
HSV
Os inibidores do vírus Herpes Simplex (HSV) são compostos que têm como alvo o vírus Herpes Simplex, que causa infecções como herpes labial e genital. Esses inibidores podem bloquear a entrada viral, a replicação ou a montagem de novas partículas virais, ajudando a reduzir a gravidade e a duração das infecções por HSV. A pesquisa sobre inibidores do HSV é essencial para desenvolver terapias antivirais que possam gerenciar e tratar tanto as infecções agudas quanto as latentes pelo HSV. Na CymitQuimica, oferecemos uma seleção de inibidores do HSV para apoiar sua pesquisa em virologia, terapia antiviral e doenças infecciosas.
Foram encontrados 87 produtos para "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.Fórmula:C33H58N6O5Pureza:99.18% - >99.99%Cor e Forma:Blue SolidPeso molecular: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.Fórmula:C11H15N5O4Pureza:98%Cor e Forma:SolidPeso molecular:281.27Omaciclovir
CAS:Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.Fórmula:C10H15N5O3Pureza:99.46% - 99.46%Cor e Forma:SolidPeso molecular: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).Fórmula:C11H13N5O3Pureza:98%Cor e Forma:SolidPeso molecular: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).Fórmula:C23H24ClN3O3Peso molecular: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.Fórmula:C21H32O3Cor e Forma:SolidPeso molecular: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).Fórmula:C23H30O5Cor e Forma:SolidPeso molecular:386.48
