On the public citation graph
Synthesis, Stereochemical Separation, and Biological Evaluation of Selective Inhibitors of Human MAO-B: 1-(4-Arylthiazol-2-yl)-2-(3-methylcyclohexylidene)hydrazines
0 signed · 74 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1531-8257(199903)14:2<219::aid-mds1003>3.0.co;2-9openalex-snapshot
Variations in the monoamine oxidase B lpar;MAOB) gene are associated with Parkinson's disease
inferredcites →https://doi.org/10.1002/jhet.110openalex-snapshot
Synthesis and biological evaluation of novel conjugated coumarin‐thiazole systems
inferredcites →https://doi.org/10.1007/978-3-7091-9050-0_27openalex-snapshot
From moclobemide to Ro 19-6327 and Ro 41-1049: the development of a new class of reversible, selective MAO-A and MAO-B inhibitors
inferredcites →https://doi.org/10.1007/s00702-007-0674-zopenalex-snapshot
New insights into the structures and functions of human monoamine oxidases A and B
inferredcites →https://doi.org/10.1016/j.addr.2008.06.002openalex-snapshot
Monoamine oxidase inactivation: From pathophysiology to therapeutics
inferredcites →https://doi.org/10.1016/j.amjopharm.2006.12.001openalex-snapshot
Rasagiline (TVP-1012): A new selective monoamine oxidase inhibitor for Parkinson's disease
inferredcites →https://doi.org/10.1016/j.bbrc.2006.03.190openalex-snapshot
Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity
inferredcites →https://doi.org/10.1016/j.bmcl.2007.05.078openalex-snapshot
Synthesis and in vitro activity of 2-thiazolylhydrazone derivatives compared with the activity of clotrimazole against clinical isolates of Candida spp.
inferredcites →https://doi.org/10.1016/j.chroma.2007.10.009openalex-snapshot
High-performance liquid chromatographic separation of enantiomers and diastereomers of 2-methylcyclohexanone thiosemicarbazone, and determination of absolute configuration and configurational stability
inferredcites →https://doi.org/10.1016/s0006-2952(99)00340-8openalex-snapshot
Drug treatment of Parkinson’s disease
inferredcites →https://doi.org/10.1021/bi051847gopenalex-snapshot
Functional Role of the “Aromatic Cage” in Human Monoamine Oxidase B: Structures and Catalytic Properties of Tyr435 Mutant Proteins,
inferredcites →https://doi.org/10.1021/bi900413gopenalex-snapshot
Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases
inferredcites →https://doi.org/10.1021/jm031087copenalex-snapshot
Crystal Structures of Monoamine Oxidase B in Complex with Four Inhibitors of the N -Propargylaminoindan Class
inferredcites →https://doi.org/10.1021/jm060869dopenalex-snapshot
Selective Inhibitory Activity against MAO and Molecular Modeling Studies of 2-Thiazolylhydrazone Derivatives
inferredcites →https://doi.org/10.1021/jm800132gopenalex-snapshot
Synthesis, Stereochemical Identification, and Selective Inhibitory Activity against Human Monoamine Oxidase-B of 2-Methylcyclohexylidene-(4-arylthiazol-2-yl)hydrazones
inferredcites →https://doi.org/10.1021/jm800885dopenalex-snapshot
A Novel Histone Acetyltransferase Inhibitor Modulating Gcn5 Network: Cyclopentylidene-[4-(4′-chlorophenyl)thiazol-2-yl)hydrazone
inferredcites →https://doi.org/10.1038/nrn1883openalex-snapshot
The therapeutic potential of monoamine oxidase inhibitors
inferredcites →https://doi.org/10.1038/sj.bjp.0703826openalex-snapshot
Rasagiline [N‐propargyl‐1R(+)‐aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B
inferredcites →https://doi.org/10.1039/c0md00014kopenalex-snapshot
Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl)hydrazones
inferredcites →https://doi.org/10.1073/pnas.0710626105openalex-snapshot
Structure of human monoamine oxidase A at 2.2-Å resolution: The control of opening the entry for substrates/inhibitors
inferredcites →https://doi.org/10.1074/jbc.m500949200openalex-snapshot
Demonstration of Isoleucine 199 as a Structural Determinant for the Selective Inhibition of Human Monoamine Oxidase B by Specific Reversible Inhibitors
inferredcites →https://doi.org/10.1107/s1600536811042486openalex-snapshot
(E)-2-(2-Methylcyclohexylidene)hydrazinecarbothioamide
inferredcites →https://doi.org/10.1111/j.1527-3458.2005.tb00269.xopenalex-snapshot
Neuroprotection by Rasagiline: A New Therapeutic Approach to Parkinson's Disease?
inferredcites →https://doi.org/10.1136/bmj.310.6979.575openalex-snapshot
Fortnightly Review: Drug treatment of Parkinson's disease
inferredcites →https://doi.org/10.1146/annurev.neuro.22.1.197openalex-snapshot
MONOAMINE OXIDASE: From Genes to Behavior
inferredcites →https://doi.org/10.1517/13543776.15.12.1763openalex-snapshot
Recent development of monoamine oxidase inhibitors
inferredcites →https://doi.org/10.2174/0929867043364757openalex-snapshot
Regulation of MAO-A and MAO-B Gene Expression
inferredcites →https://doi.org/10.2174/0929867043364775openalex-snapshot
Clinical Applications of MAO-Inhibitors
inferredcites →https://doi.org/10.2174/0929867043364784openalex-snapshot
Structure and Mechanism of Monoamine Oxidase
inferredcites →https://doi.org/10.2174/1381612043383421openalex-snapshot
Recent Approaches to Novel Anti-Alzheimer Therapy
inferredcites →https://doi.org/10.2174/1570159x15666171128145423openalex-snapshot
Computer-aided Drug Design Applied to Parkinson Targets
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.4782909openalex-extracted
New 2-Hydrazinothiazole Derivatives as Potential Mao-A, Mao-B, Ache, and Bche Inhibitorsri
inferred← citeshttps://doi.org/10.1002/ardp.201200318openalex-snapshot
Synthesis and Selective Human Monoamine Oxidase B Inhibition of Heterocyclic Hybrids Based on Hydrazine and Thiazole Scaffolds
inferred← citeshttps://doi.org/10.1002/jhet.1856openalex-snapshot
Microwave and Ultrasound‐Assisted Synthesis of Thiosemicarbazones and Their Corresponding (4,5‐Substituted‐thiazol‐2‐yl)hydrazines
inferred← citeshttps://doi.org/10.1007/s00044-019-02388-4openalex-snapshot
Novel isoxazole derivatives as potential antiparkinson agents: synthesis, evaluation of monoamine oxidase inhibitory activity and docking studies
inferred← citeshttps://doi.org/10.1016/j.arabjc.2012.12.034openalex-snapshot
Nitrogen heterocycles as potential monoamine oxidase inhibitors: Synthetic aspects
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.12.019openalex-snapshot
In vitro and in silico evaluation of new thiazole compounds as monoamine oxidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103299openalex-snapshot
Critical evaluation of current Alzheimer’s drug discovery (2018–19) & futuristic Alzheimer drug model approach
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.01.022openalex-snapshot
Synthesis of a novel series of thiazole-based histone acetyltransferase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.03.042openalex-snapshot
Identification of the stereochemical requirements in the 4-aryl-2-cycloalkylidenhydrazinylthiazole scaffold for the design of selective human monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.01.038openalex-snapshot
A novel library of saccharin and acesulfame derivatives as potent and selective inhibitors of carbonic anhydrase IX and XII isoforms
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128994openalex-snapshot
Design, synthesis, in-vitro, in-vivo and ex-vivo pharmacology of thiazolidine-2,4-dione derivatives as selective and reversible monoamine oxidase-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.chroma.2012.08.007openalex-snapshot
3-Methylcyclohexanone thiosemicarbazone: Determination of E/Z isomerization barrier by dynamic high-performance liquid chromatography, configuration assignment and theoretical study of the mechanisms involved by the spontaneous, acid and base catalyzed processes
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.04.006openalex-snapshot
Synthesis, anti-Candida activity, and cytotoxicity of new (4-(4-iodophenyl)thiazol-2-yl)hydrazine derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.10.032openalex-snapshot
Recent advances in the development of selective human MAO-B inhibitors: (Hetero)arylidene-(4-substituted-thiazol-2-yl)hydrazines
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.10.035openalex-snapshot
Combining QSAR classification models for predictive modeling of human monoamine oxidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.05.032openalex-snapshot
Exploring 4-substituted-2-thiazolylhydrazones from 2-, 3-, and 4-acetylpyridine as selective and reversible hMAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.10.050openalex-snapshot
Design, synthesis and biochemical evaluation of novel multi-target inhibitors as potential anti-Parkinson agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.12.013openalex-snapshot
Design, synthesis and biological assessment of new thiazolylhydrazine derivatives as selective and reversible h MAO-A inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.05.078openalex-snapshot
Histone acetyltransferase inhibitors: An overview in synthesis, structure-activity relationship and molecular mechanism
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112787openalex-snapshot
A comprehensive review of monoamine oxidase inhibitors as Anti-Alzheimer’s disease agents: A review
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.141154openalex-snapshot
Synthesis, biological evaluation, molecular docking, molecular dynamics, and ADME studies of novel thiouracil derivatives as dual inhibitors of butyrylcholinesterase and acetylcholinesterase enzymes
inferred← citeshttps://doi.org/10.1021/jm200716yopenalex-snapshot
Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors
inferred← citeshttps://doi.org/10.1021/jm400336xopenalex-snapshot
Dual Targeting of Adenosine A2A Receptors and Monoamine Oxidase B by 4H-3,1-Benzothiazin-4-ones
inferred← citeshttps://doi.org/10.1021/jm501690ropenalex-snapshot
New Frontiers in Selective Human MAO-B Inhibitors
inferred← citeshttps://doi.org/10.1039/c0cc05804aopenalex-snapshot
Enantioselective aza-Michael reaction of hydrazide to chalcones through the nonactivated amine moiety conjugated addition
inferred← citeshttps://doi.org/10.1080/10426507.2020.1722667openalex-snapshot
Synthesis and monoamine oxidase A/B inhibitory evaluation of new benzothiazole-thiazolylhydrazine derivatives
inferred← citeshttps://doi.org/10.1080/10426507.2024.2427148openalex-snapshot
New 2-hydrazinothiazole derivatives as potential MAO-A, MAO-B, AChE, and BChE inhibitors
inferred← citeshttps://doi.org/10.1080/14756366.2019.1571272openalex-snapshot
4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis
inferred← citeshttps://doi.org/10.1107/s1600536811042486openalex-snapshot
(E)-2-(2-Methylcyclohexylidene)hydrazinecarbothioamide
inferred← citeshttps://doi.org/10.1111/cbdd.12629openalex-snapshot
Coumarin: A Privileged Scaffold for the Design and Development of Antineurodegenerative Agents
inferred← citeshttps://doi.org/10.1248/cpb.c14-00616openalex-snapshot
Synthesis, Antibacterial, Antioxidant Activity and QSAR Studies of Novel 2-Arylidenehydrazinyl-4-arylthiazole Analogues
inferred← citeshttps://doi.org/10.1515/znc-2021-0058openalex-snapshot
New indane derivatives containing 2-hydrazinothiazole as potential acetylcholinesterase and monoamine oxidase-B inhibitors
inferred← citeshttps://doi.org/10.1515/znc-2021-0223openalex-snapshot
Novel thiazolyl-hydrazone derivatives including piperazine ring: synthesis, in vitro evaluation, and molecular docking as selective MAO-A inhibitor
inferred← citeshttps://doi.org/10.1517/13543776.2012.698613openalex-snapshot
Patent-related survey on new monoamine oxidase inhibitors and their therapeutic potential
inferred← citeshttps://doi.org/10.15272/ajbps.v4i36.577openalex-snapshot
Molecular Docking Studies on (Hetero)arlylidene(4-substituted-thiazol-2-yl)hydrazines as MAO-B Inhibitors
inferred← citeshttps://doi.org/10.2139/ssrn.7417609openalex-snapshot
Unlocking Triplet Carbene Reactivity: Photocatalyst-Free Synthesis of 1,1-Disubstituted Hydrazines via Visible-Light N–H Insertion
inferred← citeshttps://doi.org/10.2174/0929867327666200121165931openalex-snapshot
New Aspects of Monoamine Oxidase B Inhibitors: The Key Role of Halogens to Open the Golden Door
inferred← citeshttps://doi.org/10.2174/1570159x15666170116145316openalex-snapshot
Chemoinformatics Profiling of the Chromone Nucleus as a MAO-B/A2AAR Dual Binding Scaffold
inferred← citeshttps://doi.org/10.2174/1570159x15666171128145423openalex-snapshot
Computer-aided Drug Design Applied to Parkinson Targets
inferred← citeshttps://doi.org/10.3109/14756366.2016.1156103openalex-snapshot
Identification of new anti- Candida compounds by ligand-based pharmacophore virtual screening
inferred← citeshttps://doi.org/10.3390/molecules22081381openalex-snapshot
Synthesis of New Hydrazone Derivatives for MAO Enzymes Inhibitory Activity
inferred← citeshttps://doi.org/10.5772/62077openalex-snapshot
Significance of Thiazole-based Heterocycles for Bioactive Systems
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.