On the public citation graph

Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors

https://doi.org/10.1016/j.bmc.2012.12.054

0 signed · 51 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/bip.20670openalex-snapshot

Kojic acid–tripeptide amide as a new tyrosinase inhibitor

inferredcites →https://doi.org/10.1007/s00044-009-9202-zopenalex-snapshot

Synthesis and evaluation of antiinflammatory activity of substituted chalcone derivatives

inferredcites →https://doi.org/10.1016/j.bmc.2005.03.012openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.bmc.2006.05.014openalex-snapshot

Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships

inferredcites →https://doi.org/10.1016/j.bmc.2007.01.017openalex-snapshot

Synthesis and evaluation of 2′,4′,6′-trihydroxychalcones as a new class of tyrosinase inhibitors

inferredcites →https://doi.org/10.1016/j.bmc.2010.06.046openalex-snapshot

Synthesis of novel 3,5-diaryl pyrazole derivatives using combinatorial chemistry as inhibitors of tyrosinase as well as potent anticancer, anti-inflammatory agents

inferredcites →https://doi.org/10.1016/j.bmc.2010.12.051openalex-snapshot

Benzyl benzoates: New phlorizin analogs as mushroom tyrosinase inhibitors

inferredcites →https://doi.org/10.1016/j.bmc.2012.07.001openalex-snapshot

Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors

inferredcites →https://doi.org/10.1016/j.bmcl.2006.02.018openalex-snapshot

N-Benzylbenzamides: A new class of potent tyrosinase inhibitors

inferredcites →https://doi.org/10.1016/j.bmcl.2007.10.014openalex-snapshot

Discovery of small-molecule inhibitors of tyrosinase

inferredcites →https://doi.org/10.1016/j.bmcl.2012.04.046openalex-snapshot

Depigmenting activities of kojic acid derivatives without tyrosinase inhibitory activities

inferredcites →https://doi.org/10.1016/j.bmcl.2012.10.050openalex-snapshot

Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors

inferredcites →https://doi.org/10.1021/jf020826fopenalex-snapshot

Mushroom Tyrosinase: Recent Prospects

inferredcites →https://doi.org/10.1021/jf051258hopenalex-snapshot

Isolation and Identification of Flavonoids in Licorice and a Study of Their Inhibitory Effects on Tyrosinase

inferredcites →https://doi.org/10.1021/jf8033286openalex-snapshot

Tyrosinase Inhibitory Polyphenols from Roots ofMorus lhou

inferredcites →https://doi.org/10.1074/jbc.m202461200openalex-snapshot

Structural Basis and Mechanism of the Inhibition of the Type-3 Copper Protein Tyrosinase from Streptomyces antibioticusby Halide Ions

inferredcites →https://doi.org/10.1248/bpb.30.1135openalex-snapshot

Inhibitory Effect of p-Hydroxybenzyl Alcohol on Tyrosinase Activity and Melanogenesis

inferredcites →https://doi.org/10.3390/ijms10062440openalex-snapshot

An Updated Review of Tyrosinase Inhibitors

inferredcites →https://doi.org/10.3724/sp.j.1009.2010.00047openalex-snapshot

GC-MS Analysis of Cortex Magnolia Officinalis Oil Separated by Molecular Distillation

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/cmdc.202400314openalex-snapshot

Tyrosinase Inhibition and Antimelanogenic Effects of Resorcinol‐Containing Compounds

inferred← citeshttps://doi.org/10.1002/jbt.22285openalex-snapshot

Synthesis and biological evaluation of novel indenopyrazole derivatives

inferred← citeshttps://doi.org/10.1002/mrc.4367openalex-snapshot

1H and 13C NMR spectral assignments of 19 novel polymethoxylated diphenylnaphthylpyrazolinylcarbothioamides

inferred← citeshttps://doi.org/10.1007/s00044-014-1001-5openalex-snapshot

Synthesis and cytotoxicity studies of 3,5-diaryl N-acetyl pyrazoline—isatin hybrids

inferred← citeshttps://doi.org/10.1007/s11998-019-00312-4openalex-snapshot

Exploration of high corrosion resistance property of less hazardous pyrazolidine-based benzoxazines in comparison with bisphenol-F derivatives

inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115574openalex-snapshot

Targeting tyrosinase in hyperpigmentation: Current status, limitations and future promises

inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103259openalex-snapshot

Tyrosinase inhibitory effects of Vinca major and its secondary metabolites: Enzyme kinetics and in silico inhibition model of the metabolites validated by pharmacophore modelling

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.bmc.2014.04.060openalex-snapshot

Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted 5-benzylidene(thio) barbiturates as novel tyrosinase inhibitors

inferred← citeshttps://doi.org/10.1016/j.bmc.2016.03.013openalex-snapshot

Design and synthesis of thiourea derivatives with sulfur-containing heterocyclic scaffolds as potential tyrosinase inhibitors

inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2018.03.007openalex-snapshot

In silico modelling of azole derivatives with tyrosinase inhibition ability: Application of the models for activity prediction of new compounds

inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.08.048openalex-snapshot

Design, synthesis and molecular docking study of novel quinoxalin-2(1H)-ones as anti-tumor active agents with inhibition of tyrosine kinase receptor and studying their cyclooxygenase-2 activity

inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.10.030openalex-snapshot

Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors

inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114525openalex-snapshot

Azole inhibitors of mushroom and human tyrosinases: Current advances and prospects of drug development for melanogenic dermatological disorders

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2017.11.147openalex-snapshot

Evaluation of thiazolidinone derivatives as a new class of mushroom tyrosinase inhibitors

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.02.050openalex-snapshot

Novel piperonal 1,3,4-thiadiazolium-2-phenylamines mesoionic derivatives: Synthesis, tyrosinase inhibition evaluation and HSA binding study

inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.11.073openalex-snapshot

Synthesis, spectroscopic characterization, DFT study and antimicrobial activity of novel alkylaminopyrazole derivatives

inferred← citeshttps://doi.org/10.1016/j.phymed.2017.11.012openalex-snapshot

Predicting tyrosinase inhibition by 3D QSAR pharmacophore models and designing potential tyrosinase inhibitors from Traditional Chinese medicine database

inferred← citeshttps://doi.org/10.1021/acs.iecr.9b03440openalex-snapshot

Synthesis of Nontoxic Pyrazolidine-Based Benzoxazine-Coated Cotton Fabric for Oil–Water Separation

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/10.1080/1062936x.2020.1862297openalex-snapshot

SAR and QSAR research on tyrosinase inhibitors using machine learning methods

inferred← citeshttps://doi.org/10.1080/14756366.2018.1545767openalex-snapshot

A comprehensive review on tyrosinase inhibitors

inferred← citeshttps://doi.org/10.1111/cbdd.14209openalex-snapshot

Synthesis and discovery of potential tyrosinase inhibitor of new coumarin‐based thiophenyl‐pyrazolylthiazole nuclei: In vitro evaluation, cytotoxicity, kinetic, and computational studies

inferred← citeshttps://doi.org/10.1517/17460441.2014.907789openalex-snapshot

Design and discovery of mushroom tyrosinase inhibitors and their therapeutic applications

inferred← citeshttps://doi.org/10.25077/jrk.v13i1.486openalex-snapshot

Synthesis of 4-(5-(2,3-Dimenthoxyphenyl)-3-(4-Methoxyphenyl)-4,5-Dihydro-1H-Pyrazol-1-y1) Benzenesulfonamide as a Promosing Tyrosinase Inhibitor Candidate

inferred← citeshttps://doi.org/10.29228/jrp.100openalex-snapshot

Synthesis and antimicrobial activity of [1,2,4]triazіno[2,3-c]quinazoline – pyrazoline hybrids

inferred← citeshttps://doi.org/10.3109/14756366.2015.1004058openalex-snapshot

Natural, semisynthetic and synthetic tyrosinase inhibitors

inferred← citeshttps://doi.org/10.3329/dujps.v24i1.82414openalex-snapshot

Synthesis and Assessment of Antiproliferative, Antioxidant, and In Silico Features of (E)-3-(4-nitrophenyl)-1-phenyl-prop-2-en-1-one and Its Two Pyrazole Derivatives

inferred← citeshttps://doi.org/10.3389/fphar.2024.1332184openalex-snapshot

Design and synthesis of novel dihydropyridine- and benzylideneimine-based tyrosinase inhibitors

inferred← citeshttps://doi.org/10.3390/app9081704openalex-snapshot

Synthesis, Tyrosinase Inhibiting Activity and Molecular Docking of Fluorinated Pyrazole Aldehydes as Phosphodiesterase Inhibitors

inferred← citeshttps://doi.org/10.3390/molecules28155762openalex-snapshot

Tyrosinase Inhibitors: A Perspective

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.