-
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
Human immunodeficiency Virus (HIV)
CAS No. | Product Name | Inquiry |
---|---|---|
1155419-89-8 |
BI 224436BI 224436 is a novel HIV-1 non-catalytic-site integrase inhibitor; has antiviral EC50s of <15 nM against different HIV-1 laboratory strains and cellular cytotoxicity of >90 μM. |
|
1159840-61-5 |
Gardiquimod-diTFAGardiquimod diTFA, an imidazoquinoline analog, is a TLR7/8 agonist. Gardiquimod diTFA could inhibit HIV-1 infection of macrophages and activated peripheral blood mononuclear cells (PBMCs). Gardiquimod diTFA specifically activates TLR7 when used at concentrations below 10 μM. |
|
116249-65-1 |
Benanomicin ABenanomicin A is produced by the strain of Actinomadura sp. MH193-16F4. A and B have anti-candida, Cryptococcus neoforme, Saccharomyces cerevisiae and other fungal activities, while A has stronger activity. Xylose benamycin A and B showed similar or slightly stronger activity against candida, yeast and Cryptococcus, but decreased activity against aspergillus. The antifungal activity of 2-demethylbenamycin was similar to that of xylose Benamycin A. The synthesized 7-methoxybenamycin had little antifungal activity, but showed inhibitory activity of glucosinolase (EC 3.2.1.20) with IC50 of 60μg/mL. |
|
1174719-68-6 |
WRNA10WRNA10 is a potent HIV-1 TAR RNA binder with an IC50 of 10 µM and an CC50 of 40 µM. |
|
117704-65-1 |
Pradimicin APradimicin A is an antibiotic produced by Actinomadura hibisca. It has strong antifungal and yeast activity. |
|
1185237-51-7 |
Panobinostat-[d4]Panobinostat-[d4], is the labelled analogue of Panobinostat. Panobinostat is a drug for the treatment of various cancers. It is a hydroxamic acid and acts as a non-selective histone deacetylase inhibitor. |
|
1185451-72-2 |
CXCR4 antagonist 7 |
|
1185878-98-1 |
Pentoxifylline-[d6]Pentoxifylline-[d6] is the labelled analogue of Pentoxifylline which is a competitive nonselective phosphodiesterase inhibitor. |
|
1185995-18-9 |
Pentoxifylline-[d5]Pentoxifylline-[d5] is the labelled analogue of Pentoxifylline. Pentoxifylline can be used for the treatment of muscle pain in people with peripheral artery disease. |
|
1187917-12-9 |
AIC-292AIC-292 is a potent and selective inhibitor of HIV-1 nonnucleoside reverse transcriptase. It inhibits wild-type HIV-1 laboratory strains at low nanomolar concentrations. AIC-292 displays potent antiviral in vivo efficacy in a mouse xenograft model. |
|
1189471-66-6 |
rac α-Lipoic Acid-[d5]rac α-Lipoic Acid-[d5] is the labelled analogue of rac α-Lipoic Acid, which is a fat-metabolism stimulator. |
|
1189657-87-1 |
Probenecid-d14Probenecid-[d14] is the labelled analogue of Probenecid. Probenecid is a drug that increases the excretion of uric acid in the urine and can be used to treat gout and hyperuricemia. |
|
1189994-89-5 |
5-Hydroxy Valproic acid-[d7] sodium salt5-Hydroxy Valproic acid-[d7] sodium salt is the labelled analogue of 5-Hydroxy Valproic acid sodium salt, which is a metabolite of Valproic Acid. |
|
119139-55-8 |
InteriorinInteriorin is a lignan isolated from Kadsura heteroclita. Interiorin exhibits anti-HIV activity. |
|
1192224-24-0 |
Dealkyl AtazanavirAn impurity of Atazanavir |
|
1206161-97-8 |
FilgotinibFilgotinib is a potent and selective JAK1 inhibitor exhibiting 30-fold selectivity over JAK2. It was shown to inhibit Th1 and Th2 differentiation and to a lesser extent the differentiation of Th17 cells in vitro. Filgotinib has the potential for the treatment of rheumatoid arthritis and possibly other immune-inflammatory diseases. |
|
121104-96-9 |
6-O-butyl castanospermineCelgosivir, an effective α-glucosidase I inhibitor, has been found to be related to viral maturation and is still under Phase I/II trial against Dengue. IC50: 16 and 47 umol/L (through plaque assay and a cytopathic assay). |
|
1217629-70-3 |
Nelfinavir-[d3]Nelfinavir-[d3] is the labelled analogue of Nelfinavir, which is a potent and orally bioavailable human immunodeficiency virus HIV-1 protease inhibitor. |
|
1217661-20-5 |
Amprenavir-[d4]Amprenavir-[d4] is a labelled analogue of Amprenavir. Amprenavir promotes the specific interactions between the nuclear receptor pregnane X receptor (PXR) and the coactivators SRC-1 and PBP. |
|
1217819-15-2 |
Tipranavir-[d4]Tipranavir-[d4] is the labelled analogue of Tipranavir, which is a nonpeptidic HIV protease inhibitor and has been found to be effective as an antiviral. |
※ Please kindly note that our services are for research use only.