Identification of chemically diverse Chk1 inhibitors by receptor-based virtual screening.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Bioorganic & Medicinal Chemistry

• Publication date

  2006-07-15

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1016/J.BMC.2006.03.021PMID 16574416
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Synthesis and biological evaluation of 3-ethylidene-1,3-dihydro-indol-2-ones as novel checkpoint 1 inhibitors.

  2006cited by this paper
• A comprehensive listing of bioactivation pathways of organic functional groups.

  2005cited by this paper
• Structure-based design of novel Chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity.

  2005cited by this paper
• Comparative virtual and experimental high-throughput screening for glycogen synthase kinase-3beta inhibitors.

  2005cited by this paper
• 1-(5-Chloro-2-alkoxyphenyl)-3-(5-cyanopyrazin-2-yl)ureas [correction of cyanopyrazi] as potent and selective inhibitors of Chk1 kinase: synthesis, preliminary SAR, and biological activities.

  2005cited by this paper
• Identification of a buried pocket for potent and selective inhibition of Chk1: prediction and verification.

  2005cited by this paper
• Identification of compounds with nanomolar binding affinity for checkpoint kinase-1 using knowledge-based virtual screening.

  2004cited by this paper
• Filtering databases and chemical libraries

  2004cited by this paper
• Drug-like Annotation and Duplicate Analysis of a 23-Supplier Chemical Database Totalling 2.7 Million Compounds

  2004cited by this paper
• Docking and scoring in virtual screening for drug discovery: methods and applications

  2004cited by this paper
• Protein Kinase Inhibitors: Insights into Drug Design from Structure

  2004cited by this paper
• Virtual screening in structure-based drug discovery.

  2004cited by this paper
• G2 checkpoint abrogators as anticancer drugs.

  2004cited by this paper
• A structure-based strategy to identify new molecular scaffolds targeting the bacterial ribosomal A-site.

  2004cited by this paper
• Glide: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy.

  2004cited by this paper
• Novel technologies for virtual screening.

  2004cited by this paper
• Validation of an empirical RNA-ligand scoring function for fast flexible docking using RiboDock®

  2004cited by this paper
• Conformational analysis of drug-like molecules bound to proteins: an extensive study of ligand reorganization upon binding.

  2004cited by this paper
• Human Chk1 expression is dispensable for somatic cell death and critical for sustaining G2 DNA damage checkpoint.

  2003cited by this paper
• Chk1‐deficient tumour cells are viable but exhibit multiple checkpoint and survival defects

  2003cited by this paper
• Chemical substructures in drug discovery.

  2003cited by this paper
• The protein kinase C inhibitor Gö6976 is a potent inhibitor of DNA damage-induced S and G2 cell cycle checkpoints.

  2003cited by this paper
• Nonleadlikeness and leadlikeness in biochemical screening.

  2003cited by this paper
• Structural biology in drug design: selective protein kinase inhibitors.

  2002cited by this paper
• Structural basis for Chk1 inhibition by UCN-01.

  2002cited by this paper
• Kinase inhibitors and the case for CH…O hydrogen bonds in protein–ligand binding

  2002cited by this paper
• A unified view of the DNA-damage checkpoint.

  2002cited by this paper
• Latest developments in crystallography and structure-based design of protein kinase inhibitors as drug candidates.

  2002cited by this paper
• A new test set for validating predictions of protein–ligand interaction

  2002cited by this paper
• Virtual screening and fast automated docking methods.

  2002cited by this paper
• A novel indolocarbazole, ICP-1, abrogates DNA damage-induced cell cycle arrest and enhances cytotoxicity: similarities and differences to the cell cycle checkpoint abrogator UCN-01.

  2002cited by this paper
• Targeting serine/threonine protein kinase B/Akt and cell-cycle checkpoint kinases for treating cancer.

  2002cited by this paper
• Structural Basis for Chk1 Inhibition by UCN-01*

  2002cited by this paper
• Successful virtual screening for novel inhibitors of human carbonic anhydrase: strategy and experimental confirmation.

  2002cited by this paper
• Why do we need so many chemical similarity search methods?

  2002cited by this paper
• The cell cycle as a target for cancer therapy: basic and clinical findings with the small molecule inhibitors flavopiridol and UCN-01.

  2002cited by this paper
• Is There a Difference between Leads and Drugs? A Historical Perspective

  2001cited by this paper
• Molecular Complexity and Its Impact on the Probability of Finding Leads for Drug Discovery

  2001cited by this paper
• QSAR prediction of toxicity of nitrobenzenes.

  2001cited by this paper
• High-throughput docking for lead generation.

  2001cited by this paper
• Chemical inhibitors of protein kinases.

  2001cited by this paper
• Blocking Chk1 expression induces apoptosis and abrogates the G2 checkpoint mechanism.

  2001cited by this paper
• Phase I trial of 72-hour continuous infusion UCN-01 in patients with refractory neoplasms.

  2001cited by this paper
• Serine-345 is required for Rad3-dependent phosphorylation and function of checkpoint kinase Chk1 in fission yeast

  2001cited by this paper
• Flexible alignment of small molecules.

  2001cited by this paper
• Inhibition of the G2 DNA Damage Checkpoint and of Protein Kinases Chk1 and Chk2 by the Marine Sponge Alkaloid Debromohymenialdisine*

  2001cited by this paper
• The Protein Data Bank

  2000cited by this paper
• The 1.7 A crystal structure of human cell cycle checkpoint kinase Chk1: implications for Chk1 regulation.

  2000cited by this paper
• The radiosensitizing agent 7-hydroxystaurosporine (UCN-01) inhibits the DNA damage checkpoint kinase hChk1.

  2000cited by this paper
• The Chk1 Protein Kinase and the Cdc25C Regulatory Pathways Are Targets of the Anticancer Agent UCN-01*

  2000cited by this paper
• Chk1 and Cds1: linchpins of the DNA damage and replication checkpoint pathways.

  2000cited by this paper
• An indolocarbazole inhibitor of human checkpoint kinase (Chk1) abrogates cell cycle arrest caused by DNA damage.

  2000cited by this paper
• Determinants of ligand binding to cAMP-dependent protein kinase.

  1999cited by this paper
• The structure-based design of ATP-site directed protein kinase inhibitors.

  1999cited by this paper
• Prediction of Physicochemical Parameters by Atomic Contributions

  1999cited by this paper
• Evaluation of the FLEXX incremental construction algorithm for protein–ligand docking

  1999cited by this paper
• Chk1 complements the G2/M checkpoint defect and radiosensitivity of ataxia-telangiectasia cells

  1999cited by this paper
• Hydrogen Bonding, Hydrophobic Interactions, and Failure of the Rigid Receptor Hypothesis.

  1999cited by this paper
• All-atom empirical potential for molecular modeling and dynamics studies of proteins.

  1998cited by this paper
• High-throughput assay for G2 checkpoint inhibitors and identification of the structurally novel compound isogranulatimide.

  1998cited by this paper
• Development of filter functions for protein-ligand docking.

  1998cited by this paper
• Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25.

  1997cited by this paper
• Cdc25 mitotic inducer targeted by chk1 DNA damage checkpoint kinase.

  1997cited by this paper
• Predicting modes of toxic action from chemical structure: Acute toxicity in the fathead minnow (Pimephales promelas)

  1997cited by this paper
• Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94

  1996cited by this paper
• A genetic algorithm for flexible molecular overlay and pharmacophore elucidation

  1995cited by this paper
• Molecular recognition of receptor sites using a genetic algorithm with a description of desolvation.

  1995cited by this paper
• Structure-based discovery of inhibitors of thymidylate synthase.

  1993cited by this paper
• Structure-based design of nonpeptide inhibitors specific for the human immunodeficiency virus 1 protease.

  1990cited by this paper
• Electronic Reprint Biological Crystallography the Protein Data Bank Biological Crystallography the Protein Data Bank

  year unknowncited by this paper

• Ethylenediamine Diacetate (EDDA): A Highly Efficient Catalyst for the Synthesis of Dihydropyrano[2,3- c ]pyrazoles via a Four-component Reaction

  2026cites this paper
• Design, Synthesis, Molecular Modeling, and Evaluation of Larvicidal Efficacy of Novel Dihydropyrano[2,3- c ]Pyrazole Derivatives Against Culex pipiens L. larvae (Diptera: Culicidae)

  2026cites this paper
• Synthesis, Characterization, Antimicrobial Activity and Molecular Docking Studies of Novel Pyrano[2,3-c]Pyrazole Derivatives

  2025cites this paper
• Efficient Ag/La-ZnO core–shell catalyst for green synthesis of 4H-pyrano[2,3-c] pyrazoles

  2025cites this paper
• Extended insight into the catalytic activity of boron-doped graphitic carbon nitride for the synthesis of bis-pyrazolyl methanes and pyranopyrazoles

  2025cites this paper
• A green marriage: the union of theophylline's catalytic activity and healing potential

  2025cites this paper
• Efficient and Environmentally Benign One-Pot Multicomponent Synthesis of Pyranopyrazole Derivatives Using Theophylline as a Recyclable Catalyst

  2025cites this paper
• Base-promoted [4 + 2] cycloaddition of alkynyl 1,3-dithianes and chalcones to access highly substituted pyran derivatives.

  2025cites this paper
• Determination of Antimicrobial Effects of Dihydropyrano [2, 3-c] Pyrazole Derivatives Catalysed by MnFe₂O₄

  2025cites this paper
• Recent Advances in Catalytic Approaches for Pyrano[2,3‐c]Pyrazole Synthesis: Green and Sustainable Perspectives

  2025cites this paper
• Synthesis of Dihydropyrano[2,3-c]pyrazoles with Trifluoroethanol as a Reusable Promoting Medium: A Green Protocol

  2025cites this paper
• Simple Preparation of Dihydropyrano[2,3-c]pyrazoles in Aqueous Ethanol Promoted by Dibutylamine

  2025cites this paper
• Characterization of the Trimethylsilyl Derivatives of 6-Amino-3-methyl-1,4-diphenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile and Its Analogs by Electron Ionization Gas Chromatography/Mass Spectrometry.

  2025cites this paper
• Aqueous extract of Areca nut as a sustainable and highly efficient green catalyst for the synthesis of pyrazole and isoxazolone derivatives

  2025cites this paper
• Synthesis, Characterization, and Anticancer Effect of Novel Pyrazolopyranopyrimidines

  2024cites this paper
• Photoredox Catalyzed Multi Component Synthesis of Indolyl-4H-Chromenes via HAT

  2024cites this paper
• Novel pyrano[2,3-c]pyrazolopyrimidines as promising anticancer agents: Design, synthesis, and cell cycle arrest of HepG2 cells at S phase

  2024cites this paper
• Crystal structure of 6-amino-3-methyl-4-phenyl-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile

  2024cites this paper
• Molecular Investigations of Novel Pyrano[2,3-c]Pyrazole Congeners as Potential HCoV-229E Inhibitors: synthesis, Molecular Modeling, 3D QSAR, and ADMET Screening

  2024cites this paper
• 'Synthesis and biological (in vitro and in silico) screening of the 4-aryl-fused pyranopyrazole derivatives as enzyme (α-amylase, α-glucosidase, acetylcholinesterase & proteinase) inhibitors with as anti-oxidant and cytotoxicity activities

  2024cites this paper
• Copper Acetylacetonate–Immobilized Halloysite Nanotube: An Efficient Natural and Green Catalyst for the Synthesis of 4H‐Chromenes at Room Temperature

  2024cites this paper
• MnFe2O4 nanoparticle as a new and magnetically separable nanocatalyst for solvent-free synthesis of dihydropyrano [2,3-c]pyrazole derivatives

  2024cites this paper
• Visible Light Assisted Synthesis of Tetrahydrobenzo[b]pyrans Using 4CzIPN, a Carbazole-Based Photocatalyst

  2024cites this paper
• TCAA-promoted novel approach synthesis and in vitro anti-cancer activity evaluation of spiro[indolo[2,1-b]quinazoline-6,4′-pyrano[2,3-c]pyrazole]-5′-carboxamides

  2024cites this paper
• Eco-friendly and benign synthesis of 5-(aryl)alkyl substituted NH-tetrazoles via protonated MCM-41@Silyl-nPr-DABCO-H nanocatalyst and DFT study

  2024cites this paper
• Lewis acid type promoted MCM-41@SnPr-DABCO-H: a robust, metal-free and reusable nanocatalyst for clean in situ synthesis of CH-tetrazoles

  2024cites this paper
• H6P2W18O62·18H2O as a Recyclable Catalyst for Synthesis of Tetrahydrobenzo[b]pyrans

  2024cites this paper
• Organobase catalyzed synthesis of pyranopyrazoles with X-ray crystallography, docking and ADME studies

  2024cites this paper
• Ultrasound assisted multicomponent synthesis of 4H-furo[3,4-b]pyran derivatives by using Fe3O4 Schiff base-Ni(II) complex

  2024cites this paper
• 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-Me+ClO4−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway

  2024cites this paper
• Green Pathway for Solvent-free Synthesis of Tetrahydrobenzo[b]pyrans Promoted by Carboxymethyl Cellulose (CMC) as a Recyclable and Biodegradable Catalyst

  2024cites this paper
• Review on advancements of pyranopyrazole: synthetic routes and their medicinal applications

  2024cites this paper
• 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP) as a reusable promoting medium for the catalyst-free and green synthesis of dihydropyrano[2,3-c]pyrazole scaffolds

  2024cites this paper
• Synthesis of dihydropyrano[2,3-c]pyrazole scaffolds by methylene blue (MB+) as a photo-redox catalyst via a single-electron transfer (SET)/energy transfer (EnT) pathway

  2023cites this paper
• Melamine, a Recyclable Catalyst for the Synthesis of Dihydropyrano[2,3-c]pyrazoles in Aqueous Ethanol

  2023cites this paper
• Green multicomponent synthesis of pyrano[2,3-c]pyrazole derivatives: current insights and future directions

  2023cites this paper
• Anticancer Activity and Molecular Targets of Piper cernuum Substances in Oral Squamous Cell Carcinoma Models

  2023cites this paper
• A new role for concentrated solar radiation (CSR) as a renewable heat source for the catalyst-solvent free synthesis of tetrahydrobenzo[b]pyran scaffolds

  2023cites this paper
• Tandem Aqueous Extract of Onion Catalyzed Knoevenagel Condensation-Michel Addition-Cyclization: A Green Synthesis of 2-Amino- 3-Cyano-4H-Pyran derivatives and their Anti-oxidant and Molecular Docking studies

  2023cites this paper
• Carbazole-based photocatalyst (4CzIPN) as a novel donor-acceptor fluorophore-catalyzed visible-light-induced photosynthesis of dihydropyrano[2,3-c]pyrazole scaffolds via a proton-coupled electron transfer process

  2023cites this paper
• Synthesis of Tetrahydrobenzo[b]pyrans Promoted by Sodium Stearate as a Lewis Base-Surfactant Combined Catalyst in an Aqueous Micellar Medium

  2023cites this paper
• Synthesis, Antimicrobial Studies, and Molecular Docking Simulation of Novel Pyran, Pyrazole, and Pyranopyrazole Derivatives

  2023cites this paper
• Visible-light induced acridinium catalysed synthesis of biologically active dihydropyranopyrazoles scaffolds via HAT

  2023cites this paper
• Unraveling the access to the regioselective synthesis of highly functionalized pyranopyrazoles using an ionic liquid catalyst

  2023cites this paper
• Synthesis and characterization of Co-MOF@Ag2O nanocomposite and its application as a nano-organic catalyst for one-pot synthesis of pyrazolopyranopyrimidines

  2023cites this paper
• Acridine yellow G as a photo-induced electron transfer catalyzed radical metal-free synthesis of tetrahydrobenzo[b]pyran scaffolds in an aqueous media

  2023cites this paper
• SO3H‐Functionalized Carbon Materials: A Versatile and sustainable heterogeneous Catalyst for Diverse Organic Transformations

  2023cites this paper
• Targeted materials discovery using Bayesian algorithm execution

  2023cites this paper
• Assessment of catalytic and antibacterial activity of biocompatible agar supported ZnS/CuFe2O4 magnetic nanotubes

  2022cites this paper
• Ultrasound promoted synthesis of new azo fused dihydropyrano[2,3-c]pyrazole derivatives: In vitro antimicrobial, anticancer, DFT, in silico ADMET and Molecular docking studies.

  2022cites this paper
• Synthetic strategies of pyran derivatives by multicomponent reaction (MCR) approach

  2022cites this paper
• A phenylazophenylenediamine-based La-complex as a superb nanocatalyst for the synthesis of diverse pyrano[2,3-c]pyrazoles

  2022cites this paper
• Green Approach for Metal-free One-pot Synthesis of Tetrahydrobenzo[b]pyrans with Sodium Alginate as a Reusable Bifunctional Biopolymeric Catalyst

  2022cites this paper
• Novel ionic liquid dihydrogen 4,4′-trimethylenedipiperidine phosphate-catalyzed greener and efficient synthesis of dihydro pyrano [2,3-c] pyrazole

  2022cites this paper
• Pyrazole and pyrazoline derivatives as antimalarial agents: A key review.

  2022cites this paper
• Ionic Liquid [(EMIM)Ac] Catalyzed Green and Efficient Synthesis of Pyrano[2,3-c]Pyrazole Derivatives

  2022cites this paper
• A Guide to In Silico Drug Design

  2022cites this paper
• Hierarchical Virtual Screening Based on Rocaglamide Derivatives to Discover New Potential Anti-Skin Cancer Agents

  2022cites this paper
• Asymmetric Synthesis of Structurally Sophisticated Spirocyclic Pyrano[2,3-c]pyrazole Derivatives Bearing a Chiral Quaternary Carbon Center.

  2022cites this paper
• Facile synthesis and antimicrobial activity of pyrazol-4-yl- and 2H-chromene-based substituted anilines via Michael addition followed by aromatization

  2022cites this paper
• Synthesis, larvicidal efficiency and molecular docking studies of novel annulated pyrano[2,3-c]pyrazoles against Culex pipiens L. and Musca domestica L. larvae.

  2022cites this paper
• Multicomponent reactions through pristine and modified chitosans: current status and future prospects

  2022cites this paper
• Methylene Blue as a Photo-Redox Catalyst: The Development Synthesis of Tetrahydrobenzo[b]pyran Scaffolds via a Single-Electron Transfer/Energy Transfer

  2022cites this paper
• Synthesis of 1,4-dihydropyrano[2,3-c]pyrazole derivatives and exploring molecular and cytotoxic properties based on DFT and molecular docking studies

  2022cites this paper
• Synthesis, Structural Elucidation, Spectral Studies and Antimicrobial Activity of Pyrano-Pyrazole Derivatives

  2022cites this paper
• Recent advances in the synthesis of pyrazole scaffolds via nanoparticles: A review

  2022cites this paper
• Eco-friendly design of TiO2 nanoparticles supported on Fe3O4 coated carbon-based biochar substrate for the synthesis of pyrano-[2, 3-c]-pyrazole derivatives

  2022cites this paper
• Emerging Promise of Computational Techniques in Anti-Cancer Research: At a Glance

  2022cites this paper
• Synthesis of Dihydropyrano[2,3-c]pyrazoles Using Carboxymethyl Cellulose as a Recyclable Catalyst

  2022cites this paper
• Microwave-assisted synthesis of pyrano[2,3-c]-pyrazole derivatives and their anti-microbial, anti-malarial, anti-tubercular, and anti-cancer activities

  2022cites this paper
• AC-SO3H/[CholineCl][Urea]2 as a green catalytic system for the synthesis of pyrano[2,3-c]pyrazole scaffolds

  2021cites this paper
• Rapid four-component synthesis of dihydropyrano[2,3-c]pyrazoles using nano-eggshell/Ti(IV) as a highly compatible natural based catalyst

  2021cites this paper
• Tungstic acid (H 4 WO 5 ) immobilized on magnetic‐based zirconium amino acid metal–organic framework: An efficient heterogeneous Brønsted acid catalyst for l‐(4‐phenyl)‐2,4‐dihydropyrano[2,3c]pyrazole derivatives preparation

  2021cites this paper
• Synthesis of Dihydropyrano[2,3-C]pyrazoles Using Mandelic Acid as an Efficient Catalyst

  2021cites this paper
• Green synthetic approaches for biologically relevant 2-amino-4H-pyrans and 2-amino-4H-pyran-annulated heterocycles in aqueous media

  2021cites this paper
• Exploring the Effects of Water on the Mechanism of the Catalyst-Free Reaction between Isatin and 3-Methyl-2-pyrazolin-5-one from the Mixed Implicit/Explicit Multiple Types of Water Clusters.

  2021cites this paper
• ZIF-8-Incorporated Nanoparticles of MgFe2O4 Supported on Graphene Oxide: A Ternary Hybrid Catalyst for the Efficient Synthesis of Pyrazole-Based Pyrido[2,3-d]pyrimidine-diones

  2021cites this paper
• Catalyst-Free and Solvent-Free Visible Light Assisted Synthesis of Tetrahydrobenzo[b]Pyran Scaffolds at Room Temperature

  2021cites this paper
• Micelle‐Mediated Trimerization of Ynals to Orthogonally Substituted 4 H ‐Pyrans in Water: Downstream Rearrangement to Bioactive 2,8‐dioxabicyclo[3.3.1]nona‐3,6‐diene Frameworks

  2021cites this paper
• H3PMo7W5O40·24H2O catalyzed access to fused pyrazolopyranopyrimidine derivatives via one-pot multicomponent synthesis: green chemistry

  2021cites this paper
• Computer-Aided Drug Designing

  2021cites this paper
• Photoexcited Na2 eosin Y as direct hydrogen atom transfer (HAT) photocatalyst promoted photochemical metal-free synthesis of tetrahydrobenzo[b]pyran scaffolds via visible light-mediated under air atmosphere

  2021cites this paper
• A new role for photoexcited Na2 eosin Y as direct hydrogen atom transfer (HAT) photocatalyst in photochemical synthesis of dihydropyrano[2,3-c]pyrazole scaffolds promoted by visible light irradiation under air atmosphere

  2021cites this paper
• Novel 2‐Pyrazolin‐5‐one Derivative through Unforeseen Orthoamide Intermediate: Mechanistic Insights on Isocyanide Based [4+1] Cycloaddition

  2021cites this paper
• Concentrated solar radiation-assisted one-pot/multicomponent synthesis of pyranopyrazole derivatives under neat condition

  2021cites this paper
• Oximes: Novel Therapeutics with Anticancer and Anti-Inflammatory Potential

  2021cites this paper
• An Efficient One Pot Four-Component Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] Derivatives via Electrochemical Approach

  2021cites this paper
• Virtual screening in drug discovery: a precious tool for a still-demanding challenge

  2020cites this paper
• SO3H@carbon powder derived from waste orange peel: An efficient, nano-sized greener catalyst for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives

  2020cites this paper
• Catalyst‐free one‐pot synthesis of a new class of2H‐furo[3,2‐c]chromene‐2,4(3H)‐dione and arylamino‐bis(coumarin)methane derivatives on water

  2020cites this paper
• Uric Acid as a Naturally Biodegradable and Reusable Catalyst for the Convenient and Eco-Safe Synthesis of Biologically Active Pyran Annulated Heterocyclic Systems

  2020cites this paper
• Spectroscopic and Structural Investigations on Novel 6-Amino-3-Phenyl-4-(Pyridin-4-yl)-2,4-Dihydropyrano[2,3-c] Pyrazole-5-Carbonitrile by FT-IR, NMR, Docking, and DFT Methods

  2020influential citation
• Validation of ligands targeting metacaspase-2 (MCA2) from Trypanosoma brucei brucei and their application to MCA5 from T. congolense as possible trypanocides.

  2020cites this paper
• Visible light irradiation promoted catalyst-free and solvent-free synthesis of pyrano[2,3-d]pyrimidine scaffolds at room temperature

  2020cites this paper
• An expedient and eco-friendly approach for multicomponent synthesis of dihydropyrano[2,3-c]pyrazoles using nano-Al2O3/BF3/Fe3O4 as reusable catalyst

  2020cites this paper
• Synthesis of Some Novel 2-{Pyrano[2,3-c]Pyrazoles-4-Ylidene}Malononitrile Fused with Pyrazole, Pyridine, Pyrimidine, Diazepine, Chromone, Pyrano[2,3-c]Pyrazole and Pyrano[2,3-d]Pyrimidine Systems as Anticancer Agents

  2020cites this paper
• Tuning the Chemoselectivity of Dehydroacetic Acid Derived Enones by Isoniazid and Phenylhydrazines: An Efficient Access to 3-Styryl Pyrano[2,3-c ]pyrazolones

  2020cites this paper
• DABCO-catalyzed Five-component Domino Protocol for the Synthesis of Novel Benzo[a]pyrazolo[4’,3’:5,6]pyrano[2,3-c]phenazines in PEG-400 as an Efficient Green Reaction Medium

  2020cites this paper
• Caffeine as a Naturally Green and Biodegradable Catalyst for Preparation of Dihydropyrano[2,3-c]pyrazoles

  2020cites this paper
• Ultrasound-assisted multicomponent synthesis of 4H-pyrans in water and DNA binding studies

  2020cites this paper