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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
SARS-CoV
CAS No. | Product Name | Inquiry |
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1"-α-Azido-RDPr |
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28-O-Imidazolyl-azepano-betulin |
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2'-RIBOTAC-U |
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AMY-101 acetateAMY-101 acetate inhibits naturally occurring periodontitis in non-human primates (NHPs). AMY-101 acetate exhibits a favorable anti-inflammatory activity in models with COVID-19 severe pneumonia with systemic hyper inflammation. |
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AMY-101-acetateAMY-101 acetate (Cp40 acetate), a peptidic inhibitor of the central complement component C3 (KD = 0.5 nM), inhibits naturally occurring periodontitis in non-human primates (NHPs). AMY-101 acetate (Cp40 acetate) exhibits a favorable anti-inflammatory activity in models with COVID-19 severe pneumonia with systemic hyper inflammation. |
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AnsabananinAnsabananin is a weak inhibitor of the ATPase activity of the SARS Coronavirus helicase, with an IC50 value of 51 μM. |
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Anti-MERS-2E6-mAbAnti-MERS-2E6 mAb, a human neutralizing antibody IgG1 (CHO expressed) that can compete for the binding of the virus Spike protein to the receptor (CD26), thereby inhibiting virus invasion into host cells. |
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Anti-MERS-3A1-mAbAnti-MERS-3A1 mAb (MERS-3A1) is a human monoclonal IgG1 antibody with the high binding affinity produced in CHO cells. Anti-MERS-3A1 mAb bocks the binding of MERS-CoV spike protein to DPP4 receptor. |
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Antimicrobial agent-10 |
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Antimicrobial agent-11 |
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Antimicrobial agent-12 |
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1070773-09-9 |
RK-33RK-33 is a first-in-class inhibitor of DDX3. It causes G1 cell cycle arrest, induces apoptosis, and promotes radiation sensitization in DDX3-overexpressing cells, which has therapeutic use in cancers. |
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1005304-44-8 |
SARS-CoV-2-nsp13-IN-1SARS-CoV-2 nsp13-IN-1 (compound C1) is a potent nsp13 (non-structural protein 13) inhibitor. SARS-CoV-2 nsp13-IN-1 only inhibits nsp13 ssDNA+ ATPase, with an IC50 of 6 μM. SARS-CoV-2 nsp13-IN-1 does not inhibit ssDNA- ATPase. SARS-CoV-2 nsp13-IN-1 can be used for COVID-19 research. |
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1015582-31-6 |
SARS-CoV-2-nsp13-IN-3SARS-CoV-2 nsp13-IN-3 (Compound C3) is a SARS-CoV-2 non-structural protein 13 (nsp13) small-molecule inhibitor with an IC50 of 32 μM against nsp13 ssDNA+ ATPase. |
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1016762-41-6 |
SARS-CoV-2-IN-89 |
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1017691-52-9 |
SARS-CoV-2-IN-31 |
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1029939-86-3 |
ArtefenomelArtefenomel (OZ439) is an orally active, synthetic anti-malarial compound containing an artemisinin pharmacophore with a mechanism of action similar to that of artemisinin. Artefenomel has antiviral activity against SARS-CoV-2. |
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10371-86-5 |
SMU-CX1 |
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104494-35-1 |
Kazinol F |
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1052540-65-4 |
Debrisoquin hydroiodideDebrisoquin is an adrenergic neuron-blocking drug similar in effects to guanethidine. It is an antihypertensive drug with antioxidant, anti-inflammatory, and neuroprotective properties. It can regulate the activity of certain neurotransmitters, including dopamine and serotonin, which makes it a promising candidate for treating neurological disorders, such as Parkinson's disease and depression. |
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