Medicinal Chemistry Research

Papers
(The median citation count of Medicinal Chemistry Research is 2. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
Synthesis, characterization and in vitro antitumor activity of asiatic acid derivatives120
Potent α-glucosidase inhibitory activity of inoscavin A from fruiting bodies of Fulvifomes fastuosus: Mechanism of action, molecular docking and ADMET104
Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment88
Synthesis and antitumor activity evaluation in vitro of 4-aminoquinazoline derivatives containing 1,3,4-thiadiazole78
Computer-aided design, synthesis and evaluation of new SARS-CoV-2 Mpro inhibitors based on 1,5,6,7-tetrahydro-4H-indazol-4-one scaffold68
Structural simplification and ester bond flipping lead to bis-benzodioxole derivatives as potential hypolipidemic and hepatoprotective agent62
Design, synthesis, and antitumor activity evaluation of carbazole derivatives with potent HDAC inhibitory activity58
Carbamoyl flavonoids as dual inhibitors of acetylcholinesterase and monoacylglycerol lipase: synthesis, in vitro evaluation, and computational studies54
Antibacterial, antifungal activities and toxicity of new synthetic fatty acid salicylate esters51
Evaluation of a series of nucleoside analogs as effective anticoronaviral-2 drugs against the Omicron-B.1.1.529/BA.2 subvariant: A repurposing research study51
Synthesis of novel benzothieno-[3,2’-f][1,3] oxazepines and their isomeric 2-oxo-2H-spiro[benzothiophene-3,3’-pyrrolines] via 1,4-dipolar cycloaddition reaction and their evaluation as cytotoxic antic47
Asciminib: first FDA approved allosteric inhibitor of BCR-ABL1 for the treatment of chronic myeloid leukemia44
Anticancer activity of amide and ester derivatives of the ent-labdane 2α-hydroxyeperuic acid obtained via sonochemical synthesis39
Synthesis of the dibenzylbutane lignan LCA derivatives and evaluation of their anti-inflammatory activities39
Monoamine oxidase inhibition by thiazole derivatives substituted with the benzenesulfonamide moiety38
Synthesis of berberine derivatives and their antiviral activity toward respiratory syncytial virus38
Novel imino-thiazoloquinoxaline derivatives against renal cell carcinoma: less radiation-damaging approach35
Glutathione and glutathione disulfide – their biomedical and pharmaceutical applications34
Design, synthesis and anti-breast cancer properties of butyric ester tethered dihydroartemisinin-isatin hybrids34
Screening of small molecule compounds targeting hnRNPA2 protein33
Synthesis of tetrahydro-β-carboline analogs with N11 modifications and study of their antimalarial activities33
Bio-guided isolation of anti-Alzheimer’s compounds from Phyllanthus niruri and role of niruriflavone in the reversal of aluminum chloride-induced neurobehavioral and biochemical changes in an animal m33
Contrasting effect of different crowding agents on pseudoknot RNA stability30
Design and synthesis of diphenyl-1H-imidazole analogs targeting Mpro/3CLpro enzyme of SARS-CoV-230
Evaluation of benzoylacetonitriles as novel anti-neuroinflammatory agents29
A versatile strategy for the synthesis of various lumazine peptides29
Plant-derived pyroptosis inducers as a therapeutic strategy in drug-resistant cancers29
Utilizing mechanistic organic chemistry training to study drug metabolism in preclinical drug discovery/development24
4’-Thionucleosides as adenosine A3 receptor ligands: a medicinal chemistry perspective23
Synthesis, crystal structure, and anticancer activity of organotin(IV) complexes based on chlorine substituted aryl ligands22
Recent advances in triazole-benzenesulfonamide hybrids and their biological activities21
Pyrrolobenzodiazepines: natural sources, therapeutic uses, and future in neurological treatments20
Design, Synthesis, and biological evaluation of pyrazolo-benzothiazole derivatives as a potential therapeutic agent for the treatment of Alzheimer’s disease20
Synthesis, inhibition effects, molecular docking and theoretical studies as Paraoxonase 1 (PON1) inhibitors of novel 1,4-dihydropyridine substituted sulfonamide derivatives20
Discovery of 3-(N-phenylsulfamoyl)-l-phenylalanine derivatives as novel and orally available LAT1-selective inhibitors20
Enantioselectivity of pinene against Leishmania amazonensis18
Synthesis and antihepatoma activity of dimeric 1-O-acetylbritannilactone derivatives18
Synthesis of nitrogen-containing oleanolic acid derivatives as carbonic anhydrase and acetylcholinesterase inhibitors18
Dual-PROTACs based on natural product derivative potassium dehydrographolide succinate: design, synthesis, and antitumor activity of a novel EGFR degrader18
Medicinal uses, phytochemistry, pharmacology, and taxonomy of Poygonum aviculare L.: a comprehensive review18
Synthesis and biological evaluation of esculetin derivatives as potential anti-HBV agents17
Synthesis, bacteria activity and molecular simulation of D-galactose-conjugated thiosemicarbazones of 3-aryl-4-formylsydnones17
α-Glucosidase inhibitory activities of aromatic compounds from the rhizomes of Alpinia galanga17
Novel conjugated 5-alkenyl rhodanine tethered 1,4-benzodioxane derivatives as dual-chitinases inhibitors to hinder the growth of Asian corn borer17
Synthetic studies toward a simplified eleuthoside core17
Design, synthesis and evaluation of salicylic acid-donepezil hybrids as functional agents for the treatment of Alzheimer’s disease17
Pks 13 inhibitors—a promising target for future antitubercular agents16
Synthesis and in vitro anti-trypanosomal evaluation of quinolone hydrazide analogues16
Acylhydrobenzoquinones influence the susceptibility of Staphylococcus aureus towards abietanes and the speciation within Plectranthus sensus lato16
Development of new donepezil analogs: synthesis, biological screening and in silico study rational16
Design, synthesis and insecticidal activities of novel meta-diamide compounds containing ethyl group16
Role of natural secondary metabolites as HIF-1 inhibitors in cancer therapy16
Design, synthesis, and activity study of heterocyclic derivatives as JAK inhibitors15
1,2,3-triazenes and 1,2,3-triazoles as antileishmanial, antitrypanosomal, and antiplasmodial agents15
Exploring thiazole-linked thioureas using alkaline phosphatase assay, biochemical evaluation, computational analysis and structure–activity relationship (SAR) studies15
Novel indanone-chalcone esters with potential anti-Alzheimer effects designed using hybridization and bioisosteric replacement approaches14
A Click Synthesis, Molecular Docking and Biological Evaluation of 1,2,3-triazoles-benzoxazepine hybrid as potential anticancer agents13
Synthesis and biological evaluation of coumarin derivatives as anti-lung adenocarcinoma agents via induction of apoptosis and autophagy: in vitro and in vivo studies13
In vitro cytotoxicity evaluation of triphenylphosphonium (TPP) conjugates of some acetylenated nucleic bases and their analogues13
Polyketides from Neohelicosporium griseum: structure assignment and bioactivity investigation13
Antitumor studies on celastrol and its derivatives as RORα agonists and RORγ inhibitors based on Alphafold reverse docking strategy13
Molecular hybridization method for obtaining paeonol-based fibrate derivatives with potent lipid-lowering and hepatoprotective activity13
Synthesis, antiviral evaluation, molecular docking study and cytotoxicity of 5′-phosphorylated 1,2,3-triazolyl nucleoside analogues with thymine and 6-methyl uracil moieties13
Synthesis, characterization, and anticancer activity of syringaldehyde-derived chalcones against female cancers12
Novel 2-aminopyrimidine Schiff bases as possible GABA-AT inhibitors: molecular docking, MAOS, and pharmacological screening12
Synthesis and biological evaluation of triazole alcohols containing an indole-3-methyl(phenyl)amino side chain against fluconazole-resistant Candida albicans12
Dual-target inhibitors based on brpf1: a review from medicinal chemistry perspectives12
Design, synthesis and antitumor activity evaluation of 2,4,6-trisubstituted quinazoline derivatives containing piperidine moiety12
New structural scaffold discovery via fragment-based drug design: Hydroxymethyl indazole derivatives as XOR/URAT1 dual inhibitors12
Synthesis and biological assessment of triazolo-quinazoline carbothioamide derivatives for p38 MAP kinase inhibition: in-silico and in-vitro approaches11
A fast high-throughput logP estimation method for peptide molecules based on liquid chromatography-mass spectrometry method11
A potent therapeutic scaffold fusing quinazolinone/melatonin for future colorectal cancer interventions: design, one-pot synthesis, biological and ADME-tox modeling studies11
Biological evaluation of imidazopyridine derivatives as potential anticancer agents against breast cancer cells11
Development of new coumarin-piperazine-N-phenylacetamid derivatives as potent tyrosinase inhibitors: In vitro and in silico evaluations11
Site-Specific incorporation of lysine acetyl-methylation into proteins11
The metabolic fate of izencitinib, a gut-selective pan-JAK inhibitor, in humans. Identification of unusual fecal metabolites and implications for MIST evaluation11
Designations of new biological drugs11
Dynamic tail amine interactions drive isoform selectivity for potent human neuronal nitric oxide synthase inhibitors11
Insights on synthetic strategies and structure-activity relationship of donepezil and its derivatives11
Discovery of quinazoline-based derivatives as novel autophagy inhibitors in pancreatic cancer11
Antivirulence therapy: type IV pilus as a druggable target for bacterial infections10
Antiproliferative effect, cell cycle arrest and apoptosis generation of novel 6-substituted N5-formyltetrahydropyrido[3,2-d]pyrimidine derivatives10
A comprehensive review of 11C-, 18F-, and 123/124/125I-labeled radiotracers targeting cyclooxygenase-2 over the past two decades10
Rehmannia glutinosa polysaccharides: a review on structure-activity relationship and biological activity10
Glycyrrhizin and its derivatives: an emerging secondary metabolite arsenal of Glycyrrhiza glabra10
Discovery of novel HCV inhibitors: design, synthesis and biological activity of phthalamide derivatives10
Design, synthesis and evaluation of aurone and indanone derivatives as novel antitumor agents10
Synthesis and pharmacological evaluation of new disulfides linked to 1,2,4-triazole bearing urea moiety10
Discovery of α-methylene-γ-lactone-δ-epoxy derivatives with anti-cancer activity: synthesis, SAR study, and biological activity10
Kaempferia diterpenoids and flavonoids: an overview on phytochemistry, biosynthesis, synthesis, pharmacology, and pharmacokinetics9
Discovery of potent maternal embryonic leucine zipper kinase (MELK) inhibitors of novel chemotypes using structure-based pharmacophores9
Pharmacological assessment of disulfide–triazine hybrids: synthesis, enzyme inhibition, and molecular docking study9
Discovery of mobocertinib, a new irreversible tyrosine kinase inhibitor indicated for the treatment of non-small-cell lung cancer harboring EGFR exon 20 insertion mutations9
Polyalthia longifolia: phytochemistry, ethnomedicinal importance, nutritive value, and pharmacological activities review9
Synthesis and in vitro biological activity of chalcone derivatives as potential antiparasitic agents9
Synthesis, in vitro activity, and molecular docking of caffeic acid and resveratrol derivatives against Alzheimer’s disease-related enzymes9
CYP3A4 drug metabolism considerations in pediatric pharmacotherapy9
Design, synthesis and molecular docking studies of novel benzimidazole-1,3,4-oxadiazole hybrids for their carbonic anhydrase inhibitory and antioxidant effects9
Structural modification of (‒)-xanthorrhizol isolated from Curcuma aromatica rhizomes to analogs with potent nitric oxide inhibitory activities9
Assessment of the α-glucosidase and α-amylase inhibitory potential of Paliurus spina-christi Mill. and its terpenic compounds9
Lipase inhibitory activity of constituents of Physalis glutinosa and Physalis latiphysa8
Unrevealing the Role of Flavonoids in Mitigation of Non-Alcoholic Fatty Liver Disease8
The potential of chalcone derivatives as human carbonic anhydrase inhibitors in the therapy of glaucoma8
Design, synthesis, stereochemical characterization, in vitro α-glucosidase, and α-amylase inhibition and in silico studies of novel pyrazole-hydrazide hydrazones8
Discovery of novel pterostilbene/biphenyl tethered 5-FU based conjugates targeting colorectal cancer: synthesis, cytotoxic and ADMET modeling studies8
Synthesis and inhibitory activity against enzymes responsible for Type 2 diabetes mellitus of lactose-conjugated thiosemicarbazones from substituted acetophenones8
The potential of major kavalactones in modulating cytochrome P450 enzymes8
Advances in quercetin-based therapeutics for breast cancer: natural, synthetic, and nanotechnology-driven approaches8
Integrated 3D-QSAR and cellular profiling of sulfated and hydrophobic aminoglycoside glycans to modulate heparanase activity8
Sphingosine 1-phosphate receptor modulators for the treatment of inflammatory bowel disease and other immune-mediated diseases8
Tranilast-tyrosine hybrid molecule exhibits dual activity: suppression of epithelial-mesenchymal transition and induction of cytotoxicity in cancer cells8
From empirical screening to lipid trolling: the evolution of extrahelical allosteric modulators of A1 and A3 adenosine receptors8
Sulfonamide-substituted oxindoles as inhibitors of carbonic anhydrase II with potential antiglaucoma activity8
In silico drug discovery: a machine learning-driven systematic review8
Design, synthesis, and neuroprotective activity of salidroside-based dual inhibitors of selective monoamine oxidase B and amyloid-β aggregation8
Synthesis, theoretical investigations and biological evaluation of ibuprofen drug hybrids8
Stable isotope applications in drug development and the elucidation of mechanisms of drug metabolism8
Synthesis, and docking studies of arylhydrazone compounds and evaluation of their platelet aggregation inhibitory effect and cytotoxicity7
Synthesis, characterization and biological evaluation of formononetin derivatives as anticancer agents7
Synthesis and evaluation of tetrahydrobenzo[cd]indole derivatives as glycogen phosphorylase inhibitors7
Hit-to-lead optimization of amino-carboxamide benzothiazoles as LSD1 inhibitors7
Ferrocene-based compounds: promising anticancer and antimalarial agents in modern therapeutics7
Tropanes in natural products, syntheses, and drugs: some insights from the new millennium7
ATP-hydrolyzing, DNA-damaging and cytotoxic activities of peptide-targeted cobalt(III) complex with diethylentriamine7
Discovery of phenylacetamide derivatives as novel STAT3 antagonists7
A glance into Schiff-based α-glucosidase inhibitors in medicinal chemistry7
Synthesis, structure-activity relationship and evaluation of antifungal activity of tryptanthrin derivatives against drug-resistant Candida albicans7
Design, synthesis, in vitro evaluation, and molecular dynamics simulation studies of novel coumarin-acetohydrazide Schiff base derivatives as urease enzyme inhibitors7
The emerging role of proteolysis targeting chimeras (PROTACs) in the treatment of Alzheimer’s disease7
Does the negatively charged phosphate backbone contribute to stabilize the complex between cationic organic molecules and G-quadruplex structures? From guessing to calculating7
Translating G-quadruplex ligands from bench to bedside: a Stephen Neidle’s legacy7
Glycosylated triptolide affords a potent in vivo therapeutic activity to hepatocellular carcinoma in mouse model7
Structural optimization and biological evaluation of quinoline/naphthalene-based glyoxalase-I inhibitors as anti-cancer candidates7
Synthesis of 6-dialkylaminopyrimidine carboxamide analogues and their anti-tubercular properties7
Natural products in medicinal chemistry: targeting inflammatory pathways with plant-derived compounds7
Acetylcholinesterase Inhibitors from Carbamate and Benzo-fused Heterocyclic Scaffolds: Promising Therapeutics for Alzheimer’s Disease7
Engelheptanoxides behave as liver X receptor α agonists7
4,5-diazafenylfluorene-rhodanine conjugates promote anoikis in A375 cells via inhibiting PPAR-γ expression7
In vitro antiproliferative activity of Parrotia persica exclusive gallotannin7
Molecular sonification: a multi-modal approach for enhanced ai in drug discovery7
Exploring the latest breakthroughs in rhodesain inhibitors for African trypanosomiasis7
Novel P2X4 Receptor Antagonist MRS4719 Improves Ischemia/reperfusion Injury in Mice7
4-Phenylcoumarins from Mesua ferrea with selective CYP1B1 inhibitory activity7
Novel vitamin K3 analogs containing 3-N-substituted aromatic and piperazine rings with selective in vitro anticancer activity against HeLa, U87 MG, and MCF-7 cells6
Prenylated flavonoids icariin and icaritin for drug discovery: structural modifications and bioactivity studies6
Anticancer potential of nicotinonitrile derivatives as PIM-1 kinase inhibitors through apoptosis: in vitro and in vivo studies6
The use of single-molecule FRET for the characterization of Holliday junctions containing human telomeric DNA: a methodological approach for nanoscale distance, mobility, and stability measurements6
Identification of α-mangostin as a potent inhibitor of β-lactamase OXA-486
Benzocaine-N-acylindoline conjugates: synthesis and antiviral activity against Coxsackievirus B36
A second life for the crystallographic structure of Berenil-dodecanucleotide complex: a computational revisitation thirty years after its publication6
New indolo-β-lactam hybrids as potential anticancer and anti-inflammatory agents6
Naturally occurring plant-derived sulfonated and sulfated saponins from 1983 to 20246
CO prodrugs: a new scaffold of adamantane-fused norbornen-7-ones with tunable water solubility6
Inactivation of ornithine aminotransferase by (1R,4S)-4-Amino-3-(trifluoromethyl)cyclopent-2-ene-1-carboxylic acid via a stable quinonoid intermediate6
Lenacapavir, a first-in-class, long-acting capsid inhibitor approved for both HIV-1 treatment and prevention6
New tetracyclic systems integrated thienopyridine scaffold as an anti-dementia lead: in silico study and biological screening6
Discovery and development of inhibitors of heat shock factor 1 by a fluorescence polarization assay6
CO as a potential therapeutic agent: an initial investigation of dosing and concentration dynamics in solution6
Synthesis, pharmacological and molecular docking investigations of 1,3,4-oxadiazole-5-thionyl derivatives of extracted cis-clerodane diterpenoid from Cistus monspeliensis6
SARS-CoV-2 3CL-protease inhibitors derived from ML300: investigation of P1 and replacements of the 1,2,3-benzotriazole6
Piperazine derivatives as anticancer agents: a medicinal chemistry review of structure, mechanism, and clinical translation6
Siderophore–Porphyrin conjugates for bacteria-selective antimicrobial photodynamic therapy6
Underpinning the role of natural products against cisplatin-induced nephrotoxicity in rodent models6
Bioassay-guided fractionations of Cannabis sativa extract and HPLC-assisted purifications of anti-proliferative active fractions lead to the isolation of 16 known and one new phytomolecule and their i6
Hybrid-based design and biological evaluation of quinoline-benzoylhydrazine based derivatives as α-glucosidase inhibitors6
Synthesis of simplified didehydro-cortistatin A derivatives as anti-proliferative agents6
Substituted furan-carboxamide and Schiff base derivatives as potential hypolipidemic compounds: evaluation in Triton WR-1339 hyperlipidemic rat model6
Design, synthesis and anti-tumor activity evaluation of 4,6,7-substitute quinazoline derivatives6
Harnessing the necessary nitrogen atom in chemical biology and drug discovery6
Research progress on antidiabetic activity of apigenin derivatives6
Esters and amides of benzofuroxan-1-N–oxide derivatives as trypanocidal and leishmanicidal agents6
Development of novel fluoro-substituted rivastigmine derivatives as selective AChE inhibitors for the treatment of AD6
Design and synthesis of novel cycloalkanecarboxamide parabanic acid hybrids as anticonvulsants6
Synthesis and anti-leishmanial activities of uniflorol analogues6
An in vitro and in silico α-amylase/α-glucosidase/protein tyrosine phosphatase 1 beta & radical scavenging profiling of the 3,5,7-tricarbo substituted 1H-indazoles6
Optimization of clofibrate with natural product sesamol for reducing liver injury induced by acetaminophen6
Promising Schiff bases in antiviral drug design and discovery6
Acyl glucuronides–mediators of drug-induced toxicities?5
Preliminary structure−activity relationships analysis on N-(3,5-dichlorophenyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-amine, a disruptor of mycobacterial energetics5
Design and synthesis of aminothiazole-benzazole based amide: antiproliferative, antimigration activity and molecular docking studies5
Evaluation of homodimer 99mTc-HYNIC-E(SSSLTVPWY)2 peptide on HER2-over expressed breast cancer cells5
Design and synthesis of O-glycoside derivatives with promising antidiabetic and anticancer potential5
Correction to: Structure-activity relationships and pharmacokinetic evaluation of L-cystine diamides as L-cystine crystallization inhibitors for cystinuria5
Investigation of the monoamine oxidase inhibition properties of benzoxathiolone derivatives5
Synthesis and evaluation of new 2-oxo-1,2-dihydroquinoline-3-carboxamides as potent inhibitors against acetylcholinesterase enzyme5
The anti-inflammatory effects of iridoid glycosides: a comprehensive review of mechanisms of action and structure-activity relationships5
Translational insights from species differences in the metabolism of triclosan5
Morpholinated curcuminoids against urinary bladder cancer cells: synthesis and anticancer evaluation5
Recent pharmacological insights about imidazole hybrids: a comprehensive review5
Discovery of novel fatty acid amide hydrolase (FAAH) inhibitors as anti-Alzheimer’s agents through pharmacophore-based virtual screening, molecular docking and experimental validation5
Flavonoids as colchicine binding site inhibitors: emerging scaffolds in anticancer drug design5
Thiophene ring-opening reactions. Part VII: synthesis and antitumor, anti-inflammatory, and antioxidant properties of 1,3,4‒thiadiazoline‒6-sulfanylthiopyran-4(1H)-one hybrids5
An update on the discovery and development of reversible covalent inhibitors5
Exploring nucleoside analogs: key targets in the viral life cycle - advancing strategies against SARS-CoV-25
The emergence of sulfo-click amidation in kinetic target-guided synthesis5
Withania coagulans: a comprehensive exploration of its botanical, phytochemical, and pharmacological properties5
Correction: Substituted furan-carboxamide and Schiff base derivatives as potential hypolipidemic compounds: evaluation in Triton WR-1339 hyperlipidemic rat model5
The mechanism of resistance in Escherichia coli to ridinilazole and other antibacterial head-to-head bis-benzimidazole compounds5
Phytochemical constituents isolated from Silene popovii Schischk5
Insights into the α-amylase and α-glucosidase inhibition mechanism of 4-(4-hydroxyphenyl)-but-3-en-2-one from Scutellaria barbata D. Don: enzymatic kinetics, fluorescence spectroscopy and computationa5
Synthesis, biological evaluation, and molecular modeling studies of a new series of imidazothiazole or imidazooxazole derivatives as inhibitors of ectonucleoside triphosphate diphosphohydrolases (NTPD5
Glutathione transferases in cats and dogs: diversity, structure, and function5
4-methylbenzyl 5-arylthiophene-2-carboxylates as Multitarget Directed Ligands Scaffolds (MTDLs): Synthesis, in-silico docking studies, and evaluation of dual selective enzymatic inhibition (AChE &5
Novel Benzo[4,5]imidazo[1,2-a]pyrimidine derivatives as selective Cyclooxygenase-2 Inhibitors: Design, synthesis, docking studies, and biological evaluation5
Design, synthesis, and fungicidal activity of pyrimidinamine derivatives containing pyridin-2-yloxy moiety5
α-Glucosidase and cholinesterase inhibiting potential of a series of semisynthetic nitrogen triterpenic derivatives4
From the ethnomedicinal plants in northern Indochina to the development of novel anti-cancer therapeutic agents4
Cyclohepta[b]pyran: an important scaffold in biologically active natural products4
Investigating novel tubulin polymerization inhibitors: design, synthesis, LC/MS cellular permeability, in silico studies, and in vitro assessment4
Facile access to novel furoyl-based amide retroisoster inhibitors of LuxR-regulated quorum sensing: conformation analysis and docking studies4
Current updates on EGFR and HER2 tyrosine kinase inhibitors for the breast cancer4
A novel class of indole derivatives: enhanced bioavailability, permeability, and antioxidant efficacy for thromboembolic disease therapy4
Design, synthesis and antitumor activity evaluation of 4,6,7-trisubstituted quinazoline derivatives containing benzothiazole moiety4
Recent updates on thienopyrimidine derivatives as anticancer agents4
Synthesis, cytotoxicity, Pan-HDAC inhibitory activity and docking study of new N-(2-aminophenyl)-2-methylquinoline-4-carboxamide and (E)-N-(2-aminophenyl)-2-styrylquinoline-4-carboxamide derivatives a4
Iron porphyrin-mediated production of carbon monoxide from phenylpyruvic acid: from potential therapeutic and diagnostic use to physiological implications4
Design, synthesis and antifungal study of novel 2-aryl-3,4-dihydroisoquinolin-2-ium salts containing benzoate moieties4
Design & synthesis of hybrid pharmacophore of β-lactam, 1,8-naphthyridine, and secondary amines; Discover their in vitro antimicrobial, anticancer properties & DFT and ADMET prediction studies4
Current CMC challenges in oligonucleotide API development: from IND to NDA4
Design, synthesis and assay of 2-(4-phenylpiperazin-1-yl)pyrimidine-5- carboxamide derivatives as acetylcholinesterase inhibitors4
Unveiling the potential of prodrug and drug-conjugate strategies in treatment of diabetes mellitus and its complications4
Potential effect of novel thiadiazole derivatives against radiation induced inflammation with low cardiovascular risk in rats4
SAR exploration for 4-aminotetrahydroquinazolines with adamantyl moiety against orthoflaviviruses4
Gallic acid derived diarylpropanones exhibit synergistic antibacterial activities4
Nafithromycin (MIQNAF®): ultramodern lactone ketolide designed to treat community acquired bacterial pneumonia (CABP)4
Recent advances in piperidones as privileged scaffolds for drug discovery and development4
Design, synthesis and antitumor activity study of tubulin/HDAC6 dual targeting inhibitor4
Discovery of pyrrolo[2,1-f][1,2,4]triazine-based inhibitors of adaptor protein 2-associated kinase 1 for the treatment of pain4
Exploring the potential of isatin hybrids as anticancer agents: recent advances and future prospective4
From lipophilicity windows to decision-grade antibacterial design: the next translational step for coumarin amphiphiles4
Position switch of phenylthiazoles: novel compounds with promising anti-MRSA USA3004
Future challenges and opportunities with fluorine in drugs?4
Vital residues-orientated rational design of butenolide inhibitors targeting Of ChtI4
Synthesis, urease inhibitory and anticancer evaluation of glucosamine-sulfonylurea conjugates4
Design, synthesis and antiproliferative activity of ACY-1215 analogs as potent selective histone deacetylases 6 inhibitors4
Garcidepsidone B from Garcinia parvifolia: antimicrobial activities of the medicinal plants from East and North Kalimantan against dental caries and periodontal disease pathogen4
Design and synthesis of novel factor XIa Inhibitors with bicyclic isoquinoline and naphthalene fragments4
Identification and evaluation of potent AAK1 inhibitors through structure-based pharmacophores, virtual screening and bioassay screening4
Phenoxyalkyl cyclic and acyclic amine derivatives: what do they teach us about scaffold-based drug design?4
Triphenylphosphonium (TPP) conjugates of 1,2,3-triazolyl nucleoside analogues. Synthesis, cytotoxicity and antimicrobial activity4
Targeting MDM2 for the development of a new cancer therapy: progress and challenges4
Correction: Bioassay-guided fractionations of Cannabis sativa extract and HPLC-assisted purifications of anti-proliferative active fractions lead to the isolation of 16 known and one new phytomolecule4
Correction: Anticancer therapeutic potential of silibinin: current trends, scope and relevance4
Structure-based optimization of aminothiadiazole inhibitors of AKT4
Pharmacodynamic material basis investigations of the crude and processed Radix et Rhizoma Rhei by the immobilized β2-adrenoceptor chromatography4
The history, mechanism, and perspectives of nirmatrelvir (PF-07321332): an orally bioavailable main protease inhibitor used in combination with ritonavir to reduce COVID-19-related hospitalizations4
Biocatalytic potential of microbial CYP450s in the degradation of selected environmental pollutants4
Design, synthesis and profiling of proteolysis-targeting chimeras (PROTACs) as CDK4/6 degraders4
Development and evaluation of mitochondria-targeted caseinolytic protease (ClpP) agonist chemical probes in in vitro breast cancer models4
Integrating omics data for personalized medicine in treating psoriasis4
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