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Design, Synthesis, and Evaluation of Nonpeptidic Inhibitors of Human Rhinovirus 3C Protease
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Beiträge zur Kenntnis des Einflusses von Alkyl‐ und Alkylenmerkaptogruppen auf die therapeutische Wirkung organischer Verbindungen. I. Über Methylmerkaptoatophane
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Untersuchungen über Isatin und verwandte Verbindungen, V.: Über Nitro‐isatine
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Untersuchungen über Isatin und verwandte Verbindungen, VI: Über 5‐Jod‐isatin und 5.5′‐Dijod‐indigo
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Synthesis and Activity of Piperazine-containing Antirhinoviral Agents and Crystal Structure of SDZ 880-061 Bound to Human Rhinovirus 14
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Poliovirus‐encoded proteinase 3C: a possible evolutionary link between cellular serine and cysteine proteinase families
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A collaborative report: Rhinoviruses—Extension of the numbering system from 89 to 100
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Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyprotein
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Spiro indolinone beta-lactams, inhibitors of poliovirus and rhinovlrus 3C-proteinases
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Peptide Aldehyde Inhibitors of Hepatitis A Virus 3C Proteinase
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Bioactive marine metabolites. 33. Cyclotheonamides, potent thrombin inhibitors, from a marine sponge Theonella sp
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Chelatoselective fluorescence perturbation in anthrylazamacrocycle conjugate probes. Electrophilic aromatic cadmiation
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Stereospecific Synthesis of Peptidyl .alpha.-Keto Amides as Inhibitors of Calpain
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Synthesis of functionalized styrenes via palladium-catalyzed coupling of aryl bromides with vinyl tin reagents
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Picornaviral 3C cysteine proteinases have a fold similar to chymotrypsin-like serine proteinases
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Membrane targeting of the small GTPase Rab9 is accompanied by nucleotide exchange
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Molecular cloning and complete sequence determination of RNA genome of human rhinovirus type 14.
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Viral cysteine proteases are homologous to the trypsin-like family of serine proteases: structural and functional implications.
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Reactions of Isatin Dimethyl Ketal and Its Ethyl Imino Ether with Methyllithium
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New Soluble-Formazan Assay for HIV-1 Cytopathic Effects: Application to High-Flux Screening of Synthetic and Natural Products for AIDS-Antiviral Activity
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The complete nucleotide sequence of a common cold virus: human rhinovlrus 14
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Hydrolysis of a Series of Synthetic Peptide Substrates by the Human Rhinovirus 14 3C Proteinase, Cloned and Expressed in Escherichia coli
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Diaminomethane dihydrochloride, a novel reagent for the synthesis of primary amides of amino acids and peptides from active esters
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Role of maturation cleavage in infectivity of picornaviruses: activation of an infectosome
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Spectroscopic Studies on the Interaction of Isatin with Calf Thymus DNA
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N-Benzylindole-2,3-dione (N-benzylisatin)
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Fragment-based screening targeting an open form of the SARS-CoV-2 main protease binding pocket
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Toward development of generic inhibitors against the 3C proteases of picornaviruses
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In Vitro Antiviral Activity of AG7088, a Potent Inhibitor of Human Rhinovirus 3C Protease
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Inhibition of Human Rhinovirus-Induced Cytokine Production by AG7088, a Human Rhinovirus 3C Protease Inhibitor
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Bayesian Parameter Estimates of Nelfinavir and Its Active Metabolite, Hydroxy-tert-Butylamide, in Infants Perinatally Infected with Human Immunodeficiency Virus Type 1
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In Vitro Antiviral Activity and Single-Dose Pharmacokinetics in Humans of a Novel, Orally Bioavailable Inhibitor of Human Rhinovirus 3C Protease
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Protease Inhibitors as Antiviral Agents
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Pharmacophore Modeling and Docking Studies on Some Nonpeptide-Based Caspase-3 Inhibitors
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Imobilização de complexos oxindolimínicos de cobre e zinco em argilas beidelitas
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Peptidyl Diazomethyl Ketones Inhibit the Human Rhinovirus 3C Protease: Effect on Virus Yield by Partial Block of P3 Polyprotein Processing
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Simple isatin derivatives as free radical scavengers: Synthesis, biological evaluation and structure-activity relationship
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QSAR and molecular docking studies of isatin and indole derivatives as SARS 3CLpro inhibitors
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Synthesis and Anticancer Activity Evaluation of Azepinobisindoles; the Isomeric Iheyamine A Derivatives
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Advances in enzymatic activity regulation mechanism and inhibitor discovery of coronavirus 3C-like protease
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Utilization and simulation of innovative new binuclear Co(ii), Ni(ii), Cu(ii), and Zn(ii) diimine Schiff base complexes in sterilization and coronavirus resistance (Covid-19)
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Picornaviral 3C protease inhibitors and the dual 3C protease/coronaviral 3C-like protease inhibitors
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Recent advances in the development of human rhinovirus 3C protease inhibitors
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Pharmacophores and biological activities of severe acute respiratory syndrome viral protease inhibitors
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Human rhinovirus 3C protease inhibitors: recent developments
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Targeting Cysteine Proteases from Plasmodium falciparum: A General Overview, Rational Drug Design and Computational Approaches for Drug Discovery
inferred← citeshttps://doi.org/10.2174/1568026620666201207095117openalex-snapshot
An Updated Review on SARS-CoV-2 Main Proteinase (MPro): Protein Structure and Small-Molecule Inhibitors
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Advancements in Schiff Bases of 1H-Indole-2,3dione: A Versatile Heterocyclic Compound in Pharmacological Field
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An Insight into COVID-19 and Traditional Herbs: Bangladesh Perspective
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Design and synthesis of inhibitors of foot-and-mouth disease virus 3C protease
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Synthesis, characterization and biocidal activity of some transition metal(II) complexes with isatin salicylaldehyde acyldihydrazones
inferred← citeshttps://doi.org/10.3390/chemistry7020043openalex-snapshot
Molecular Iodine-Catalyzed Synthesis of 3,3-Disubstituted Isatins: Total Synthesis of Indole Alkaloid, 3,3-Dimethoxy-2-oxindole
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Discovery of Novel Druggable Sites on Zika Virus NS3 Helicase Using X-ray Crystallography-Based Fragment Screening
inferred← citeshttps://doi.org/10.3390/ijms25158105openalex-snapshot
Breaking the Chain: Protease Inhibitors as Game Changers in Respiratory Viruses Management
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Design, Synthesis of New 1,2,4-Triazole/1,3,4-Thiadiazole with Spiroindoline, Imidazo[4,5-b]quinoxaline and Thieno[2,3-d]pyrimidine from Isatin Derivatives as Anticancer Agents
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Recent Advancement in Synthesis of Isatin as Anticonvulsant Agents: A Review
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2, 3-Dioxoindoline Derivatives: Synthesis, Reactions and Exploring Pharmacological Activities
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Additional file 1 of QSAR and molecular docking studies of isatin and indole derivatives as SARS 3CLpro inhibitors
inferred← citeshttps://doi.org/10.70675/f693911fze603z4b8eza459ze0b2aed3432aopenalex-snapshot
Pharmacochimie radicalaire à visée antirhinovirale
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Synthesis, Characterization and Antimicrobial Activity of 5-Substituted indole-2,3-dione Based 4 -Thiazolidione Derivatives
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