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Antiviral API
- Arenavirus
- Cytomegalovirus (CMV)
- Dengue virus
- Endogenous Metabolite
- Enterovirus (EV)
- Epstein-Barr virus (EBV)
- Filovirus
- Flavivirus
- HCV Protease
- Hepatitis B Virus (HBV)
- Hepatitis C Virus (HCV)
- Herpes simplex Virus (HSV)
- HIF/HIF Prolyl-Hydroxylase
- HIV Integrase
- HIV Protease
- Human immunodeficiency Virus (HIV)
- Human papillomavirus (HPV)
- Influenza Virus
- Nipah virus
- Orthopoxvirus
- Others
- Rabies virus (RABV)
- Respiratory syncytial Virus (RSV)
- Reverse Transcriptases (RTs)
- SARS-CoV
- Tobacco mosaic virus (TMV)
- Vesicular stomatitis virus (VSV)
- Virus Protease
- West Nile virus
- Antiviral intermediates
Herpes simplex Virus (HSV)
CAS No. | Product Name | Inquiry |
---|---|---|
1246819-64-6 |
Levamisole-d5 HydrochlorideLevamisole-[d5] Hydrochloride is the labelled analogue of Levamisole, which is a biological response modifier with anthelmintic activity. |
|
124-76-5 |
IsoborneolIsoborneol is a monoterpene that can be isolated from a variety of plants. It is used as a flavor in food additive. Isoborneol acts as an inhibitor of herpes simplex virus type 1 (HSV-1) replication. It also exhibits antitumor and neuroprotective effects. |
|
124832-26-4 |
ValacyclovirValaciclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. |
|
1279033-32-7 |
Valacyclovir-[d8] HydrochlorideLabelled Valacyclovir. Valacyclovir is an antiviral drug used to treat infections caused by herpes viruses. |
|
1331910-75-8 |
Valacyclovir-[d4] HydrochlorideValacyclovir-[d4] Hydrochloride is the labelled analogue of Valacyclovir Hydrochloride, which is a derivative of valacyclovir. valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster and herpes B. |
|
1357299-45-6 |
OG-L002 hydrochloride |
|
1357302-64-7 |
OG-L002OG-L002 potently inhibits HSV IE gene expression in both HeLa and HFF cells with IC50s of ~10 μM and ~3 μM, respectively. OG-L002 is a potent and highly selective inhibitor of LSD1 (IC50 = 0.02 μM), and is a potent inhibitor of monoamine oxidases (MAO) with IC50s of 1.38 and 0.72 μM for MAO-A and MAO-B, respectively. |
|
1359968-33-4 |
Ganciclovir-hydrateGanciclovir (BW 759) hydrate, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovirhydrate 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. |
|
13677-79-7 |
Gallic aldehydeGallic aldehyde is found in the whole plants of Geum japonicum, it shows potent antiviral activity against HSV-1. |
|
1383450-81-4 |
RilematovirRilematovir (JNJ-678) is a novel fusion protein inhibitor. Rilematovir has the potential for respiratory syncytial virus (RSV) research. |
|
1428321-10-1 |
Pritelivir mesylate hydratePritelivir mesylate hydrate is an inhibitor of the viral helicase-primase complex and has activity against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) with IC50s of both 0.02 μM against HSV1-2. It shows antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection. |
|
1428333-96-3 |
Pritelivir mesylatePritelivir mesylate is a potent helicase primase inhibitor that inhibits HSV replication. Pritelivir is active against both types of herpes simplex virus (HSV-1 and HSV-2). |
|
1453834-21-3 |
LDC4297LDC4297 is a potent and selective cyclin-dependent protein kinase 7 (CDK7) inhibitor with an IC50 of 0.13 nM. |
|
147-94-4 |
CytarabineArabinofuranosyl-cytosine (ara-C) is an inhibitor of DNA synthesis used as an antineoplastic and antiviral. It is a chemotherapy agent used to treat cancers of white blood cells like acute myeloid leukemia (AML) and non-Hodgkin lymphoma. |
|
152464-78-3 |
Leachianone GLeachianone G isolated from the roots of Sophora flavescens Ait. |
|
154-17-6 |
2-Deoxy-D-glucose2-deoxy-D-glucose is a non-metabolizable glucose analog that inhibits phosphorylation of glucose by hexokinase, the first step of glycolysis. This results in the depletion in cellular ATP, the inhibition of protein glycosylation, and the disruption of ER quality control by inducing the unfolded protein response. 2-deoxy-D-glucose has been shown to cause cell cycle inhibition and cell death in in vitro models of hypoxia, induce autophagy, increase reactive oxygen species production, activate AMPK, and block tumor cell growth in animal models. |
|
155112-92-8 |
Woodorien |
|
155944-24-4 |
Cangorinine E-1Cangorinine-E-I is a natural compound which can be isolated from Picris hieracioides and Ixeris chinensis, etc. |
|
176983-21-4 |
2α,19α-Dihydroxy-3-oxo-urs-12-en-28-oic acid2α,19α-Dihydroxy-3-oxo-urs-12-en-28-oic acid is a natural compound isolated from the leaves of Eriobotrya japonica. |
|
1793003-47-0 |
11-Deoxymogroside IIIE11-Deoxymogroside IIIE is a triterpenoid isolated from Siraitia grosvenorii. |
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