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73 results for "Antiviral Compounds" in Products

Antiviral Compounds Products

Antivirals are drugs that inhibit viral infection, targeting virus entry, assembly or replication. Mechanisms of antiviral action include blocking virus replication at key points, such as interfering with DNA polymerization or protease inhibition. They are used to treat viral infections such as HIV and CMV.

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Potent inhibitor of SERCA ATPase

Chemical Name: (3S,3aR,4S,6S,6AR,7S,8S,9bS)-6-(Acetyloxy)-2,3,3a,4,5,6,6a,7,8,9b-decahydro-3,3a-dihydroxy-3,6,9-trimethyl-8-[[(2Z)-2-methyl-1-oxo-2-butenyl]oxy]-2-oxo-4-(1-oxobutoxy)azuleno[4,5-b]furan-7-yl octanoate
Purity: ≥97% (HPLC)
Potent inhibitor of SERCA ATPase

Glutathione (GSH) precursor; maintains stem cell function in culture.

Chemical Name: (2R)-2-Acetamido-3-sulfanylpropanoic acid
Purity: ≥98% (HPLC)
Adult Stem Cell-derived Lung Organoids
(5)

Selective inhibitor of Akt/PKB signaling. Antitumor and antiviral

Alternate Names: Triciribine,NSC 154020,TCN
Chemical Name: 1,5-Dihydro-5-methyl-1-β-D-ribofuranosyl-1,4,5,6,8-pentaazaacenaphthylen-3-amine
Purity: ≥98% (HPLC)
Selective inhibitor of Akt/PKB signaling. Antitumor and antiviral

Selective CCR5 antagonist

Alternate Names: UK-427857
Chemical Name: 4,4-Difluoro-N-{(1S)-3-[3-(3-isopropyl- 5-methyl-4H-1,2,4-triazol-4-yl)- 8-azabicyclo[3.2.1]oct-8-yl]-1- phenylpropyl}cyclohexanecarboxamide
Purity: ≥98% (HPLC)
Selective CCR5 antagonist

Prodrug of antiviral nucleoside analog; inhibits SARS-CoV, SARS-CoV-2 and MERS-CoV infection

Chemical Name: β-D-N4-hydroxycytidine-5'-isopropyl ester
Purity: ≥98% (HPLC)
Prodrug of antiviral nucleoside analog; inhibits SARS-CoV, SARS-CoV-2 and MERS-CoV infection

Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide prodrug

Alternate Names: GS-5734
Chemical Name: 2-Ethylbutyl (2S)-2-[[(S)-[[(2R,3S,4R,5R)-5-(4-aminopyrrolo(2,1-f)(1,2,4)triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl]methoxy]phenoxyphosphoryl]amino]propanoate
Purity: ≥98% (HPLC)
Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide prodrug

Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide

Chemical Name: (2R,3R,4S,5R)-2-(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-carbonitrile
Purity: ≥98% (HPLC)
Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide

Non-selective PI 3-kinase inhibitor

Chemical Name: 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Purity: ≥98% (HPLC)
Non-selective PI 3-kinase inhibitor

Antimicrobial peptide derivative of human cathelicidin

Purity: ≥95% (HPLC)
Antimicrobial peptide derivative of human cathelicidin

Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral

Alternate Names: BCX 4430
Chemical Name: (2S,3S,4R,5R)-2-(4-Amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-5-(hydroxymethyl)-3,4-pyrrolidinediol dihydrochloride
Purity: ≥98% (HPLC)
Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral

Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleoside

Chemical Name: N-Hydroxycytidine
Purity: ≥98% (HPLC)
Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleoside

Inhibits replication of SARS-CoV-2 in vitro; broad spectrum antiviral

Chemical Name: Ethyl 6-Bromo-4-((dimethylamino)methyl)-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-indole-3-carboxylate hydrochloride
Purity: ≥98% (HPLC)
Inhibits replication of SARS-CoV-2 in vitro; broad spectrum antiviral

α-glucosidase I and II inhibitor; also inhibits ceramide-specific glycosyltransferases and exhibits broad spectrum antiviral activity

Alternate Names: N-Butyldeoxynojirimycin hydrochloride,NB-DNJ
Chemical Name: (2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-3,4,5-piperidinetriol hydrochloride
α-glucosidase I and II inhibitor; also inhibits ceramide-specific glycosyltransferases and exhibits broad spectrum antiviral activity

Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable

Alternate Names: AZD 0530
Chemical Name: N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methyl-1-piperazinyl)ethoxy]-5-[(tetrahydro-2H-pyran-4-yl)oxy]-4-quinazolinamine
Purity: ≥98% (HPLC)
Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable

Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone

Chemical Name: Cholest-5-ene-3β,25-diol
Purity: ≥95% (HPLC)
Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone

Potent and selective herpes simplex virus (HSV) helicase primase inhibitor

Chemical Name: N-[5-(Aminosulfonyl)-4-methyl-2-thiazolyl]-N-methyl-4-(2-pyridinyl)benzeneacetamide
Purity: ≥98% (HPLC)
Potent and selective herpes simplex virus (HSV) helicase primase inhibitor

Influenza virus neuraminidase inhibitor; antiviral prodrug

Alternate Names: GS 4104
Chemical Name: Ethyl (3R,4R,5S)-4-Acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate phosphate
Purity: ≥98% (HPLC)
Influenza virus neuraminidase inhibitor; antiviral prodrug

Blocks eIF4E activity; antiviral guanosine analog

Chemical Name: 1-β-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboxamide
Purity: ≥98% (HPLC)
Blocks eIF4E activity; antiviral guanosine analog

MRP and OAT3 inhibitor

Chemical Name: 4-(Dipropylsulfamoyl)benzoic acid
Purity: ≥98% (HPLC)
MRP and OAT3 inhibitor

Core binding factor inhibitor; attenuates hematopoiesis

Alternate Names: CBF&#946-Runx1 inhibitor II
Chemical Name: 7-Chloro-1,3-dihydro-5-(1H-pyrrol-2-yl)-2H-1,4-benzodiazepin-2-one
Purity: ≥98% (HPLC)
Core binding factor inhibitor; attenuates hematopoiesis

Pyruvate flavodoxin/ferredoxin oxidoreductase inhibitor; also inhibits Wnt signaling; broad spectrum anti-infective

Chemical Name: 2-(Acetyloxy)-N-(5-nitro-2-thiazolyl)benzamide
Purity: ≥98% (HPLC)
Pyruvate flavodoxin/ferredoxin oxidoreductase inhibitor; also inhibits Wnt signaling; broad spectrum anti-infective

DNA polymerase α, δ and ε inhibitor

Chemical Name: (3R,4R,4aR,6aS,8R,9R,11aS,11bS)-Tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-8,11a-methano-11aH-cyclohepta[a]naphthalene-4,9-dimethanol
Purity: ≥98% (HPLC)
DNA polymerase α, δ and ε inhibitor

mSTING agonist; induces antitumor immunological responses

Chemical Name: 5,6-Dimethyl-9-oxo-9H-xanthene-4-acetic acid
Purity: ≥98% (HPLC)
mSTING agonist; induces antitumor immunological responses

Non-selective P2 antagonist

Chemical Name: 8,8'-[Carbonylbis[imino-3,1-phenylenecarbonylimino(4-methyl-3,1-phenylene)carbonylimino]]bis-1,3,5-naphthalenetrisulfonic acid hexasodium salt
Purity: ≥98% (HPLC)
Non-selective P2 antagonist

Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter

Alternate Names: Kempferol
Chemical Name: 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Purity: ≥98% (HPLC)
Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter
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