HSV

Herpes simplex virus

HSV

HSV Isoform Specific Products:

HSV Isoform Comparison

HSV Related Products (256)
HSV Isoform Comparison

By Effects:	Controls (2) Inhibitors (236)

Cat. No.	Product Name	Effect	Purity	Chemical Structure

HY-N7677

Isookanin	Inhibitor	99.52%
Isookanin can be used for the research of various illnesses including cancers, skin rashes, snake and insects bites, diabetes mellitus, diarrhoea. Isookanin acts as an anti-viral agent against HSV and varicella-zoster virus (VZV). Antioxidant activity.

HY-13605S

Cytarabine-d₂	Inhibitor	≥98.0%
Cytarabine-d₂ is the deuterium labeled Cytarabine. Cytarabine, a nucleoside analog, causes S phase cell cycle arrest and inhibits DNA polymerase. Cytarabine inhibits DNA synthesis with an IC50 of 16 nM. Cytarabine has antiviral effects against HSV[1][2].

HY-N6666

Vidarabine monohydrate	Inhibitor	99.96%
Vidarabine monohydrate is an adenine arabinoside. Vidarabine monohydrate an antiviral agent which is active against herpes simplex viruses (HSV) and varicella zoster viruses.

HY-163529

HN0037	Inhibitor	99.46%
HN0037 is a selective and orally active helicase-primase inhibitor. HN0037 inhibits HSV replication by targeting the viral helicase-primase enzyme complex.

HY-U00124

Tromantadine	Inhibitor	≥99.0%
Tromantadine hydrochloride, an Amantadine derivative with antiherpetic activity, inhibits herpes simplex virus type 1 (HSV-1) and HSV-2 replication.

HY-113135R

5-Methylcytidine (Standard)	Inhibitor
5-Methylcytidine (Standard) is the analytical standard of 5-Methylcytidine. This product is intended for research and analytical applications. 5-Methylcytidine is a nucleoside compound. 5-Methylcytidine has antiviral activity, and its IC₅₀ against HSV-1 is 0.06 μM.

HY-N7346

Lucidadiol	Inhibitor	≥98.0%
Lucidadiol is a natural compound isolated from Ganoderma lucidum. Lucidadiol exhibits acetylcholinesterase-inhibitory activity, with IC₅₀ values of 31 μM. Lucidadiol shows antiviral activity against influenza virus type A and HSV type 1.

HY-50735

Fiacitabine	Inhibitor	99.27%
Fiacitabine(NSC 382097; FIAC; FOAC) is a selective inhibitior of DNA replication of herpes simplex virus(HSV) with IC50 values of 2.

HY-14809R

Amenamevir (Standard)	Inhibitor
Amenamevir (Standard) is the analytical standard of Amenamevir. This product is intended for research and analytical applications. Amenamevir is a helicase-primase inhibitor which has potent antiviral activity against HSVs with an EC₅₀ of 14 ng/mL.

HY-A0181S2

Adenosine monophosphate-d₁₂ dilithium	Inhibitor
Adenosine monophosphate-d₁₂ (AMP-d₁₂) dilithium is deuterium labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction.

HY-N0097S4

Guanosine-¹³C₁₀	Inhibitor
Guanosine-¹³C₁₀ is the ¹³C labeled Guanosine (HY-N0097). Guanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond. Guanosine possesses anti-HSV activity.

HY-W017522S4

Adipic acid-d₈	Inhibitor	98.64%
Adipic acid-d₈ (Hexanedioic acid-d₈) is the deuterium labeled Adipic acid (HY-W017522). Adipic acid (Hexanedioic acid) is an orally active compound with anti-HSV-1 activity. Adipic acid has low toxicity and can be used as a food additive and a gelling agent. Adipic acid can also be used in the synthesis of lubricants, artificial resins, plastics, etc.

HY-17422A

Acyclovir sodium	Inhibitor
Acyclovir (Aciclovir) sodium is a potent, orally active antiviral agent. Acyclovir sodium has antiherpetic activity with IC₅₀ values of 0.85 μM and 0.86 μM for HSV-1 and HSV-2, respectively. Acyclovir sodium induces cell cycle perturbation and apoptosis. Acyclovir sodium prevents bacterial infections during induction therapy for acute leukaemia.

HY-107739

Penciclovir sodium	Inhibitor
Penciclovir (VSA 671) sodium is a potent and selective anti-herpesvirus agent with EC₅₀ values of 0.5, 0.8 µg/ml for HSV-1 (HFEM), HSV-2 (MS), respectively. Penciclovir sodium shows anti-herpesvirus activity with no-toxic. Penciclovir sodium preventes mortality in mouse.

HY-13637B

Ganciclovir hydrate	Inhibitor
Ganciclovir (BW 759) hydrate, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir hydrate also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir hydrate inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir hydrate has an IC₅₀ of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain.

HY-17425B

Valacyclovir hydrochloride hydrate	Inhibitor
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 research of ocular herpes. Valacyclovir hydrochloride hydrate is a precursor and can be rapidly converted into acyclovir in vivo.

HY-131606

Cidofovir diphosphate
Cidofovir diphosphate is an active intracellular metabolite of Cidofovir. Cidofovir diphosphate is a selective inhibitor of viral DNA polymerases with K_i values of 6.6, 0.86 and 1.4 μM for HCMV, HSV-1 and HSV-2 DNA polymerase, respectively.

HY-19288

Valomaciclovir stearate	Inhibitor
Valomaciclovir stearate (ABT 606), a nucleoside analog, is the Omaciclovir (HY-116174) prodrug. Valomaciclovir stearate has antiviral activity against HSV-1 and varicella zoster virus (VZV).

HY-17426S

Famciclovir-d₄	Inhibitor
Famciclovir-d₄ is the deuterium labeled Famciclovir. Famciclovir (BRL 42810) is a guanine analogue antiviral agent used for the treatment of various herpesvirus infections[1][2].

HY-P5693

HBA(111–142)	Inhibitor
HBA(111-142), an antimicrobial peptide, is a C-terminal 32-mer fragment of alpha-hemoglobin. HBA(111-142) has antibacterial activity against the ESKAPE panel of pathogens. HBA(111-142) forms amyloid fibrils, and has antiviral activities. HBA(111-142) inhibits measles and herpes viruses (HSV-1, HSV-2, HCMV).

2-Deoxy-D-glucose	HSV-1			99.93%
Brefeldin A	HSV-1			99.82%
Cytarabine	HSV-1			99.98%
Dynasore	HSV-1	HSV-2		99.66%
Imiquimod	HSV-1			99.96%
Ivermectin	HSV-1			98.28%
Ganciclovir	HSV-1	HSV-2		99.89%
Salubrinal	HSV-1			99.58%
Acyclovir	HSV-1, IC₅₀: 0.85 μM	HSV-2, IC₅₀: 0.86 μM		99.34%
Floxuridine			HSV	99.97%
Ginsenoside Rb1	HSV-1			98.75%
Imiquimod hydrochloride	HSV-1			99.77%
Digitoxin	HSV-1			99.36%
Trifluridine	HSV-1	HSV-2		99.98%
Xanthohumol	HSV-1	HSV-2		99.97%
Surfactin	HSV-1	HSV-2		98.96%
Levamisole hydrochloride	HSV-1			99.87%
Theaflavin 3,3'-digallate			HSV	99.73%
Surfen dihydrochloride	HSV-1			≥99.0%
Ganciclovir sodium	HSV-1	HSV-2		99.92%
5-Methylcytidine	HSV-1, IC₅₀: 0.06 μM			99.72%
Betulonic acid	HSV-1			98.06%
FSL-1 TFA		HSV-2		99.65%
Pritelivir	HSV-1, IC₅₀: 0.02 μM	HSV-2, IC₅₀: 0.02 μM		99.94%
Oxytetracycline	HSV-1			99.05%
Oxyresveratrol	HSV-1	HSV-2		99.73%
Valacyclovir hydrochloride	HSV-1, IC₅₀: 2.9 μg/mL			99.85%
Adenosine 5'-monophosphate monohydrate	HSV-1	HSV-2		99.07%
Vidarabine	HSV-1, IC₅₀: 9.3 μg/mL	HSV-2, IC₅₀: 11.3 μg/mL		99.35%
Amenamevir	HSV-1, IC₅₀: 7.7-20 ng/mL	HSV-2, IC₅₀: 15-58 ng/mL		99.89%
Penciclovir	HSV-1, EC₅₀: 0.5 μg/mL	HSV-2, EC₅₀: 0.8 μg/mL		99.92%
Octyl gallate	HSV-1			98.01%
Pinostrobin	HSV-1			99.98%
BIO-acetoxime	HSV-1			≥98.0%
Brassicasterol	HSV-1, IC₅₀: 1.2 μM			98.71%
Soyasaponin II	HSV-1, IC₅₀: 54 μM			99.81%
Oxytetracycline hydrochloride	HSV-1			98.92%
LDC4297	HSV-1, EC₅₀: 0.02 μM	HSV-2, EC₅₀: 0.27 μM		98.25%
Imiquimod maleate	HSV-1			99.25%
FIT-039	HSV-1, IC₅₀: 0.69 μM			99.56%
SIBA	HSV-1			99.64%
AT-533	HSV-1			98.86%
Histone H4 (2-21)	HSV-1			98.17%
Isoxanthohumol	HSV-1	HSV-2		99.91%
LDC4297 hydrochloride	166v VP22-GFP, EC₅₀: 0.02 μM	01-6332, EC₅₀: 0.27 μM		98.23%
Manzamine A hydrochloride	HSV-1			99.66%
Isoborneol	HSV-1			98.45%
Docusate Sodium	HSV-1	HSV-2		≥98.0%
Tromantadine hydrochloride	HSV-1	HSV-2		≥98.0%
Soyasapogenol C	HSV-1			≥99.0%
Pritelivir mesylate hydrate	HSV-1, IC₅₀: 0.02 μM	HSV-2, IC₅₀: 0.02 μM		99.51%
Valacyclovir	HSV-1, IC₅₀: 2.9 μg/mL
Pritelivir mesylate	HSV-1, IC₅₀: 0.02 μM	HSV-2, IC₅₀: 0.02 μM		99.51%
Oxytetracycline calcium	HSV-1
5-Nitrobarbituric acid	HSV-1, IC₅₀: 1.7 μM			99.91%
Leachianone G	HSV-1, IC₅₀: 1.6 μg/mL
B220	HSV-1	HSV-2		≥99.0%
Manzamine A	HSV-1
Stearyl gallate	HSV-1			99.50%
Tromantadine	HSV-1	HSV-2		≥99.0%
Fiacitabine	HSV-1	HSV-2		99.27%
Acyclovir sodium	HSV-1, IC₅₀: 0.85 μM	HSV-2, IC₅₀: 0.86 μM
Penciclovir sodium	HSV-1, EC₅₀: 0.5 μg/mL	HSV-2, EC₅₀: 0.8 μg/mL
Ganciclovir hydrate	HSV-1	HSV-2
Perillic acid	HSV-1
Ganoderone A			HSV, IC₅₀: 0.3 μg/mL
Kushenol K		HSV-2, EC₅₀: 147 μM
Ginsenoside Rb1 (Standard)	HSV-1
Peniterphenyl A	HSV-1
WAY-150138	HSV-1, IC₅₀: 0.2 μg/mL	HSV-2, IC₅₀: 6.8 μg/mL
HSV-1/HSV-2-IN-2	HSV-1, EC₅₀: 6.8 μM	HSV-2, EC₅₀: 8.9 μM
Yatein	HSV-1			99.76%
HSV-1-IN-1	HSV-1, IC₅₀: 0.5 nM	HSV-2, IC₅₀: 16 nM
HSV-1/HSV-2-IN-1	HSV-1	HSV-2
Oxytetracycline dihydrate	HSV-1
Surfen	HSV-1
17,17-Ethylendioxyandrost-5-en-3β-ol	HSV-1
SCH-43478		HSV-2, IC₅₀: 1.8 μg/mL
BRL44385	HSV-1	HSV-2

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HSV

HSV

HSV Isoform Specific Products:

HSV Isoform Specific Products:

HSV Related Products (256)

HSV Isoform Comparison

HSV Related Products (256):