Bioorganic Chemistry

Papers
(The TQCC of Bioorganic Chemistry is 9. 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
Water-soluble pillar[5]arene sulfo-derivatives self-assemble into biocompatible nanosystems to stabilize therapeutic proteins218
(±)-Caryopterisines A and B, dimeric monoterpene alkaloids with unprecedented 6/5/5/5/6 pentacyclic rings scaffold from Caryopteris glutinosa157
FPR2-based anti-inflammatory and anti-lipogenesis activities of novel meroterpenoid dimers from Ganoderma93
Recent advancements in the quest of benzazoles as anti-Mycobacterium tuberculosis agents90
Design, synthesis, and biological evaluation of novel thiourea derivatives as small molecule inhibitors for prostate specific membrane antigen86
Exploration of triazole derivatives, SAR profiles, and clinical pipeline against Mycobacterium tuberculosis84
Design, synthesis, and biological evaluation of novel FGFR1 PROTACs84
Synthesis and biological evaluation of 4-((3-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-4-yl)oxy)quinoline derivatives as novel potential transforming growth factor-β type 1 receptor inhibitors for hepatoc82
Heterologous expression of calcium-independent mesophilic α-amylase from Priestia megaterium: Immobilization on genipin-modified multi-walled carbon nanotubes and silica supports to enhance thermostab75
Triazole derivatives inhibit the VOR complex-mediated nuclear transport of extracellular particles: Potential application in cancer and HIV-1 infection71
Development and therapeutic potential of DNA-dependent protein kinase inhibitors70
Nicotinonitrile-derived apoptotic inducers: Design, synthesis, X-ray crystal structure and Pim kinase inhibition66
Impact of sulfur substitution on biotin binding affinity to streptavidin66
Development of new chiral 1,2,4-triazole-3-thiones and 1,3,4-thiadiazoles with promising in vivo anticonvulsant activity targeting GABAergic system and voltage-gated sodium channels (VGSCs)65
Aromatase inhibitors for the treatment of breast cancer: An overview (2019–2023)63
Design and synthesis of new 2-oxoquinoxalinyl-1,2,4-triazoles as antitumor VEGFR-2 inhibitors61
Mahanimbine isolated from Murraya koenigii inhibits P-glycoprotein involved in lung cancer chemoresistance61
Synthesis of indole-based-thiadiazole derivatives as a potent inhibitor of α-glucosidase enzyme along with in silico study60
Structural characteristics of a low molecular weight velvet antler protein and the anti-tumor activity on S180 tumor-bearing mice60
Discovery of novel dihydropyrazole-stilbene derivatives for ameliorating heart failure through modulation of p38/NF-κB signaling pathway60
SAR study of oxidative DIMs analogs targeting the Nur77-mediated apoptotic pathway of cancer cells59
Multi-component forms of the 2nd generation H1 receptor antagonist drug, Bilastine and its enhanced physicochemical characteristics59
Advancements in folate receptor targeting for anti-cancer therapy: A small molecule-drug conjugate approach57
Recent developments of P-glycoprotein inhibitors and its structure–activity relationship (SAR) studies57
Cholinesterase inhibitors assessment of aporphine alkaloids from Annona crassiflora and molecular docking studies56
Novel heptafluoroisopropyl N-phenylpyrazole aryl amides containing cyanoalkyl groups: Design, synthesis, insecticidal activity, docking studies and theoretical calculations55
Discovery of new small molecule inhibitors of the BPTF bromodomain54
Nematocidal alkaloids from the roots of Stemona mairei (H.Lév.)K.Krause and identification of their pharmacophoric moiety54
Editorial Board52
Oxazolo[5,4-f]quinoxaline-type selective inhibitors of glycogen synthase kinase-3α (GSK-3α): Development and impact on temozolomide treatment of glioblastoma cells52
Inhibition of staphylococcal nuclease by benzimidazole-based Ligand: Implications in DNA-Mediated entrapment and uptake of MRSA by Macrophage-like cells52
Inhibitors of bacterial RNA polymerase transcription complex52
Discovery of novel selective phosphodiesterase‑1 inhibitors for the treatment of acute myelogenous leukemia52
Monoamine oxidase A and B inhibitory activities of 3,5-diphenyl-1,2,4-triazole substituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives52
An efficient and concise synthesis of a selective small molecule non-peptide inhibitor of cathepsin L: KGP9451
Hybridization of amantadine with gardenamide A enhances NMDA antagonism and in vivo anti-PD effects51
N-(3-cyano-1H-indol-5-yl)isonicotinamide and N-(3-cyano-1H-indol-5-yl)-1H-benzo[d]imidazole-5-carboxamide derivatives: Novel amide-based xanthine oxidase inhibitors50
Identification of (E)-1-((1H-indol-3-yl)methylene)-4-substitute-thiosemicarbazones as potential anti-hepatic fibrosis agents49
Discovery of N-arylcinnamamides as novel erythroblast enucleation inducers49
Design, synthesis and biological evaluation of hybrid of ubenimex-fluorouracil for hepatocellular carcinoma therapy48
Design, synthesis and biological evaluation of alkynyl-containing maleimide derivatives for the treatment of drug-resistant tuberculosis48
Light and hydrogen peroxide dual-responsive DNA interstrand crosslink precursors with potent cytotoxicity48
Synthesis of N-methylpyridine-chlorofuranformamide analogs as novel OPG up-regulators and inhibitors of RANKL-induced osteoclastogenesis48
Receptor mapping using methoxy phenyl piperazine derivative: Preclinical PET imaging47
Advanced high-affinity glycoconjugate ligands of galectins47
Isolation and target identification of anti-renal fibrosis compounds from Cordyceps militaris47
6-C-Linked trehalose glycolipids signal through Mincle and exhibit potent adjuvant activity46
Glycomimetic inhibitors of tandem-repeat galectins: Simple and efficient46
Thioether-based novel transition metal complexes: Synthesis, DNA interaction, in vitro biological assay, DFT calculations, and molecular docking studies46
Issue TOC45
A chemoenzymatic process for preparation of highly purified dehydroepiandrosterone in high space-time yield45
Onychiol B attenuates lipopolysaccharide-induced inflammation via MAPK/NF-κB pathways and acute lung injury in vivo45
Buffalo colostrum peptide mitigates Parkinson's disease pathophysiology through Cullin-3 inhibition45
seco-Sesquiterpenes and acorane-type sesquiterpenes with antiviral activity from the twigs and leaves of Illicium henryi Diels44
Design, synthesis, biological evaluation and docking study of some new aryl and heteroaryl thiomannosides as FimH antagonists44
Synthesis of new phenoxymethylcoumarin clubbed 4-arylthiazolylhydrazines as α-glucosidase inhibitors and their kinetics and molecular docking studies44
3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactions43
Proteasome activation: A novel strategy for targeting undruggable intrinsically disordered proteins43
Peptide inhibitors of angiotensin-I converting enzyme based on angiotensin (1–7) with selectivity for the C-terminal domain43
Guided rational design with scaffold hopping leading to novel histamine H3 receptor ligands43
A novel NIR fluorescent probe inhibits melanoma progression through apoptosis and ERK/DRP1-mediated mitochondrial fission43
The C-terminal segment of Leishmania major HslU: Toward potential inhibitors of LmHslVU activity42
Iron chelation and inhibition of metallopeptidases mediate anti-Trichomonas vaginalis activity by a novel 8-hydroxyquinoline derivative42
New enantiomeric lignans and new meroterpenoids with nitric oxide release inhibitory activity from Piper puberulum42
pH-promoted O-α-glucosylation of flavonoids using an engineered α-glucosidase mutant42
Issue TOC41
4-Chlorophenylthioacetone-derived thiosemicarbazones as potent antitrypanosomal drug candidates: Investigations on the mode of action41
Efficient synthesis of artificial pharmaceutical solid-phase modules for constructing aptamer-drug conjugates41
Natural product protulactone A: Total synthesis from D-galactose, X-ray analysis and biological evaluation41
Editorial Board41
Study of G protein-coupled receptors dimerization: From bivalent ligands to drug-like small molecules41
Nanotechnology applications for treatment of hepatic infections via modulating Hepatic histopathological and DNA alterations41
Protecting-group free synthesis of glycoconjugates displaying dual fungicidal and plant defense-eliciting activities41
Discovery of novel 1H-benzo[d]imidazole-4,7-dione based transglutaminase 2 inhibitors as p53 stabilizing anticancer agents in renal cell carcinoma40
Identification of diverse sesquiterpenoids with anti-fibrotic potential from Inula japonica Thunb.40
Incorporation of a FRET pair within a phosphonate diester40
A comprehensive review of small molecules targeting PI3K pathway: Exploring the structural development for the treatment of breast cancer40
Design, synthesis and biological evaluation of acyl hydrazones-based derivatives as RXRα-targeted anti-mitotic agents39
A possible covalent xanthine oxidase inhibitor TS10: Inhibition mechanism, metabolites identification and PDPK assessment39
SKLB-14b, a novel oral microtubule-destabilizing agent based on hydroxamic acid with potent anti-tumor and anti-multidrug resistance activities39
Development of fluorescent dual-FRET probe for simultaneous detection of caspase-8 and caspase-9 activities and their relative quantification39
Probing naphthalene diimide and 3-hydroxypropylphosphate as end-conjugating moieties for improved thrombin binding aptamers: Structural and biological effects38
Synthesis and biological evaluation of novel 3-(5-substituted-1H-indol-3-yl)pyrrolidine-2,5-dione derivatives with a dual affinity for serotonin 5-HT1A receptor and SERT38
Synthesis of mitochondria-targeted ferulic acid amide derivatives with antioxidant, anti-inflammatory activities and inducing mitophagy38
Euryfuranyl compounds from edible species of cuttlefish as potential anti-inflammatory leads attenuating NF-κB signaling cascade in lipopolysaccharide-activated macrophages38
Design, expression and biological evaluation of DX-88mut as a novel selective factor XIa inhibitor for antithrombosis37
Mn-doped bimetallic synergistic catalysis boosts for enzymatic phosphorylation of N-Acetylglucosamine/ N-Acetylgalactosamine and their derivatives37
Isolation, identification, and activity evaluation of antioxidant components from Inula viscosa: A bioguided approach37
Optimization of a cell surface vimentin binding peptoid to extract antagonist effect on lung cancer cells36
Development of novel androgen receptor antagonists based on the structure of darolutamide36
Identification of selective ligands targeting two GPCRs by receptor-affinity chromatography coupled with high-throughput sequencing techniques36
Discovery of stylissatin A analogs exhibiting potent nitric oxide inhibition36
Discovery of linear unnatural peptides as potent mutant isocitrate dehydrogenase 1 inhibitors by Ugi reaction36
Issue TOC36
Novel thiazolopyridine derivatives of diflapolin as dual sEH/FLAP inhibitors with improved solubility36
Antibiotic resistance and drug modification: Synthesis, characterization and bioactivity of newly modified potent ciprofloxacin derivatives35
Disaccharide-polyethylenimine organic nanoparticles as non-toxic in vitro gene transporters and their anticancer potential35
Minor immunosuppressive spiroorthoester group-containing pregnane glycosides from the root barks of Periploca sepium35
Design, synthesis and biological evaluation of novel pleuromutilin derivatives possessing 4-aminothiophenol linker as promising antibacterial agents35
Procerolides A-B from Microcionidae marine sponge Clathria procera: Anti-inflammatory macrocylic lactones with selective cyclooxygenase-2 attenuation properties35
Synthesis of 6-epi-tuberiferin and the biological activities of tuberiferin, dehydrobrabrachylaenolide, 6-epi-tuberiferin, and their synthetic intermediates35
Issue TOC34
Design, synthesis, and cytotoxic activity of novel 2H-imidazo[1,2-c]pyrazolo[3,4-e]pyrimidine derivatives34
Novel antimicrobial peptide DvAMP serves as a promising antifungal agent against Cryptococcus neoformans34
Synthesis, biological evaluation, pharmacokinetic studies and molecular docking of 4′′′-acetyl-delicaflavone as antitumor agents34
Synthesis and biological evaluation of novel withangulatin A derivatives as potential anticancer agents34
Synthesis and antitubercular activity of novel 4-arylalkyl substituted thio-, oxy- and sulfoxy-quinoline analogues targeting the cytochrome bc1 complex34
Identification of a promising hit from a new series of pyrazolo[1,5-a]pyrimidine based compounds as a potential anticancer agent with potent CDK1 inhibitory and pro-apoptotic properties through a mult34
Editorial Board34
Synthesis, bio-physical and anti-leishmanial studies of some novel indolo[3,2-a]phenanthridine derivatives33
Design and synthesis of β-carboline and combretastatin derivatives as anti-neutrophilic inflammatory agents32
Tubulin degradation: Principles, agents, and applications32
Bioisosteric ferrocenyl 1,3-thiazolidine-4-carboxylic acid derivatives: In vitro antiproliferative and antimicrobial evaluations32
Discovery of diverse sesquiterpenoids from Magnolia grandiflora with cytotoxic activities by inducing cell apoptosis32
Unsaturated lipids modulating the interaction of the antileishmanial isolinderanolide E with models of cellular membranes31
Discovery of aminothiazole derivatives as novel human enterovirus A71 capsid protein inhibitors31
The discovery of novel sanjuanolide derivatives as chemotherapeutic agents targeting castration-resistant prostate cancer31
Design, synthesis and biological evaluation of selective histone deacetylase 6 (HDAC6) inhibitors bearing benzoindazole or pyrazoloindazole scaffold as surface recognition motif31
Issue TOC31
New benzothienopyran and benzothienopyranopyrimidine derivatives as topoisomerase I inhibitors: Design, synthesis, anticancer screening, apoptosis induction and molecular modeling studies31
Discovery of pyrrolo[1,2-a]quinoxalin-4(5H)-one derivatives as novel non-covalent Bruton’s tyrosine kinase (BTK) inhibitors31
Discovery of hepatoprotective activity components from Thymus quinquecostatus celak. by molecular networking, biological evaluation and molecular dynamics studies30
Efficient biosynthesis of Vibegron intermediate using a novel carbonyl reductase based on molecular modification of hydrogen bonding network regulation30
Issue TOC30
Discovery of novel benzofuro[3,2-b]quinoline derivatives as dual CDK2/Topo I inhibitors30
Small organic molecules accelerate the expansion of regulatory T cells30
EZH2 serves as a promising therapeutic target for fibrosis30
Unleashing the potential of natural biological peptide Macropin: Hydrocarbon stapling for effective breast cancer treatment30
Arylacryl amides: Design, synthesis and the protection against cisplatin-induced acute kidney injury via TLR4/STING/NF-κB pathway29
A novel benzothiophene incorporated Schiff base acting as a “turn-on” sensor for the selective detection of Serine in organic medium29
Genome-directed discovery of antiproliferative bafilomycins from a deepsea-derived Streptomyces samsunensis29
Novel 4-Amino-Quinazoline moieties ligated Platinum(IV) prodrugs overcome cisplatin resistance in EGFRWT human lung cancer29
Discovery of berberine analogs as potent and highly selective p300/CBP HAT inhibitors29
B13, a well-tolerated inhibitor of hedgehog pathway, exhibited potent anti-tumor effects against colorectal carcinoma in vitro and in vivo29
Regioselectivity in inhibition of peptide deformylase from Haemophilus influenzae by 4- vs 5-azaindole hydroxamic acid derivatives: Biochemical, structural and antimicrobial studies29
Discovery of isoliquiritigenin analogues that reverse acute hepatitis by inhibiting macrophage polarization28
Development of fluorinated and methoxylated benzothiazole derivatives as highly potent and selective cannabinoid CB2 receptor ligands28
Energy metabolism as a target for cyclobenzaprine: A drug candidate against Visceral Leishmaniasis28
Novel 4-phenoxypyridine derivatives bearing imidazole-4-carboxamide and 1,2,4-triazole-3-carboxamide moieties: Design, synthesis and biological evaluation as potent antitumor agents28
Biological activity and ADME/Tox prediction of some 2-substituted benzoxazole derivatives28
Novel bisubstrate uridine-peptide analogues bearing a pyrophosphate bioisostere as inhibitors of human O-GlcNAc transferase28
Dissection of phospholipases A2 reveals multifaceted peptides targeting cancer cells, Leishmania and bacteria28
Synthesis and structure–activity relationships of ticlopidine derivatives and analogs as inhibitors of ectonucleotidase CD3928
Discovery of a novel GRPR antagonist for protection against cisplatin-induced acute kidney injury28
Lipopeptides production by a newly Halomonas venusta strain: Characterization and biotechnological properties28
1,2-Isoselenazol-3(2H)-one derivatives as NDM-1 inhibitors displaying synergistic antimicrobial effects with meropenem on NDM-1 producing clinical isolates28
Synthesis, structure and acetylcholinesterase inhibition activity of new diarylpyrazoles28
Scaffold overlay of flavonoid-inspired molecules: Discovery of 2,3-diaryl-pyridopyrimidin-4-imine/ones as dual hTopo-II and tubulin targeting anticancer agents28
Design, synthesis, modelling studies and biological evaluation of 1,3,4-oxadiazole derivatives as potent anticancer agents targeting thymidine phosphorylase enzyme27
Biphenyl substituted lysine derivatives as recognition elements for the matrix metalloproteinases MMP-2 and MMP-927
Synthesis and biological evaluation of new nicotinate derivatives as potential anti-inflammatory agents targeting COX-2 enzyme27
Structural modification of natural axinelline A: Achieving reduced colitis side effects through balanced COX inhibition27
Discovery of novel TLR4/MD-2 inhibitors: Receptor structure-based virtual screening studies and anti-inflammatory evaluation27
A NMR study of binding the metabolite of SN38 derivatives to a model nicked DNA decamer mimicking target of Topo I inhibitors27
Coumarins-lipophilic cations conjugates: Efficient mitocans targeting carbonic anhydrases26
Identification of FTY720 and COH29 as novel topoisomerase I catalytic inhibitors by experimental and computational studies26
Membrane interactions in Alzheimer’s disease treatment strategies with multitarget molecules26
Rational development of an ESIPT-based fluorescent probe with large Stokes shift for imaging of hydrogen sulfide in live cells26
Design, synthesis and evaluation of EZH2-based PROTACs targeting PRC2 complex in lymphoma26
Discovery of a new class of potent pyrrolo[3,4-c]quinoline-1,3-diones based inhibitors of human dihydroorotate dehydrogenase: Synthesis, pharmacological and toxicological evaluation26
Carbazole-based mitochondria-targeted fluorescent probes for in vivo viscosity and cyanide detection in cells and zebrafish26
Synthesis and in vitro cytotoxic activity of dye-linker-macrocycle conjugates with variable linker length and components26
Exploration and structure–activity relationship research of benzenesulfonamide derivatives as potent TRPV4 inhibitors for treating acute lung injury26
Counterion influence on near-infrared-II heptamethine cyanine salts for photothermal therapy25
Nitroreductase-induced bioorthogonal ligation for prodrug activation: A traceless strategy for cancer-specific imaging and therapy25
Unveiling a new strategy for PDIA1 inhibition: Integration of activity-based probes profiling and targeted degradation25
Selective activation of prodrugs in breast cancer using metabolic glycoengineering and the tetrazine ligation bioorthogonal reaction25
Discovery of novel oxazole-based macrocycles as anti-coronaviral agents targeting SARS-CoV-2 main protease25
Discovery of a highly selective fluorescent probe for hydrogen peroxide and its biocompatibility evaluation and bioimaging applications in cells and zebrafish25
Inhibition of TGF-β1/Smad3 signaling by compound 5aa: A potential treatment for idiopathic pulmonary fibrosis25
Water-soluble alkaloids isolated from Portulaca oleracea L.25
Synthesis and characterization of organoselenium based BODIPY and its application in living cells25
Unlocking the potential of higher-molecular-weight 5-HT7R ligands: Synthesis, affinity, and ADMET examination24
A new strategy for the treatment of Parkinson’s disease: Discovery and bio-evaluation of the first central-targeting tyrosinase inhibitor24
Structurally various p-terphenyls with neuraminidase inhibitory from a sponge derived fungus Aspergillus sp. SCSIO4131524
Rosmarinic acid turned α-syn oligomers into non-toxic species preserving microtubules in Raw 264.7 cells24
Screening and characterization of a β-xylosidase from Bifidobacterium breve K-110 and its application in the biotransformation of the total flavonoids of epimedium to icariin with α-l-rhamnosidase24
Structural optimization and biological evaluation of ML364 based derivatives as USP2a inhibitors24
Design, synthesis, and biological evaluation of carbonyl-hydrazine-1-carboxamide derivatives as anti-hepatic fibrosis agents targeting Nur7724
Synthesis of novel oxazol-5-one derivatives containing chiral trifluoromethyl and isoxazole moieties as potent antitumor agents and the mechanism investigation24
Carbazole alkaloids with potential cytotoxic activities targeted on PCK2 protein from Murraya microphylla24
Novel 131-iodine labeled and ultrasound-responsive nitric oxide and reactive oxygen species controlled released nanoplatform for synergistic sonodynamic/nitric oxide/chemodynamic/radionuclide therapy24
Design and synthesis of 9-phenanthranilamide derivatives and the study of anti-inflammatory, antioxidant and neuroprotective activities24
Potent antiplasmodial alkaloids from the rhizobacterium Pantoea agglomerans as hemozoin modulators23
Synthesis and biological evaluation of heterocyclic ring-fused dammarane-type ginsenoside derivatives as potential anti-tumor agents23
Expansion of targeted degradation by Gilteritinib-Warheaded PROTACs to ALK fusion proteins23
Design and synthesis of pyrimidine-5-carbonitrile hybrids as COX-2 inhibitors: Anti-inflammatory activity, ulcerogenic liability, histopathological and docking studies23
Design, synthesis and biological evaluation of 7–(5–((substituted – amino)-methyl)-thiophen–2–yl)-spiro-[chroman–2,4′–piperidin]–4–one hydrochloride analogues as anticancer agents23
Heteryunine A, an amidated tryptophan-catechin-spiroketal hybrid with antifibrotic activity from Heterosmilax yunnanensis23
Design, synthesis and anticancer evaluation of novel oncolytic peptide-chlorambucil conjugates23
Design, synthesis and biological evaluation of novel bischalcone derivatives as potential anticancer agents23
Exploring the potential intracellular targets of vascular normalization based on active candidates23
Transforming iodoquinol into broad spectrum anti-tumor leads: Repurposing to modulate redox homeostasis23
Astraoleanosides E–P, oleanane-type triterpenoid saponins from the aerial parts of Astragalus membranaceus Bunge and their β-glucuronidase inhibitory activity23
Telomerase activators from 20(27)-octanor-cycloastragenol via biotransformation by the fungal endophytes23
Design, synthesis and antitumor activities of phthalazinone derivatives as PARP-1 inhibitors and PARP-1/HDAC-1 inhibitors22
Novel mandelic acid derivatives containing piperazinyls as potential candidate fungicides against Monilinia fructicola: Design, synthesis and mechanism study22
Design, synthesis, and biological activities of arecoline derivatives containing 1,3,4-oxadiazole structure22
Acovenosigenin A β-glucoside mediates JAK2-STAT3 signaling pathway by targeting GP130 in A549 and H460 cells based on integrative analysis of transcriptome and proteome and biological verification22
Discovery and evolution of berberine analogues as anti-Helicobacter pylori agents with multi-target mechanisms22
Antiproliferative activity, enzymatic inhibition and apoptosis-promoting effects of benzoxazole-based hybrids on human breast cancer cells22
Design, synthesis, biological activity evaluation and structure-activity relationships of new steroidal aromatase inhibitors. The case of C-ring and 7β substituted steroids22
Structure-activity relationship studies of dipeptide-based hepsin inhibitors with Arg bioisosteres22
Metal-free internal nucleophile-triggered domino route for synthesis of fused quinoxaline [1,4]-diazepine hybrids and the evaluation of their DNA binding properties22
Cephalostatins and ritterazines: Distinctive dimeric marine-derived steroidal pyrazine alkaloids with intriguing anticancer activities22
Tetrahydropyridine appended 8-aminoquinoline derivatives: Design, synthesis, in silico, and in vitro antimalarial studies22
Identification of diterpenoids from Salvia castanea Diels f. tomentosa Stib and their antitumor activities22
THP as a sensor for the electrochemical detection of H2O222
Design, synthesis and in silico insights of new 7,8-disubstituted-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione derivatives with potent anticancer and multi-kinase inhibitory activities22
Synthesis, in vitro anticancer activity and in silico studies of certain isoxazole-based carboxamides, ureates, and hydrazones as potential inhibitors of VEGFR222
Design, synthesis and biological evaluation of anilide (dicarboxylic acid) shikonin esters as antitumor agents through targeting PI3K/Akt/mTOR signaling pathway22
Design, synthesis, molecular docking and in silico ADMET profile of pyrano[2,3-d]pyrimidine derivatives as antimicrobial and anticancer agents22
Saponins from Dolichos lablab seeds with anti-inflammatory activity22
The utility of Streptococcus mutans undecaprenol kinase for the chemoenzymatic synthesis of diverse non-natural isoprenoids22
Cedrol in ginger (Zingiber officinale) as a promising hair growth drug: The effects of oral and external administration on hair regeneration and its mechanism22
Synthesis and evaluation of the anti-inflammatory activity of novel 8-quinolinesulfonamide derivatives as TLR4/MD-2 inhibitors with efficacy in adjuvant-induced arthritis22
New Smoothened ligands based on the purine scaffold as potential agents for treating pancreatic cancer22
Synthetic access to syn-functionalised chiral hydroxy pyrrolidines and pyrrolidones: Evaluation of α-glucosidase inhibition activity, docking studies and pharmacokinetics prediction22
X-ray crystallography study and optimization of novel benzothiophene analogs as potent selective estrogen receptor covalent antagonists (SERCAs) with improved potency and safety profiles22
Combining photo-redox and enzyme catalysis for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives in one pot22
Unusual polyoxygenated casbane diterpenoids from the South China Sea soft coral Sinularia erecta21
Synthesis and biological evaluation of 1-phenyl-4,6-dihydrobenzo[b]pyrazolo[3,4-d]azepin-5(1H)-one/thiones as anticancer agents21
Design, synthesis, and biological evaluation of hydroxamic acid-substituted 2,4-diaryl aminopyrimidines as potent EGFRT790M/L858R inhibitors for the treatment of NSCLC21
Synthesis and anticancer evaluation of 6-azacyclonol-2,4,6-trimethylpyridin-3-ol derivatives: M3 muscarinic acetylcholine receptor-mediated anticancer activity of a cyclohexyl derivative in androgen-r21
Casuattimines A–N, fourteen new Lycopodium alkaloids from Lycopodiastrum casuarinoides with Cav3.1 channel inhibitory activity21
Novel indazole derivatives as potent apoptotic antiproliferative agents by multi-targeted mechanism: Synthesis and biological evaluation21
Design, synthesis, and biological evaluation of novel EGFR inhibitors containing 5-chloro-3-hydroxymethyl-indole-2-carboxamide scaffold with apoptotic antiproliferative activity21
Identification of new lead molecules against anticancer drug target TFIIH subunit P8 using biophysical and molecular docking studies21
Self-assembled dehydropeptide nanocarrier as a delivery system for antitumor drug temozolomide21
Synthesis, biological evaluation, and molecular docking study of some new rohitukine analogs as protein tyrosine phosphatase 1B inhibitors21
Discovery of new pyrimido[5,4-c]quinolines as potential antiproliferative agents with multitarget actions: Rapid synthesis, docking, and ADME studies21
Design, synthesis, cytotoxic activities, and molecular docking of chalcone hybrids bearing 8-hydroxyquinoline moiety with dual tubulin/EGFR kinase inhibition21
Structural simplification and bioisostere principle lead to Bis-benzodioxole-fibrate derivatives as potential hypolipidemic and hepatoprotective agents21
Design, synthesis, and evaluation of proliferation inhibitory activity of novel L-shaped ortho-quinone analogs as anticancer agents20
The cryptic metabolites and anti-phytopathogenic activities from Nigrospora lacticolonia and Penicillium rubens uncovered by the synergism with host Paris polyphylla, monoculture, and co-culture20
Diversity-oriented synthesis through gamma radiolysis: Preparation of unusual ecdysteroid derivatives activating Akt and AMPK in skeletal muscle cells20
Discovery of new chalone adamantyl arotinoids having RXRα-modulating and anticancer activities20
Novel metronidazole-derived three-component hybrids as promising broad-spectrum agents to combat oppressive bacterial resistance20
Novel dual-target μ‑opioid and TRPV1 ligands as potential pharmacotherapeutics for pain management20
Biotransformations of anthranilic acid and phthalimide to potent antihyperlipidemic alkaloids by the marine-derived fungus Scedosporium apiospermum F41-120
Antimicrobial macrozones interact with biological macromolecules via two-site binding mode of action: Fluorimetric, NMR and docking studies20
Design, synthesis and structure-activity relationship optimization of phenanthridine derivatives as new anti-vitiligo compounds20
Synthesis and evaluation of novel fluorinated hematoporphyrin ether derivatives for photodynamic therapy20
Design, synthesis and biological evaluation of oxadiazole clubbed piperazine derivatives as potential antidepressant agents20
Application of cyclohexane-1,3-diones for six-membered oxygen-containing heterocycles synthesis20
Design and synthesis of novel benzimidazole-iminosugars linked a substituted phenyl group and their inhibitory activities against β-glucosidase20
Novel isatin-based hybrids as potential anti-rheumatoid arthritis drug candidates: Synthesis and biological evaluation20
Evaluation of honokiol, magnolol and of a library of new nitrogenated neolignans as pancreatic lipase inhibitors20
Coumarin thiazoles as unique structural skeleton of potential antimicrobial agents20
Novel natural scaffold as hURAT1 inhibitor identified by 3D-shape-based, docking-based virtual screening approach and biological evaluation20
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