On the public citation graph

Comparative Quantitative Structure−Activity Relationship Studies (QSAR) on Non-Benzodiazepine Compounds Binding to Benzodiazepine Receptor (BzR)

0 signed · 115 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9780470171912.ch4openalex-snapshot

Quantitative Models of Steric Effects

inferredcites →https://doi.org/10.1002/qsar.19880070105openalex-snapshot

Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR Studies

inferredcites →https://doi.org/10.1002/qsar.19910100410openalex-snapshot

Comprehensive Medicinal Chemistry

inferredcites →https://doi.org/10.1002/qsar.19960150104openalex-snapshot

Quantitative Structure ‐ Activity Relationship Studies on Benzodiazepine Receptor Binding of Some Nonbenzodiazepine Series of Ligands

inferredcites →https://doi.org/10.1002/qsar.19970160503openalex-snapshot

Quantitative Structure–Activity Relationship Studies on Some Nonbenzodiazepines Binding to Benzodiazepine Receptor

inferredcites →https://doi.org/10.1002/qsar.2660110403openalex-snapshot

Study of Benzodiazepines Receptor Sites Using a Combined QSAR‐CoMFA Approach

inferredcites →https://doi.org/10.1007/bf00498510openalex-snapshot

A three-state model of the benzodiazepine receptor explains the interactions between the benzodiazepine antagonist Ro 15-1788, benzodiazepine tranquilizers, ?-carbolines, and phenobarbitone

inferredcites →https://doi.org/10.1016/0006-2952(88)90079-2openalex-snapshot

The influence of lipophilic character on receptor binding affinity of a series of β- carbolines

inferredcites →https://doi.org/10.1016/0006-2952(90)90321-bopenalex-snapshot

Identification and distribution of peripheral benzodiazepine binding sites in male rat genital tract

inferredcites →https://doi.org/10.1016/0014-5793(78)80331-7openalex-snapshot

Diazepam receptor: Specific binding of [3H]diazepam and [3H]flunitrazepam to rat brain subfractions

inferredcites →https://doi.org/10.1016/0024-3205(91)90533-hopenalex-snapshot

Molecular models for recognition and activation at the benzodiazepine receptor: A review

inferredcites →https://doi.org/10.1016/0028-3908(78)90125-9openalex-snapshot

Effects of flurazepam on amino acid-evoked responses recorded from the lobster muscle and the frog spinal cord

inferredcites →https://doi.org/10.1016/0165-6147(92)90027-4openalex-snapshot

Multiple benzodiazepine receptors: no reason for anxiety

inferredcites →https://doi.org/10.1016/0166-2236(83)90119-4openalex-snapshot

Multiple GABA receptors and associated regulatory sites

inferredcites →https://doi.org/10.1016/0169-409x(91)90053-fopenalex-snapshot

Forthcoming events

inferredcites →https://doi.org/10.1016/0223-5234(92)90058-9openalex-snapshot

Synthesis and benzodiazepine receptor binding of some 4H-pyrimido[2,1-b]benzothiazol-4-ones

inferredcites →https://doi.org/10.1016/0223-5234(96)80363-1openalex-snapshot

Benzodiazepine receptor ligands. Synthesis and pharmacological evaluation of 3-, 7- and 8-substituted [5,1-c][1,2,4]benzotriazines and 5-oxide derivatives. Part I

inferredcites →https://doi.org/10.1016/0223-5234(96)85873-9openalex-snapshot

Syntheses, pharmacological evaluation and molecular modelling of substituted 6-alkoxyimidazo[1,2-b]pyridazines as new ligands for the benzodiazepine receptor

inferredcites →https://doi.org/10.1016/0223-5234(96)88259-6openalex-snapshot

Syntheses of 5-thienyl and 5-furyl-substituted benzodiazepines: probes of the pharmacophore for benzodiazepine receptor agonists

inferredcites →https://doi.org/10.1016/0223-5234(96)89169-0openalex-snapshot

Oxadiazoles as bioisosteric transformations of carboxylic functionalities. II

inferredcites →https://doi.org/10.1016/s0021-9258(17)36131-8openalex-snapshot

The peripheral-type benzodiazepine receptor. Localization to the mitochondrial outer membrane.

inferredcites →https://doi.org/10.1016/s0021-9258(19)84763-4openalex-snapshot

Subcellular Distribution of “Peripheral Type” Binding Sites for [3H]Ro5-4864 in guinea pig lung

inferredcites →https://doi.org/10.1016/s0022-3565(25)33552-4openalex-snapshot

Specific high-affinity binding sites for [3H]Ro 5-4864 in rat brain and kidney.

inferredcites →https://doi.org/10.1016/s0026-895x(25)15026-8openalex-snapshot

Characterization of peripheral-type benzodiazepine binding sites in brain using [3H]Ro 5-4864.

inferredcites →https://doi.org/10.1016/s0306-4522(03)00288-4openalex-snapshot

Comparative modeling of GABAA receptors: limits, insights, future developments

inferredcites →https://doi.org/10.1016/s0968-0896(00)82154-9openalex-snapshot

2-Aryl-2,5-dihydropyridazino[4,3-b]lindol-3(3H)-ones: Novel rigid planar benzodiazepine receptor ligands

inferredcites →https://doi.org/10.1016/s0968-0896(96)00220-9openalex-snapshot

Structure-activity relationships of 2-Aryl-2,5-dihydropyridazino[4,3-b]indol-3(3H)-ones at the benzodiazepine receptor

inferredcites →https://doi.org/10.1016/s0968-0896(97)10039-6openalex-snapshot

High affinity central benzodiazepine receptor ligands: synthesis and structure–activity relationship studies of a new series of pyrazolo[4,3-c]quinolin-3-ones

inferredcites →https://doi.org/10.1016/s0968-0896(99)00093-0openalex-snapshot

Synthesis and structure–affinity relationships at the central benzodiazepine receptor of pyridazino[4,3-b]indoles and Indeno[1,2-c]pyridazines

inferredcites →https://doi.org/10.1016/s0968-0896(99)00232-1openalex-snapshot

Synthesis and BZR affinity of pyrazolo[1,5-a]pyrimidine derivatives. part 1: study of the structural features for BZR recognition

inferredcites →https://doi.org/10.1016/s1471-4892(01)00008-xopenalex-snapshot

GABAA-receptor subtypes: a new pharmacology

inferredcites →https://doi.org/10.1021/ar50020a002openalex-snapshot

Quantitative approach to biochemical structure-activity relationships

inferredcites →https://doi.org/10.1021/cr00002a004openalex-snapshot

A survey of Hammett substituent constants and resonance and field parameters

inferredcites →https://doi.org/10.1021/jm00036a007openalex-snapshot

Novel Ligands Specific for Mitochondrial Benzodiazepine Receptors: 6-arylpyrrolo[2,1-d][1,5]benzothiazepine Derivatives. Synthesis, Structure-Activity Relationships, and Molecular Modeling Studies

inferredcites →https://doi.org/10.1021/jm00044a004openalex-snapshot

Structure-Activity Relationships of 1,2,4-Triazolo[1,5-a]quinoxalines and Their 1-Deaza Analogs Imidazo[1,2-a]quinoxalines at the Benzodiazepine Receptor

inferredcites →https://doi.org/10.1021/jm00050a007openalex-snapshot

A Comparative Molecular Field Analysis Model for 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines Binding Selectively to the Mitochondrial Benzodiazepine Receptor

inferredcites →https://doi.org/10.1021/jm00060a007openalex-snapshot

Synthesis and evaluation of imidazo[1,5-a][1,4]benzodiazepine esters with high affinities and selectivities at "diazepam-insensitive" benzodiazepine receptors

inferredcites →https://doi.org/10.1021/jm00065a004openalex-snapshot

Synthetic and computer-assisted analysis of the structural requirements for selective, high-affinity ligand binding to diazepam-insensitive benzodiazepine receptors

inferredcites →https://doi.org/10.1021/jm00072a012openalex-snapshot

QSAR's from similarity matrices. Technique validation and application in the comparison of different similarity evaluation methods

inferredcites →https://doi.org/10.1021/jm0009742openalex-snapshot

Mapping and Fitting the Peripheral Benzodiazepine Receptor Binding Site by Carboxamide Derivatives. Comparison of Different Approaches to Quantitative Ligand−Receptor Interaction Modeling

inferredcites →https://doi.org/10.1021/jm00117a029openalex-snapshot

Synthesis of novel 3-substituted .beta.-carbolines as benzodiazepine receptor ligands: probing the benzodiazepine receptor pharmacophore

inferredcites →https://doi.org/10.1021/jm00125a015openalex-snapshot

Benzodiazepine receptor binding activity of 6,9-disubstituted purines

inferredcites →https://doi.org/10.1021/jm00132a004openalex-snapshot

Specific inhibition of benzodiazepine receptor binding by some N-(indol-3-ylglyoxylyl) amino acid derivatives: stereoselective interactions

inferredcites →https://doi.org/10.1021/jm00163a032openalex-snapshot

Benzodiazepine receptor binding activity of 8-substituted-9-(3-substituted-benzyl)-6-(dimethylamino)-9H-purines

inferredcites →https://doi.org/10.1021/jm00165a028openalex-snapshot

Structural requirements for agonist actions at the benzodiazepine receptor: studies with analogs of 6-(benzyloxy)-4-(methoxymethyl)-.beta.-carboline-3-carboxylic acid ethyl ester

inferredcites →https://doi.org/10.1021/jm00169a013openalex-snapshot

Benzodiazepine receptor-binding activity of 9-(1-phenylethyl)purines

inferredcites →https://doi.org/10.1021/jm00171a007openalex-snapshot

Synthetic and computer-assisted analyses of the pharmacophore for the benzodiazepine receptor inverse agonist site

inferredcites →https://doi.org/10.1021/jm00171a015openalex-snapshot

Synthesis of substituted 7,12-dihydropyrido[3,2-b:5,4-b']diindoles: rigid planar benzodiazepine receptor ligands with inverse agonist/antagonist properties

inferredcites →https://doi.org/10.1021/jm00219a019openalex-snapshot

Electronic factors in the structure-activity relations of some 1,4-benzodiazepin-2-ones

inferredcites →https://doi.org/10.1021/jm00393a009openalex-snapshot

1,3-Diarylpyrazolo[4,5-c]- and -[5,4-c]quinolin-4-ones. 4. Synthesis and specific inhibition of benzodiazepine receptor binding

inferredcites →https://doi.org/10.1021/jm00401a025openalex-snapshot

(Imidazo[1,2-a]pyrimidin-2-yl)phenylmethanones and related compounds as potential nonsedative anxiolytics

inferredcites →https://doi.org/10.1021/jm9600609openalex-snapshot

Synthesis and Structure−Activity Relationships of Fused Imidazopyridines: A New Series of Benzodiazepine Receptor Ligands

inferredcites →https://doi.org/10.1021/jm970112+openalex-snapshot

Synthesis and Binding Affinity of 2-Phenylimidazo[1,2-a]pyridine Derivatives for both Central and Peripheral Benzodiazepine Receptors. A New Series of High-Affinity and Selective Ligands for the Peripheral Type

inferredcites →https://doi.org/10.1021/jm970487vopenalex-snapshot

Three-Dimensional Quantitative Structure−Activity Relationships from Molecular Similarity Matrices and Genetic Neural Networks. 1. Method and Validations

inferredcites →https://doi.org/10.1021/jm970488nopenalex-snapshot

Three-Dimensional Quantitative Structure−Activity Relationships from Molecular Similarity Matrices and Genetic Neural Networks. 2. Applications

inferredcites →https://doi.org/10.1021/jm980317yopenalex-snapshot

Predictive Models for GABAA/Benzodiazepine Receptor Subtypes: Studies of Quantitative Structure−Activity Relationships for Imidazobenzodiazepines at Five Recombinant GABAA/Benzodiazepine Receptor Subtypes [αxβ3γ2 (x = 1−3, 5, and 6)] via Comparative Molecular Field Analysis

inferredcites →https://doi.org/10.1021/jm990341ropenalex-snapshot

Pharmacophore/Receptor Models for GABAA/BzR Subtypes (α1β3γ2, α5β3γ2, and α6β3γ2) via a Comprehensive Ligand-Mapping Approach

inferredcites →https://doi.org/10.1021/jm991010hopenalex-snapshot

Structure−Activity Relationships and Molecular Modeling Analysis of Flavonoids Binding to the Benzodiazepine Site of the Rat Brain GABAA Receptor Complex

inferredcites →https://doi.org/10.1021/jm991035gopenalex-snapshot

Novel 2-Phenylimidazo[1,2-a]pyridine Derivatives as Potent and Selective Ligands for Peripheral Benzodiazepine Receptors: Synthesis, Binding Affinity, and in Vivo Studies

inferredcites →https://doi.org/10.1038/274383a0openalex-snapshot

GABAergic modulation of benzodiazepine binding site sensitivity

inferredcites →https://doi.org/10.1073/pnas.89.11.5113openalex-snapshot

Pregnenolone biosynthesis in C6-2B glioma cell mitochondria: regulation by a mitochondrial diazepam binding inhibitor receptor.

inferredcites →https://doi.org/10.1111/j.1432-1033.1988.tb14211.xopenalex-snapshot

The subcellular location in rat kidney of the peripheral benzodiazepine acceptor

inferredcites →https://doi.org/10.1111/j.1471-4159.1986.tb12965.xopenalex-snapshot

Subcellular Localization of “Peripheral‐Type” Binding Sites for Benzodiazepines in Rat Brain

inferredcites →https://doi.org/10.1111/j.1476-5381.1983.tb09380.xopenalex-snapshot

Characteristics of GABAB receptor binding sites on rat whole brain synaptic membranes

inferredcites →https://doi.org/10.1124/jpet.300.1.2openalex-snapshot

A New Benzodiazepine Pharmacology

inferredcites →https://doi.org/10.1126/science.6101294openalex-snapshot

Receptors for the Age of Anxiety: Pharmacology of the Benzodiazepines

inferredcites →https://doi.org/10.3109/03602539308993972openalex-snapshot

Quantitative Structure-Activity Relationships of Cytochrome P-450

inferredcites →https://doi.org/10.7270/q2pn945popenalex-snapshot

BindingDB Entry 5122: [3H]RY 80: A high-affinity, selective ligand for gamma-aminobutyric acidA receptors containing alpha-5 subunits.

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9780470116449.ch6openalex-snapshot

Applications of Support Vector Machines in Chemistry

inferred← citeshttps://doi.org/10.1002/chin.200450258openalex-snapshot

Comparative Quantitative Structure—Activity Relationship Studies (QSAR) on Non‐Benzodiazepine Compounds Binding to Benzodiazepine Receptor (BzR)

inferred← citeshttps://doi.org/10.1002/cjoc.200890127openalex-snapshot

Quantitative Retention‐Activity Relationship Studies by Liposome Electrokinetic Chromatography to Predict Skin Permeability

inferred← citeshttps://doi.org/10.1002/ejoc.201100710openalex-snapshot

Temperature‐Dependent Regioselective Synthesis of 1,2,4‐Triazino[2,3‐b]indazoles and 3H‐1,4‐Benzodiazepines by Domino‐Staudinger/Aza‐Wittig/Isomerization Reaction

inferred← citeshttps://doi.org/10.1002/qsar.200530204openalex-snapshot

Quantitative Structure–Activity Relationship Studies for the Binding Affinities of Imidazobenzodiazepines for the α6 Benzodiazepine Receptor Isoform Utilizing Optimized Blockwise Variable Combination by Particle Swarm Optimization for Partial Least Squares Modeling

inferred← citeshttps://doi.org/10.1002/qsar.200630059openalex-snapshot

Quantitative Structure–Activity Relationship Study on a Series of Novel Ligands Binding to Central Benzodiazepine Receptor By Using the Combination of Heuristic Method and Support Vector Machines

inferred← citeshttps://doi.org/10.1002/qua.21474openalex-snapshot

3D‐quantitative structure activity analysis and quantum chemical analysis of pyrido‐di‐indoles

inferred← citeshttps://doi.org/10.1007/978-3-319-56850-8_1openalex-snapshot

Towards the Revival of Interpretable QSAR Models

inferred← citeshttps://doi.org/10.1007/978-981-16-7857-8_16openalex-snapshot

QSAR—An Important In-Silico Tool in Drug Design and Discovery

inferred← citeshttps://doi.org/10.1007/s00044-008-9111-6openalex-snapshot

2D-QSAR of non-benzodiazepines to benzodiazepines receptor (BZR)

inferred← citeshttps://doi.org/10.1007/s00044-010-9306-5openalex-snapshot

3D-QSAR studies of 4-quinolone derivatives as high-affinity ligands at the benzodiazepine site of brain GABAA receptors

inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00242-xopenalex-snapshot

Quantitative Structure–Activity Relationship – A Historical Perspective and the Future

inferred← citeshttps://doi.org/10.1016/j.aca.2005.07.033openalex-snapshot

QSAR analysis of a series of 2-aryl(heteroaryl)-2,5-dihydropyrazolo[4,3-c]quinolin-3-(3H)-ones using piecewise hyper-sphere modeling by particle swarm optimization

inferred← citeshttps://doi.org/10.1016/j.bmc.2007.10.037openalex-snapshot

Synthesis and structure–activity relationships of N-(3-phenylpropyl)-N′-benzylpiperazines: Potent ligands for σ1 and σ2 receptors

inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.07.107openalex-snapshot

Flavylium salts as in vitro precursors of potent ligands to brain GABA-A receptors

inferred← citeshttps://doi.org/10.1016/j.comptc.2012.05.019openalex-snapshot

On substituent effect on the benzodiazepinone system

inferred← citeshttps://doi.org/10.1016/j.crci.2014.01.007openalex-snapshot

Synthesis of novel O-alkylbenzochromeno-1,5-benzodiazepinones. Study of the N–H····N and CO····HN hydrogen bonding interactions with 2-aminopyridines

inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.09.004openalex-snapshot

Quantitative structure–activity relationship studies of a series of non-benzodiazepine structural ligands binding to benzodiazepine receptor

inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.11.009openalex-snapshot

QSAR modeling of the interaction of flavonoids with GABA(A) receptor

inferred← citeshttps://doi.org/10.1016/j.ejmech.2008.01.030openalex-snapshot

3D and quantum QSAR of non-benzodiazepine compounds

inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173837openalex-snapshot

Neuropharmacological potentials of β-carboline alkaloids for neuropsychiatric disorders

inferred← citeshttps://doi.org/10.1016/j.jtusci.2016.06.005openalex-snapshot

Combining DFT and QSAR computation to predict the interaction of flavonoids with the GABA (A) receptor using electronic and topological descriptors

inferred← citeshttps://doi.org/10.1016/j.mencom.2007.01.016openalex-snapshot

Unexpected formation of 4-methyl-1-vinyl-δ-carboline in the reaction of 3-acetylindole oxime with acetylene

inferred← citeshttps://doi.org/10.1016/j.talanta.2006.05.058openalex-snapshot

Artificial neural network-based transformation for nonlinear partial least-square regression with application to QSAR studies

inferred← citeshttps://doi.org/10.1016/j.tet.2010.09.077openalex-snapshot

Me3SiCl-promoted intramolecular cyclization of aromatic compounds tethered with N,O-acetals leading to the facile preparation of 1,4-benzodiazepine skeletons

inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.088openalex-snapshot

Recent developments in the chemistry of pyrazolo[4,3-c]quinolines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.064openalex-snapshot

Synthesis of 3-aryl substituted benzo[1,2,5]triazepin-4-ones via intramolecular imine formation

inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.123openalex-snapshot

An alternative approach toward 2-aryl-2H-pyrazolo[4,3-c]-quinolin-3-ones by a multistep synthesis

inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.132openalex-snapshot

Rapid access to pyrido[1,2,5]triazepin-4-ones through intramolecular nucleophilic aromatic substitution

inferred← citeshttps://doi.org/10.1016/s0065-2725(06)92004-2openalex-snapshot

The Literature of Heterocyclic Chemistry, Part IX, 2002–2004

inferred← citeshttps://doi.org/10.1021/cb800054wopenalex-snapshot

A Cellular Conformation-Based Screen for Androgen Receptor Inhibitors

inferred← citeshttps://doi.org/10.1021/ci900075fopenalex-snapshot

New Hybrid Genetic Based Support Vector Regression as QSAR Approach for Analyzing Flavonoids-GABA(A) Complexes

inferred← citeshttps://doi.org/10.1021/cr800229sopenalex-snapshot

Route to Novel Auxin: Auxin Chemical Space toward Biological Correlation Carriers

inferred← citeshttps://doi.org/10.1021/je100738hopenalex-snapshot

Automated Potentiometric Titration Method for Determination of pKValues: An Application to Benzodiazepines

inferred← citeshttps://doi.org/10.1021/ol302837hopenalex-snapshot

Multicomponent Synthesis of Diverse 1,4-Benzodiazepine Scaffolds

inferred← citeshttps://doi.org/10.1038/s41573-024-00981-wopenalex-snapshot

New epilepsy therapies in development

inferred← citeshttps://doi.org/10.1038/srep12131openalex-snapshot

Regioselective Halogenation of 1,4-Benzodiazepinones via CH Activation

inferred← citeshttps://doi.org/10.1055/a-0652-5290openalex-snapshot

QSAR Models for Nitrogen Containing Monophosphonate and Bisphosphonate Derivatives as Human Farnesyl Pyrophosphate Synthase Inhibitors Based on Monte Carlo Method

inferred← citeshttps://doi.org/10.1080/1062936x.2018.1564067openalex-snapshot

Design and development of novel focal adhesion kinase (FAK) inhibitors using Monte Carlo method with index of ideality of correlation to validate QSAR

inferred← citeshttps://doi.org/10.1080/10826070701191052openalex-snapshot

Structure‐Retention Correlation in Liquid Chromatography for Pharmaceutical Applications

inferred← citeshttps://doi.org/10.1134/s0012501607090060openalex-snapshot

Simulation of biological activity of some conformationally variable organophosphorus compounds

inferred← citeshttps://doi.org/10.12677/hjmce.2017.51001openalex-snapshot

The Development of Therapeutic Drugs for Insomnia

inferred← citeshttps://doi.org/10.2174/092986709787002817openalex-snapshot

Topological Polar Surface Area: A Useful Descriptor in 2D-QSAR

inferred← citeshttps://doi.org/10.2174/157340609788681494openalex-snapshot

QSAR Studies on 4-Quinolone Derivatives as High-Affinity Ligands at the Benzodiazepine Site of Brain GABAA Receptors

inferred← citeshttps://doi.org/10.3390/cells9061469openalex-snapshot

High Content Screening Using New U2OS Reporter Cell Models Identifies Harmol Hydrochloride as a Selective and Competitive Antagonist of the Androgen Receptor

inferred← citeshttps://doi.org/10.5012/bkcs.2009.30.11.2717openalex-snapshot

Classification and Regression Tree Analysis for Molecular Descriptor Selection and Binding Affinities Prediction of Imidazobenzodiazepines in Quantitative Structure-Activity Relationship Studies

inferred← citeshttps://doi.org/10.70675/dade83e0zd417z4190zb0a0zf6a5e174c2aeopenalex-snapshot

Identification de nouveaux inhibiteurs de l'axe androgénique pour contourner la résistance à la castration des cancers de la prostate

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.