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LIFE SCIENCES > Immunodetection Tools > COVID-19 RESEARCH > Chemicals
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Covid-19: Chemicals
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SARS-CoV-2, the cause of the COVID-19 pandemic currently affecting all countries in the world, belongs to the beta-coronaviruses genus, which also includes the SARS CoV (2003) and the MERS CoV (2012).
If vaccines have arrived to undermine the pandemic, the development of a curative treatment would be an answer to all unvaccinated people. And at a time when many variants are spreading, vaccination cannot be the answer on its own.
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| There are many molecules being tested and we offer you a wide choice of molecules that could play a role in the development of an effective treatment against covid-19. |
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For more information, please see our Covid-19 related article (in french).
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In progress. Due to the current situation, this page may be subject to frequent updates.
For any request please contact-us.
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INTERCHIM BIOSCIENCE ARBIDOL (HYDROCHLORIDE), TARGET: INFLUENZA VIRUS P/N : HY-14904A Pack : 1 x 10 mg P/N : HY-14904A Item : VIF014 Pack : 1 x 10 mg Cat. Price :  Umifenovir hydrochloride is a potent, orally active broad-spectrum antiviral with activity against a number of enveloped and non-enveloped viruses. Umifenovir hydrochloride is used as an anti-influenza virus agent. Umifenovir hydrochloride could effectively inhibit the fusion of virus with host cells. Umifenovir hydrochloride is an efficient inhibitor of SARS-CoV-2 in vitro. Anti-inflammatory activity.IC50 & Target: Antiviral, Anti-influenza agentIn Vitro: Umifenovi CAS : 131707-23-8 INTERCHIM BIOSCIENCE ARBIDOL (HYDROCHLORIDE), TARGET: INFLUENZA VIRUS P/N : HY-14904A Pack : 1 x 50 mg P/N : HY-14904A Item : VIF015 Pack : 1 x 50 mg Cat. Price : Umifenovir hydrochloride is a potent, orally active broad-spectrum antiviral with activity against a number of enveloped and non-enveloped viruses. Umifenovir hydrochloride is used as an anti-influenza virus agent. Umifenovir hydrochloride could effectively inhibit the fusion of virus with host cells. Umifenovir hydrochloride is an efficient inhibitor of SARS-CoV-2 in vitro. Anti-inflammatory activity.IC50 & Target: Antiviral, Anti-influenza agentIn Vitro: Umifenovi CAS : 131707-23-8 INTERCHIM BIOSCIENCE ARBIDOL (HYDROCHLORIDE), TARGET: INFLUENZA VIRUS P/N : HY-14904A Pack : 1 x 100 mg P/N : HY-14904A Item : VIF016 Pack : 1 x 100 mg Cat. Price : Umifenovir hydrochloride is a potent, orally active broad-spectrum antiviral with activity against a number of enveloped and non-enveloped viruses. Umifenovir hydrochloride is used as an anti-influenza virus agent. Umifenovir hydrochloride could effectively inhibit the fusion of virus with host cells. Umifenovir hydrochloride is an efficient inhibitor of SARS-CoV-2 in vitro. Anti-inflammatory activity.IC50 & Target: Antiviral, Anti-influenza agentIn Vitro: Umifenovi CAS : 131707-23-8 INTERCHIM BIOSCIENCE CAMOSTAT (MESYLATE) P/N : HY-13512 Pack : 1 x 50 mg P/N : HY-13512 Item : STF825 Pack : 1 x 50 mg Cat. Price : Camostat mesylate (Camostat mesilate) is an orally active, synthetic serine protease inhibitor for chronic pancreatitis. Camostat mesylate, an inhibitor of TMPRSS2, shows antiviral activity against SARS-CoV-2. Camostat mesylate also inhibits the activity of prostasin, trypsin, and matriptase.In Vitro: Camostat mesylate (Camostat mesilate) inhibits both monocyte chemoattractant protein-1 (MCP-1) and TNF-α production from monocytes, and proliferation and MCP-1 p Molecular formula : C21H26N4O8S CAS : 59721-29-8 INTERCHIM BIOSCIENCE CAMOSTAT (MESYLATE) P/N : HY-13512 Pack : 1 x 100 mg P/N : HY-13512 Item : STF826 Pack : 1 x 100 mg Cat. Price : Camostat mesylate (Camostat mesilate) is an orally active, synthetic serine protease inhibitor for chronic pancreatitis. Camostat mesylate, an inhibitor of TMPRSS2, shows antiviral activity against SARS-CoV-2. Camostat mesylate also inhibits the activity of prostasin, trypsin, and matriptase.In Vitro: Camostat mesylate (Camostat mesilate) inhibits both monocyte chemoattractant protein-1 (MCP-1) and TNF-α production from monocytes, and proliferation and MCP-1 p Molecular formula : C21H26N4O8S CAS : 59721-29-8 INTERCHIM BIOSCIENCE CAMOSTAT (MESYLATE) P/N : HY-13512 Pack : 1 x 10 mg P/N : HY-13512 Item : STF824 Pack : 1 x 10 mg Cat. Price : Camostat mesylate (Camostat mesilate) is an orally active, synthetic serine protease inhibitor for chronic pancreatitis. Camostat mesylate, an inhibitor of TMPRSS2, shows antiviral activity against SARS-CoV-2. Camostat mesylate also inhibits the activity of prostasin, trypsin, and matriptase.In Vitro: Camostat mesylate (Camostat mesilate) inhibits both monocyte chemoattractant protein-1 (MCP-1) and TNF-α production from monocytes, and proliferation and MCP-1 p Molecular formula : C21H26N4O8S CAS : 59721-29-8 INTERCHIM BIOSCIENCE HYDROXYCHLOROQUINE (SULFATE) P/N : HY-B1370 Pack : 1 x 50 mg P/N : HY-B1370 Item : XMN535 Pack : 1 x 50 mg Cat. Price : Hydroxychloroquine sulfate (HCQ sulfate) is a synthetic antimalarial agent which can also inhibit Toll-like receptor 7/9 (TLR7/9) signaling. Hydroxychloroquine sulfate is efficiently inhibits SARS-CoV-2 infection in vitro.IC50 & Target: Antimalarial, TLR7/9In Vitro: Hydroxychloroquine sulfate is a synthetic antimalarial drug derived from 4-aminoquinoline, it has been used for several decades for the treatment of some rheumatic diseases such as rheumato CAS : 747-36-4 INTERCHIM BIOSCIENCE IMATINIB MESYLATE P/N : AZ876D Pack : 1 x 1 g P/N : AZ876D Item : AZ876D Pack : 1 x 1 g Cat. Price : Molecular formula : C30H35N7O4S CAS : 220127-57-1 INTERCHIM BIOSCIENCE LOPINAVIR TARGET: HIV PROTEASE,HIV P/N : HY-14588 Pack : 1 x 100 mg P/N : HY-14588 Item : PO407T Pack : 1 x 100 mg Cat. Price : Lopinavir is a potent HIV protease inhibitor with Ki of 1.3 pM.Target: HIV proteaseLopinavir is a potent inhibitor of Rh123 efflux in Caco-2 monolayers with IC50 of 1.7 mM. Lopinavir exposure (72 hours) in LS 180V cells reduces the content of intracellular Rh123. Lopinavir induces P-glycoprotein immunoreactive protein and messenger RNA levels in LS 180V cells. Lopinavir inhibits subtype C clone C6 with IC50 of 9.4 nM. Lopinavir inhibits CYP3A with IC50 of 7.3 mM in human liver microsomes, whil Molecular formula : C37H48N4O5 CAS : 192725-17-0 INTERCHIM BIOSCIENCE LOPINAVIR TARGET: HIV PROTEASE,HIV P/N : HY-14588 Pack : 1 x 250 mg P/N : HY-14588 Item : PO407U Pack : 1 x 250 mg Cat. Price : Lopinavir is a potent HIV protease inhibitor with Ki of 1.3 pM.Target: HIV proteaseLopinavir is a potent inhibitor of Rh123 efflux in Caco-2 monolayers with IC50 of 1.7 mM. Lopinavir exposure (72 hours) in LS 180V cells reduces the content of intracellular Rh123. Lopinavir induces P-glycoprotein immunoreactive protein and messenger RNA levels in LS 180V cells. Lopinavir inhibits subtype C clone C6 with IC50 of 9.4 nM. Lopinavir inhibits CYP3A with IC50 of 7.3 mM in human liver microsomes, whil Molecular formula : C37H48N4O5 CAS : 192725-17-0 INTERCHIM BIOSCIENCE LOPINAVIR TARGET: HIV PROTEASE,HIV P/N : HY-14588 Pack : 1 x 50 mg P/N : HY-14588 Item : PO407S Pack : 1 x 50 mg Cat. Price : Lopinavir is a potent HIV protease inhibitor with Ki of 1.3 pM.Target: HIV proteaseLopinavir is a potent inhibitor of Rh123 efflux in Caco-2 monolayers with IC50 of 1.7 mM. Lopinavir exposure (72 hours) in LS 180V cells reduces the content of intracellular Rh123. Lopinavir induces P-glycoprotein immunoreactive protein and messenger RNA levels in LS 180V cells. Lopinavir inhibits subtype C clone C6 with IC50 of 9.4 nM. Lopinavir inhibits CYP3A with IC50 of 7.3 mM in human liver microsomes, whil Molecular formula : C37H48N4O5 CAS : 192725-17-0 INTERCHIM BIOSCIENCE NICLOSAMIDE, TARGET: STAT,PARASITE P/N : HY-B0497 Pack : 1 x 5 g P/N : HY-B0497 Item : 22774M Pack : 1 x 5 g Cat. Price : Niclosamide (BAY2353)?is an orally bioavailable chlorinated salicylanilide, with anthelmintic and potential antineoplastic activity. Niclosamide (BAY2353) inhibits STAT3 with IC50 of 0.25 Î?M in HeLa cells and inhibits DNA replication in a cell-free assay.IC50 & Target: IC50: 0.25 Î?M (STAT3)In Vitro: Niclosamide is an inhibitor of STAT3, inhibiting STAT3-mediated luciferase reporter activity with an IC50 of 0.25 Î?M in HeLa cells. Niclosamide (1 Molecular formula : C13H8Cl2N2O4 CAS : 50-65-7 INTERCHIM BIOSCIENCE NICLOSAMIDE, TARGET: STAT,PARASITE P/N : HY-B0497 Pack : 1 x 10 g P/N : HY-B0497 Item : 22774L Pack : 1 x 10 g Cat. Price : Niclosamide (BAY2353)?is an orally bioavailable chlorinated salicylanilide, with anthelmintic and potential antineoplastic activity. Niclosamide (BAY2353) inhibits STAT3 with IC50 of 0.25 Î?M in HeLa cells and inhibits DNA replication in a cell-free assay.IC50 & Target: IC50: 0.25 Î?M (STAT3)In Vitro: Niclosamide is an inhibitor of STAT3, inhibiting STAT3-mediated luciferase reporter activity with an IC50 of 0.25 Î?M in HeLa cells. Niclosamide (1 Molecular formula : C13H8Cl2N2O4 CAS : 50-65-7 INTERCHIM BIOSCIENCE NITAZOXANIDE, TARGET: AUTOPHAGY,INFLUENZA VIRUS P/N : HY-B0217 Pack : 1 x 10 mg P/N : HY-B0217 Item : RQ550T Pack : 1 x 10 mg Cat. Price : Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. (IC50 for canine influenza virus ranges from 0.17 to 0.21 Î?M).Target: OthersNitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. In vitro studies demonstrated much broader activity. Dr. Rossignol co-founded Romark Laboratories, with the goal of bringing nitazoxanide to market as an anti-parasitic drug. Initial studies in the USA were conducted in collaboratio Molecular formula : C12H9N3O5S CAS : 55981-09-4 INTERCHIM BIOSCIENCE NITAZOXANIDE, TARGET: AUTOPHAGY,INFLUENZA VIRUS P/N : HY-B0217 Pack : 1 x 100 mg P/N : HY-B0217 Item : RQ550V Pack : 1 x 100 mg Cat. Price : Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. (IC50 for canine influenza virus ranges from 0.17 to 0.21 Î?M).Target: OthersNitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. In vitro studies demonstrated much broader activity. Dr. Rossignol co-founded Romark Laboratories, with the goal of bringing nitazoxanide to market as an anti-parasitic drug. Initial studies in the USA were conducted in collaboratio Molecular formula : C12H9N3O5S CAS : 55981-09-4 INTERCHIM BIOSCIENCE NITAZOXANIDE, TARGET: AUTOPHAGY,INFLUENZA VIRUS P/N : HY-B0217 Pack : 1 x 50 mg P/N : HY-B0217 Item : RQ550U Pack : 1 x 50 mg Cat. Price : Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. (IC50 for canine influenza virus ranges from 0.17 to 0.21 Î?M).Target: OthersNitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent. In vitro studies demonstrated much broader activity. Dr. Rossignol co-founded Romark Laboratories, with the goal of bringing nitazoxanide to market as an anti-parasitic drug. Initial studies in the USA were conducted in collaboratio Molecular formula : C12H9N3O5S CAS : 55981-09-4 INTERCHIM BIOSCIENCE REMDESIVIR , TARGET: SARS-COV P/N : B60DF5 Pack : 01 x 1 g P/N : B60DF5 Item : B60DF5 Pack : 01 x 1 g Cat. Price : Molecular formula : C27H35N6O8P CAS : 1809249-37-3 INTERCHIM BIOSCIENCE REMDESIVIR , TARGET: SARS-COV P/N : B60DF4 Pack : 1 x 100 mg P/N : B60DF4 Item : B60DF4 Pack : 1 x 100 mg Cat. Price : Molecular formula : C27H35N6O8P CAS : 1809249-37-3 INTERCHIM BIOSCIENCE REMDESIVIR , TARGET: SARS-COV P/N : B60DF2 Pack : 1 x 50 mg P/N : B60DF2 Item : B60DF2 Pack : 1 x 50 mg Cat. Price : Molecular formula : C27H35N6O8P CAS : 1809249-37-3 INTERCHIM BIOSCIENCE REMDESIVIR , TARGET: SARS-COV P/N : HY-104077 Pack : 1 x 1 ml P/N : HY-104077 Item : B60DFA Pack : 1 x 1 ml Cat. Price : Remdesivir (GS-5734), a nucleoside analogue with effective antiviral activity, has EC50s of 74 nM for SARS-CoV and MERS-CoV in HAE cells, and 30 nM for murine hepatitis virus in delayed brain tumor cells. Remdesivir is highly effective in the control of SARS-CoV-2 (COVID-19) infection in vitro.IC50 & Target: EC50: 30 nM (murine hepatitis virus, delayed brain tumor cell), 74 nM (SARS-CoV, HAE cell), 74 nM (MERS-CoV, HAE cell)In Vitro: Remdesi Molecular formula : C27H35N6O8P CAS : 1809249-37-3 INTERCHIM BIOSCIENCE REMDESIVIR , TARGET: SARS-COV P/N : HY-104077 Pack : 1 x 1 mg P/N : HY-104077 Item : B60DFF Pack : 1 x 1 mg Cat. Price : Remdesivir (GS-5734), a nucleoside analogue with effective antiviral activity, has EC50s of 74 nM for SARS-CoV and MERS-CoV in HAE cells, and 30 nM for murine hepatitis virus in delayed brain tumor cells. Remdesivir is highly effective in the control of SARS-CoV-2 (COVID-19) infection in vitro.IC50 & Target: EC50: 30 nM (murine hepatitis virus, delayed brain tumor cell), 74 nM (SARS-CoV, HAE cell), 74 nM (MERS-CoV, HAE cell)In Vitro: Remdesi Molecular formula : C27H35N6O8P CAS : 1809249-37-3 INTERCHIM BIOSCIENCE TOCILIZUMAB, TARGET: INTERLEUKIN RELATED P/N : B5ZX74 Pack : 01 x 25 mg P/N : B5ZX74 Item : B5ZX74 Pack : 01 x 25 mg Cat. Price : CAS : 375823-41-9 INTERCHIM BIOSCIENCE TOCILIZUMAB, TARGET: INTERLEUKIN RELATED P/N : HY-P9917 Pack : 1 x 1 mg P/N : HY-P9917 Item : B5ZX70 Pack : 1 x 1 mg Cat. Price : Tocilizumab (Anti-Human IL6R, Humanized Antibody) is an anti-human interleukin-6 receptor (IL-6R) neutralizing antibody, prevents binding of IL-6 to the IL-6R, thereby inhibiting both classic and trans-signaling. Tocilizumab (Anti-Human IL6R, Humanized Antibody) can be used for the treatment of rheumatoid arthritis. Tocilizumab is remarkablely effective for the study of severe COVID-19 (coronavirus disease).IC50 & Target: IC50: IL-6RIn Vitro: Tocilizumab (Anti-Human IL6R, CAS : 375823-41-9 INTERCHIM BIOSCIENCE TOCILIZUMAB, TARGET: INTERLEUKIN RELATED P/N : B5ZX73 Pack : 01 x 10 mg P/N : B5ZX73 Item : B5ZX73 Pack : 01 x 10 mg Cat. Price : CAS : 375823-41-9 INTERCHIM BIOSCIENCE TOCILIZUMAB, TARGET: INTERLEUKIN RELATED P/N : HY-P9917 Pack : 1 x 25 mg P/N : HY-P9917 Item : B5ZX72 Pack : 1 x 25 mg Cat. Price : Tocilizumab (Anti-Human IL6R, Humanized Antibody) is an anti-human interleukin-6 receptor (IL-6R) neutralizing antibody, prevents binding of IL-6 to the IL-6R, thereby inhibiting both classic and trans-signaling. Tocilizumab (Anti-Human IL6R, Humanized Antibody) can be used for the treatment of rheumatoid arthritis. Tocilizumab is remarkablely effective for the study of severe COVID-19 (coronavirus disease).IC50 & Target: IC50: IL-6RIn Vitro: Tocilizumab (Anti-Human IL6R, CAS : 375823-41-9
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