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Strategies in the design of antiviral drugs

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.282.13.1240openalex-snapshot
Use of the Oral Neuraminidase Inhibitor Oseltamivir in Experimental Human Influenza
inferredcites →https://doi.org/10.1002/(sici)1098-1128(200003)20:2<129::aid-med2>3.0.co;2-aopenalex-snapshot
The HIV-1 Reverse Transcription (RT) Process as Target for RT Inhibitors
inferredcites →https://doi.org/10.1002/rmv.1980030205openalex-snapshot
Therapeutic potential of HPMPC as an antiviral drug
inferredcites →https://doi.org/10.1006/bbrc.1997.6552openalex-snapshot
Models Which Explain the Inhibition of Reverse Transcriptase by HIV-1-Specific (Thio)carboxanilide Derivatives1
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NS3 Serine Protease of Bovine Viral Diarrhea Virus: Characterization of Active Site Residues, NS4A Cofactor Domain, and Protease–Cofactor Interactions
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Viral Entry as the Primary Target for the Anti-HIV Activity of Chicoric Acid and Its Tetra-Acetyl Esters
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Cyclosaligenyl-2′,3′-didehydro-2′,3′-dideoxythymidine Monophosphate: Efficient Intracellular Delivery of d4TMP
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Characterization of the Activation Pathway of Phosphoramidate Triester Prodrugs of Stavudine and Zidovudine
inferredcites →https://doi.org/10.1016/s0026-895x(24)13282-8openalex-snapshot
Inhibition of Human Immunodeficiency Virus Type 1 Replication and Cytokine Production by Fluoroquinoline Derivatives
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Mutation of Asp171 and Asp262 of the Chemokine Receptor CXCR4 Impairs Its Coreceptor Function for Human Immunodeficiency Virus-1 Entry and Abrogates the Antagonistic Activity of AMD3100
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A Second Target for the Peptoid Tat/Transactivation Response Element Inhibitor CGP64222: Inhibition of Human Immunodeficiency Virus Replication by Blocking CXC-Chemokine Receptor 4-Mediated Virus Entry
inferredcites →https://doi.org/10.1016/s0026-895x(24)26490-7openalex-snapshot
Inhibition of HIV Infection by Bicyclams, Highly Potent and Specific CXCR4 Antagonists
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Mutational Analysis of Trp-229 of Human Immunodeficiency Virus Type 1 Reverse Transcriptase (RT) Identifies This Amino Acid Residue as a Prime Target for the Rational Design of New Non-Nucleoside RT Inhibitors
inferredcites →https://doi.org/10.1016/s0092-8674(00)80058-6openalex-snapshot
A Novel Role for 3-O-Sulfated Heparan Sulfate in Herpes Simplex Virus 1 Entry
inferredcites →https://doi.org/10.1016/s0092-8674(00)80066-5openalex-snapshot
Inhibiting HIV-1 Entry
inferredcites →https://doi.org/10.1016/s0092-8674(00)81275-1openalex-snapshot
Structure and Mechanism of Inosine Monophosphate Dehydrogenase in Complex with the Immunosuppressant Mycophenolic Acid
inferredcites →https://doi.org/10.1016/s0140-6736(00)02288-1openalex-snapshot
Efficacy and safety of oseltamivir in treatment of acute influenza: a randomised controlled trial
inferredcites →https://doi.org/10.1016/s0166-3542(00)00066-8openalex-snapshot
Treatment of lethal Ebola virus infection in mice with a single dose of an S-adenosyl-l-homocysteine hydrolase inhibitor
inferredcites →https://doi.org/10.1016/s0166-3542(00)00112-1openalex-snapshot
Retroviral integrase inhibitors year 2000: update and perspectives
inferredcites →https://doi.org/10.1016/s0166-3542(98)00025-4openalex-snapshot
The role of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection1Presented at the Eleventh International Conference on Antiviral Research, San Diego, CA, 5–10 April 1998.1
inferredcites →https://doi.org/10.1016/s0960-894x(00)00465-0openalex-snapshot
Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: towards smaller inhibitors
inferredcites →https://doi.org/10.1016/s0960-894x(00)00610-7openalex-snapshot
Arylalkylidene rhodanine with bulky and hydrophobic functional group as selective HCV NS3 protease inhibitor
inferredcites →https://doi.org/10.1016/s0960-894x(00)00654-5openalex-snapshot
The identification of α-ketoamides as potent inhibitors of hepatitis c virus nS3-4a proteinase
inferredcites →https://doi.org/10.1016/s0960-894x(02)00008-2openalex-snapshot
Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. Part 7: Structure–Activity Studies of Bicyclic 2-Pyridone-Containing Peptidomimetics
inferredcites →https://doi.org/10.1016/s0960-894x(99)00004-9openalex-snapshot
Inhibition of herpes proteases and antiviral activity of 2-substituted thieno[2,3-d]oxazinones
inferredcites →https://doi.org/10.1016/s0960-894x(99)00539-9openalex-snapshot
The inhibition of human cytomegalovirus (hCMV) protease by hydroxylamine derivatives
inferredcites →https://doi.org/10.1016/s0968-0896(99)00094-2openalex-snapshot
Synthesis and antiviral activity of monobactams inhibiting the human cytomegalovirus protease
inferredcites →https://doi.org/10.1016/s1386-6532(01)00167-6openalex-snapshot
Antiviral drugs: current state of the art
inferredcites →https://doi.org/10.1021/bi991992sopenalex-snapshot
Only a Small Fraction of Purified Hepatitis C RNA-Dependent RNA Polymerase Is Catalytically Competent: Implications for Viral Replication and in Vitro Assays
inferredcites →https://doi.org/10.1021/ja963036topenalex-snapshot
Influenza Neuraminidase Inhibitors Possessing a Novel Hydrophobic Interaction in the Enzyme Active Site: Design, Synthesis, and Structural Analysis of Carbocyclic Sialic Acid Analogues with Potent Anti-Influenza Activity
inferredcites →https://doi.org/10.1021/jm000078qopenalex-snapshot
Design and Synthesis of Pyrrolidine-5,5-trans-lactams (5-Oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as Novel Mechanism-Based Inhibitors of Human Cytomegalovirus Protease. 1. The α-Methyl-trans-lactam Template
inferredcites →https://doi.org/10.1021/jm000176bopenalex-snapshot
4-Aryl-2,4-dioxobutanoic Acid Inhibitors of HIV-1 Integrase and Viral Replication in Cells
inferredcites →https://doi.org/10.1021/jm000210mopenalex-snapshot
Highly Potent and Selective Inhibition of Varicella-Zoster Virus by Bicyclic Furopyrimidine Nucleosides Bearing an Aryl Side Chain
inferredcites →https://doi.org/10.1021/jm0003844openalex-snapshot
4-Hydroxy-5,6-dihydropyrones as Inhibitors of HIV Protease: The Effect of Heterocyclic Substituents at C-6 on Antiviral Potency and Pharmacokinetic Parameters
inferredcites →https://doi.org/10.1021/jm970664sopenalex-snapshot
cycloSal-2‘,3‘-dideoxy-2‘,3‘-didehydrothymidine Monophosphate (cycloSal-d4TMP): Synthesis and Antiviral Evaluation of a New d4TMP Delivery System
inferredcites →https://doi.org/10.1021/jm980068dopenalex-snapshot
Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 1. Michael Acceptor Structure−Activity Studies
inferredcites →https://doi.org/10.1021/jm9800696openalex-snapshot
Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 2. Peptide Structure−Activity Studies
inferredcites →https://doi.org/10.1021/jm9802158openalex-snapshot
Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIV Protease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class
inferredcites →https://doi.org/10.1021/jm980537bopenalex-snapshot
Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 3. Structure−Activity Studies of Ketomethylene-Containing Peptidomimetics
inferredcites →https://doi.org/10.1021/jm9805384openalex-snapshot
Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 4. Incorporation of P1 Lactam Moieties as l -Glutamine Replacements
inferredcites →https://doi.org/10.1021/jm9807104openalex-snapshot
Design and Synthesis of Lipophilic Phosphoramidate d4T-MP Prodrugs Expressing High Potency Against HIV in Cell Culture: Structural Determinants for in Vitro Activity and QSAR
inferredcites →https://doi.org/10.1021/jm990346oopenalex-snapshot
Potent and Selective Inhibition of Varicella-Zoster Virus (VZV) by Nucleoside Analogues with an Unusual Bicyclic Base
inferredcites →https://doi.org/10.1021/jm991171lopenalex-snapshot
The Cyclohexene Ring System as a Furanose Mimic: Synthesis and Antiviral Activity of Both Enantiomers of Cyclohexenylguanine
inferredcites →https://doi.org/10.1038/323464a0openalex-snapshot
A novel selective broad-spectrum anti-DNA virus agent
inferredcites →https://doi.org/10.1038/3293openalex-snapshot
Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry
inferredcites →https://doi.org/10.1038/363418a0openalex-snapshot
Rational design of potent sialidase-based inhibitors of influenza virus replication
inferredcites →https://doi.org/10.1038/82191openalex-snapshot
The broad-spectrum antiviral ribonucleoside ribavirin is an RNA virus mutagen
inferredcites →https://doi.org/10.1038/nm0897-866openalex-snapshot
Dengue virus infectivity depends on envelope protein binding to target cell heparan sulfate
inferredcites →https://doi.org/10.1053/jhep.2001.25636openalex-snapshot
A Randomized 4–Arm Multicenter Study of Interferon Alfa-2B Plus Ribavirin in the Treatment of Patients With Chronic Hepatitis C Not Responding to Interferon Alone
inferredcites →https://doi.org/10.1056/nejm199709253371302openalex-snapshot
Efficacy and Safety of the Neuraminidase Inhibitor Zanamivir in the Treatment of Influenzavirus Infections
inferredcites →https://doi.org/10.1073/pnas.090576697openalex-snapshot
A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5
inferredcites →https://doi.org/10.1073/pnas.111085598openalex-snapshot
RNA virus error catastrophe: Direct molecular test by using ribavirin
inferredcites →https://doi.org/10.1073/pnas.221375398openalex-snapshot
SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo
inferredcites →https://doi.org/10.1073/pnas.88.4.1499openalex-snapshot
Intracellular metabolism and mechanism of anti-retrovirus action of 9-(2-phosphonylmethoxyethyl)adenine, a potent anti-human immunodeficiency virus compound.
inferredcites →https://doi.org/10.1073/pnas.93.5.2186openalex-snapshot
Peptides from conserved regions of paramyxovirus fusion (F) proteins are potent inhibitors of viral fusion.
inferredcites →https://doi.org/10.1073/pnas.94.8.3548openalex-snapshot
An inhibitor of the Tat/TAR RNA interaction that effectively suppresses HIV-1 replication
inferredcites →https://doi.org/10.1073/pnas.96.10.5698openalex-snapshot
A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity
inferredcites →https://doi.org/10.1073/pnas.96.20.11000openalex-snapshot
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes
inferredcites →https://doi.org/10.1074/jbc.275.19.14316openalex-snapshot
Binding of the Second Generation Non-nucleoside Inhibitor S-1153 to HIV-1 Reverse Transcriptase Involves Extensive Main Chain Hydrogen Bonding
inferredcites →https://doi.org/10.1074/jbc.c000446200openalex-snapshot
Flavopiridol Inhibits P-TEFb and Blocks HIV-1 Replication
inferredcites →https://doi.org/10.1084/jem.186.8.1383openalex-snapshot
Inhibition of T-tropic HIV Strains by Selective Antagonization of the Chemokine Receptor CXCR4
inferredcites →https://doi.org/10.1086/315228openalex-snapshot
Poly(Sodium 4‐Styrene Sulfonate): An Effective Candidate Topical Antimicrobial for the Prevention of Sexually Transmitted Diseases
inferredcites →https://doi.org/10.1086/514292openalex-snapshot
A Mouse Model for Evaluation of Prophylaxis and Therapy of Ebola Hemorrhagic Fever
inferredcites →https://doi.org/10.1086/514316openalex-snapshot
Antiviral Drug Therapy of Filovirus Infections: S‐Adenosylhomocysteine Hydrolase Inhibitors Inhibit Ebola Virus In Vitro and in a Lethal Mouse Model
inferredcites →https://doi.org/10.1086/515386openalex-snapshot
A Mouse Model for Evaluation of Prophylaxis and Therapy of Ebola Hemorrhagic Fever
inferredcites →https://doi.org/10.1089/088922299309829openalex-snapshot
Resistance of the Human Immunodeficiency Virus to the Inhibitory Action of Negatively Charged Albumins on Virus Binding to CD4
inferredcites →https://doi.org/10.1089/aid.1995.11.191openalex-snapshot
A General Model for the Surface Glycoproteins of HIV and Other Retroviruses
inferredcites →https://doi.org/10.1097/00042560-199908150-00002openalex-snapshot
Abacavir and Mycophenolic Acid, an Inhibitor of Inosine Monophosphate Dehydrogenase, Have Profound and Synergistic Anti-HIV Activity
inferredcites →https://doi.org/10.1097/00126334-199908150-00002openalex-snapshot
Abacavir and Mycophenolic Acid, an Inhibitor of Inosine Monophosphate Dehydrogenase, Have Profound and Synergistic Anti-HIV Activity
inferredcites →https://doi.org/10.1099/0022-1317-81-5-1335openalex-snapshot
Enzymatic properties of hepatitis C virus NS3-associated helicase
inferredcites →https://doi.org/10.1124/mol.52.1.98openalex-snapshot
Development of Resistance of Human Immunodeficiency Virus Type 1 to Dextran Sulfate Associated with the Emergence of Specific Mutations in the Envelope gp120 Glycoprotein
inferredcites →https://doi.org/10.1124/mol.53.2.340openalex-snapshot
Human Immunodeficiency Virus Glycoprotein gp120 as the Primary Target for the Antiviral Action of AR177 (Zintevir)
inferredcites →https://doi.org/10.1126/science.1057453openalex-snapshot
Protein Design of an HIV-1 Entry Inhibitor
inferredcites →https://doi.org/10.1126/science.287.5453.646openalex-snapshot
Inhibitors of Strand Transfer That Prevent Integration and Inhibit HIV-1 Replication in Cells
inferredcites →https://doi.org/10.1128/aac.33.8.1291openalex-snapshot
Broad-spectrum antiviral activities of neplanocin A, 3-deazaneplanocin A, and their 5'-nor derivatives
inferredcites →https://doi.org/10.1128/aac.35.4.679openalex-snapshot
Antiviral activities of 5-ethynyl-1-beta-D-ribofuranosylimidazole-4- carboxamide and related compounds
inferredcites →https://doi.org/10.1128/aac.41.3.594openalex-snapshot
Effect of incorporation of cidofovir into DNA by human cytomegalovirus DNA polymerase on DNA elongation
inferredcites →https://doi.org/10.1128/aac.42.2.216openalex-snapshot
The Novel Immunosuppressive Agent Mycophenolate Mofetil Markedly Potentiates the Antiherpesvirus Activities of Acyclovir, Ganciclovir, and Penciclovir In Vitro and In Vivo
inferredcites →https://doi.org/10.1128/aac.42.3.487openalex-snapshot
Inhibition of Acute-, Latent-, and Chronic-Phase Human Immunodeficiency Virus Type 1 (HIV-1) Replication by a Bistriazoloacridone Analog That Selectively Inhibits HIV-1 Transcription
inferredcites →https://doi.org/10.1128/aac.42.3.640openalex-snapshot
Oral Administration of a Prodrug of the Influenza Virus Neuraminidase Inhibitor GS 4071 Protects Mice and Ferrets against Influenza Infection
inferredcites →https://doi.org/10.1128/aac.42.7.1666openalex-snapshot
Antiherpesvirus Activities of (1′ S ,2′ R )-9-{[1′,2′-Bis(hydroxymethyl)cycloprop-1′-yl]methyl}guanine (A-5021) in Cell Culture
inferredcites →https://doi.org/10.1128/aac.42.8.2095openalex-snapshot
Mode of Action of (1′ S ,2′ R )-9-{[1′,2′-Bis(hydroxymethyl) cycloprop-1′-yl]methyl}guanine (A-5021) against Herpes Simplex Virus Type 1 and Type 2 and Varicella-Zoster Virus
inferredcites →https://doi.org/10.1128/aac.43.10.2444openalex-snapshot
In Vitro Antiviral Activity of AG7088, a Potent Inhibitor of Human Rhinovirus 3C Protease
inferredcites →https://doi.org/10.1128/aac.44.1.78-87.2000openalex-snapshot
Zanamivir Susceptibility Monitoring and Characterization of Influenza Virus Clinical Isolates Obtained during Phase II Clinical Efficacy Studies
inferredcites →https://doi.org/10.1128/aac.44.4.859-866.2000openalex-snapshot
Broad-Spectrum Antiviral Activity of the IMP Dehydrogenase Inhibitor VX-497: a Comparison with Ribavirin and Demonstration of Antiviral Additivity with Alpha Interferon
inferredcites →https://doi.org/10.1128/aac.45.3.743-748.2001openalex-snapshot
Cyclopentane Neuraminidase Inhibitors with Potent In Vitro Anti-Influenza Virus Activities
inferredcites →https://doi.org/10.1128/aac.45.3.749-757.2001openalex-snapshot
In Vivo Influenza Virus-Inhibitory Effects of the Cyclopentane Neuraminidase Inhibitor RWJ-270201
inferredcites →https://doi.org/10.1128/aac.45.4.1162-1167.2001openalex-snapshot
Comparison of the Anti-Influenza Virus Activity of RWJ-270201 with Those of Oseltamivir and Zanamivir
inferredcites →https://doi.org/10.1128/cmr.11.4.614openalex-snapshot
Protease Inhibitors as Antiviral Agents
inferredcites →https://doi.org/10.1128/cmr.14.2.382-397.2001openalex-snapshot
Vaccinia Virus Inhibitors as a Paradigm for the Chemotherapy of Poxvirus Infections
inferredcites →https://doi.org/10.1128/jvi.75.9.4117-4128.2001openalex-snapshot
Herpes Simplex Virus Type 1 Entry Is Inhibited by the Cobalt Chelate Complex CTC-96
inferredcites →https://doi.org/10.1146/annurev.pa.36.040196.002553openalex-snapshot
Structural Mechanisms of HIV Drug Resistance
inferredcites →https://doi.org/10.1177/095632020001100101openalex-snapshot
The Herpesvirus Proteases as Targets for Antiviral Chemotherapy
inferredcites →https://doi.org/10.1177/095632020001100201openalex-snapshot
Novel Approaches to the Treatment of Hepatitis C Virus Infection
inferredcites →https://doi.org/10.1177/095632029700800601openalex-snapshot
HIV-1 Integrase as a Target for Antiviral Drugs
inferredcites →https://doi.org/10.1177/095632029901000101openalex-snapshot
Human Immunodeficiency Virus Gene Regulation as a Target for Antiviral Chemotherapy
inferredcites →https://doi.org/10.1248/bpb.24.236openalex-snapshot
Selective Nonpeptidic Inhibitors of Herpes Simplex Virus Type 1 and Human Cytomegalovirus Proteases.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/cssc.200900221openalex-snapshot
Suzuki–Miyaura Cross‐Coupling Reactions in Aqueous Media: Green and Sustainable Syntheses of Biaryls
inferred← citeshttps://doi.org/10.1002/ejoc.200500532openalex-snapshot
Synthesis and Properties of Fluorescent cycloSal Nucleotides Based on the Pyrimidine Nucleoside m5K and Its 2′,3′‐Dideoxy Analog dm5K
inferred← citeshttps://doi.org/10.1002/ejoc.200500671openalex-snapshot
cycloSal Phosphates as Chemical Trojan Horses for Intracellular Nucleotide and Glycosylmonophosphate Delivery — Chemistry Meets Biology
inferred← citeshttps://doi.org/10.1002/ejoc.201001473openalex-snapshot
Synthesis of 2′,3′‐Modified Carbocyclic L ‐Nucleoside Analogues
inferred← citeshttps://doi.org/10.1002/ejoc.201100334openalex-snapshot
Linear Synthesis of Chiral cycloSal‐Pronucleotides
inferred← citeshttps://doi.org/10.1002/ejoc.201301097openalex-snapshot
Synthesis, Antiviral Evaluation, and Computational Studies of Cyclobutane and Cyclobutene L ‐Nucleoside Analogues
inferred← citeshttps://doi.org/10.1002/ejoc.201402106openalex-snapshot
Synthesis and Biological Activity of Triazole‐Appended N,O‐Nucleosides
inferred← citeshttps://doi.org/10.1002/ejoc.201403648openalex-snapshot
Synthesis of C6‐Pyridylpurine Nucleosides by Reaction of Nebularine N1‐Oxide with Pyridinyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/hlca.200490079openalex-snapshot
Design, Synthesis, and Characterization of Photolabeling Probes for the Study of the Mechanisms of the Antiviral Effects of Ribavirin
inferred← citeshttps://doi.org/10.1002/hlca.200490201openalex-snapshot
7‐Iodo‐5‐aza‐7‐deazaguanine: Syntheses of Anomeric D ‐ and L ‐Configured 2‐Deoxyribonucleosides
inferred← citeshttps://doi.org/10.1002/hlca.201100366openalex-snapshot
Synthesis and Anti‐HIV Activity of Triazolo‐Fused 3′,5′‐Cyclic Nucleoside Analogues Derived from an Intramolecular Huisgen 1,3‐Dipolar Cycloaddition
inferred← citeshttps://doi.org/10.1002/hlca.201200285openalex-snapshot
Synthesis and Anti‐HIV Activity of Triazolo‐Fused 2′,3′‐Cyclic Nucleoside Analogs Prepared by an Intramolecular Huisgen 1,3‐Dipolar Cycloaddition
inferred← citeshttps://doi.org/10.1002/hlca.201500149openalex-snapshot
Copper/Graphene/Clay Nanohybrid: A Highly Efficient Heterogeneous Nanocatalyst for the Synthesis of Novel 1,2,3‐Triazolyl Carboacyclic Nucleosides via ‘Click’ Huisgen 1,3‐Dipolar Cycloaddition
inferred← citeshttps://doi.org/10.1002/jhet.5570410516openalex-snapshot
Synthesis and antiviral activity of new benzothiadiazine dioxide derivatives
inferred← citeshttps://doi.org/10.1002/jmv.28652openalex-snapshot
Repurposing of the antibiotic nitroxoline for the treatment of mpox
inferred← citeshttps://doi.org/10.1002/jobm.70057openalex-snapshot
A Comprehensive Review of Antimicrobial Drugs: Mechanisms of Action and Specific Targets in Microorganisms
inferred← citeshttps://doi.org/10.1002/mabi.201400298openalex-snapshot
Polymeric Anti‐HIV Therapeutics
inferred← citeshttps://doi.org/10.1002/med.10047openalex-snapshot
Protease inhibitors of the sulfonamide type: Anticancer, antiinflammatory, and antiviral agents
inferred← citeshttps://doi.org/10.1002/med.20021openalex-snapshot
Sulfamates and their therapeutic potential
inferred← citeshttps://doi.org/10.1002/med.20173openalex-snapshot
Yet another ten stories on antiviral drug discovery (part D): Paradigms, paradoxes, and paraductions
inferred← citeshttps://doi.org/10.1002/med.21340openalex-snapshot
Curious Discoveries in Antiviral Drug Development: The Role of Serendipity
inferred← citeshttps://doi.org/10.1002/med.21997openalex-snapshot
COVID‐19 cooling: Nanostrategies targeting cytokine storm for controlling severe and critical symptoms
inferred← citeshttps://doi.org/10.1002/minf.201300185openalex-snapshot
Interaction of Flaviviruses with Reproduction Inhibitors Binding in β‐OG Pocket: Insights from Molecular Dynamics Simulations
inferred← citeshttps://doi.org/10.1002/ppsc.202100044openalex-snapshot
From Bulk to Nanoparticles: An Overview of Antiviral Materials, Its Mechanisms, and Applications
inferred← citeshttps://doi.org/10.1002/prot.20392openalex-snapshot
Linking tumor cell cytotoxicity to mechanism of drug action: An integrated analysis of gene expression, small‐molecule screening and structural databases
inferred← citeshttps://doi.org/10.1002/ptr.1912openalex-snapshot
Antiviral activity and constituent of Ardisia chinensis benth against coxsackie B3 virus
inferred← citeshttps://doi.org/10.1002/ptr.1962openalex-snapshot
Antiviral triterpenoids from the medicinal plant Schefflera heptaphylla
inferred← citeshttps://doi.org/10.1002/qua.21192openalex-snapshot
Parameterization of AZT—A widely used nucleoside inhibitor of HIV‐1 reverse transcriptase
inferred← citeshttps://doi.org/10.1002/rmv.539openalex-snapshot
HIV integrase inhibitors as therapeutic agents in AIDS
inferred← citeshttps://doi.org/10.1002/slct.201701111openalex-snapshot
Microwave‐Assisted Synthesis of C ‐4′‐(1,5‐disubstituted)‐triazole ‐ spiro‐ α ‐L‐arabinofuranosyl Nucleosides
inferred← citeshttps://doi.org/10.1002/slct.202302295openalex-snapshot
Evaluating the Antiviral Potential of Phytocompounds from Mesua ferrea against SARS‐CoV‐2 Main Protease: Structure‐Based Virtual Screening and Molecular Dynamics Simulation Investigations
inferred← citeshttps://doi.org/10.1002/slct.202304774openalex-snapshot
Nucleoside‐Based Drug Target with General Antimicrobial Screening and Specific Computational Studies against SARS‐CoV‐2 Main Protease
inferred← citeshttps://doi.org/10.1002/smll.201501914openalex-snapshot
Plasmonic Nanohole Sensor for Capturing Single Virus‐Like Particles toward Virucidal Drug Evaluation
inferred← citeshttps://doi.org/10.1002/tcr.202200218openalex-snapshot
Exploring Nucleobase Modifications in Oligonucleotide Analogues for Use as Environmentally Responsive Fluorophores and Beyond
inferred← citeshttps://doi.org/10.1007/0-387-28146-0_14openalex-snapshot
Defining Drug Interactions with the Viral Membrane Protein Vpu from HIV-1
inferred← citeshttps://doi.org/10.1007/3-540-29456-2_5openalex-snapshot
Strukturproteomik mikrobieller Genome
inferred← citeshttps://doi.org/10.1007/3-7985-1560-3_5openalex-snapshot
NO-Donoren als Inhibitoren von viralen Proteasen — Ein mögliches therapeutisches Prinzip bei enteroviralen Herzerkrankungen
inferred← citeshttps://doi.org/10.1007/978-1-0716-4546-8_3openalex-snapshot
Deciphering Host Differential Gene Expression in Viral Infections Through Public RNA-Seq Data from NCBI GEO
inferred← citeshttps://doi.org/10.1007/978-1-4614-7291-9_8openalex-snapshot
Targeting Small Molecules and Peptides to the p66-p51 Reverse Transcriptase Interface
inferred← citeshttps://doi.org/10.1007/978-1-4939-8618-7_8openalex-snapshot
An Integrative Approach to Virus–Host Protein–Protein Interactions
inferred← citeshttps://doi.org/10.1007/978-1-59745-148-2_15openalex-snapshot
ThecycloSal-Nucleotide Delivery System
inferred← citeshttps://doi.org/10.1007/978-1-60761-931-4_9openalex-snapshot
Structure-Based Library Design in Efficient Discovery of Novel Inhibitors
inferred← citeshttps://doi.org/10.1007/978-1-61779-965-5_10openalex-snapshot
Advances in Nuclear Magnetic Resonance for Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-3-030-76320-6_12openalex-snapshot
Drug Resistance in Liver Diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-83350-3_29-1openalex-snapshot
Coumarins as Emerging Antiviral Compounds from Natural Origins: Ethnopharmacology, Chemistry, Mechanism of Action, Clinical, Preclinical Studies, and Future Perspectives
inferred← citeshttps://doi.org/10.1007/978-3-031-12199-9_29openalex-snapshot
Coumarins as Emerging Anti-Viral Compounds from Natural Origins: Ethnopharmacology, Chemistry, Mechanism of Action, Clinical and Preclinical Studies, and Future Perspectives
inferred← citeshttps://doi.org/10.1007/978-3-032-18894-6_1openalex-snapshot
Exploring Deep Learning for De Novo Drug Design: A Brief Review of Chemical Property Optimization
inferred← citeshttps://doi.org/10.1007/978-3-032-23507-7_5openalex-snapshot
Immunomodulatory and Antiviral Fungal Metabolites
inferred← citeshttps://doi.org/10.1007/978-3-319-47266-9_26openalex-snapshot
Hepatitis B Virus Drug Resistance
inferred← citeshttps://doi.org/10.1007/978-3-540-69182-2_12openalex-snapshot
Investigating Protein-Protein and Protein-Ligand Interactions by Molecular Dynamics Simulations
inferred← citeshttps://doi.org/10.1007/978-3-540-75546-3_8openalex-snapshot
The Impact of CVB3 Infection on Host Cell Biology
inferred← citeshttps://doi.org/10.1007/978-3-540-79086-0_3openalex-snapshot
Antiviral Agents Acting as DNA or RNA Chain Terminators
inferred← citeshttps://doi.org/10.1007/978-981-15-1761-7_14openalex-snapshot
Bioactive Phytocompounds to Fight Against Antimicrobial Resistance
inferred← citeshttps://doi.org/10.1007/978-981-16-1313-5_67-1openalex-snapshot
Flex-Nucleosides – A Strategic Approach to Antiviral Therapeutics
inferred← citeshttps://doi.org/10.1007/978-981-19-9776-1_67openalex-snapshot
Flex-Nucleosides: A Strategic Approach to Antiviral Therapeutics
inferred← citeshttps://doi.org/10.1007/bf02990895openalex-snapshot
Steered molecular dynamics simulations of protein-ligand interactions
inferred← citeshttps://doi.org/10.1007/s00044-013-0684-3openalex-snapshot
Synthesis of thiocarbohydrazide and carbohydrazide derivatives as possible biologically active agents
inferred← citeshttps://doi.org/10.1007/s00044-021-02700-1openalex-snapshot
Synthesis and biological evaluation of pyrrolidine-functionalized nucleoside analogs
inferred← citeshttps://doi.org/10.1007/s00106-010-2253-0openalex-snapshot
Wirksamkeit von Pflanzenprodukten gegen Herpesinfektionen
inferred← citeshttps://doi.org/10.1007/s00253-015-7242-5openalex-snapshot
Antiviral activity and specific modes of action of bacterial prodigiosin against Bombyx mori nucleopolyhedrovirus in vitro
inferred← citeshttps://doi.org/10.1007/s00262-004-0558-0openalex-snapshot
Analysis of the autoantibody repertoire in Burkitt?s lymphoma patients: frequent response against the transcription factor ATF-2
inferred← citeshttps://doi.org/10.1007/s00430-003-0198-6openalex-snapshot
Nitric oxide donors inhibit the coxsackievirus B3 proteinases 2A and 3C in vitro, virus production in cells, and signs of myocarditis in virus-infected mice
inferred← citeshttps://doi.org/10.1007/s00705-003-0213-7openalex-snapshot
AZT inhibits Visna/maedi virus -induced apoptosis
inferred← citeshttps://doi.org/10.1007/s00705-017-3511-1openalex-snapshot
HSP90: a promising broad-spectrum antiviral drug target
inferred← citeshttps://doi.org/10.1007/s00705-024-05979-8openalex-snapshot
Identification and characterization of a marine bacterium extract from Mameliella sp. M20D2D8 with antiviral effects against influenza A and B viruses
inferred← citeshttps://doi.org/10.1007/s00706-018-2234-7openalex-snapshot
Antiviral activities of 5-chlorobenzotriazole derivatives
inferred← citeshttps://doi.org/10.1007/s10534-025-00702-9openalex-snapshot
Exploring the antitumor effects of Pd(II) complexes with nitrogen donor ligands towards breast carcinoma
inferred← citeshttps://doi.org/10.1007/s10600-015-1479-1openalex-snapshot
Activity of Thermopsis schischkinii Alkaloids Against Influenza A(H1N1)pdm09 Virus
inferred← citeshttps://doi.org/10.1007/s10616-014-9740-1openalex-snapshot
Discovery of a new antiviral protein isolated Lonomia obliqua analysed by bioinformatics and real-time approaches
inferred← citeshttps://doi.org/10.1007/s10822-016-9901-8openalex-snapshot
Conformational flexibility of DENV NS2B/NS3pro: from the inhibitor effect to the serotype influence
inferred← citeshttps://doi.org/10.1007/s10904-022-02411-zopenalex-snapshot
New Antimicrobial Polymeric Microspheres Containing Azomethine
inferred← citeshttps://doi.org/10.1007/s11030-013-9448-8openalex-snapshot
Aldol-type compounds from water-soluble indole-3,4-diones: synthesis, kinetics, and antiviral properties
inferred← citeshttps://doi.org/10.1007/s11030-020-10118-xopenalex-snapshot
Structure-based screening of novel lichen compounds against SARS Coronavirus main protease (Mpro) as potentials inhibitors of COVID-19
inferred← citeshttps://doi.org/10.1007/s11094-019-02079-9openalex-snapshot
Specific Antiviral Activity of Pyrimidinedispirotripiperazinium Alone and in Combination with Acyclovir on a Herpes-Simplex-Virus Infection Model
inferred← citeshttps://doi.org/10.1007/s11101-025-10078-wopenalex-snapshot
A systematic review on the research status of quercetagetin: resources, biosynthesis, bioavailability, bioactive-delivery systems, health effects, marketed functional products and patents
inferred← citeshttps://doi.org/10.1007/s11171-005-0076-7openalex-snapshot
Synthesis and Antiviral Activity of New 5-Substituted 2′-Deoxyuridine Derivatives
inferred← citeshttps://doi.org/10.1007/s11172-008-0346-7openalex-snapshot
Synthesis of acyclic nucleosides based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones
inferred← citeshttps://doi.org/10.1007/s11172-010-0056-9openalex-snapshot
Synthesis and antiviral activity of nucleoside analogs based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones
inferred← citeshttps://doi.org/10.1007/s11224-011-9853-5openalex-snapshot
A curious conformational property of 2-amino-4-thiazolyl-methoxyimino polymers exhibiting activity against HIV-1 reverse transcriptase
inferred← citeshttps://doi.org/10.1007/s11274-016-2092-6openalex-snapshot
Studies on the production of shikimic acid using the aroK knockout strain of Bacillus megaterium
inferred← citeshttps://doi.org/10.1007/s13205-021-02644-8openalex-snapshot
Mechanistic insight into anti-COVID-19 drugs: recent trends and advancements
inferred← citeshttps://doi.org/10.1007/s13318-016-0390-xopenalex-snapshot
In Vitro Evaluation of Absorption Characteristics of Peramivir for Oral Delivery
inferred← citeshttps://doi.org/10.1007/s13659-020-00275-9openalex-snapshot
Hordatines as a Potential Inhibitor of COVID-19 Main Protease and RNA Polymerase: An In-Silico Approach
inferred← citeshttps://doi.org/10.1007/s13758-011-0018-2openalex-snapshot
Model Membrane Platforms for Biomedicine: Case Study on Antiviral Drug Development
inferred← citeshttps://doi.org/10.1007/s40242-013-2375-5openalex-snapshot
Synthesis and anti-HIV activity of Triazolo-fused 3′,4′-cyclic and 4′-spiro nucleoside analogues
inferred← citeshttps://doi.org/10.1007/s40265-017-0830-1openalex-snapshot
Middle East Respiratory Syndrome and Severe Acute Respiratory Syndrome: Current Therapeutic Options and Potential Targets for Novel Therapies
inferred← citeshttps://doi.org/10.1007/s40495-025-00390-6openalex-snapshot
Unravelling the Potential of Anticancer Drugs for SARS-CoV-2
inferred← citeshttps://doi.org/10.1007/s42979-024-03335-wopenalex-snapshot
In-silico screening of phytocomponents from Phlogacanthus thyrsiformis and Tinospora cordifolia for antiviral efficacy against duck enteritis virus
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00212-1openalex-snapshot
Deoxyribonucleic Acid Viruses: Antivirals for Herpesviruses and Hepatitis B Virus
inferred← citeshttps://doi.org/10.1016/b978-0-12-405880-4.00009-3openalex-snapshot
The Nucleoside Reverse Transcriptase Inhibitors, Nonnucleoside Reverse Transcriptase Inhibitors, and Protease Inhibitors in the Treatment of HIV Infections (AIDS)
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12406-0openalex-snapshot
Direct-Acting Antiviral Agents for the Treatment of Hepatitis C Virus Infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12407-2openalex-snapshot
New Antiretrovirals for HIV and Antivirals for HBV
inferred← citeshttps://doi.org/10.1016/b978-0-12-411492-0.00034-1openalex-snapshot
Antiviral Drugs
inferred← citeshttps://doi.org/10.1016/b978-0-12-813667-6.00014-0openalex-snapshot
Lipid-based colloidal carriers for topical application of antiviral drugs
inferred← citeshttps://doi.org/10.1016/b978-0-323-91245-7.00024-9openalex-snapshot
Management of plant diseases using endophytes as biocontrol agents: Present status and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-323-91814-5.00020-9openalex-snapshot
Anti-herpes virus agents
inferred← citeshttps://doi.org/10.1016/b978-0-323-99314-2.00010-3openalex-snapshot
Fungal endophytes’ secondary metabolism: Regulation, function and drug discovery
inferred← citeshttps://doi.org/10.1016/b978-0-443-06911-6.50052-9openalex-snapshot
Antiviral drugs
inferred← citeshttps://doi.org/10.1016/b978-0-443-15241-2.00008-9openalex-snapshot
Selecting target stages in the viral life cycle for antiviral vaccine design
inferred← citeshttps://doi.org/10.1016/b978-0-443-51186-8.00010-5openalex-snapshot
Antiviral drugs
inferred← citeshttps://doi.org/10.1016/b978-0-7020-3471-8.00051-2openalex-snapshot
Antiviral drugs
inferred← citeshttps://doi.org/10.1016/b978-0-7216-0693-4.50058-xopenalex-snapshot
Antiviral Agents
inferred← citeshttps://doi.org/10.1016/j.actatropica.2014.02.003openalex-snapshot
Molecular cloning and characterization of Brugia malayi thymidylate kinase
inferred← citeshttps://doi.org/10.1016/j.addr.2009.11.021openalex-snapshot
Surface modifications of nanocarriers for effective intracellular delivery of anti-HIV drugs
inferred← citeshttps://doi.org/10.1016/j.ajoms.2023.02.005openalex-snapshot
Herpes gladiatorum in sports: An appraisal for health care worker and team dentists
inferred← citeshttps://doi.org/10.1016/j.antiviral.2003.09.004openalex-snapshot
A novel approach to develop anti-HIV drugs: adapting non-nucleoside anticancer chemotherapeutics
inferred← citeshttps://doi.org/10.1016/j.antiviral.2004.05.004openalex-snapshot
Mycophenolic acid inhibits avian reovirus replication
inferred← citeshttps://doi.org/10.1016/j.antiviral.2005.02.006openalex-snapshot
Mesuol, a natural occurring 4-phenylcoumarin, inhibits HIV-1 replication by targeting the NF-κB pathway
inferred← citeshttps://doi.org/10.1016/j.antiviral.2005.05.001openalex-snapshot
Antiviral drug discovery and development: Where chemistry meets with biomedicine
inferred← citeshttps://doi.org/10.1016/j.antiviral.2005.06.004openalex-snapshot
Antiviral activity and mode of action of caffeoylquinic acids from Schefflera heptaphylla (L.) Frodin
inferred← citeshttps://doi.org/10.1016/j.antiviral.2006.04.011openalex-snapshot
Application of the cycloSal-prodrug approach for improving the biological potential of phosphorylated biomolecules
inferred← citeshttps://doi.org/10.1016/j.antiviral.2006.05.007openalex-snapshot
Aspects of successful drug discovery and development
inferred← citeshttps://doi.org/10.1016/j.antiviral.2008.12.010openalex-snapshot
Design, synthesis, molecular modeling, and anti-HIV-1 integrase activity of a series of photoactivatable diketo acid-containing inhibitors as affinity probes
inferred← citeshttps://doi.org/10.1016/j.antiviral.2011.07.005openalex-snapshot
4-[1-(4-Fluorobenzyl)-4-hydroxy-1H-indol-3-yl]-2-hydroxy-4-oxobut-2-enoic acid as a prototype to develop dual inhibitors of HIV-1 integration process
inferred← citeshttps://doi.org/10.1016/j.antiviral.2016.07.014openalex-snapshot
Artificial ribonucleases inactivate a wide range of viruses using their ribonuclease, membranolytic, and chaotropic-like activities
inferred← citeshttps://doi.org/10.1016/j.antiviral.2018.04.004openalex-snapshot
The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold
inferred← citeshttps://doi.org/10.1016/j.apsb.2015.09.001openalex-snapshot
An Odyssey in antiviral drug development—50 years at the Rega Institute: 1964–2014
inferred← citeshttps://doi.org/10.1016/j.apsb.2022.05.020openalex-snapshot
Carbohydrate-based drugs launched during 2000−2021
inferred← citeshttps://doi.org/10.1016/j.bbapap.2010.01.007openalex-snapshot
A mechanistic view of human mitochondrial DNA polymerase γ: Providing insight into drug toxicity and mitochondrial disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.08.251openalex-snapshot
HIV-1-infected macrophages induce astrogliosis by SDF-1α and matrix metalloproteinases
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.12.145openalex-snapshot
In vivo dynamics of enterovirus protease revealed by fluorescence resonance emission transfer (FRET) based on a novel FRET pair
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.05.049openalex-snapshot
Insights into the mechanism of drug resistance: X-ray structure analysis of G48V/C95F tethered HIV-1 protease dimer/saquinavir complex
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.11.043openalex-snapshot
Remdesivir: From Ebola to COVID-19
inferred← citeshttps://doi.org/10.1016/j.bcab.2021.102056openalex-snapshot
Evidence-based traditional Siddha formulations for prophylaxis and management of respiratory symptoms in COVID-19 pandemic-a review
inferred← citeshttps://doi.org/10.1016/j.bcp.2005.11.024openalex-snapshot
Anti-Tat and anti-HIV activities of trimers of n-alkylglycines
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.01.005openalex-snapshot
Thiopurine analogues inhibit papain-like protease of severe acute respiratory syndrome coronavirus
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.09.006openalex-snapshot
Denbinobin, a naturally occurring 1,4-phenanthrenequinone, inhibits HIV-1 replication through an NF-κB-dependent pathway
inferred← citeshttps://doi.org/10.1016/j.biocel.2004.02.027openalex-snapshot
Designing anti-AIDS drugs targeting the major mechanism of HIV-1 RT resistance to nucleoside analog drugs
inferred← citeshttps://doi.org/10.1016/j.bioorg.2010.08.001openalex-snapshot
Synthesis of 3-fluoro-6-S-(2-S-pyridyl) nucleosides as potential lead cytostatic agents
inferred← citeshttps://doi.org/10.1016/j.biortech.2012.05.100openalex-snapshot
Deletion of the aroK gene is essential for high shikimic acid accumulation through the shikimate pathway in E. coli
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.04.015openalex-snapshot
Synthesis of glycoporphyrin derivatives and their antiviral activity against herpes simplex virus types 1 and 2
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.01.040openalex-snapshot
Mining the NCI antiviral compounds for HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.09.007openalex-snapshot
Synthesis of neplanocin F analogues as potential antiviral agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.08.026openalex-snapshot
Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: Synthesis via the azide-alkyne ‘click’ reaction
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.088openalex-snapshot
Design and synthesis of novel dihydroquinoline-3-carboxylic acids as HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.06.061openalex-snapshot
Synthesis and evaluation of novel 3-(3,5-dimethylbenzyl)uracil analogs as potential anti-HIV-1 agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.11.012openalex-snapshot
Synthesis and biological evaluation of pyridinone analogues as novel potent HIV-1 NNRTIs
inferred← citeshttps://doi.org/10.1016/j.bmc.2024.117605openalex-snapshot
Medicinal chemistry perspectives on the development of piperazine-containing HIV-1 inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.12.095openalex-snapshot
A possible improvement for structure-based drug design illustrated by the discovery of a Tat HIV-1 inhibitor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.12.107openalex-snapshot
A new approach to the synthesis of optically active alkylated adenine derivatives
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.10.019openalex-snapshot
5′-Homoaristeromycin. Synthesis and antiviral activity against orthopox viruses
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.12.068openalex-snapshot
Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure–activity relationship studies
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.12.093openalex-snapshot
β-Diketo acids with purine nucleobase scaffolds: Novel, selective inhibitors of the strand transfer step of HIV integrase
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.02.023openalex-snapshot
Discovery of bitriazolyl compounds as novel antiviral candidates for combating the tobacco mosaic virus
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.08.056openalex-snapshot
Structure-based design of a novel thiazolone scaffold as HCV NS5B polymerase allosteric inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.09.095openalex-snapshot
Novel thiazolones as HCV NS5B polymerase allosteric inhibitors: Further designs, SAR, and X-ray complex structure
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.12.009openalex-snapshot
A novel diketo phosphonic acid that exhibits specific, strand-transfer inhibition of HIV integrase and anti-HIV activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.02.060openalex-snapshot
Identification of acridinyl hydrazides as potent aspartic protease inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.01.108openalex-snapshot
N-Alkyldeoxynojirimycin derivatives with novel terminal tertiary amide substitution for treatment of bovine viral diarrhea virus (BVDV), Dengue, and Tacaribe virus infections
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.08.009openalex-snapshot
Synthesis, conformational study and antiviral activity of l-like neplanocin derivatives
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127539openalex-snapshot
Synthesis and biological evaluation of 5′-C-methyl nucleotide prodrugs for treating HCV infections
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128518openalex-snapshot
4-Oxooctahydroquinoline-1(2H)-carboxamides as hepatitis B virus (HBV) capsid core protein assembly modulators
inferred← citeshttps://doi.org/10.1016/j.bsheal.2022.03.008openalex-snapshot
Constructive strategies for drug delivery systems in antivirus disease therapy by biosafety materials
inferred← citeshttps://doi.org/10.1016/j.carbpol.2018.11.093openalex-snapshot
Exopolysaccharides of lactic acid bacteria: Structure, bioactivity and associations: A review
inferred← citeshttps://doi.org/10.1016/j.carres.2006.11.015openalex-snapshot
Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations
inferred← citeshttps://doi.org/10.1016/j.carres.2019.03.012openalex-snapshot
Divalent oseltamivir analogues as potent influenza neuraminidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110738openalex-snapshot
In‐vitro antiviral screening of some thiopyranothiazoles
inferred← citeshttps://doi.org/10.1016/j.cclet.2013.11.029openalex-snapshot
An H-phosphonate strategy for the synthesis of 2′,3′-dideoxynucleoside triphosphates and homodinucleotides
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108254openalex-snapshot
Furin Inhibitors Block SARS-CoV-2 Spike Protein Cleavage to Suppress Virus Production and Cytopathic Effects
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.131047openalex-snapshot
Development and validation of sensitive methods for simultaneous determination of 9 antiviral drugs in different various environmental matrices by UPLC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.chroma.2005.05.099openalex-snapshot
Separation of 3′-azido-2′,3′-dideoxythymidine pronucleotide diastereoisomers in biological samples by CZE with cyclodextrin addition
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2025.108663openalex-snapshot
Structure-based drug design; Computational strategies in drug discovery; Antihypertensive agents; Antiviral drugs; Molecular docking; QSAR; Pharmacological insights
inferred← citeshttps://doi.org/10.1016/j.ddstr.2006.06.008openalex-snapshot
Beyond interferon and ribavirin: Antiviral therapies for hepatitis C virus
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