73 results for "Antiviral Compounds" in Products

Antiviral Compounds

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%
Potent inhibitor of SERCA ATPase
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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%
Selective CCR5 antagonist
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Non-selective PI 3-kinase inhibitor

Chemical Name: 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Purity: ≥98%
Non-selective PI 3-kinase inhibitor
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Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone

Chemical Name: Cholest-5-ene-3β,25-diol
Purity: ≥95%
Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone
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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%
Selective inhibitor of Akt/PKB signaling. Antitumor and antiviral
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Toll-like receptor 7 (TLR7) agonist

Alternate Names: R 848
Chemical Name: 1-[4-Amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol
Purity: ≥98%
Toll-like receptor 7 (TLR7) agonist
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Potent and selective VPAC2 agonist

Purity: ≥95%
Potent and selective VPAC2 agonist
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MRP and OAT3 inhibitor

Chemical Name: 4-(Dipropylsulfamoyl)benzoic acid
Purity: ≥98%
MRP and OAT3 inhibitor
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Specific inhibitor of NF-κB activation

Alternate Names: CAPE
Chemical Name: 3-(3,4-Dihydroxyphenyl)-2-propenoic acid 2-phenylethyl ester
Purity: ≥98%
Specific inhibitor of NF-κB activation
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Antimicrobial peptide derivative of human cathelicidin

Purity: ≥95%
Antimicrobial peptide derivative of human cathelicidin
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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%
Non-selective P2 antagonist
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Selective PC-PLC inhibitor

Chemical Name: O-(Octahydro-4,7-methano-1H-inden-5-yl) carbonopotassium dithioate
Purity: ≥98%
Selective PC-PLC inhibitor
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Toll-like receptor 7 (TLR7) agonist

Alternate Names: R 837
Chemical Name: 1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine
Purity: ≥98%
Toll-like receptor 7 (TLR7) agonist
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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%
Core binding factor inhibitor; attenuates hematopoiesis
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mSTING agonist; induces antitumor immunological responses

Chemical Name: 5,6-Dimethyl-9-oxo-9H-xanthene-4-acetic acid
Purity: ≥98%
mSTING agonist; induces antitumor immunological responses
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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%
Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide prodrug
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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
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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%
Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter
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Reverse transcriptase inhibitor

Alternate Names: PMPA,(R)-9-(2-Phosphonoylmethoxypropyl)adenine
Chemical Name: (R)-[[2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]phosphonic acid
Purity: ≥98%
Reverse transcriptase inhibitor
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Potent Aurora kinase B inhibitor

Chemical Name: N-[2,3-Dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]-ethanesulfonamide hydrochloride
Purity: ≥98%
Potent Aurora kinase B inhibitor
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Potent CXCR4 antagonist

Chemical Name: N,N'-Dicyclohexylcarbamimidothioic acid (5,6-dihydro-6,6-dimethylimidazo[2,1-b]thiazol-3-yl)methyl ester dihydrochloride
Purity: ≥98%
Potent CXCR4 antagonist
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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%
DNA polymerase α, δ and ε inhibitor
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HIV-1 and HIV-2 protease inhibitor

Alternate Names: ABT-538,A-84538,Abbot 84538
Chemical Name: 5-Thiazolylmethyl (3S,4S,6S,9S)-4-hydroxy-12-methyl-9-(1-methylethyl)-13-[2-(1-methylethyl)-4-thiazolyl]-8,11-dioxo-3,6-bis(phenylmethyl)-2,7,10,12-tetraazatridecanoate
Purity: ≥98%
HIV-1 and HIV-2 protease inhibitor
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Potent and selective HIV-1 and HIV-2 protease inhibitor

Chemical Name: 2,3,5-Trideoxy-N-[(1S,2R)-2,3-dihydro-2-hydroxy-1H-inden-1-yl]-5-[(2S)-2-[[(1,1-dimethylethyl)amino]carbonyl]-4-(3-pyridinylmethyl)-1-piperazinyl]-2-(phenylmethyl)-D-erythro-pentonamide sulfate
Purity: ≥98%
Potent and selective HIV-1 and HIV-2 protease inhibitor
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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%
Influenza virus neuraminidase inhibitor; antiviral prodrug
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