On the public citation graph

Structure–activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues

0 signed · 219 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf02979054openalex-snapshot
Relationship between tyrosinase inhibitory action and oxidation-reduction potential of cosmetic whitening ingredients and phenol derivatives
inferredcites →https://doi.org/10.1016/s0968-0896(01)00003-7openalex-snapshot
Synthesis of N-substituted N-nitrosohydroxylamines as inhibitors of Mushroom Tyrosinase
inferredcites →https://doi.org/10.1021/jf011230fopenalex-snapshot
Tyrosinase Inhibitors of Pulsatilla cernua Root-Derived Materials
inferredcites →https://doi.org/10.1021/np50106a021openalex-snapshot
Tyrosinase Inhibitors from Anacardium occidentale Fruits
inferredcites →https://doi.org/10.1023/b:jopc.0000032649.60933.58openalex-snapshot
Inhibitory Effects of 4-Halobenzoic Acids on the Diphenolase and Monophenolase Activity of Mushroom Tyrosinase
inferredcites →https://doi.org/10.1042/bj2570289openalex-snapshot
The inhibition of tyrosinase by pyridinones
inferredcites →https://doi.org/10.1080/14756360409162449openalex-snapshot
Mushroom Tyrosinase Inhibition by Two Potent Uncompetitive Inhibitors
inferredcites →https://doi.org/10.1080/14786410310001620628openalex-snapshot
Biotransformation of (+)-androst-4-ene-3,17-dione
inferredcites →https://doi.org/10.1111/j.1600-0749.1999.tb00756.xopenalex-snapshot
Effects of 4‐Tertiary Butylphenol on the Tyrosinase Activity in Human Melanocytes
inferredcites →https://doi.org/10.1248/cpb.52.1458openalex-snapshot
Tyrosinase Inhibitors from Rhododendron collettianum and Their Structure-Activity Relationship (SAR) Studies
inferredcites →https://doi.org/10.1248/cpb.53.86openalex-snapshot
Tyrosinase-Inhibitory Long-Chain Esters from Amberboa ramosa
inferredcites →https://doi.org/10.2174/1570178043488608openalex-snapshot
Microwave-Assisted Synthesis of 2,5-Disubstituted-1,3,4-Oxadiazoles

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4760920openalex-extracted
Kinetic Studies, Molecular Docking, and Antioxidant Activity of Novel 1,3-Diphenyl Pyrazole Derivatives Coupled with Thiosemicarbazide with Anti-Tyrosinase and Anti-Melanogenesis Properties
inferred← citeshttps://doi.org/10.1002/9781118939901.ch5openalex-snapshot
Beckmann Rearrangements and Fragmentations in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/ardp.200600100openalex-snapshot
Synthesis and Antiviral Evaluation of Some Sugar Arylglycinoylhydrazones and Their Oxadiazoline Derivatives
inferred← citeshttps://doi.org/10.1002/ardp.201300231openalex-snapshot
Oxadiazoles as Privileged Motifs for Promising Anticancer Leads: Recent Advances and Future Prospects
inferred← citeshttps://doi.org/10.1002/ardp.70188openalex-snapshot
Activity Profiling of Nitro‐Substituted Di(Hetero)Aryl 1,3,4‐ and 1,2,4‐Oxadiazoles: Antimicrobial, Cholinesterase Inhibition and Antioxidant Potential
inferred← citeshttps://doi.org/10.1002/cmdc.200600186openalex-snapshot
Prediction of Tyrosinase Inhibition Activity Using Atom‐Based Bilinear Indices
inferred← citeshttps://doi.org/10.1002/cmdc.201200363openalex-snapshot
A Facile Synthesis of Novel Bis‐(indolyl)‐1,3,4‐oxadiazoles as Potent Cytotoxic Agents
inferred← citeshttps://doi.org/10.1002/jhet.1048openalex-snapshot
The First Synthesis of Furoxan and 1,3,4‐Oxadiazole Ring Ensembles
inferred← citeshttps://doi.org/10.1002/jhet.2110openalex-snapshot
New Pyrazolyl‐Nicotinic Acids, Methyl Esters, and 1,3,4‐Oxadiazolyl‐pyrazolyl‐pyridine Tricyclic Scaffold Derivatives from 6‐Hydrazinylnicotinic Acid Hydrazide Hydrate
inferred← citeshttps://doi.org/10.1002/jhet.3409openalex-snapshot
Synthesis and Biological Evaluation of New Ibuprofen‐1,3,4‐oxadiazole‐1,2,3‐triazole Hybrids
inferred← citeshttps://doi.org/10.1002/jhet.3725openalex-snapshot
NO2‐Fe (II)Pc‐catalyzed synthesis of 2‐ferrocenyl‐5‐aryl‐1,3,4‐oxadiazoles and study of antifungal activity
inferred← citeshttps://doi.org/10.1002/slct.201600465openalex-snapshot
Rationale Design, Synthesis And In Vitro Anticancer Activity of New 2,5‐Disubstituted‐1,3,4‐Oxadiazole Analogues
inferred← citeshttps://doi.org/10.1002/slct.201801213openalex-snapshot
Copper‐Catalyzed Three‐Component Reaction of Oxadiazoles, Elemental Se/S and Aryl Iodides: Synthesis of Chalcogenyl (Se/S)‐Oxadiazoles
inferred← citeshttps://doi.org/10.1002/slct.201904412openalex-snapshot
Design and Ultrasound Assisted Synthesis of Novel 1,3,4‐Oxadiazole Drugs for Anti‐Cancer Activity
inferred← citeshttps://doi.org/10.1007/7081_2007_077openalex-snapshot
Heterocyclic Compounds Against the Enzyme Tyrosinase Essential for Melanin Production: Biochemical Features of Inhibition
inferred← citeshttps://doi.org/10.1007/978-94-007-1485-4_5openalex-snapshot
Oxadiazoles
inferred← citeshttps://doi.org/10.1007/978-981-16-4655-3_4openalex-snapshot
Thiadiazole Synthesis
inferred← citeshttps://doi.org/10.1007/s00044-013-0588-2openalex-snapshot
2,5-Disubstituted-1,3,4-oxadiazoles: thymidine phosphorylase inhibitors
inferred← citeshttps://doi.org/10.1007/s00044-015-1476-8openalex-snapshot
Synthesis of 2-(2-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole derivatives and evaluation of their antiglycation potential
inferred← citeshttps://doi.org/10.1007/s00280-009-0992-yopenalex-snapshot
Antiangiogenic and antiproliferative effects of substituted-1,3,4-oxadiazole derivatives is mediated by down regulation of VEGF and inhibition of translocation of HIF-1α in Ehrlich ascites tumor cells
inferred← citeshttps://doi.org/10.1007/s00339-019-2692-8openalex-snapshot
Solvatochromic analysis and DFT computational study of N-(hexyl)-N-(5-(3-hydroxynaphthyl-2-yl)-1,3,4-oxadiazol-2-yl)amine
inferred← citeshttps://doi.org/10.1007/s00706-008-0099-xopenalex-snapshot
Synthesis and antimicrobial evaluation of some 1,3-thiazole, 1,3,4-thiadiazole, 1,2,4-triazole, and 1,2,4-triazolo[3,4-b][1,3,4]-thiadiazine derivatives including a 5-(benzofuran-2-yl)-1-phenylpyrazole moiety
inferred← citeshttps://doi.org/10.1007/s10593-011-0847-4openalex-snapshot
Synthesis of novel 1,3,4-oxadiazole derivatives and their nucleoside analogs with antioxidant and antitumor activities
inferred← citeshttps://doi.org/10.1007/s10637-008-9116-5openalex-snapshot
Growth inhibition and induction of apoptosis in MCF-7 breast cancer cells by a new series of substituted-1,3,4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.1007/s10930-009-9182-3openalex-snapshot
In Vitro Effect of Ozagrel on Mushroom Tyrosinase
inferred← citeshttps://doi.org/10.1007/s11224-022-02052-5openalex-snapshot
Cluster formation between an oxadiazole derivative with metal nanoclusters (Ag/Au/Cu), graphene quantum dot sheets, SERS studies, and solvent effects
inferred← citeshttps://doi.org/10.1007/s11696-024-03861-0openalex-snapshot
Design, synthesis, in-vitro and in-silico anticancer studies on amide derivatives of 1,3,4-oxadiazole-isoxazol-pyridine-benzimidazole
inferred← citeshttps://doi.org/10.1007/s11696-026-04859-6openalex-snapshot
Synthesis, in-vitro anticancer evaluation and in-silico molecular docking studies of oxazol-2-yl)pyrazin-2-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.1007/s12039-014-0625-9openalex-snapshot
Synthesis and evaluation of 2-(5-(aryl)-1,3,4-oxadiazol-2-ylthio)-N-(3-(trifluoromethyl)phenyl)acetamides and N-(4-chloro-3-fluorophenyl)-2-(5-(aryl)-1,3,4-oxadiazol-2-ylthio)acetamides as antimicrobial agents
inferred← citeshttps://doi.org/10.1007/s42452-020-2511-zopenalex-snapshot
Synthesis, characterisation and evaluation of oxadiazole as promising anticancer agent
inferred← citeshttps://doi.org/10.1007/s44344-025-00018-3openalex-snapshot
Sulfonated grapheneoxide as a sustainable metal free acid catalyst: a smart approach for synthesizing 1, 3, 4-oxadiazole derivatives from carboxylic acids: antimicrobial activities
inferred← citeshttps://doi.org/10.1016/b978-0-12-822895-1.00006-0openalex-snapshot
Microwave-assisted synthesis of N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.arabjc.2011.02.006openalex-snapshot
Synthesis and biological significances of 1,3,4-thiadiazolines and related heterocyclic compounds
inferred← citeshttps://doi.org/10.1016/j.arabjc.2013.11.010openalex-snapshot
A facile one-pot synthesis of novel 2,5-disubstituted-1,3,4-oxadiazoles under conventional and microwave conditions and evaluation of their in vitro antimicrobial activities
inferred← citeshttps://doi.org/10.1016/j.arabjc.2013.12.020openalex-snapshot
Synthesis and biological evaluation of newer analogues of 2,5-disubstituted 1,3,4-oxadiazole containing pyrazole moiety as antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.bbapap.2016.12.013openalex-snapshot
Modifying effects of carboxyl group on the interaction of recombinant S100A8/A9 complex with tyrosinase
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.10.026openalex-snapshot
Carbazole and hydrazone derivatives as new competitive inhibitors of tyrosinase: Experimental clues to binuclear copper active site binding
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107586openalex-snapshot
Highly potent anti-melanogenic effect of 2-thiobenzothiazole derivatives through nanomolar tyrosinase activity inhibition
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107722openalex-snapshot
Kinetic studies, molecular docking, and antioxidant activity of novel 1,3-diphenyl pyrazole-thiosemicarbazone with anti-tyrosinase and anti-melanogenesis properties
inferred← citeshttps://doi.org/10.1016/j.biopha.2014.11.010openalex-snapshot
Compounds isolated from the aerial part of Crataegus azarolus inhibit growth of B16F10 melanoma cells and exert a potent inhibition of the melanin synthesis
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.05.014openalex-snapshot
Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.10.067openalex-snapshot
TOMOCOMD-CARDD descriptors-based virtual screening of tyrosinase inhibitors: Evaluation of different classification model combinations using bond-based linear indices
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.05.053openalex-snapshot
Synthesis and antimycobacterial activity of 4-(5-substituted-1,3,4-oxadiazol-2-yl)pyridines
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.10.102openalex-snapshot
1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.04.021openalex-snapshot
New potent inhibitors of tyrosinase: Novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.07.067openalex-snapshot
Synthesis, anticancer activity and mitochondrial mediated apoptosis inducing ability of 2,5-diaryloxadiazole–pyrrolobenzodiazepine conjugates
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.09.051openalex-snapshot
Synthesis, biological evaluation, and molecular docking studies of 2-chloropyridine derivatives possessing 1,3,4-oxadiazole moiety as potential antitumor agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.06.061openalex-snapshot
Oxadiazole derivatives containing 1,4-benzodioxan as potential immunosuppressive agents against RAW264.7 cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.08.013openalex-snapshot
Synthesis, biological evaluation, and molecular docking studies of 1,3,4-oxadiazole derivatives possessing 1,4-benzodioxan moiety as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.03.064openalex-snapshot
Synthesis, biological evaluation and molecular docking studies of 1,3,4-oxadiazole derivatives as potential immunosuppressive agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.08.059openalex-snapshot
Design, synthesis and biological evaluation of heterocyclic azoles derivatives containing pyrazine moiety as potential telomerase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.12.054openalex-snapshot
Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.04.043openalex-snapshot
Synthesis, biological evaluation, and molecular docking studies of novel 1,3,4-oxadiazole derivatives possessing benzotriazole moiety as FAK inhibitors with anticancer activity
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.11.004openalex-snapshot
Synthesis, molecular modeling and biological evaluation of N-benzylidene-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetohydrazide derivatives as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.03.009openalex-snapshot
Inhibitory effects of novel synthetic methimazole derivatives on mushroom tyrosinase and melanogenesis
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.07.032openalex-snapshot
Oxadiazoles and thiadiazoles: Novel α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.07.068openalex-snapshot
2-(4-Fluorophenyl)-quinazolin-4(3H)-one as a novel tyrosinase inhibitor: Synthesis, inhibitory activity, and mechanism
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.09.085openalex-snapshot
New tyrosinase inhibitors selected by atomic linear indices-based classification models
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.03.172openalex-snapshot
An efficient synthesis and biological study of novel indolyl-1,3,4-oxadiazoles as potent anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.04.067openalex-snapshot
Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.04.146openalex-snapshot
Ketonethiosemicarbazones: Structure–activity relationships for their melanogenesis inhibition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.12.035openalex-snapshot
Structure–activity relationship of naphthaldehydethiosemicarbazones in melanogenesis inhibition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.11.029openalex-snapshot
Novel pyrazole integrated 1,3,4-oxadiazoles: Synthesis, characterization and antimicrobial evaluation
inferred← citeshttps://doi.org/10.1016/j.cdc.2020.100570openalex-snapshot
Synthesis, anticancer evaluation and molecular docking studies of 1,3,4-oxadiazole linked resveratrol derivatives
inferred← citeshttps://doi.org/10.1016/j.cdc.2022.100971openalex-snapshot
Design, Synthesis and Anticancer Evaluation of Benzoxazole Resemble Substituted Arylamide Derivatives of Bis-1,3,4-Oxadiazole-oxazolo[4,5-b]pyridin-2-yl) as Anticancer Agents
inferred← citeshttps://doi.org/10.1016/j.cdc.2022.100981openalex-snapshot
Synthesis and biological evaluation of 1,3,4-oxadiazole linked azaindole derivatives as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.comche.2005.05.001openalex-snapshot
Combinatorial Chemistry Online Volume 7, Issue 6, June 2005
inferred← citeshttps://doi.org/10.1016/j.comche.2005.12.001openalex-snapshot
Combinatorial Chemistry Online
inferred← citeshttps://doi.org/10.1016/j.ejmech.2006.03.002openalex-snapshot
Synthesis and antimicrobial studies of a new series of 2-{4-[2-(5-ethylpyridin-2-yl)ethoxy]phenyl}-5-substituted-1,3,4-oxadiazoles
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.01.026openalex-snapshot
Dragon method for finding novel tyrosinase inhibitors: Biosilico identification and experimental in vitro assays
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.04.006openalex-snapshot
Synthesis and pharmacological evaluation of 1,3,4-oxadiazole bearing bis(heterocycle) derivatives as anti-inflammatory and analgesic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.06.023openalex-snapshot
Hypervalent iodine(III) mediated synthesis of novel unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles as antibacterial and antifungal agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.11.013openalex-snapshot
Novel 1,3,4-heterodiazole analogues: Synthesis and in-vitro antitumor activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.12.013openalex-snapshot
Synthesis and antitumor evaluation of some new 1,3,4-oxadiazole-based heterocycles
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.03.056openalex-snapshot
Design, synthesis and biological evaluation of a novel series of 1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl)phenyl pyrazole moiety as cytotoxic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.09.026openalex-snapshot
Design, synthesis, and evaluation of (E)-N-substituted benzylidene–aniline derivatives as tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.11.039openalex-snapshot
Synthesis, molecular modeling and biological evaluation of 2-aminomethyl-5-(quinolin-2-yl)-1,3,4-oxadiazole-2(3H)-thione quinolone derivatives as novel anticancer agent
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.018openalex-snapshot
Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.04.051openalex-snapshot
1,3,4-Oxadiazoles: An emerging scaffold to target growth factors, enzymes and kinases as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.07.029openalex-snapshot
Design, synthesis and biological evaluation of novel α-aminophosphonate oxadiazoles via optimized iron triflate catalyzed reaction as apoptotic inducers
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.05.019openalex-snapshot
Synthesis and in vitro antibacterial activity of new oxoethylthio-1,3,4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.06.020openalex-snapshot
Synthesis and antimicrobial screening of 1,3,4-oxadiazole and clubbed thiophene derivatives
inferred← citeshttps://doi.org/10.1016/j.matpr.2022.05.092openalex-snapshot
Design, synthesis, in silico study and preliminary pharmacological evaluation of ibuprofen derivatives containing 1, 3, 4-Oxadiazole moiety
inferred← citeshttps://doi.org/10.1016/j.medidd.2020.100017openalex-snapshot
Design, synthesis and SAR bioevaluation of benzophenone-mercaptooxadiazole analogs
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.127875openalex-snapshot
Synthesis, anticancer evaluation and molecular docking studies of 2,5-bis(indolyl)-1,3,4-oxadiazoles, Nortopsentin analogues
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128705openalex-snapshot
Design and synthesis of triazole conjugated novel 2,5-diaryl substituted 1,3,4-oxadiazoles as potential antimicrobial and anti-fungal agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.132216openalex-snapshot
Synthesis, spectral analysis, antibacterial, antifungal, antioxidant and hemolytic activity studies of some new 2,5-disubstituted-1,3,4-oxadiazoles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133017openalex-snapshot
Synthesis, molecular structure, electronic, spectroscopic, NLO and antimicrobial study of N-benzyl-2-(5-aryl-1,3,4-oxadiazol-2-yl)aniline derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139578openalex-snapshot
Exploring target site interactions of 1,3,4-Oxadiazole/1,3,4-thiadiazole derivatives: Synthesis, characterization in vitro anti-urease and in silico molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.phytochem.2006.08.006openalex-snapshot
Polyphenol oxidases in plants and fungi: Going places? A review
inferred← citeshttps://doi.org/10.1016/j.rechem.2020.100045openalex-snapshot
Synthesis, docking and biological evaluation of thiadiazole and oxadiazole derivatives as antimicrobial and antioxidant agents
inferred← citeshttps://doi.org/10.1016/j.scp.2020.100279openalex-snapshot
Facile preparation of cesium salt of tungstophosphoric acid for catalytic synthesis of one-pot two-component 1,3,4-oxadiazole derivatives in water: A doubly green approach
inferred← citeshttps://doi.org/10.1016/j.tet.2012.11.071openalex-snapshot
A new and efficient synthesis of 1,3,4-oxadiazole derivatives using TBTU
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.127openalex-snapshot
A facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.054openalex-snapshot
Convenient preparation of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles promoted by Dess–Martin reagent
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.086openalex-snapshot
A novel one-pot synthesis of α-keto-1,3,4-oxadiazole derivatives based on isocyanide-Nef reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.064openalex-snapshot
Ligand-free copper(0) catalyzed direct C–H arylation of 1,2,4-triazoles and 1,3,4-oxadiazoles with aryl iodides in PEG-400
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.018openalex-snapshot
Oxidation of sp3 C H bonds in N-alkylhydrazides: Access to 2,5-disubstituted 1,3,4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.1016/s1359-6446(05)03708-6openalex-snapshot
Monitor
inferred← citeshttps://doi.org/10.1021/jf203494topenalex-snapshot
Solid-Phase Synthesis of Mimosine Tetrapeptides and Their Inhibitory Activities on Neuraminidase and Tyrosinase
inferred← citeshttps://doi.org/10.1021/jf800109aopenalex-snapshot
Enzyme, Protein, Carbohydrate, and Phenolic Contaminants in Commercial Tyrosinase Preparations: Potential Problems Affecting Tyrosinase Activity and Inhibition Studies
inferred← citeshttps://doi.org/10.1021/ol100931qopenalex-snapshot
Novel One-Pot, Four-Component Condensation Reaction: An Efficient Approach for the Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazole Derivatives by a Ugi-4CR/aza-Wittig Sequence
inferred← citeshttps://doi.org/10.1021/ol202409ropenalex-snapshot
Cu(II) Catalyzed Imine C–H Functionalization Leading to Synthesis of 2,5-Substituted 1,3,4-Oxadiazoles
inferred← citeshttps://doi.org/10.1039/c3ra44897eopenalex-snapshot
Iodine-catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles
inferred← citeshttps://doi.org/10.1039/c4ra02672aopenalex-snapshot
Synthesis, photophysical and electrochemical properties of chiral and achiral thiadiazolophanes
inferred← citeshttps://doi.org/10.1039/c5nj02566dopenalex-snapshot
Novel 1,3,4-oxadiazole motifs bearing a quinoline nucleus: synthesis, characterization and biological evaluation of their antimicrobial, antitubercular, antimalarial and cytotoxic activities
inferred← citeshttps://doi.org/10.1039/c5ra23282aopenalex-snapshot
Novel benzimidazole–oxadiazole hybrid molecules as promising antimicrobial agents
inferred← citeshttps://doi.org/10.1039/c6ra12754aopenalex-snapshot
Synthesis and effects of oxadiazole derivatives on tyrosinase activity and human SK-MEL-28 malignant melanoma cells
inferred← citeshttps://doi.org/10.1039/c7ce00678kopenalex-snapshot
Complex electronic interplay of σ-hole and π-hole interactions in crystals of halogen substituted 1,3,4-oxadiazol-2(3H)-thiones
inferred← citeshttps://doi.org/10.1039/c7qo00348jopenalex-snapshot
Photoredox catalytic intramolecular imine C–H bond functionalization using ligand free Cu( ii ) salts
inferred← citeshttps://doi.org/10.1039/c9ra09016aopenalex-snapshot
Synthesis of new oxadiazol-phthalazinone derivatives with anti-proliferative activity; molecular docking, pro-apoptotic, and enzyme inhibition profile
inferred← citeshttps://doi.org/10.1039/d3ob01964kopenalex-snapshot
Phenyliodine bis(trifluoroacetate) as a sustainable reagent: exploring its significance in organic synthesis
inferred← citeshttps://doi.org/10.1063/5.0324010openalex-snapshot
Synthesis and antibacterial study of some novel β-lactam derivatives via imine intermediates
inferred← citeshttps://doi.org/10.1071/ch08243openalex-snapshot
A New Synthetic Route of 2-Aroyl- and 2-Benzyl-Benzofurans and their Application in the Total Synthesis of a Metabolite Isolated from Dorstenia gigas
inferred← citeshttps://doi.org/10.1071/ch15116openalex-snapshot
Indole-3-carbinol and 1,3,4-Oxadiazole Hybrids: Synthesis and Study of Anti-Proliferative and Anti-Microbial Activity
inferred← citeshttps://doi.org/10.1080/00397910701199151openalex-snapshot
Silica Sulfuric Acid: An Efficient and Versatile Acidic Catalyst for the Rapid and Ecofriendly Synthesis of 1,3,4‐Oxadiazoles at Ambient Temperature
inferred← citeshttps://doi.org/10.1080/00397911.2013.879901openalex-snapshot
Review of Synthesis of 1,3,4-Oxadiazole Derivatives
inferred← citeshttps://doi.org/10.1080/00397911.2018.1432761openalex-snapshot
Design, synthesis and biological evaluation of novel N1,N8-bis(((4-((5-aryl-1,3,4-oxadiazol-2-yl)methoxy)phenyl)amino)oxy)-1-naphthamide derivatives
inferred← citeshttps://doi.org/10.1080/00397911.2018.1535076openalex-snapshot
Synthesis and biological evaluation of 1,2,4-oxadiazole linked 1,3,4-oxadiazole derivatives as tubulin binding agents
inferred← citeshttps://doi.org/10.1080/00397911.2025.2457440openalex-snapshot
Design, synthesis, anticancer evaluation and molecular docking studies of different aryl derivatives of azaindole-pyrimidine-1,3,4-oxadiazoles
inferred← citeshttps://doi.org/10.1080/07328300802262778openalex-snapshot
Synthesis and Antiviral Evaluation of Some 5‐N‐Arylaminomethyl‐2‐glycosylsulphanyl‐1,3,4‐oxadiazoles and Their Analogs against Hepatitis A and Herpes Simplex Viruses
inferred← citeshttps://doi.org/10.1080/07388551.2025.2583450openalex-snapshot
Beyond traditional cosmetics: exploring endophytic fungal-derived tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1080/07391102.2023.2274973openalex-snapshot
Design and synthesis of 4-aminophenol-1,3,4-oxadiazole derivative potentiates apoptosis by targeting MAP kinase in triple negative breast cancer cells
inferred← citeshttps://doi.org/10.1080/10408398.2021.1871724openalex-snapshot
A systematic review of synthetic tyrosinase inhibitors and their structure-activity relationship
inferred← citeshttps://doi.org/10.1080/10426500902840887openalex-snapshot
A Novel, One-Pot Synthesis of 2,5-Disubstituted-1,3,4-Oxadiazoles Using 1,4-Bis(Triphenylphosphonium)-2-Butene Peroxodisulfate
inferred← citeshttps://doi.org/10.1080/10426507.2011.568026openalex-snapshot
(N-Isocyanimino)Triphenylphosphorane as an Efficient Reagent for the Preparation of N-Benzyl-1-Phenyl-1-(5-Phenyl-1,3,4-Oxadiazol- 2-yl)Methanamine Derivatives via in-Situ Generation of Densely Functionalized Iminophosphoranes
inferred← citeshttps://doi.org/10.1080/10426507.2014.903488openalex-snapshot
The Reaction of N -Isocyaniminotriphenylphosphorane with Cyclopentanone and A Primary Amine in the Presence of An E -Cinnamic Acid Derivative
inferred← citeshttps://doi.org/10.1080/10426507.2015.1085047openalex-snapshot
Synthesis, Crystal Structures, Fluorescence and Xanthine Oxidase Inhibitory of Sulfur-Containing Pyrazole Derivatives Incorporated with Oxadiazole and Triazole
inferred← citeshttps://doi.org/10.1080/10601325.2012.642210openalex-snapshot
Metal Complexes of New Tetraazamacrocyclic Constrained Oxadiazole Ring as Subunits: Synthesis, DNA Binding and Photonuclease Activity
inferred← citeshttps://doi.org/10.1080/1062936x.2020.1862297openalex-snapshot
SAR and QSAR research on tyrosinase inhibitors using machine learning methods
inferred← citeshttps://doi.org/10.1080/17415993.2015.1114117openalex-snapshot
Utility involving thioacetoacetanilides as precursors for synthesis of new thiazole, thiadiazole and thiophene derivatives with antimicrobial activity
inferred← citeshttps://doi.org/10.1080/23312009.2017.1303909openalex-snapshot
Design and synthesis of 1,4-benzothiazine derivatives with promising effects against colorectal cancer cells
inferred← citeshttps://doi.org/10.1093/bbb/zbab084openalex-snapshot
Structure–activity relationships of antityrosinase and antioxidant activities of cinnamic acid and its derivatives
inferred← citeshttps://doi.org/10.1107/s1600536809029894openalex-snapshot
5-[1-(3,4-Dichlorophenoxy)ethyl]-1,3,4-oxadiazole-2(3H)-thione hemihydrate
inferred← citeshttps://doi.org/10.1107/s1600536809030190openalex-snapshot
2-(4-Bromophenyl)-5-fluoro-3-methylsulfinyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s160053680905418xopenalex-snapshot
5-Bromo-2-(4-fluorophenyl)-7-methyl-3-methylsulfinyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810008627openalex-snapshot
5-Chloro-3-ethylsulfinyl-2-(4-fluorophenyl)-7-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810012869openalex-snapshot
3-(4-Fluorophenylsulfonyl)-5-isopropyl-2-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810021823openalex-snapshot
5-Fluoro-3-(4-fluorophenylsulfinyl)-2-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810022397openalex-snapshot
2-(4-Fluorophenyl)-5-iodo-7-methyl-3-methylsulfinyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810024190openalex-snapshot
3-Ethylsulfinyl-5-iodo-2-phenyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810025468openalex-snapshot
5-Fluoro-3-(4-fluorophenylsulfonyl)-2-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810028308openalex-snapshot
3-Ethylsulfanyl-2,5-diphenyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810034069openalex-snapshot
3-[(4-Fluorophenyl)sulfonyl]-5-iodo-2-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810035932openalex-snapshot
3-(4-Chlorophenylsulfinyl)-2,5-dimethyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536810042339openalex-snapshot
3-[(4-Chlorophenyl)sulfinyl]-2,4,6,7-tetramethyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536811018654openalex-snapshot
3-(3-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s160053681200027xopenalex-snapshot
3-(3-Chlorophenylsulfinyl)-2,4,6-trimethyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s1600536812039463openalex-snapshot
3-Ethylsulfinyl-2-(3-fluorophenyl)-5-iodo-7-methyl-1-benzofuran
inferred← citeshttps://doi.org/10.1107/s2056989017003978openalex-snapshot
Crystal structure and Hirshfeld surface analysis of 1-(4-chlorophenyl)-2-{[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl}ethanone
inferred← citeshttps://doi.org/10.1109/icaect49130.2021.9392393openalex-snapshot
Substituent Effect on the Chalcones and their DFT Studies
inferred← citeshttps://doi.org/10.1111/cbdd.12297openalex-snapshot
A Facile One‐Pot Synthesis of 2‐Arylamino‐5‐Aryloxylalkyl‐1,3,4‐Oxadiazoles and Their Urease Inhibition Studies
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2007.05944.xopenalex-snapshot
Functional interaction of diphenols with polyphenol oxidase
inferred← citeshttps://doi.org/10.1134/s1068162021030092openalex-snapshot
Chemistry of Oxadiazole Analogues: Current Status and Applications
inferred← citeshttps://doi.org/10.1134/s1070363220120221openalex-snapshot
Design, Synthesis, and Anticancer Activity of 1,3,4-Oxadiazole Incorporated 5-(Pyrimidin-5-yl)benzo[d]oxazole Derivatives
inferred← citeshttps://doi.org/10.1134/s107036322205019xopenalex-snapshot
Design and Synthesis of Different Aryl Substituted 1,3,4-Oxadiazole-imidazo[1,5-a]pyridine Derivatives as Anticancer Agents
inferred← citeshttps://doi.org/10.1134/s1070428024601997openalex-snapshot
Design and Synthesis of 1,3,4-Oxadiazole–Quinazolinone Hybrids, Evaluation of Their Anticancer and Antimicrobial Activities, and Docking Studies
inferred← citeshttps://doi.org/10.1142/s1088424621500863openalex-snapshot
New water soluble magnesium phthalocyanine as a potential anticancer drug: Cytotoxic and apoptotic effect on different cancer cell lines
inferred← citeshttps://doi.org/10.1155/2011/751894openalex-snapshot
Microwave-Assisted Solution Phase Synthesis of Novel 2-{4-[2-(N-Methyl-2-pyridylamino)ethoxy]phenyl}-5-Substituted 1,3,4-Oxadiazole Library
inferred← citeshttps://doi.org/10.1351/pac200779122277openalex-snapshot
Molecular design of tyrosinase inhibitors: A critical review of promising novel inhibitors from synthetic origins
inferred← citeshttps://doi.org/10.14233/ajchem.2020.22680openalex-snapshot
Synthesis and Biological Evaluation of 1,3,4-Oxadiazole Fused Resveratrol Derivatives as Anticancer Agents
inferred← citeshttps://doi.org/10.1515/ncrs-2016-0262openalex-snapshot
Crystal structure of 2-(1-benzyl-3-phenyl-1H-pyrazol-5-yl)-5-(4-nitrobenzylthio)-1,3,4-oxadiazole, C25H19N5O3S
inferred← citeshttps://doi.org/10.1515/tjb-2016-0240openalex-snapshot
Synthesis and biological evaluation of some new pyrimidine bearing 2,5-disubstituted 1,3,4-oxadiazole derivatives as cytotoxic agents
inferred← citeshttps://doi.org/10.1515/znc-2008-9-1010openalex-snapshot
Anti-Hepatitis B Virus Activity of New 1,2,4-Triazol-2-yl- and 1,3,4-Oxadiazol-2-yl-2-pyridinone Derivatives
inferred← citeshttps://doi.org/10.18185/erzifbed.823431openalex-snapshot
Synthesis and Antioxidant Activities of New 2-(4-methylphenylsulphonyl)-5-Aryl-1,3,4-Oxadiazole Compounds
inferred← citeshttps://doi.org/10.19261/cjm.2012.07(2).03openalex-snapshot
Synthesis of Mono-Substituted and Simmetrically 2, 5-Disubstituted 1, 3, 4-Oxadiazoles
inferred← citeshttps://doi.org/10.20944/preprints202308.1064.v1openalex-snapshot
Emerging Oxygen Based Heterocyclic Scaffolds as Potential Anticancer Candidates
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1517144/v1openalex-snapshot
Cluster formation between an oxadiazole derivative with metal nanoclusters (Ag/Au/Cu), graphene quantum dot sheets, SERS studies and solvent effects
inferred← citeshttps://doi.org/10.21608/ejchem.2014.1044openalex-snapshot
Synthesis of 5-(1,2,3-Triazol-4-yl)-1,3,4-Oxa(thia) diazol-2-Amines as Antimicrobial Agents
inferred← citeshttps://doi.org/10.2174/0113852728383478251027072653openalex-snapshot
Insights into the Recent Research Progress on the Synthesis and Pharmacology Approaches of 1,3,4-oxadiazole: A Comprehensive Review
inferred← citeshttps://doi.org/10.2174/0115680266337405240926114604openalex-snapshot
Computational Studies in Dermo-cosmetics: In silico Discovery of Therapeutic Agents Targeting a Variety of Proteins for Skin Diseases
inferred← citeshttps://doi.org/10.2174/1381612827666210803113506openalex-snapshot
Synthesis of Novel NSAIDs Linked to Triazolyl-oxadiazole Heterocyclic Compounds as more Comprehensive Antimicrobial Agents: A Computational Molecular Docking
inferred← citeshttps://doi.org/10.2174/138527212799958011openalex-snapshot
Microwave Assisted Synthesis of Five Membered Azaheterocyclic Systems
inferred← citeshttps://doi.org/10.2174/1389557511313070007openalex-snapshot
Recent Updates on Biological Activities of Oxadiazoles
inferred← citeshttps://doi.org/10.2174/1570180816666181031125946openalex-snapshot
Novel 1,3,4-Oxadiazole Fused Thiadiazole Derivatives: Synthesis and study of Anticancer Activities
inferred← citeshttps://doi.org/10.2174/1570180816666190611162355openalex-snapshot
Tyrosinase Inhibitory Activity of S-Naproxen Derivatives
inferred← citeshttps://doi.org/10.22270/jddt.v13i3.5749openalex-snapshot
Novel 1, 3, 4-Oxadiazole-pyridine hybrids as potential DNA gyrase B inhibitors (5D7R): ADMET prediction and molecular docking study
inferred← citeshttps://doi.org/10.30970/vch.6002.256openalex-snapshot
Methods of obtaining and possible directions of chemical modifications of 1,3,4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.3109/14756366.2010.550890openalex-snapshot
Synthesis and biological evaluation of 2,5-disubstituted 1,3,4-oxadiazole derivatives with both COX and LOX inhibitory activity
inferred← citeshttps://doi.org/10.3109/14756366.2012.670806openalex-snapshot
Tyrosinase inhibitory activities of the compounds isolated fromNeolitsea aciculata(Blume) Koidz.
inferred← citeshttps://doi.org/10.3109/14756366.2015.1004058openalex-snapshot
Natural, semisynthetic and synthetic tyrosinase inhibitors
inferred← citeshttps://doi.org/10.3184/174751913x13603559594859openalex-snapshot
Use of Ester Formylhydrazones for the Synthesis of 1,2,4-triazole and 1,3,4-oxadiazole Derivatives
inferred← citeshttps://doi.org/10.32352/10.32352/0367-3057.6.19.05openalex-snapshot
Biological activity of heterocyclic systems based on functionally substituted 1,3,4-thia(oxa)diazoles (a review)
inferred← citeshttps://doi.org/10.32628/ijsrst52411174openalex-snapshot
The Synthesis, Characterization, and Biological Activities of Some Novel Schiff Bases Derived From 3-Acetyl-4-Hydroxy-2H-Chromen-2-One And 2-Aminooxadiazole Derivatives Have Been Investigated
inferred← citeshttps://doi.org/10.32628/ijsrst524112100openalex-snapshot
Synthesis, Characterization, and Biological Activities of Novel Schiff Bases Derived from 3-acetyl-4-hydroxy-2h-chromen-2-one and 5-(4-ethoxy/ halo substituted phenyl)-1,3,4-oxadiazol-2-amine
inferred← citeshttps://doi.org/10.32947/ajps.v20i4.781openalex-snapshot
Synthesis, Antibacterial study and ADME Evaluation of Novel Isonicotinoyl Hydrazide Derivative Containing 1,3,4-Oxadiazole Moiety
inferred← citeshttps://doi.org/10.32947/ajps.v25i5.1294openalex-snapshot
1,3,4-OXADIAZOLE: Synthesis Derivatives &Biological Activities. A Review article
inferred← citeshttps://doi.org/10.33263/briac104.960971openalex-snapshot
A review on synthetic routes for obtaining of 2,5-disubstituted 1,3,4-oxadiazoles via cyclodehydration and oxidative cyclization reactions
inferred← citeshttps://doi.org/10.33483/jfpau.567757openalex-snapshot
HISTOLOGICAL STUDY OF A CORRECTIVE INFLUENCE OF A COMPOUND POTASSIUM 2-((4-AMINO-5-(MORPHOLINOMETHYL)- 4H-1,2,4-TRIAZOL-3-YL)THIO)ACETATE (PKR-173) ON THE STATE OF CHICKEN'S LIVER UNDER INFECTION BY PSEUDOMONAS AERUGINOSA
inferred← citeshttps://doi.org/10.3390/ijms10062440openalex-snapshot
An Updated Review of Tyrosinase Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules170910192openalex-snapshot
Synthetic Approaches and Pharmacological Activity of 1,3,4-Oxadiazoles: A Review of the Literature from 2000–2012
inferred← citeshttps://doi.org/10.3390/molecules28155762openalex-snapshot
Tyrosinase Inhibitors: A Perspective
inferred← citeshttps://doi.org/10.3390/molecules29122887openalex-snapshot
Investigation of the Efficacy of Benzylidene-3-methyl-2-thioxothiazolidin-4-one Analogs with Antioxidant Activities on the Inhibition of Mushroom and Mammal Tyrosinases
inferred← citeshttps://doi.org/10.3390/ph16020254openalex-snapshot
An Understanding of Mechanism-Based Approaches for 1,3,4-Oxadiazole Scaffolds as Cytotoxic Agents and Enzyme Inhibitors
inferred← citeshttps://doi.org/10.3390/ph16040517openalex-snapshot
Synthesis, Anticancer, Antimicrobial and Antioxidant Potential of Novel 4-(Substituted phenyl-1,3,4-oxadiazol/thiadiazol-2-yl)-4-(4-substituted phenyl) Azetidin-2-One Derivatives
inferred← citeshttps://doi.org/10.36229/978-65-86127-73-7.cap.01openalex-snapshot
Fraturas de Fêmur – panorama das taxas de morbimortalidade e incidência entre as regiões brasileiras
inferred← citeshttps://doi.org/10.36229/978-65-86127-73-7.cap.03openalex-snapshot
Efetividade da fisioterapia preventiva no Centro de Convivência da Pessoa Idosa no município de Nova Lima, Minas Gerais.
inferred← citeshttps://doi.org/10.36229/978-65-86127-73-7.cap.04openalex-snapshot
O cuidado ao idoso portador de Esclerose Lateral Amiotrófica: Relato de experiência
inferred← citeshttps://doi.org/10.36229/978-65-86127-73-7.cap.07openalex-snapshot
Assistência de enfermagem a pessoa idosa no perioperatório: Um relato de experiência
showing the first 200 of 207 · page through all 207
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.