|Description||It is a nucleoside analogue, a modified form of deoxyuridine, similar enough to be incorporated into viral DNA replication, but the iodine atom added to the uracil component blocks base pairing.Idoxuridine is an antiviral agent for feline herpesvirus type-1 with IC50 of 4.3 μM|
|Synonyms||NSC 39661, SKF 14287|
BAY 57-1293 represents a new class of potent inhibitors of herpes simplex virus (HSV) that target the virus helicase primase complex. Potent helicase-primase in...
It is a nucleoside analogue, a modified form of deoxyuridine, similar enough to be incorporated into viral DNA replication, but the iodine atom added to the ura...
Vidarabine is a nucleoside antibiotic isolated from Streptomyces antibioticus, which is active against herpes simplex and varicella zoster viruses. It has some ...
Docosanol is a saturated fatty alcoholused traditionally as an emollient, emulsifier, and thickener in cosmetics, nutritional supplement.
Aciclovir is a synthetic nucleoside analogue active against herpesviruses.It is primarily used for the treatment of herpes simplex virus infections, chickenpox ...
Penciclovir is a guanosine analogue antiviral drug used for the treatment of various herpesvirusinfections. It is a nucleoside analogue which exhibits low toxic...
Fiacitabine is a selective inhibitior of DNA replication of herpes simplex virus(HSV). It was active at much lower concentrations than arabinosylcytosine, iodod...
Tromantadine is a topical antiherpetic drug that has two independent actions on herpes simplex virus type 1 (HSV-1) replication: early, during virus binding or ...
Famciclovir(Famvir) is a guanine analogue antiviral drug used for the treatment of various herpesvirus infections, most commonly for herpes zoster (shingles). I...
Valaciclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.
Valaciclovir HCl is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.
Ganciclovir is an antiviral drug for feline herpesvirus type-1 with IC50 of 5.2 μM.
WAY 150138, belonging to a novel group of thiourea compounds, can cause the inhibition of the herpes simplex virus.