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A Three-Dimensional Model of Lanosterol 14α-Demethylase of Candida albicans and Its Interaction with Azole Antifungals
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A three‐dimensional model of aromatase cytochrome P450
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The Ubiquitously Expressed Human CYP51 Encodes Lanosterol 14α-Demethylase, a Cytochrome P450 Whose Expression Is Regulated by Oxysterols
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The G464S Amino Acid Substitution in Candida albicans Sterol 14α-Demethylase Causes Fluconazole Resistance in the Clinic through Reduced Affinity
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Antifungal triazole alcohols: A comparative analysis of structure-activity, structure-teratogenicity and structure-therapeutic index relationships using the Multiple Computer-Automated Structure Evaluation (Multi-CASE) methodology
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A simple method for displaying the hydropathic character of a protein
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HIGH-RESOLUTION CRYSTAL STRUCTURE OF CYTOCHROME P450-CAM
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Crystal structure and refinement of cytochrome P450terp at 2·3 Å resolution
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Structural analysis of the interaction between the side-chain of substrates and the active site of lanosterol 14α-demethylase (P-45014DM) of yeast
inferredcites →https://doi.org/10.1016/0263-7855(94)80086-3openalex-snapshot
Modeling cytochrome P450 14α demethylase (Candida albicans) from P450cam
inferredcites →https://doi.org/10.1016/0960-0760(93)90243-popenalex-snapshot
A detailed molecular model for human aromatase
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A single amino acid substitution converts cytochrome P45014DM to an inactive form, cytochrome P450SG1: Complete primary structures deduced from cloned DNAs
inferredcites →https://doi.org/10.1016/s0021-9258(18)38093-1openalex-snapshot
Lanosterol 14 alpha-methyl demethylase. Isolation and characterization of the third metabolically generated oxidative demethylation intermediate.
inferredcites →https://doi.org/10.1016/s0300-483x(98)00149-8openalex-snapshot
Molecular modelling of the human cytochrome P450 isoform CYP2A6 and investigations of CYP2A substrate selectivity
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Homology modelling of human cytochromes P450 involved in xenobiotic metabolism and rationalization of substrate selectivity
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Molecular modelling of steroidogenic cytochromes P450 from families CYP11, CYP17, CYP19 and CYP21 based on the CYP102 crystal Structure
inferredcites →https://doi.org/10.1021/bi00068a013openalex-snapshot
Inhibitor-induced conformational change in cytochrome P-450CAM
inferredcites →https://doi.org/10.1021/jm00093a015openalex-snapshot
Stereoisomers of ketoconazole: preparation and biological activity
inferredcites →https://doi.org/10.1023/a:1007947411145openalex-snapshot
Three-dimensional modelling of human cytochrome P450 1A2 and its interaction with caffeine and MeIQ
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Assessment of protein models with three-dimensional profiles
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00376.xopenalex-snapshot
Optimized expression and catalytic properties of a wheat obtusifoliol 14α‐demethylase (CYP51) expressed in yeast
inferredcites →https://doi.org/10.1073/pnas.96.16.8937openalex-snapshot
Characterization and catalytic properties of the sterol 14α-demethylase from Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1074/jbc.271.21.12445openalex-snapshot
The Mechanism of the Acyl-Carbon Bond Cleavage Reaction Catalyzed by Recombinant Sterol 14α-Demethylase of Candida albicans (Other Names Are: Lanosterol 14α-Demethylase, P-45014DM, and CYP51)
inferredcites →https://doi.org/10.1080/07391102.1994.10508088openalex-snapshot
Application of 3-Dimensional Homology Modeling of Cytochrome P450 2B1 for Interpretation of Site-Directed Mutagenesis Results
inferredcites →https://doi.org/10.1093/nar/17.2.804openalex-snapshot
Nucleotide sequence of cytochrome P450 LIAI (lanosterol 14α-demethylase) fromCandida albicans
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a021331openalex-snapshot
Sterol 14-Demethylase P450 (P45014DM*) Is One of the Most Ancient and Conserved P450 Species
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a022536openalex-snapshot
Purification and Characterization of Rat Sterol 14-Demethylase P450 (CYP51) Expressed in Escherichia coli
inferredcites →https://doi.org/10.1093/protein/2.5.335openalex-snapshot
Modelling the polypeptide backbone with ‘spare parts’ from known protein structures
inferredcites →https://doi.org/10.1126/science.8342039openalex-snapshot
Crystal Structure of Hemoprotein Domain of P450BM-3, a Prototype for Microsomal P450's
inferredcites →https://doi.org/10.1128/aac.43.5.1163openalex-snapshot
Formation of Azole-Resistant Candida albicans by Mutation of Sterol 14-Demethylase P450
inferredcites →https://doi.org/10.1248/cpb.45.321openalex-snapshot
Optically Active Antifungal Azoles. VII. Synthesis and Antifungal Activity of Stereoisomers of 2-((1R,2R)-2-(2,4-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl)-4-(4-(2,2,3,3-tetrafluoropropoxy)phenyl)-3(2H,4H)-1,2,4-triazolone (TAK-187).
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inferred← citeshttps://doi.org/10.1016/j.tgchem.2024.100038openalex-snapshot
Ionic liquid Mediated Pd-catalyzed sonochemistry for facile synthesis of carbazoles: Molecular Modelling and antimicrobial studies
inferred← citeshttps://doi.org/10.1016/s0065-2911(03)47003-3openalex-snapshot
The biodiversity of microbial cytochromes P450
inferred← citeshttps://doi.org/10.1016/s0169-409x(02)00009-1openalex-snapshot
Pharmacophore modeling of cytochromes P450
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00263-8openalex-snapshot
1,4-Benzothiazine and 1,4-Benzoxazine imidazole derivatives with antifungal activity: A docking study
inferred← citeshttps://doi.org/10.1016/s1473-3099(09)70265-8openalex-snapshot
Azole resistance in Aspergillus fumigatus: a side-effect of environmental fungicide use?
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c00266openalex-snapshot
Novel Triazoles with Potent and Broad-Spectrum Antifungal Activity In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01718openalex-snapshot
Repurposing the Clinically Efficacious Antifungal Agent Itraconazole as an Anticancer Chemotherapeutic
inferred← citeshttps://doi.org/10.1021/acsomega.3c02141openalex-snapshot
Investigation of Luliconazole-Loaded Mucoadhesive Electrospun Nanofibers for Anticandidal Activity in the Management of Vaginal Candidiasis
inferred← citeshttps://doi.org/10.1021/acsomega.9b03558openalex-snapshot
Investigation of the Detailed Internal Structure and Dynamics of Itraconazole by Solid-State NMR Measurements
inferred← citeshttps://doi.org/10.1021/ci900425topenalex-snapshot
Structure-Based Rational Screening of Novel Hit Compounds with Structural Diversity for Cytochrome P450 Sterol 14α-Demethylase from Penicillium digitatum
inferred← citeshttps://doi.org/10.1021/jf103243mopenalex-snapshot
Homology Modeling and Screening of New 14α-Demethylase Inhibitor (DMI) Fungicides Based on Optimized Expression of CYP51 from Ustilago maydis in Escherichia coli
inferred← citeshttps://doi.org/10.1021/jm020980topenalex-snapshot
Synthesis, Antifungal Activity, and Molecular Modeling Studies of New Inverted Oxime Ethers of Oxiconazole
inferred← citeshttps://doi.org/10.1021/jm050441zopenalex-snapshot
The Protein Farnesyltransferase Inhibitor Tipifarnib as a New Lead for the Development of Drugs against Chagas Disease
inferred← citeshttps://doi.org/10.1021/jm4016284openalex-snapshot
Design, Synthesis, and Structure–Activity Relationship Studies of Novel Fused Heterocycles-Linked Triazoles with Good Activity and Water Solubility
inferred← citeshttps://doi.org/10.1021/jm800009ropenalex-snapshot
1-[(3-Aryloxy-3-aryl)propyl]-1H-imidazoles, New Imidazoles with Potent Activity againstCandida albicansand Dermatophytes. Synthesis, Structure−Activity Relationship, and Molecular Modeling Studies
inferred← citeshttps://doi.org/10.1038/s41564-024-01720-yopenalex-snapshot
Pan-drug resistance and hypervirulence in a human fungal pathogen are enabled by mutagenesis induced by mammalian body temperature
inferred← citeshttps://doi.org/10.1038/s41598-025-11080-0openalex-snapshot
Cell wall modifications in Saccharomyces cerevisiae wine yeast through adaptive laboratory evolution with Tebuconazole
inferred← citeshttps://doi.org/10.1039/c1md00103eopenalex-snapshot
Discovery of highly potent antifungal triazoles by structure-based lead fusion
inferred← citeshttps://doi.org/10.1039/c2md20109gopenalex-snapshot
Discovery of a new class of dithiocarbamates and rhodanine scaffolds as potent antifungal agents: synthesis, biology and molecular docking
inferred← citeshttps://doi.org/10.1039/c3md20086hopenalex-snapshot
Synthesis and antifungal activity of the novel triazole compounds
inferred← citeshttps://doi.org/10.1039/c3ra41310aopenalex-snapshot
Molecular docking, design, synthesis and antifungal activity study of novel triazole derivatives containing the 1,2,3-triazole group
inferred← citeshttps://doi.org/10.1039/c8ra08426bopenalex-snapshot
1,2,3-Triazole–quinazolin-4(3 H )-one conjugates: evolution of ergosterol inhibitor as anticandidal agent
inferred← citeshttps://doi.org/10.1073/pnas.0407790101openalex-snapshot
Biological spectra analysis: Linking biological activity profiles to molecular structure
inferred← citeshttps://doi.org/10.1073/pnas.061562898openalex-snapshot
Crystal structure of cytochrome P450 14α-sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with azole inhibitors
inferred← citeshttps://doi.org/10.1074/jbc.m413042200openalex-snapshot
Structural Diversities of Active Site in Clinical Azole-bound Forms between Sterol 14α-Demethylases (CYP51s) from Human and Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1080/07391102.2004.10506984openalex-snapshot
Homology Modeling of Lanosterol 14α-Demethylase ofCandida albicansandAspergillus fumigatusand Insights into the Enzyme-Substrate Interactions
inferred← citeshttps://doi.org/10.1080/07391102.2025.2479847openalex-snapshot
Azole resistance: insights from Y132 substitutions in Candida sterol 14α-demethylase utilizing molecular dynamics simulations
inferred← citeshttps://doi.org/10.1080/13693780500138971openalex-snapshot
An update on antifungal targets and mechanisms of resistance inCandidaalbicans
inferred← citeshttps://doi.org/10.1080/1475636021000005686openalex-snapshot
In Vitro Activity of a New Antifungal Azolyl-substituted Indole Against Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1088/1742-6596/1294/5/052049openalex-snapshot
Quantitative Structure-Activity Relationship Studies Of Amino Acids Conjugated 2-Amnio-Arylthiazole As Antifungal
inferred← citeshttps://doi.org/10.1088/2053-1591/aaee3bopenalex-snapshot
Investigation of Antimicrobial activity of CTAB assisted hydrothermally derived Nano BaTiO3
inferred← citeshttps://doi.org/10.1093/jac/dkn015openalex-snapshot
Susceptibility of clinical isolates of Candida species to fluconazole and detection of Candida albicans ERG11 mutations
inferred← citeshttps://doi.org/10.1093/jac/dku554openalex-snapshot
Identification and properties of plasma membrane azole efflux pumps from the pathogenic fungi Cryptococcus gattii and Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1094/pdis-08-20-1806-reopenalex-snapshot
Sensitivity of Pyricularia oryzae Populations to Fungicides Over a 26-Year Time Frame in Brazil
inferred← citeshttps://doi.org/10.1099/mic.0.27938-0openalex-snapshot
Altered expression profile of mycobacterial surface glycopeptidolipids following treatment with the antifungal azole inhibitors econazole and clotrimazole
inferred← citeshttps://doi.org/10.1101/2021.02.26.433138openalex-snapshot
Photochromic fluorophores enable imaging of lowly-expressed proteins in the autofluorescent fungus Candida albicans
inferred← citeshttps://doi.org/10.1107/s1600536800020699openalex-snapshot
1-{[4-(4-Chlorophenyl)-1H-pyrrol-3-yl](2,4-dichlorophenyl)methyl}-1H-imidazole (RDS 416)
inferred← citeshttps://doi.org/10.1111/1567-1364.12042openalex-snapshot
Erg11 mutations associated with azole resistance in clinical isolates of Candida albicans
inferred← citeshttps://doi.org/10.1111/apm.13336openalex-snapshot
Azole resistance in Candida auris: mechanisms and combinatorial therapy
inferred← citeshttps://doi.org/10.1111/ced.13641openalex-snapshot
Ultrastructural changes of Trichophyton rubrum in tinea unguium after itraconazole therapy in vivo observed using scanning electron microscopy
inferred← citeshttps://doi.org/10.1111/fcp.12230openalex-snapshot
Targeting CYP 51 for drug design by the contributions of molecular modeling
inferred← citeshttps://doi.org/10.1111/febs.16977openalex-snapshot
The intricate link between iron, mitochondria and azoles in Candida species
inferred← citeshttps://doi.org/10.1111/j.1439-0507.2009.01766.xopenalex-snapshot
Investigation of mutations in Erg11 gene of fluconazole resistant Candida albicans isolates from Turkish hospitals
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2009.00797.xopenalex-snapshot
Design of Conformationally Constrained Azole Antifungals: Efficient Synthesis and Antifungal Activity of trans‐3‐Imidazolylflavanones
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2010.01038.xopenalex-snapshot
Synthesis, Molecular Docking, and Biological Evaluation of Novel Triazole Derivatives as Antifungal Agents
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2011.01138.xopenalex-snapshot
Structure‐Based Design, Synthesis, and Antifungal Activity of New Triazole Derivatives
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2011.01178.xopenalex-snapshot
Synthesis, Antifungal Activity, and Docking Study of Some New 1,2,4‐triazole Analogs
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2012.01398.xopenalex-snapshot
Synthesis and Biological Evaluation of Triazole Derivatives as Potential Antifungal Agent
inferred← citeshttps://doi.org/10.1111/nph.18575openalex-snapshot
Membrane component ergosterol builds a platform for promoting effector secretion and virulence in Magnaporthe oryzae
inferred← citeshttps://doi.org/10.1111/pce.70582openalex-snapshot
Protease‐Mediated Dual Action Against Rice Blast: Suppression of Magnaporthe oryzae Ergosterol Biosynthesis Pathway and Enhancement of Rice Disease Resistance by Bacillus amyloliquefaciens SN16‐1
inferred← citeshttps://doi.org/10.1124/dmd.106.013888openalex-snapshot
Three-Dimensional Quantitative Structure-Activity Relationship Analysis of Human CYP51 Inhibitors
inferred← citeshttps://doi.org/10.1128/aac.00459-07openalex-snapshot
Cross-Resistance to Medical and Agricultural Azole Drugs in Yeasts from the Oropharynx of Human Immunodeficiency Virus Patients and from Environmental Bavarian Vine Grapes
inferred← citeshttps://doi.org/10.1128/aac.00516-13openalex-snapshot
Chromosome 5 Monosomy of Candida albicans Controls Susceptibility to Various Toxic Agents, Including Major Antifungals
inferred← citeshttps://doi.org/10.1128/aac.01383-12openalex-snapshot
Screening of Antifungal Azole Drugs and Agrochemicals with an Adapted alamarBlue-Based Assay Demonstrates Antibacterial Activity of Croconazole against Mycobacterium ulcerans
inferred← citeshttps://doi.org/10.1128/aac.01630-08openalex-snapshot
Three-Dimensional Model of Lanosterol 14α-Demethylase from Cryptococcus neoformans : Active-Site Characterization and Insights into Azole Binding
inferred← citeshttps://doi.org/10.1128/aac.05389-11openalex-snapshot
S279 Point Mutations in Candida albicans Sterol 14-α Demethylase (CYP51) Reduce In Vitro Inhibition by Fluconazole
inferred← citeshttps://doi.org/10.1128/aac.45.10.2676-2684.2001openalex-snapshot
Prevalence of Molecular Mechanisms of Resistance to Azole Antifungal Agents in Candida albicans Strains Displaying High-Level Fluconazole Resistance Isolated from Human Immunodeficiency Virus-Infected Patients
inferred← citeshttps://doi.org/10.1128/aac.45.11.2987-2990.2001openalex-snapshot
Critical Annotations to the Use of Azole Antifungals for Plant Protection
inferred← citeshttps://doi.org/10.1128/aac.46.6.1695-1703.2002openalex-snapshot
Molecular Mechanisms of Fluconazole Resistance in Candida dubliniensis Isolates from Human Immunodeficiency Virus-Infected Patients with Oropharyngeal Candidiasis
inferred← citeshttps://doi.org/10.1128/aac.47.4.1213-1219.2003openalex-snapshot
Genetic Basis for Differential Activities of Fluconazole and Voriconazole against Candida krusei
inferred← citeshttps://doi.org/10.1128/aac.48.2.568-574.2004openalex-snapshot
Three-Dimensional Models of Wild-Type and Mutated Forms of Cytochrome P450 14α-Sterol Demethylases from Aspergillus fumigatus and Candida albicans Provide Insights into Posaconazole Binding
inferred← citeshttps://doi.org/10.1128/aac.48.7.2747-2750.2004openalex-snapshot
Substitutions at Methionine 220 in the 14α-Sterol Demethylase (Cyp51A) of Aspergillus fumigatus Are Responsible for Resistance In Vitro to Azole Antifungal Drugs
inferred← citeshttps://doi.org/10.1128/mmbr.00045-10openalex-snapshot
Regulatory Circuitry Governing Fungal Development, Drug Resistance, and Disease
inferred← citeshttps://doi.org/10.1128/msphere.00146-21openalex-snapshot
Photochromic Fluorophores Enable Imaging of Lowly Expressed Proteins in the Autofluorescent Fungus Candida albicans
inferred← citeshttps://doi.org/10.1134/s0006297911020039openalex-snapshot
Molecular modeling of human lanosterol 14α-demethylase complexes with substrates and their derivatives
inferred← citeshttps://doi.org/10.11606/d.5.2011.tde-23082011-125151openalex-snapshot
Identificação e análise de mutações no gene ERG11 de isolados de Candida susceptíveis e resistentes ao fluconazol
inferred← citeshttps://doi.org/10.1186/2193-1801-3-660openalex-snapshot
Structural basis for heterogeneous phenotype of ERG11 dependent Azole resistance in C.albicans clinical isolates
inferred← citeshttps://doi.org/10.1248/bpb.29.1262openalex-snapshot
Influence of Thermodynamic Parameter in Lanosterol 14.ALPHA.-Demethylase Inhibitory Activity as Antifungal Agents: A QSAR Approach
inferred← citeshttps://doi.org/10.1248/bpb.30.1246openalex-snapshot
Identification of Y118 Amino Acid Residue in Candida albicans Sterol 14.ALPHA.-Demethylase Associated with the Enzyme Activity and Selective Antifungal Activity of Azole Analogues
inferred← citeshttps://doi.org/10.1248/cpb.54.583openalex-snapshot
QSAR Study of 3-Phenyl-5-acyloxymethyl-2H,5H-furan-2-ones as Antifungal Agents: The Dominant Role of Electronic Parameter
inferred← citeshttps://doi.org/10.1289/ehp.5785openalex-snapshot
Azole fungicides affect mammalian steroidogenesis by inhibiting sterol 14 alpha-demethylase and aromatase.
inferred← citeshttps://doi.org/10.1371/journal.pone.0021239openalex-snapshot
Amino Acid Substitutions at the Major Insertion Loop of Candida albicans Sterol 14alpha-Demethylase Are Involved in Fluconazole Resistance
inferred← citeshttps://doi.org/10.1371/journal.pone.0032278openalex-snapshot
Antifungal Susceptibility Profiles of 1698 Yeast Reference Strains Revealing Potential Emerging Human Pathogens
inferred← citeshttps://doi.org/10.1385/1-59259-802-1:449openalex-snapshot
Prediction of Drug-Like Molecular Properties
inferred← citeshttps://doi.org/10.1517/17425255.2013.794785openalex-snapshot
Itraconazole: an update on pharmacology and clinical use for treatment of invasive and allergic fungal infections
inferred← citeshttps://doi.org/10.15415/jptrm.2020.82008openalex-snapshot
Molecular Docking Approach to Identify Potential AntiCandidal Potential of Curcumin
inferred← citeshttps://doi.org/10.15575/biodjati.v9i1.32147openalex-snapshot
In Silico Studies of Bioactive Compounds from Pseudomonas azotoformans UICC B-91 in Inhibiting Candida albicans
inferred← citeshttps://doi.org/10.17582/journal.sja/2022/38.4.1235.1239openalex-snapshot
Computational Structural Calculation of N-Methyl Benzothiazolium Iodide as an Antifungal Candidate
inferred← citeshttps://doi.org/10.17721/fujcv4i2p1-27openalex-snapshot
Chemical modifications and transformations of 3-azahetarylchroman-4-ones
inferred← citeshttps://doi.org/10.18502/cmm.5.3.1739openalex-snapshot
Extensive ERG11 mutations associated with fluconazole-resistant Candida albicans isolated from HIV-infected patients
inferred← citeshttps://doi.org/10.2147/dddt.s58680openalex-snapshot
Triazole derivatives with improved in vitro antifungal activity over azole drugs
inferred← citeshttps://doi.org/10.21577/0103-5053.20230050openalex-snapshot
Solvatochromism and Thermochromism of Fluconazole: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.2174/092986711794480113openalex-snapshot
New Lead Structures in Antifungal Drug Discovery
inferred← citeshttps://doi.org/10.2174/1573407215666190131110930openalex-snapshot
3D Pharmacophore-based Ligand Alignment, Virtual Screening and Molecular Docking Protocols Towards the Discovery of 2-((1H-1,2,4-triazol-1- yl)methyl) Derivatives as Antifungal Inhibitors
inferred← citeshttps://doi.org/10.2174/1573409915666181219124956openalex-snapshot
Molecular Modelling Studies of 1,4-Diaryl-2-Mercaptoimidazole Derivatives for Antimicrobial Potency
inferred← citeshttps://doi.org/10.2217/fmb-2023-0012openalex-snapshot
Synergistic Effect of Hydralazine Associated with Triazoles on Candida spp. in Planktonic Cells
inferred← citeshttps://doi.org/10.2217/fmb.14.18openalex-snapshot
Elucidating Drug Resistance in Human Fungal Pathogens
inferred← citeshttps://doi.org/10.2217/fmb.15.47openalex-snapshot
Medically Important Fungi Respond to Azole Drugs: An Update
inferred← citeshttps://doi.org/10.3109/10408444.2013.855163openalex-snapshot
Human and ecological risk assessment of a crop protection chemical: a case study with the azole fungicide epoxiconazole
inferred← citeshttps://doi.org/10.33273/2663-9726-2021-54-1-52-61openalex-snapshot
Reproductive toxicity of triazole fungicides cyproconazole and epoxiconazole when exposed to male and female wistar rats during gametogenesis
inferred← citeshttps://doi.org/10.3389/fmicb.2016.01164openalex-snapshot
Direct Molecular Diagnosis of Aspergillosis and CYP51A Profiling from Respiratory Samples of French Patients
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00864openalex-snapshot
Palmitic Acid Inhibits the Virulence Factors of Candida tropicalis: Biofilms, Cell Surface Hydrophobicity, Ergosterol Biosynthesis, and Enzymatic Activity
inferred← citeshttps://doi.org/10.3390/jof12100728openalex-snapshot
Advances in Azole Antifungal Agents: From Structural Foundations to Resistance Challenges
inferred← citeshttps://doi.org/10.3390/molecules23030599openalex-snapshot
Synthesis, Molecular Docking, and Antimycotic Evaluation of Some 3-Acyl Imidazo[1,2-a]pyrimidines
inferred← citeshttps://doi.org/10.3390/molecules27123886openalex-snapshot
Novel α-Aminophosphonates and α-Aminophosphonic Acids: Synthesis, Molecular Docking and Evaluation of Antifungal Activity against Scedosporium Species
inferred← citeshttps://doi.org/10.3390/molecules29122839openalex-snapshot
Stereoselective Asymmetric Syntheses of Molecules with a 4,5-Dihydro-1H-[1,2,4]-Triazoline Core Possessing an Acetylated Carbohydrate Appendage: Crystal Structure, Spectroscopy, and Pharmacology
inferred← citeshttps://doi.org/10.3390/ph14111110openalex-snapshot
Three-Component Synthesis of 2-Amino-3-cyano-4H-chromenes, In Silico Analysis of Their Pharmacological Profile, and In Vitro Anticancer and Antifungal Testing
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