Medicinal Chemistry Research

Papers
(The median citation count of Medicinal Chemistry Research is 1. 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 2021-02-01 to 2025-02-01.)
ArticleCitations
Ultra-performance liquid chromatography coupled with quadrupole high-resolution time-of-flight mass spectrometry for metabolite profiling and biological activity of Stellaria pallida (Dumort) Piré75
Novel pyran derivatives as potential succinate dehydrogenase inhibitors: design, synthesis, crystal structure, biological activity, and molecular modeling74
Position switch of phenylthiazoles: novel compounds with promising anti-MRSA USA30065
Development of novel 2-acetylphenol-O-alkylhydroxyethylamine derivatives as multifunctional agents for Alzheimer’s disease treatment49
Special issue of Medicinal Chemistry Research in honor of Dr. Nicholas A. Meanwell41
Design, synthesis, and biological evaluation of catalpalactone and its analogs36
Social environment during fear extinction alters the binding of [3H] MK-801 to N-methyl-D-aspartic acid receptors in Wistar-Kyoto and Wistar rats35
Synthesis and antitumor activity evaluation in vitro of 4-aminoquinazoline derivatives containing 1,3,4-thiadiazole33
Novel potent and highly selective DDR1 inhibitors from integrated lead finding31
Structural optimization and biological evaluation of quinoline/naphthalene-based glyoxalase-I inhibitors as anti-cancer candidates28
Synthesis and evaluation of 2-methylbenzothiazole derivatives as monoamine oxidase inhibitors26
A review of trilaciclib, a first-in-class cyclin-dependent kinase 4/6 inhibitor, for the management of metastatic small-cell lung cancer26
The HBV capsid modulators derived from sulfamoylbenzamides and benzamides: an overview of the progress of patents25
Synthesis and antiproliferative activity of hybrid thiosemicarbazone derivatives bearing coumarin and d-galactose moieties with EGFR inhibitory activity and molecular docking study25
Engelheptanoxides behave as liver X receptor α agonists25
The emerging role of proteolysis targeting chimeras (PROTACs) in the treatment of Alzheimer’s disease24
Synthesis, and docking studies of arylhydrazone compounds and evaluation of their platelet aggregation inhibitory effect and cytotoxicity23
Discovery of novel donepezil-M30D hybrids with neuroprotective properties for Alzheimer’s disease treatment23
Evaluation of antibacterial, antioxidant, cytotoxic, and acetylcholinesterase inhibition activities of novel [1,4] benzoxazepines fused to heterocyclic systems with a molecular modeling study23
Antimicrobial activity of some celastroloids and their derivatives21
Quinoxaline 1,4-di-N-oxides: a review of the importance of their structure in the development of drugs against infectious diseases and cancer21
Synthesis and biological evaluation of novel 1,3-diphenylurea quinoxaline derivatives as potent anticancer agents20
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 m18
Synthesis of adamantane-monoterpene conjugates with 1,3,4-thiadiazol-2(3H)-imine linker and evaluation of their inhibitory activity against TDP118
Design and synthesis of ludartin derivatives as potential anticancer agents against hepatocellular carcinoma18
Carboxamide appended quinoline moieties as potential anti-proliferative agents, apoptotic inducers and Pim-1 kinase inhibitors18
Unlocking therapeutic potential: exploring indole scaffolds and their structural insights as pharmacophores in designing anti-breast cancer agents18
Molecular glues: enhanced protein-protein interactions and cell proteome editing17
Design, synthesis, and evaluation of potential carbamate prodrugs of 5′-methylthioadenosine (MTA)17
DNA sequence-specific ligands. XX. Synthesis, spectral properties, virological and biochemical studies of fluorescent dimeric trisbenzimidazoles DB3P(n)16
Synthesis and biological evaluation of xanthone derivatives as anti-cancer agents targeting topoisomerase II and DNA16
Increased rigidity and bioisosteric replacement in the design, synthesis and preliminary evaluation of novel, functionalized 3,3-dialkyl-γ-butyrolactones as sigma-2 ligands16
Computer-aided design, synthesis and evaluation of new SARS-CoV-2 Mpro inhibitors based on 1,5,6,7-tetrahydro-4H-indazol-4-one scaffold16
Self-assembled amphiphilic bipyridine and bisquinoline cisplatin analogues: synthesis and anticancer properties16
Synthesis, structure-activity relationship studies and evaluation of a TLR 3/8/9 agonist and its analogues15
Novel imino-thiazoloquinoxaline derivatives against renal cell carcinoma: less radiation-damaging approach15
4-Phenylcoumarins from Mesua ferrea with selective CYP1B1 inhibitory activity15
Synthesis of berberine derivatives and their antiviral activity toward respiratory syncytial virus15
Synthesis of 2-oxoquinoline derivatives as dual pim and mTORC protein kinase inhibitors14
2,3-Diketopiperazine as potential scaffold to develop new anti-Chagasic agents13
Plastoquinone analogs: a potential antimicrobial lead structure intensely suppressing Staphylococcus epidermidis and Candida albicans growth13
Synthesis of alkoxy-isoflavones as potential α-glucosidase inhibitors13
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 a13
Synthesis and evaluation of mycophenolic acid derivatives as potential anti-Toxoplasma gondii agents12
Synthesis, urease inhibitory and anticancer evaluation of glucosamine-sulfonylurea conjugates12
Acetylcholinesterase inhibition, molecular docking and ADME prediction studies of new dihydrofuran-piperazine hybrid compounds12
Synthesis and biological evaluation of (20S,24R)-epoxy-dammarane-3β,12β,25-triol derivatives as α-glucosidase and PTP1B inhibitors12
Garcidepsidone B from Garcinia parvifolia: antimicrobial activities of the medicinal plants from East and North Kalimantan against dental caries and periodontal disease pathogen12
Ellagic acid (EA), a tannin was isolated from Eucalyptus citriodora leaves and its anti-inflammatory activity12
Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment11
Ronald T. Borchardt: a pioneer in drug discovery and development11
A novel class of indole derivatives: enhanced bioavailability, permeability, and antioxidant efficacy for thromboembolic disease therapy11
Role of the Caco-2 cell culture model developed in Dr. Ronald T. Borchardt’s lab in modern drug research and development: a perspective from a practitioner11
Bexagliflozin: a comprehensive review of a recently approved SGLT2 inhibitor for the treatment of type 2 diabetes mellitus11
Sulfur (VI) fluoride exchange (SuFEx): a versatile tool to profile protein-biomolecule interactions for therapeutic development11
Design, synthesis and antitumor activity evaluation of 4,6,7-trisubstituted quinazoline derivatives containing benzothiazole moiety10
Design, synthesis and antitumor activity evaluation of novel benzamide HDAC inhibitors10
In vitro antiproliferative activity of Parrotia persica exclusive gallotannin10
Development of novel chalcone derivatives as multifunctional agents for the treatment of Alzheimer’s disease10
Discovery of cytotoxic truncated vitamin D derivatives against both bortezomib‐sensitive and bortezomib‐resistant multiple myeloma phenotypes10
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 studies10
Structural simplification and ester bond flipping lead to bis-benzodioxole derivatives as potential hypolipidemic and hepatoprotective agent10
Design, synthesis and biological evaluation of novel 2,4,6-trisubstituted quinazoline derivatives as potential antitumor agents10
Tetra-substituted pyrazole analogues: synthesis, molecular docking, ADMET prediction, antioxidant and pancreatic lipase inhibitory activities9
Design, synthesis, and antitumor activity evaluation of carbazole derivatives with potent HDAC inhibitory activity9
Synthesis, anticancer evaluation and docking studies of novel adamantanyl-1,3,4-oxadiazol hybrid compounds as Aurora-A kinase inhibitors9
Synthesis, in vitro and in silico enzymatic inhibition assays, and toxicity evaluations of new 4,5-diphenylimidazole-N-phenylacetamide derivatives as potent α-glucosidase inhibitors9
Synthesis of 6-dialkylaminopyrimidine carboxamide analogues and their anti-tubercular properties9
Design and synthesis of indole-based elipticine analogues as topoisomerase IIβ inhibitors9
Antibacterial, antifungal activities and toxicity of new synthetic fatty acid salicylate esters9
N-Benzyl, N-phenethyl and N-benzyloxybenzamide derivatives inhibit amyloid-beta (Aβ42) aggregation and mitigate Aβ42-induced neurotoxicity9
Synthesis, biological evaluation, and bioinformatics analysis of indole analogs on AChE and GST activities9
Dual inhibition strategy addressing hyperuricemia and oxidative stress: design, biological evaluation and stability studies of febuxostat-probenecid mutual prodrug9
A very promising antibiofilm activity against Candida albicans from an in vitro screening for antimicrobial, antibiofilm and antiproliferative activity of new synthesized 4-cinnamamido- and 2-phenoxya9
Synthesis, characterization and biological evaluation of Bis-benzimidazolium salts and their silver(I)-N-heterocyclic carbene complexes9
Asciminib: first FDA approved allosteric inhibitor of BCR-ABL1 for the treatment of chronic myeloid leukemia9
Pyridazinones containing the (4-methoxyphenyl)piperazine moiety as AChE/BChE inhibitors: design, synthesis, in silico and biological evaluation8
Synthesis, cytotoxicities, and carbonic anhydrase inhibition activities of pyrazoline–benzenesulfonamide derivatives harboring phenol/polyphenol moieties8
Design, synthesis and anti-breast cancer properties of butyric ester tethered dihydroartemisinin-isatin hybrids8
Synthesis, structure-activity relationship and evaluation of antifungal activity of tryptanthrin derivatives against drug-resistant Candida albicans8
FTase inhibitors and cancer: prospects for use in targeted therapies8
Design, synthesis, antibacterial evaluation and molecular docking studies of novel pyrazole/1,2,4-oxadiazole conjugate ester derivatives8
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 antic8
Glutathione and glutathione disulfide – their biomedical and pharmaceutical applications8
Design, synthesis and biological evaluation of potent thiazolidinedione salicylic acid inhibitors against glyoxalase-I as potential anticancer agents8
Design, synthesis and anticancer activity studies of novel indole derivatives as Bcl-2/Mcl-1 dual inhibitors8
Targeting disease with benzoxazoles: a comprehensive review of recent developments8
Synthesis, structural characterization and antimycobacterial evaluation of several halogenated non-nitro benzothiazinones8
Synthesis and in vitro activity of oleanolic acid derivatives against Chlamydia trachomatis and Staphylococcus aureus8
Structure activity relationship (SAR) driven design and discovery of WCK 5107 (Zidebactam): novel β-lactam enhancer, potent against multidrug-resistant gram-negative pathogens8
Extraction and purification, pharmacological action, synthesis and product development of salidroside: a review8
Drug repositioning of benzimidazole anthelmintics in the treatment of cryptococcosis: a review8
Synthesis of the dibenzylbutane lignan LCA derivatives and evaluation of their anti-inflammatory activities7
Monoamine oxidase inhibition by thiazole derivatives substituted with the benzenesulfonamide moiety7
Development of novel triconjugates fusing melatonin/isatin/N-acylhydrazone targeting colorectal cancer: design, synthesis, biological, and in silico ADME/Tox profiling7
Design, synthesis, in vitro determination and molecular docking studies of 4-(1-(tert-butyl)-3-phenyl-1H-pyrazol-4-yl) pyridine derivatives with terminal sulfonamide derivatives in LPS-induced RAW264.7
Design, synthesis, and biological evaluation of 2, 4-dichlorophenoxyacetamide chalcone hybrids as potential c-Met kinase inhibitors7
Diverse therapeutic potential of 3-hydroxy-4-pyranones and related compounds as kojic acid analogs7
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 study7
Novel MreB inhibitors with antibacterial activity against Gram (-) bacteria7
Triphenylphosphonium (TPP) conjugates of 1,2,3-triazolyl nucleoside analogues. Synthesis, cytotoxicity and antimicrobial activity7
Synthesis of hydrazine containing piperazine or benzimidazole derivatives and their potential as α-amylase inhibitors by molecular docking, inhibition kinetics and in vitro cytotoxicity activity studi7
Identification and evaluation of natural organosulfur compounds as potential dual inhibitors of α-amylase and α-glucosidase activity: an in-silico and in-vitro approach7
Lewis base-catalyzed synthesis of highly functionalized spirooxindole-pyranopyrazoles and their in vitro anticancer studies7
Synthesis and anti-inflammatory activity of chromone-sulfonamide derivatives as COXs/iNOS dual-target inhibitors7
Recent insights into antibacterial potential of benzothiazole derivatives7
2-Phenyl substituted Benzimidazole derivatives: Design, synthesis, and evaluation of their antiproliferative and antimicrobial activities7
Correction to: Design, synthesis and SAR of novel sulfonylurea derivatives for the treatment of diabetes mellitus in rats6
The versatile NDI-based compounds: emerging anticancer and antimicrobial agents6
Structural and stereochemical determinants for hGAT3 inhibition: development of novel conformationally constrained and substituted analogs of (S)-isoserine6
Dedication to Dr. Thomas Baillie in recognition of his scientific career6
Synthesis and antiproliferative activity of 7-substituted amide estradiol derivatives6
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 phytomolecule6
Ethical aspects of innovative medical and medicinal sciences6
Design, synthesis, in vitro evaluation, and molecular dynamics simulation studies of novel coumarin-acetohydrazide Schiff base derivatives as urease enzyme inhibitors6
Utilizing mechanistic organic chemistry training to study drug metabolism in preclinical drug discovery/development6
Correction: Structural and stereochemical determinants for hGAT3 inhibition: development of novel conformationally constrained and substituted analogs of (S)-isoserine6
Novel biologically active pyridine derivatives: Synthesis, structure characterization, in vitro antimicrobial evaluation and structure-activity relationship6
Design, synthesis and antifungal study of novel 2-aryl-3,4-dihydroisoquinolin-2-ium salts containing benzoate moieties6
Characterization of Allium tuberosum Rottl. peptides with dual inhibitory activities against angiotensin I converting enzyme and dipeptidyl peptidase-IV6
Novel antimicrobial ciprofloxacin-pyridinium quaternary ammonium salts with improved physicochemical properties and DNA gyrase inhibitory activity5
Exploring the latest breakthroughs in rhodesain inhibitors for African trypanosomiasis5
Dauricine: a review of natural observation, pharmacology, and pharmacokinetics5
Synthesis and antiviral property of polysulfate-grafted maleimide-based enediynes5
Advances in research of ursolic acid and its derivatives as potential drug candidates against various types of lung cancers5
Design, synthesis and biological evaluation of aminopyrimidine derivatives bearing dihydroquinoxalinone as novel EGFRL858R/T790M kinase inhibitors against non-small-cell lung cancer5
Design, synthesis and evaluation of imidazo[1,2-a]pyrazin-8(7H)-one derivatives as acetylcholinesterase inhibitors and antioxidants5
Natural products and their derivatives as anti-flavivirus drug candidates5
Structural classification of EZH2 inhibitors and prospects for the treatment of tumor: a review5
Synthesis and potential antimicrobial activity of novel α-aminophosphonates derivatives bearing substituted quinoline or quinolone and thiazole moieties5
Evaluation of benzoylacetonitriles as novel anti-neuroinflammatory agents5
Synthesis and biological evaluation of pyrrolidine-functionalized nucleoside analogs5
Discovery and exploration of monosaccharide linked dimers of galectin-3 inhibitors to target fibrosis5
Identification of novel benzoyl hydrazine derivatives as activators of neddylation pathway to inhibit the tumor progression in vitro5
Synthesis of 2-amino-4H-chromenes catalyst-free via sequential Knoevenagel-Michael reaction and evaluation of biological activity in tumor cells5
Ester tethered artemisinin-isatin hybrids: design, synthesis and anti-leukemic activity evaluation5
Structure-based discovery of new polo-like kinase 1 (PLK1) inhibitors as potential anticancer agents via docking-based comparative intermolecular contacts analysis (dbCICA)5
A reliable and automated synthesis of 6-[18F]fluoro-L-DOPA and the clinical application on the imaging of congenital hyperinsulinism of infants5
α-Glucosidase and cholinesterase inhibiting potential of a series of semisynthetic nitrogen triterpenic derivatives4
A versatile strategy for the synthesis of various lumazine peptides4
Design, synthesis, and in vitro biological evaluation of novel HDAC inhibitors bearing C-1 phenyl substituted tetrahydroisoquinoline Cap moiety as anti-tumor therapeutic agents4
Microwave-assisted synthesis and evaluation of their antiproliferative, antimicrobial, activities and DNA Binding studies of (3-Methyl-7H-furo[2,3-f]chromen-2-yl)(aryl)methanones4
Design, Synthesis, and biological evaluation of pyrazolo-benzothiazole derivatives as a potential therapeutic agent for the treatment of Alzheimer’s disease4
Indazole derivatives as selective inhibitors of butyrylcholinesterase with effective blood-brain-barrier permeability profile4
Research progress on antidiabetic activity of apigenin derivatives4
Screening of small molecule compounds targeting hnRNPA2 protein4
Development of ketoprofen-p-aminobenzoic acid co-crystal: formulation, characterization, optimization, and evaluation4
Design, synthesis and biological evaluation of indoline derivatives as multifunctional agents for the treatment of ischemic stroke4
Development of LC-MS/MS methods affording identification and measurement of active metabolites in rat and dog plasma after oral dosing of a penta-ethyl ester prodrug of diethylenetriamine pentaacetic 4
Tetrahydroquinoline/4,5-dihydroisoxazole hybrids with a remarkable effect over mitochondrial bioenergetic metabolism on melanoma cell line B16F104
Phthalamide derivatives as ACE/AChE/BuChE inhibitors against cardiac hypertrophy: an in silico, in vitro, and in vivo modeling approach4
Design, synthesis and antitumor activity evaluation of pyrimidine derivatives containing 4-hydroxypiperidine group4
From the ethnomedicinal plants in northern Indochina to the development of novel anti-cancer therapeutic agents4
Discovery of novel neuroprotective cinnamoyl-M30D hybrids targeting Alzheimer’s disease4
Design, synthesis, and antimicrobial evaluation of novel 10-Undecenoic acid-based lipidic triazoles4
Synthesis of tetrahydro-β-carboline analogs with N11 modifications and study of their antimalarial activities4
Identification of α-mangostin as a potent inhibitor of β-lactamase OXA-484
New tetracyclic systems integrated thienopyridine scaffold as an anti-dementia lead: in silico study and biological screening4
Synthesis and antitumor activity of novel silibinin and 2,3-dehydrosilybin derivatives with carbamate groups4
Inhibition of jack bean urease by amphiphilic peptides4
Semi-synthesis of novel thebaine derivatives with low cytotoxicity and their antibacterial and antihemolytic properties4
Design, synthesis, and anticancer activities of 8,9-substituted Luotonin A analogs as novel topoisomerase I inhibitors4
Evaluation of chemical constituents of Rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia) as adenosine A1/A2A receptor ligands4
Rational design and development of novel NAE inhibitors for the treatment of pancreatic cancer4
2-substituted 4-aminoquinazoline derivatives as potential dual inhibitors of EGFR and HER2: an in silico and in vitro study4
Mannose: a potential saccharide candidate in disease management4
2-Styrylchromones as inhibitors of α-amylase and α-glucosidase enzymes for the management of type 2 diabetes mellitus4
Harnessing the necessary nitrogen atom in chemical biology and drug discovery4
Glycosylated triptolide affords a potent in vivo therapeutic activity to hepatocellular carcinoma in mouse model4
Naturally occurring organosulfur for treating metabolic disorders and infectious diseases4
Study on synthesis and anticancer activity of 17beta-estradiol-phenol/aniline nitrogen mustard derivatives4
Inhibition of protein kinases by proton pump inhibitors: computational screening and in vitro evaluation4
Pyrrolo[2,1-f][1,2,4]triazine: a promising fused heterocycle to target kinases in cancer therapy4
Design, synthesis, and biological evaluation of pyrimidine analogs as SecA inhibitors4
Invalidation of dieckol and 1,2,3,4,6-pentagalloylglucose (PGG) as SARS-CoV-2 main protease inhibitors and the discovery of PGG as a papain-like protease inhibitor4
Synthesis and antitumor activity of novel pyridoxine-based structural analogs of saccharumoside-B4
Novel Curcumin Monocarbonyl Analogue-Dithiocarbamate hybrid molecules target human DNA ligase I and show improved activity against colon cancer4
Integrating omics data for personalized medicine in treating psoriasis3
Strong in vitro and in vivo cytotoxic effects of two platinum(II) complexes with cryptolepine derivatives3
Chemical composition and vasodilator activity of different Alpinia zerumbet leaf extracts, a potential source of bioactive flavonoids3
Medicinal uses, phytochemistry, pharmacology, and taxonomy of Poygonum aviculare L.: a comprehensive review3
Facile access to novel furoyl-based amide retroisoster inhibitors of LuxR-regulated quorum sensing: conformation analysis and docking studies3
Gallic acid derived diarylpropanones exhibit synergistic antibacterial activities3
Anticancer and antimicrobial activities of new thiazolyl-urea derivatives: gene expression, DNA damage, DNA fragmentation and SAR studies3
Cyclohepta[b]pyran: an important scaffold in biologically active natural products3
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 measurements3
What’s been Hapten-ing over the last 88 years?3
Benzothiazole derivatives as effective α-glucosidase inhibitors: an insight study of structure-activity relationships and molecular targets3
Bioassay-guided isolation and identification of anti-Alzheimer’s active compounds from Spiranthes sinensis (Pers.) Ames3
Design, synthesis, and biological evaluation of novel 2-acetylphenol-rivastigmine hybrids as potential multifunctional agents for the treatment of Alzheimer’s disease3
Enantioselectivity of pinene against Leishmania amazonensis3
Pyrrolobenzodiazepines: natural sources, therapeutic uses, and future in neurological treatments3
Synthesis, bacterial and fungal inhibition assay, molecular docking study of substituted isatin (N-substituted 1,2,3,4-tetra-O-acetyl-β-glucopyranosyl)thiosemicarbazones3
Design, synthesis, molecular docking study and molecular dynamics simulation of new coumarin-pyrimidine hybrid compounds having anticancer and antidiabetic activity3
Synthesis and characterization of new tetrakisphosphonic acid derivatives as FPPS inhibitors and evaluation of their anti-osteoclastogenic potential for prevention of osteoporosis3
Synthesis, inhibition effects, molecular docking and theoretical studies as Paraoxonase 1 (PON1) inhibitors of novel 1,4-dihydropyridine substituted sulfonamide derivatives3
Review: Chemical and biological features of genus Paralemnalia soft corals3
Synthesis and biological evaluations of novel pyrazinoic acid derivatives as anticancer agents3
Design, synthesis and investigating the in vitro and in silico HDAC8 inhibitory activities of derivatives of [6]-shogaol and [6]-gingerol isolated from ginger (Zingiber officinale)3
Recent advances in triazole-benzenesulfonamide hybrids and their biological activities3
Design and synthesis of novel factor XIa Inhibitors with bicyclic isoquinoline and naphthalene fragments3
Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant S. aureus3
Pyrrolidine-based cationic γ-peptide: a DNA-binding molecule works as a potent anti-gene agent3
Sulfonamide derivatives of cis-imidazolines as potent p53-MDM2/MDMX protein-protein interaction inhibitors3
Contrasting effect of different crowding agents on pseudoknot RNA stability3
New class of hybrids based on chalcone and melatonin: a promising therapeutic option for the treatment of colorectal cancer3
Synthesis and biological activity of amide derivatives derived from natural product Waltherione F3
The trimethoxyphenyl (TMP) functional group: a versatile pharmacophore3
Semi-synthesis and cytotoxicity evaluation of pyrimidine, thiazole, and indole analogues of argentatins A–C from guayule (Parthenium argentatum) resin3
Design and synthesis of new 1,4,5-trisubstituted triazole-bearing benzenesulphonamide moiety as selective COX-2 inhibitors3
Design and synthesis of diphenyl-1H-imidazole analogs targeting Mpro/3CLpro enzyme of SARS-CoV-23
Design, synthesis and assay of 2-(4-phenylpiperazin-1-yl)pyrimidine-5- carboxamide derivatives as acetylcholinesterase inhibitors3
Potential effect of novel thiadiazole derivatives against radiation induced inflammation with low cardiovascular risk in rats3
Synthesis, trypanocidal and cytotoxic activities of α,β-unsaturated ketones derived from eugenol and analogues3
Synthesis of nitrogen-containing oleanolic acid derivatives as carbonic anhydrase and acetylcholinesterase inhibitors3
Synthesis and in vitro antiproliferative evaluation of novel drimane oxepinyl triazoles from labdane diterpene sclareol3
Synthesis, antibacterial evaluation and in silico study of DOTA-fluoroquinolone derivatives3
Synthesis and anticancer activity of novel hydrazone linkage-based aryl sulfonate derivatives as apoptosis inducers3
Novel fluorinated pyrazole-based heterocycles scaffold: cytotoxicity, in silico studies and molecular modelling targeting double mutant EGFR L858R/T790M as antiproliferative and apoptotic agents3
Unveiling the potential of prodrug and drug-conjugate strategies in treatment of diabetes mellitus and its complications3
Translating G-quadruplex ligands from bench to bedside: a Stephen Neidle’s legacy3
Synthesis, pharmacological and molecular docking investigations of 1,3,4-oxadiazole-5-thionyl derivatives of extracted cis-clerodane diterpenoid from Cistus monspeliensis3
Phenylpropanoids from Liparis nervosa and their in vitro antioxidant and α-glucosidase inhibitory activities3
Loading harmine on nanographene changes the inhibitory effects of free harmine against MCF-7 and fibroblast cells3
Clerodendrum viscosum: a critical review on phytochemistry, pharmacology, quality assurance, and safety data3
The past decade of Genentech experience in elucidation of novel reaction mechanisms in drug metabolism3
Different barbiturate derivatives linked to aryl hydrazone moieties as urease inhibitors; design, synthesis, urease inhibitory evaluations, and molecular dynamic simulations3
Synthesis and biological evaluation of chromone derivatives against triple-negative breast cancer cells3
ATP-hydrolyzing, DNA-damaging and cytotoxic activities of peptide-targeted cobalt(III) complex with diethylentriamine3
Design, synthesis and antiproliferative activity of ACY-1215 analogs as potent selective histone deacetylases 6 inhibitors3
Effect of a hexacyclic triterpenic acid from Euscaphis japonica on the oleic acid induced HepG2 cellular model of non-alcoholic fatty liver disease3
Novel monastrol/melatonin hybrids as a new approach for colorectal cancer intervention: design, synthesis, biological activity, and drug-likeness modeling studies2
A vitamin D C/D ring-derived compound with cytotoxicity2
Design and synthesis of novel pyrazolopyrimidine-based derivatives as reversible BTK inhibitors with potent antiproliferative activity in mantle cell lymphoma2
Discovery of HNPC-A188: a novel acaricide containing trifluoroethyl thioether and pyrimidin-4-amine2
Synthesis and analgesic potential of 4-[4–chloro-3- (trifluoromethyl)-phenyl]-4-piperidinol analogues against pain model in mice2
Clathrolides A–B: previously undescribed macrocylic lactones from marine demosponge Clathria (Thalysias) vulpina (Lamarck, 1814) as potential antihypertensive leads attenuating angiotensin converting 2
Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1,2,4-triazoles: their structure-activity relationship and SwissADME predictions2
Novel 2-[(8-hydroxyquinolin-7-yl)(phenyl)methylamino]benzoic acid analogs targeting the active site of botulinum neurotoxins: designing, synthesis, and biological evaluation2
Design, synthesis, antiproliferative and antimicrobial evaluation of a new class of disulfides containing 1,3,4-thiadiazole units2
Candida albicans ergosterol disorders as a consequence of the new sulfone derivative action mode2
Characterization of the CO release properties of a common CO donor, CORM-401, in the context of its application in studying CO biology2
Exploring the potential of chromone scaffold compounds in cancer therapy: targeting key kinase pathways2
Identification of potential natural product derivatives as CK2 inhibitors based on GA-MLR QSAR modeling, synthesis and biological evaluation2
Design, synthesis, biological evaluation and in silico studies of EGFR inhibitors based on 4-oxo-chromane scaffold targeting resistance in non-small cell lung cancer (NSCLC)2
Dual HDAC–BRD4 inhibitors endowed with antitumor and antihyperalgesic activity2
A new cadinane sesquiterpenoid from Eupatorium adenophorum and α-glycosidase and AChE inhibitory activities of a gossypetin acylglucoside2
Innovation in the discovery of the HIV-1 attachment inhibitor temsavir and its phosphonooxymethyl prodrug fostemsavir2
Phosphoryl prodrugs: characteristics to improve drug development2
Synthesis, in vitro and in silico enzyme (COX-1/2 & LOX-5), free radical scavenging and cytotoxicity profiling of the 2,4-dicarbo substituted quinazoline 3-oxides2
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