Herpes simplex Virus (HSV)

CAS No.	Product Name	Inquiry
1020719-42-9	Famciclovir-[d4] Famciclovir-[d4] is the labelled analogue of Famciclovir, which is used for the treatment of various herpesvirus infections, most commonly for herpes zoster.
1020719-72-5	Penciclovir-[d4] Penciclovir-[d4] is the labelled analogue of Penciclovir, which is a guanosine analogue antiviral drug used for the treatment of various herpesvirusinfections.
1034-01-1	Octyl Gallate Octyl Gallate is an octyl ester of gallic acid that is commonly used as a food preservative such as a thickener, bulking agent, or emulsifier in processed foods. Octyl Gallate exhibits antifungal activity against Zygosaccharomyces bailii, Aspergillus niger, Candida albicans, and Saccharomyces cerevisiae, as well as antibacterial and antiviral activities against Enterococcus facealis, poliovirus herpes simplex virus type 1, and stomatitis virus.
10361-12-3	Gallic acid stearyl ester Gallic acid stearyl ester, a long chain alkyl gallate (carbon number of 18), has antioxidant activity and weak antiviral activity against HSV-1.
1036-49-3	Isookanin
104227-87-4	Famciclovir Famciclovir(Famvir) is a guanine analogue antiviral drug used for the treatment of various herpesvirus infections, most commonly for herpes zoster (shingles). It is a prodrug form of penciclovir with improved oral bioavailability.
1054312-81-0	FK-3000
107910-75-8	Ganciclovir Sodium Ganciclovir Sodium is a potent inhibitor of the Herpesvirus family including cytomegalovirus. It is an acyclovir analog. It is used to treat complications from AIDS-associated cytomegalovirus infections. It was developed by Roche and has been listed.
1113044-49-7	FIT-039 FIT-039 is a potent and selective inhibitor of cyclin-dependent kinase 9 (CDK9), which suppresses replication of a broad spectrum of DNA viruses through inhibition of mRNA transcription.
111687-37-7	6H-Purin-6-one, 2-amino-9-[(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]-1,9-dihydro- HSV-TK substrate is a substrate for HSV-TK, and induces multi-log cytotoxicity in HSV-TK-expressing and bystander cells.
112228-65-6	B220 B220 is an antiviral agent which can inhibit the growth of HSV-1, HSV-2 and human cytomegalovirus (CMV).
112246-15-8	20(R)Ginsenoside Rh2 Ginsenoside Rh2 possesses matrix metalloproteinase inhibitory, anti-inflammatory and antioxidative activity. It had a significant inhibitory effect on the proliferation. It has been shown to have anticancer effects and to be capable of increasing inchoate apoptotic rate, reducing apoptotic rate significantly, enhancing the activity of Caspase-3 and inducing apoptosis in human lung adenocarcinoma A549 cells.
112446-99-8	SCH-43478
114778-60-8	BRL44385 BRL44385, a novel guanine analogue, is a potent and selective inhibitor of herpes simplex virus types 1 and 2 and varicella zoster virus.
118-00-3	Guanosine Guanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond.
1185179-33-2	Acyclovir-[d4] Acyclovir-[d4] is the labelled analogue of Acyclovir. Acyclovir is a medication against infections caused by virus. It is indiacated for the treatment of herpes simplex virus infections, chickenpox, and shingles.
119670-30-3	Z-LVG-CHN2 Z-LVG-CHN2 is a tripeptide derivative that mimics part of the human cysteine proteinase-binding center. Z-LVG-CHN2 effectively blocks SARS-COV-2 replication (EC50 = 190 nM) via inhibition of SARS-COV-2 3CL pro protease.
119897-50-6	2-Deoxy-D-glucose-[6-13C] 2-Deoxy-D-glucose-[6-13C], is the labelled analogue of 2-Deoxy-D-glucose. 2-deoxy-D-Glucose is a non-metabolizable glucose analog that inhibits phosphorylation of glucose by hexokinase, the first step of glycolysis.
1218948-84-5	Valacyclovir-hydrochloride-hydrate Valacyclovir hydrochloride hydrate is a potent antiviral agent. Valacyclovir hydrochloride hydrate can be used in the management of herpes simplex, herpes zoster and herpes B. Valacyclovir hydrochloride hydrate can be formulate ocular inserts for the treatment of ocular herpes. Valacyclovir hydrochloride hydrate is a prodrug and can be rapidly converted into acyclovir in vivo.
124265-89-0	Omaciclovir This active molecular is a DNA-directed DNA polymerase inhibitor potentially originated by Medivir AB. Omaciclovir can be selectively phosphorylated by viral thymidine kinase to its monophosphate form and it is further modified to a triphosphate, which is an inhibitor of VZV DNA polymerase. Preclinical trials for Herpes simplex virus infections, HIV infections and Varicella zoster virus infections were discontinued.

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