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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
Influenza Virus
CAS No. | Product Name | Inquiry |
---|---|---|
3022924-04-2 |
ZIKV-IN-8 |
|
3031330-66-9 |
PROTAC Hemagglutinin Degrader-1 |
|
303175-44-2 |
zapnometinibzapnometinib is an ATP non-competitive MEK1/2 inhibitor that can treat respiratory viral infections by inhibiting MEK. |
|
3033379-90-4 |
MI-1904 |
|
3033567-35-7 |
Dihydromaniwamycin E |
|
3055-98-9 |
Octaethylene glycol monododecyl etherOctaethylene glycol monododecyl ether, a non-ionic surfactant formed by the ethoxylation of dodecanol (lauryl alcohol), is a non-ionic detergent for the solubilization of membrane bound proteins, as well as the viral membranes of intact influenza viruses. |
|
31377-23-8 |
1-Adamantanamine sulfateAmantadine (1-Adamantanamine) sulfate is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine sulfate inhibits several ion channels such as NMDA and M2, and also inhibits Coronavirus ion channels. It also has anti-orthopoxvirus and anticancer activity. Amantadine sulfate can be used for Parkinson's disease, postoperative cognitive dysfunction (POCD) and COVID-19 research. |
|
3160-91-6 |
Moroxydine hydrochlorideMoroxydine HCl is a synthetic antiviral compound chemically belonging to the series of the heterocyclic biguanidines. |
|
327-57-1 |
L-NorleucineL-Norleucine, an isomer of leucine, specifically affects skeletal muscle protein synthesis and has antiviral activity. |
|
330600-85-6 |
PeramivirPeramivir is an antiviral inhibitor with an IC50 of median 0.09 nM. It prevents the virus from infecting cells. |
|
332108-65-3 |
ABMAABMA is a broad-spectrum inhibitor of intracellular toxin and pathogens. It efficiently protects cells against various pathogens including viruses, intracellular bacteria, and parasite. ABMA selectively acts at host cell late endosomes rather than targeting toxin or pathogen itself. |
|
335679-69-1 |
A-315675 |
|
33830-10-3 |
1-Adamantanamine-[d15]1-Adamantanamine-[d15] is a labelled form of Amantadine. Amantadine can be used as an antiviral and an antiparkinsonian drug. It is an NMDA receptor antagonist. Amantadine is also a useful building block in organic synthesis, allowing the insertion of an adamantyl group. |
|
3411-37-8 |
SophoranolSophoranol is an alkaloid isolated from S. flavescens. Sophoranol shows potent antiviral activities against respiratory syncytial virus (RSV) with an IC50 of 10.4 μg/mL. |
|
345267-14-3 |
BCX-1898 |
|
34580-13-7 |
KetotifenKetotifen is a cycloheptathiophene blocker of histamine H1 receptors and release of inflammatory mediators, used as self-medication for the temporary relief of itching of the eye due to allergic conjunctivitis (ophthalmic). |
|
350818-67-6 |
Rimantadine-[d4] HydrochlorideRimantadine-[d4] Hydrochloride is the labelled analogue of Rimantadine. Rimantadine is an antiviral drug used to treat influenzavirus A infection. |
|
352000-07-8 |
Baicalein hydrate |
|
35891-70-4 |
MyriocinMyriocin is an unsaturated hydrocarbon and fatty acid derivative produced by Myriococcum albomyces NRRL 3858. It has antifungal activity. |
|
371942-69-7 |
YM-201636YM201636 is an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, can halt glucose entry by insulin in adipocytes. YM201636 almost completely inhibited basal and insulin-activated 2-deoxyglucose uptake at doses as low as 160 nM, with IC(50)=54+/-4 nM for the net insulin response. Insulin-induced GLUT4 translocation was partially inhibited at substantially higher doses, comparable to those required for inhibition of insulin-induced phosphorylation of Akt/PKB. In addition to PIKfyve, YM201636 also completely inhibited insulin-dependent activation of class IA PI 3-kinase. |
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