiting avian myeloblastosis virus (AMV) protease with an IC50 of 7.8 μM. It also inhibits sialyltransferases ST6N, ST3O, and ST3N with IC50 values of 0.61, 6.7, and 10 μg/mL, respectively, and fucosyltransferase with an IC50 of 11.3 μg/mL. Additionally, Mer-NF5003F exhibits in vitro activity against herpes simplex virus HSV-1 (IC50=4.32 μg/mL) and multi-drug-resistant Plasmodium falciparum K1 strain (IC50=0.85 μg/mL).Formula:C23H30O5Color and Shape:SolidMolecular weight:386.48
