On the public citation graph
Benzimidazole Derivatives as New Serotonin 5-HT6Receptor Antagonists. Molecular Mechanisms of Receptor Inactivation
0 signed · 118 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known work and none has been retracted — and get a dated CiteStamped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/cbic.200600429openalex-snapshot
The Role of Internal Water Molecules in the Structure and Function of the Rhodopsin Family of G Protein‐Coupled Receptors
inferredcites →https://doi.org/10.1002/jcc.10349openalex-snapshot
A point‐charge force field for molecular mechanics simulations of proteins based on condensed‐phase quantum mechanical calculations
inferredcites →https://doi.org/10.1002/jcc.20035openalex-snapshot
Development and testing of a general amber force field
inferredcites →https://doi.org/10.1006/bbrc.1993.1619openalex-snapshot
A Novel Rat Serotonin (5-HT6) Receptor: Molecular Cloning, Localization and Stimulation of cAMP Accumulation
inferredcites →https://doi.org/10.1007/bf02450276openalex-snapshot
Cellule enterocromaffini e cellule basigranulose acidofile nei Vertebrati
inferredcites →https://doi.org/10.1007/s10540-005-2896-3openalex-snapshot
Transmembrane Signaling in the Brain by Serotonin, A Key Regulator of Physiology and Emotion
inferredcites →https://doi.org/10.1016/0006-2952(73)90196-2openalex-snapshot
Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
inferredcites →https://doi.org/10.1016/0924-977x(96)83212-3openalex-snapshot
5-HT6 and 5-HT7 receptors: New targets for neuropsychiatry
inferredcites →https://doi.org/10.1016/j.bmc.2008.10.041openalex-snapshot
The importance of CH/π hydrogen bonds in rational drug design: An ab initio fragment molecular orbital study to leukocyte-specific protein tyrosine (LCK) kinase
inferredcites →https://doi.org/10.1016/j.bmcl.2004.05.076openalex-snapshot
Possible differences in modes of agonist and antagonist binding at human 5-HT6 receptors
inferredcites →https://doi.org/10.1016/j.drudis.2006.02.004openalex-snapshot
Medicinal chemistry strategies to 5-HT6 receptor ligands as potential cognitive enhancers and antiobesity agents
inferredcites →https://doi.org/10.1016/j.jmb.2005.12.046openalex-snapshot
Location of Trp265 in Metarhodopsin II: Implications for the Activation Mechanism of the Visual Receptor Rhodopsin
inferredcites →https://doi.org/10.1016/j.pharmthera.2005.05.001openalex-snapshot
5-HT6 receptors: a novel target for cognitive enhancement
inferredcites →https://doi.org/10.1016/j.pharmthera.2007.08.006openalex-snapshot
Selective 5-HT6 receptor ligands: Progress in the development of a novel pharmacological approach to the treatment of obesity and related metabolic disorders
inferredcites →https://doi.org/10.1016/j.tips.2009.02.006openalex-snapshot
Ligand binding and micro-switches in 7TM receptor structures
inferredcites →https://doi.org/10.1016/s0006-8993(96)01224-3openalex-snapshot
Immuno-localization of serotonin 5-HT6 receptor-like material in the rat central nervous system
inferredcites →https://doi.org/10.1016/s0021-9258(18)57137-4openalex-snapshot
SERUM VASOCONSTRICTOR (SEROTONIN)
inferredcites →https://doi.org/10.1016/s0022-3565(25)10539-9openalex-snapshot
Determination of the role of the 5-ht6 receptor in the rat brain: a study using antisense oligonucleotides.
inferredcites →https://doi.org/10.1016/s0026-895x(25)13130-1openalex-snapshot
Molecular cloning of a mammalian serotonin receptor that activates adenylate cyclase.
inferredcites →https://doi.org/10.1016/s0026-895x(25)13616-xopenalex-snapshot
Cloning and expression of a novel serotonin receptor with high affinity for tricyclic psychotropic drugs.
inferredcites →https://doi.org/10.1016/s0028-3908(97)00036-1openalex-snapshot
5-HT Receptor Classification and Nomenclature: Towards a Harmonization with the Human Genome
inferredcites →https://doi.org/10.1016/s0040-4020(00)00225-8openalex-snapshot
Pd(0) Amination of Benzimidazoles as an Efficient Method towards New (Benzimidazolyl)piperazines with High Affinity for the 5-HT1A Receptor
inferredcites →https://doi.org/10.1016/s0149-7634(96)00022-xopenalex-snapshot
Multiple Serotonin Receptors: Too Many, Not Enough, or Just the Right Number?
inferredcites →https://doi.org/10.1016/s0169-328x(01)00090-0openalex-snapshot
Cloning of the mouse 5-HT6 serotonin receptor and mutagenesis studies of the third cytoplasmic loop
inferredcites →https://doi.org/10.1016/s0960-894x(00)00453-4openalex-snapshot
N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists
inferredcites →https://doi.org/10.1021/jm010943mopenalex-snapshot
N-Arylsulfonylindole Derivatives as Serotonin 5-HT6Receptor Ligands
inferredcites →https://doi.org/10.1021/jm030030nopenalex-snapshot
Higher-End Serotonin Receptors: 5-HT5, 5-HT6, and 5-HT7
inferredcites →https://doi.org/10.1021/jm048999eopenalex-snapshot
Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 8. Computational Simulation of Ligand−Receptor Interaction of 5-HT1AR Agonists with Selectivity over α1-Adrenoceptors
inferredcites →https://doi.org/10.1021/jm050247copenalex-snapshot
A Three-Dimensional Pharmacophore Model for 5-Hydroxytryptamine6(5-HT6) Receptor Antagonists
inferredcites →https://doi.org/10.1021/jm070910sopenalex-snapshot
Binding of Serotonin and N1-Benzenesulfonyltryptamine-Related Analogs at Human 5-HT6 Serotonin Receptors: Receptor Modeling Studies
inferredcites →https://doi.org/10.1021/jm980532eopenalex-snapshot
5-Chloro-N-(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): A Potent, Selective, and Orally Bioavailable 5-HT6 Receptor Antagonist
inferredcites →https://doi.org/10.1021/jm990550bopenalex-snapshot
2-Substituted Tryptamines: Agents with Selectivity for 5-HT6Serotonin Receptors
inferredcites →https://doi.org/10.1038/nature06325openalex-snapshot
Crystal structure of the human β2 adrenergic G-protein-coupled receptor
inferredcites →https://doi.org/10.1038/nature07101openalex-snapshot
Structure of a β1-adrenergic G-protein-coupled receptor
inferredcites →https://doi.org/10.1038/nature08144openalex-snapshot
The structure and function of G-protein-coupled receptors
inferredcites →https://doi.org/10.1038/nchembio714openalex-snapshot
Linking agonist binding to histamine H1 receptor activation
inferredcites →https://doi.org/10.1038/sj.bjp.0701851openalex-snapshot
Characterization of Ro 04‐6790 and Ro 63‐0563: potent and selective antagonists at human and rat 5‐HT6 receptors
inferredcites →https://doi.org/10.1038/sj.emboj.7600374openalex-snapshot
Electron crystallography reveals the structure of metarhodopsin I
inferredcites →https://doi.org/10.1046/j.1471-4159.1996.66010047.xopenalex-snapshot
Cloning, Characterization, and Chromosomal Localization of a Human 5‐HT6 Serotonin Receptor
inferredcites →https://doi.org/10.1071/ch9940247openalex-snapshot
DNA Binding Compounds. V. Synthesis and Characterization of Boron Containing Bibenzimidazoles Related to the DNA Minor Groove Binder, Hoechst-33258
inferredcites →https://doi.org/10.1074/jbc.m310888200openalex-snapshot
Sequential Binding of Agonists to the β2 Adrenoceptor
inferredcites →https://doi.org/10.1074/jbc.m502272200openalex-snapshot
Uncoupling and Endocytosis of 5-Hydroxytryptamine 4 Receptors
inferredcites →https://doi.org/10.1097/00001756-199412000-00037openalex-snapshot
5-HT6 receptors positively coupled to adenylyl cyclase in striatal neurones in culture
inferredcites →https://doi.org/10.1124/mol.108.053686openalex-snapshot
Conformational Toggle Switches Implicated in Basal Constitutive and Agonist-Induced Activated States of 5-Hydroxytryptamine-4 Receptors
inferredcites →https://doi.org/10.1124/mol.64.6.1295openalex-snapshot
Differences in the Central Nervous System Distribution and Pharmacology of the Mouse 5-Hydroxytryptamine-6 Receptor Compared with Rat and Human Receptors Investigated by Radioligand Binding, Site-Directed Mutagenesis, and Molecular Modeling
inferredcites →https://doi.org/10.1126/science.1150577openalex-snapshot
High-Resolution Crystal Structure of an Engineered Human β 2 -Adrenergic G Protein–Coupled Receptor
inferredcites →https://doi.org/10.1126/science.1150609openalex-snapshot
GPCR Engineering Yields High-Resolution Structural Insights into β 2 -Adrenergic Receptor Function
inferredcites →https://doi.org/10.1146/annurev.biophys.29.1.291openalex-snapshot
Comparative Protein Structure Modeling of Genes and Genomes
inferredcites →https://doi.org/10.1146/annurev.pharmtox.42.091101.144224openalex-snapshot
The Binding Site of Aminergic G Protein–Coupled Receptors: The Transmembrane Segments and Second Extracellular Loop
inferredcites →https://doi.org/10.1146/annurev.pharmtox.46.120604.141218openalex-snapshot
MOLECULAR MECHANISM OF 7TM RECEPTOR ACTIVATION—A GLOBAL TOGGLE SWITCH MODEL
inferredcites →https://doi.org/10.1146/annurev.pharmtox.47.120505.105126openalex-snapshot
Pharmacogenomic and Structural Analysis of Constitutive G Protein–Coupled Receptor Activity
inferredcites →https://doi.org/10.1358/dof.2005.030.05.907630openalex-snapshot
Drug discovery targets: 5-HT6 receptor
inferredcites →https://doi.org/10.1517/13543776.12.4.513openalex-snapshot
Recent progress in 5-HT6receptor antagonists for the treatment of CNS diseases
inferredcites →https://doi.org/10.1517/13543776.8.10.1217openalex-snapshot
The 5-hydroxytryptamine 6 receptor: localisation and function
inferredcites →https://doi.org/10.2174/092986706775197953openalex-snapshot
Heptahelical and Other G-Protein-Coupled Receptors (GPCRs) Signaling
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adsc.201401110openalex-snapshot
Phenyliodine Diacetate‐Mediated Intramolecular C(sp2)H Amidation for 1,2‐Disubstituted Benzimidazole Synthesis under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ange.202306176openalex-snapshot
Mit sichtbarem Licht schaltbare Benzimidazol‐Azo‐Arene wirken als β‐Arrestin2 funktionell selektive Cannabinoid‐Rezeptor 2 Agonisten
inferred← citeshttps://doi.org/10.1002/anie.202306176openalex-snapshot
Visible‐Light Photoswitchable Benzimidazole Azo‐Arenes as β‐Arrestin2‐Biased Selective Cannabinoid 2 Receptor Agonists
inferred← citeshttps://doi.org/10.1002/aoc.3747openalex-snapshot
Two silver(I) complexes with bis(benzimidazole)‐2‐oxopropane ligands: Syntheses, crystal structures and DNA binding studies
inferred← citeshttps://doi.org/10.1002/ejoc.201800688openalex-snapshot
An Intramolecular C(sp2)–H Amidation Using N‐Iodosuccinimide
inferred← citeshttps://doi.org/10.1002/jcc.21857openalex-snapshot
Importance of CH/π hydrogen bonds in recognition of the core motif in proline‐recognition domains: An Ab initio fragment molecular orbital study
inferred← citeshttps://doi.org/10.1002/mrc.4463openalex-snapshot
Separation and identification of the mixture of 2‐(3,4‐dimethoxyphenyl)‐1‐n‐propyl or (4‐chlorobenzyl)‐5 and (6)‐1H‐benzimidazolecarbonitriles
inferred← citeshttps://doi.org/10.1002/open.202000261openalex-snapshot
Kinetic Target‐Guided Synthesis of Small‐Molecule G‐Quadruplex Stabilizers
inferred← citeshttps://doi.org/10.1007/978-1-4939-7404-7_15openalex-snapshot
Computational Modeling of Drugs for Alzheimer’s Disease: Design of Serotonin 5-HT6 Antagonists
inferred← citeshttps://doi.org/10.1007/978-94-007-7423-0_2openalex-snapshot
Modeling of G Protein-Coupled Receptors Using Crystal Structures: From Monomers to Signaling Complexes
inferred← citeshttps://doi.org/10.1007/s10822-015-9883-yopenalex-snapshot
Dynamics and structural determinants of ligand recognition of the 5-HT6 receptor
inferred← citeshttps://doi.org/10.1007/s11164-023-05011-9openalex-snapshot
Vitamin B1-catalyzed one-pot ultrasound-assisted synthesis of 1,2-disubstituted benzimidazole and its selective recognition of metal ions
inferred← citeshttps://doi.org/10.1007/s11224-020-01513-zopenalex-snapshot
Drug design of new 5-HT6 antagonists: a QSAR study of arylsulfonamide derivatives
inferred← citeshttps://doi.org/10.1007/s11243-015-9948-8openalex-snapshot
Three- and four-coordinate Ag(I) complexes of crotonate and bis(benzimidazole)-2-oxapropane ligands: syntheses, crystal structures, DNA-binding studies and antioxidant activities
inferred← citeshttps://doi.org/10.1016/b978-0-12-384976-2.00001-0openalex-snapshot
5-HT6 Medicinal Chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-391861-1.00005-8openalex-snapshot
The Role of Hydrophobic Amino Acids in the Structure and Function of the Rhodopsin Family of G Protein-Coupled Receptors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.12.019openalex-snapshot
A simple and efficient synthesis of benzimidazoles containing piperazine or morpholine skeleton at C-6 position as glucosidase inhibitors with antioxidant activity
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.07.004openalex-snapshot
CH/π hydrogen bonds play a role in ligand recognition and equilibrium between active and inactive states of the β2 adrenergic receptor: An ab initio fragment molecular orbital (FMO) study
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.02.020openalex-snapshot
Synthesis and biological evaluation of benzoisothiazole derivatives possessing N,N-dimethylformimidamide group as 5-HT6 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.01.003openalex-snapshot
Structure activity relationship studies of 3-arylsulfonyl-pyrido[1,2-a]pyrimidin-4-imines as potent 5-HT6 antagonists
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.11.050openalex-snapshot
Novel brain penetrant benzofuropiperidine 5-HT6 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.12.026openalex-snapshot
Discovery of 7-arylsulfonyl-1,2,3,4, 4a,9a-hexahydro-benzo[4,5]furo[2,3-c]pyridines: Identification of a potent and selective 5-HT6 receptor antagonist showing activity in rat social recognition test
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.05.100openalex-snapshot
Synthesis and the 5-HT6 receptor antagonistic effect of 3-arylsulfonylamino-5,6-dihydro-6-substituted pyrazolo[3,4]pyridinones for neuropathic pain treatment
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.04.033openalex-snapshot
The computer-aided discovery of novel family of the 5-HT6 serotonin receptor ligands among derivatives of 4-benzyl-1,3,5-triazine
inferred← citeshttps://doi.org/10.1016/j.ica.2012.09.013openalex-snapshot
Non-symmetrically substituted N-heterocyclic carbene–Ag(I) complexes of benzimidazol-2-ylidenes: Synthesis, crystal structures, anticancer activity and transmetallation studies
inferred← citeshttps://doi.org/10.1016/j.ica.2021.120548openalex-snapshot
Competition between electrocatalytic CO2 reduction and H+ reduction by Cu(II), Co(II) complexes containing redox-active ligand
inferred← citeshttps://doi.org/10.1016/j.jmgm.2021.107844openalex-snapshot
Drug design of new 5-HT6R antagonists aided by artificial neural networks
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127424openalex-snapshot
Synthesis, crystal structure, fluorescent and electrochemical properties of three silver(I) complexes with 2,2’-(1,4-butanediyl)bis-1,3-benzimidazole bridging ligand
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137714openalex-snapshot
Synthesis of benzimidazoles containing piperazine ring as potential therapeutic agents against diabetes mellitus and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156086openalex-snapshot
Carbamoyldithioesters as new suppliers of one‑carbon fragment in the benzimidazoles and benzoxazoles synthesis
inferred← citeshttps://doi.org/10.1016/j.tranon.2020.100854openalex-snapshot
Synthesis of 99mTc-labeled 2-Mercaptobenzimidazole as a novel radiotracer to diagnose tumor hypoxia
inferred← citeshttps://doi.org/10.1021/acs.jctc.2c00371openalex-snapshot
Induced-Fit Docking Enables Accurate Free Energy Perturbation Calculations in Homology Models
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c02148openalex-snapshot
First-in-Class Selenium-Containing Potent Serotonin Receptor 5-HT 6 Agents with a Beneficial Neuroprotective Profile against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00179openalex-snapshot
Therapeutic Potential of 5-HT6Receptor Agonists
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.8b00836openalex-snapshot
Aminergic GPCR–Ligand Interactions: A Chemical and Structural Map of Receptor Mutation Data
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01465openalex-snapshot
Copper-Catalyzed Inter/Intramolecular N-Alkenylation of Benzimidazoles via Tandem Processes Involving Selectively Mild Iodination of sp3 C–H Bond at α-Position of Ester
inferred← citeshttps://doi.org/10.1021/acschemneuro.1c00037openalex-snapshot
DARK Classics in Chemical Neuroscience: Etonitazene and Related Benzimidazoles
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.6b00482openalex-snapshot
Pyrano[2,3,4-cd]indole as a Scaffold for Selective Nonbasic 5-HT6R Ligands
inferred← citeshttps://doi.org/10.1021/ci500001fopenalex-snapshot
Impact of Template Choice on Homology Model Efficiency in Virtual Screening
inferred← citeshttps://doi.org/10.1021/jm1007177openalex-snapshot
Development of Molecular Probes for the Human 5-HT6 Receptor
inferred← citeshttps://doi.org/10.1021/jm200371qopenalex-snapshot
Progress in Structure Based Drug Design for G Protein-Coupled Receptors
inferred← citeshttps://doi.org/10.1021/jm200466ropenalex-snapshot
N′-(Arylsulfonyl)pyrazoline-1-carboxamidines as Novel, Neutral 5-Hydroxytryptamine 6 Receptor (5-HT6R) Antagonists with Unique Structural Features
inferred← citeshttps://doi.org/10.1021/jm2007886openalex-snapshot
New Serotonin 5-HT1A Receptor Agonists with Neuroprotective Effect against Ischemic Cell Damage
inferred← citeshttps://doi.org/10.1021/jm401895uopenalex-snapshot
Novel Arylsulfonamide Derivatives with 5-HT6/5-HT7Receptor Antagonism Targeting Behavioral and Psychological Symptoms of Dementia
inferred← citeshttps://doi.org/10.1021/jm5003952openalex-snapshot
Serotonin 5-HT6Receptor Antagonists for the Treatment of Cognitive Deficiency in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1038/srep41293openalex-snapshot
A new serotonin 5-HT6 receptor antagonist with procognitive activity – Importance of a halogen bond interaction to stabilize the binding
inferred← citeshttps://doi.org/10.1039/c0md00258eopenalex-snapshot
The importance of solvation in the design of ligands targeting membrane proteins
inferred← citeshttps://doi.org/10.1039/c3ra22435jopenalex-snapshot
A simple and straightforward synthesis of substituted 2-arylbenzimidazoles over silica gel
inferred← citeshttps://doi.org/10.1039/c4cp00099dopenalex-snapshot
CH–π hydrogen bonds in biological macromolecules
inferred← citeshttps://doi.org/10.1039/c6ra09733bopenalex-snapshot
Mono-, bi- and multi-nuclear silver complexes constructed from bis(benzimidazole)-2-oxapropane ligands and methacrylate: syntheses, crystal structures, DNA-binding properties and antioxidant activities
inferred← citeshttps://doi.org/10.1039/d1ra07978fopenalex-snapshot
Synthesis of 7-amino-6-halogeno-3-phenylquinoxaline-2-carbonitrile 1,4-dioxides: a way forward for targeting hypoxia and drug resistance of cancer cells
inferred← citeshttps://doi.org/10.1039/d3sc05246jopenalex-snapshot
Arylazobenzimidazoles: versatile visible-light photoswitches with tuneable Z -isomer stability
inferred← citeshttps://doi.org/10.1039/d4nj03105aopenalex-snapshot
Cyclocondensation of o -phenylenediamines with α-ketothioesters: a novel approach for the synthesis of 2-acylbenzimidazoles
inferred← citeshttps://doi.org/10.1107/s205322961402405xopenalex-snapshot
Structure determination of three furan-substituted benzimidazoles and calculation of π–π and C—H...π interaction energies
inferred← citeshttps://doi.org/10.2165/11590190-000000000-00000openalex-snapshot
Role of Serotonin in Alzheimerʼs Disease
inferred← citeshttps://doi.org/10.2174/092986711796011283openalex-snapshot
Serotonin Receptors of Type 6 (5-HT6): What can we Expect from them?
inferred← citeshttps://doi.org/10.3390/ijms23169443openalex-snapshot
Serotonin 5-HT6 Receptor Ligands and Butyrylcholinesterase Inhibitors Displaying Antioxidant Activity—Design, Synthesis and Biological Evaluation of Multifunctional Agents against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules23102529openalex-snapshot
Computer-Aided Studies for Novel Arylhydantoin 1,3,5-Triazine Derivatives as 5-HT6 Serotonin Receptor Ligands with Antidepressive-Like, Anxiolytic and Antiobesity Action In Vivo
inferred← citeshttps://doi.org/10.3390/molecules27092626openalex-snapshot
In Silico Screening of Natural Compounds for Candidates 5HT6 Receptor Antagonists against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ph14060528openalex-snapshot
Novel N-Arylsulfonylindoles Targeted as Ligands of the 5-HT6 Receptor. Insights on the Influence of C-5 Substitution on Ligand Affinity
inferred← citeshttps://doi.org/10.5772/intechopen.87068openalex-snapshot
Catalytic Intermolecular Functionalization of Benzimidazoles
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.