On the public citation graph
Medicinal chemistry updates on quinoline- and endoperoxide-based hybrids with potent antimalarial activity
0 signed · 113 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known work and none has been retracted — and get a dated CiteStamped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/anie.201907224openalex-snapshot
Artemisinin–(Iso)quinoline Hybrids by C−H Activation and Click Chemistry: Combating Multidrug‐Resistant Malaria
inferredcites →https://doi.org/10.1002/cbic.200400347openalex-snapshot
Design, Synthesis and Antimalarial Activity of Trifluoromethylartemisinin–Mefloquine Dual Molecules
inferredcites →https://doi.org/10.1002/cmdc.201200536openalex-snapshot
Artemisinin–Polypyrrole Conjugates: Synthesis, DNA Binding Studies and Preliminary Antiproliferative Evaluation
inferredcites →https://doi.org/10.1002/cmdc.201800728openalex-snapshot
Targeting Asexual and Sexual Blood Stages of the Human Malaria Parasite P. falciparum with 7‐Chloroquinoline‐Based 1,2,3‐Triazoles
inferredcites →https://doi.org/10.1002/ddr.20345openalex-snapshot
Next‐generation antimalarial drugs: hybrid molecules as a new strategy in drug design
inferredcites →https://doi.org/10.1002/jhet.3617openalex-snapshot
Design, Synthesis, and Biological andIn SilicoStudy of Fluorine‐Containing Quinoline Hybrid Thiosemicarbazide Analogues
inferredcites →https://doi.org/10.1002/jhet.3855openalex-snapshot
Synthesis of novel quinoline‐thiosemicarbazide hybrids and evaluation of their biological activities, molecular docking, molecular dynamics, pharmacophore model studies, and ADME‐Tox properties
inferredcites →https://doi.org/10.1002/med.21643openalex-snapshot
Hybrid molecules with potential in vitro antiplasmodial and in vivo antimalarial activity against drug‐resistant Plasmodium falciparum
inferredcites →https://doi.org/10.1007/978-1-59259-111-4_10openalex-snapshot
Artemisinin and Its Derivatives
inferredcites →https://doi.org/10.1016/j.bioorg.2020.104142openalex-snapshot
Identification and structure–activity relationship (SAR) studies of carvacrol derivatives as potential anti-malarial against Plasmodium falciparum falcipain-2 protease
inferredcites →https://doi.org/10.1016/j.bmc.2011.06.025openalex-snapshot
Synthesis and antimalarial activity of new heterocyclic hybrids based on chloroquine and thiazolidinone scaffolds
inferredcites →https://doi.org/10.1016/j.bmc.2015.04.017openalex-snapshot
From hybrid compounds to targeted drug delivery in antimalarial therapy
inferredcites →https://doi.org/10.1016/j.bmc.2015.06.056openalex-snapshot
Anti-Plasmodium falciparum activity of quinoline–sulfonamide hybrids
inferredcites →https://doi.org/10.1016/j.bmc.2016.05.060openalex-snapshot
Synthesis, antimalarial properties and 2D-QSAR studies of novel triazole-quinine conjugates
inferredcites →https://doi.org/10.1016/j.bmc.2019.01.044openalex-snapshot
New hybrid trifluoromethylquinolines as antiplasmodium agents
inferredcites →https://doi.org/10.1016/j.bmcl.2007.04.054openalex-snapshot
A novel artemisinin–quinine hybrid with potent antimalarial activity
inferredcites →https://doi.org/10.1016/j.bmcl.2008.11.047openalex-snapshot
Chloroquine–astemizole hybrids with potent in vitro and in vivo antiplasmodial activity
inferredcites →https://doi.org/10.1016/j.bmcl.2009.02.013openalex-snapshot
Semi-synthetic and synthetic 1,2,4-trioxaquines and 1,2,4-trioxolaquines: synthesis, preliminary SAR and comparison with acridine endoperoxide conjugates
inferredcites →https://doi.org/10.1016/j.bmcl.2009.10.010openalex-snapshot
Synthesis of 9-anilinoacridine triazines as new class of hybrid antimalarial agents
inferredcites →https://doi.org/10.1016/j.bmcl.2011.01.103openalex-snapshot
Synthesis, in vitro antimalarial and cytotoxicity of artemisinin-aminoquinoline hybrids
inferredcites →https://doi.org/10.1016/j.bmcl.2015.04.014openalex-snapshot
New quinoline derivatives demonstrate a promising antimalarial activity against Plasmodium falciparum in vitro and Plasmodium berghei in vivo
inferredcites →https://doi.org/10.1016/j.bmcl.2018.08.037openalex-snapshot
Synthesis, antimalarial activities and cytotoxicities of amino-artemisinin-1,2-disubstituted ferrocene hybrids
inferredcites →https://doi.org/10.1016/j.ejmech.2010.04.011openalex-snapshot
Quinolines and structurally related heterocycles as antimalarials
inferredcites →https://doi.org/10.1016/j.ejmech.2010.12.003openalex-snapshot
4-Anilinoquinoline triazines: A novel class of hybrid antimalarial agents
inferredcites →https://doi.org/10.1016/j.ejmech.2012.01.039openalex-snapshot
Novel hybrid molecules based on 15-membered azalide as potential antimalarial agents
inferredcites →https://doi.org/10.1016/j.ejmech.2014.07.064openalex-snapshot
β-amino-alcohol tethered 4-aminoquinoline-isatin conjugates: Synthesis and antimalarial evaluation
inferredcites →https://doi.org/10.1016/j.ejmech.2016.11.057openalex-snapshot
Design, synthesis and evaluation of 4-aminoquinoline-purine hybrids as potential antiplasmodial agents
inferredcites →https://doi.org/10.1016/j.ejmech.2017.07.061openalex-snapshot
Quinoline hybrids and their antiplasmodial and antimalarial activities
inferredcites →https://doi.org/10.1016/j.ejmech.2018.11.021openalex-snapshot
N-Substituted aminoquinoline-pyrimidine hybrids: Synthesis, in vitro antimalarial activity evaluation and docking studies
inferredcites →https://doi.org/10.1016/j.ejmech.2018.12.007openalex-snapshot
Current scenario of artemisinin and its analogues for antimalarial activity
inferredcites →https://doi.org/10.1016/j.ejmech.2020.112330openalex-snapshot
Synthesis and biological evaluation of novel quinoline-piperidine scaffolds as antiplasmodium agents
inferredcites →https://doi.org/10.1016/j.ejps.2014.01.014openalex-snapshot
Synthesis and in vitro biological evaluation of aminoacridines and artemisinin–acridine hybrids
inferredcites →https://doi.org/10.1016/j.exppara.2016.01.010openalex-snapshot
Design, synthesis and antimalarial screening of some hybrid 4-aminoquinoline-triazine derivatives against pf-DHFR-TS
inferredcites →https://doi.org/10.1016/j.ijmm.2013.07.005openalex-snapshot
A primaquine–chloroquine hybrid with dual activity against Plasmodium liver and blood stages
inferredcites →https://doi.org/10.1016/j.pt.2019.05.002openalex-snapshot
Ozonide Antimalarial Activity in the Context of Artemisinin-Resistant Malaria
inferredcites →https://doi.org/10.1016/s2214-109x(17)30333-9openalex-snapshot
Outbreak of human malaria caused by Plasmodium simium in the Atlantic Forest in Rio de Janeiro: a molecular epidemiological investigation
inferredcites →https://doi.org/10.1021/acsmedchemlett.0c00196openalex-snapshot
Synthesis of Novel Ciprofloxacin-Based Hybrid Molecules toward Potent Antimalarial Activity
inferredcites →https://doi.org/10.1021/acsmedchemlett.8b00381openalex-snapshot
Synthesis of Artemisinin–Estrogen Hybrids Highly Active against HCMV, P. falciparum, and Cervical and Breast Cancer
inferredcites →https://doi.org/10.1021/acsmedchemlett.9b00669openalex-snapshot
Synthesis of Novel G Factor or Chloroquine-Artemisinin Hybrids and Conjugates with Potent Antiplasmodial Activity
inferredcites →https://doi.org/10.1021/acsomega.7b00310openalex-snapshot
Synthesis of Novel Hybrids of Quinazoline and Artemisinin with High Activities against Plasmodium falciparum , Human Cytomegalovirus, and Leukemia Cells
inferredcites →https://doi.org/10.1021/jm100117eopenalex-snapshot
Trioxaferroquines as New Hybrid Antimalarial Drugs
inferredcites →https://doi.org/10.1021/jm1009567openalex-snapshot
Endoperoxide Carbonyl Falcipain 2/3 Inhibitor Hybrids: Toward Combination Chemotherapy of Malaria through a Single Chemical Entity
inferredcites →https://doi.org/10.1021/jm4014778openalex-snapshot
Quinoline–Pyrimidine Hybrids: Synthesis, Antiplasmodial Activity, SAR, and Mode of Action Studies
inferredcites →https://doi.org/10.1038/nrmicro2239openalex-snapshot
Artemisinin-based combination therapies: a vital tool in efforts to eliminate malaria
inferredcites →https://doi.org/10.1038/s41598-018-36493-yopenalex-snapshot
Genetically diverse Plasmodium falciparum infections, within-host competition and symptomatic malaria in humans
inferredcites →https://doi.org/10.1038/s41598-019-42495-1openalex-snapshot
Electrical percolation threshold of carbon black in a polymer matrix and its application to antistatic fibre
inferredcites →https://doi.org/10.1039/c1md00188dopenalex-snapshot
Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparumtransketolase and β-hematin inhibitors
inferredcites →https://doi.org/10.1039/c5ra19673fopenalex-snapshot
A structure guided drug-discovery approach towards identification of Plasmodium inhibitors
inferredcites →https://doi.org/10.1039/c6ra00846aopenalex-snapshot
N-(7-Chloroquinolinyl-4-aminoalkyl)arylsulfonamides as antimalarial agents: rationale for the activity with reference to inhibition of hemozoin formation
inferredcites →https://doi.org/10.1073/pnas.0804338105openalex-snapshot
Selection of a trioxaquine as an antimalarial drug candidate
inferredcites →https://doi.org/10.1111/cbdd.12108openalex-snapshot
4‐Aminoquinoline‐Triazine‐Based Hybrids with Improved In Vitro Antimalarial Activity Against CQ ‐Sensitive and CQ ‐Resistant Strains of P lasmodium falciparum
inferredcites →https://doi.org/10.1128/aac.00249-17openalex-snapshot
Are Antimalarial Hybrid Molecules a Close Reality or a Distant Dream?
inferredcites →https://doi.org/10.1128/aac.05133-11openalex-snapshot
Design and Evaluation of Primaquine-Artemisinin Hybrids as a Multistage Antimalarial Strategy
inferredcites →https://doi.org/10.1186/1475-2875-10-144openalex-snapshot
Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria
inferredcites →https://doi.org/10.1186/1475-2875-12-71openalex-snapshot
Potent in vivo anti-malarial activity and representative snapshot pharmacokinetic evaluation of artemisinin-quinoline hybrids
inferredcites →https://doi.org/10.1186/s12936-019-2724-zopenalex-snapshot
The past, present and future of anti-malarial medicines
inferredcites →https://doi.org/10.17179/excli2016-677openalex-snapshot
Synthesis and antimalarial potential of some novel quinoline-pyrazolopyridine derivatives
inferredcites →https://doi.org/10.2174/1568026620666200130162347openalex-snapshot
Inhibition of Hemoglobin Degrading Protease Falcipain-2 as a Mechanism for Anti-Malarial Activity of Triazole-Amino Acid Hybrids
inferredcites →https://doi.org/10.3390/molecules21121629openalex-snapshot
Design, Synthesis and Biological Evaluation of Novel Primaquine-Cinnamic Acid Conjugates of the Amide and Acylsemicarbazide Type
inferredcites →https://doi.org/10.3390/molecules22122268openalex-snapshot
Quinoline-Based Hybrid Compounds with Antimalarial Activity
inferredcites →https://doi.org/10.3390/tropicalmed4010026openalex-snapshot
Resistance to Artemisinin Combination Therapies (ACTs): Do Not Forget the Partner Drug!
inferredcites →https://doi.org/10.3390/tropicalmed4040139openalex-snapshot
Strengthening Surveillance Systems for Malaria Elimination by Integrating Molecular and Genomic Data
inferredcites →https://doi.org/10.4155/fmc-2018-0337openalex-snapshot
Artemisinin and Its Derivatives; Ancient Tradition Inspiring the Latest Therapeutic Approaches Against Malaria
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.4675637openalex-extracted
Design, Synthesis and Anticancer Activity of New Quinolines, Quinazolines and 1,2,4-Triazoles with Pyrido[2,3-d] Pyrimidines
inferred← citeshttps://doi.org/10.1002/cbdv.202300156openalex-snapshot
An Efficient Approach for the Synthesis and Antitumor Evaluation of Novel Azo‐ and Anil‐Linked with 3‐Aminopyrazolo[3,4‐b]pyridine
inferred← citeshttps://doi.org/10.1002/cctc.202500620openalex-snapshot
A Multicomponent Synthetic Strategy for 2‐Pyrazolines and Pyrimidines Through Activation of Renewable Alcohols by a Versatile Fe(III) Catalyst and Friedländer Quinoline Synthesis
inferred← citeshttps://doi.org/10.1002/jccs.202300212openalex-snapshot
Synthesis, design, and antimicrobial activity of pyrido[2,3‐d][1,2,4]triazolo[4,3‐a]pyrimidinones based on quinoline derivatives
inferred← citeshttps://doi.org/10.1002/med.21979openalex-snapshot
An overview on the antimalarial activity of 1,2,4‐trioxanes, 1,2,4‐trioxolanes and 1,2,4,5‐tetraoxanes
inferred← citeshttps://doi.org/10.1002/slct.202504720openalex-snapshot
Targeting Plasmodium Falciparum Asexual and Sexual Stages with Melatonin‐Based Indole Compounds
inferred← citeshttps://doi.org/10.1007/s00044-022-02866-2openalex-snapshot
Design, synthesis and biological evaluation of 8-aminoquinoline-1,2,3-triazole hybrid derivatives as potential antimicrobial agents
inferred← citeshttps://doi.org/10.1007/s11030-024-11013-5openalex-snapshot
Fe3O4@SiO2@[Aminoglycol][Formate] as a new superparamagnetic nanocatalyst and [Aminoglycol][Formate] as a novel ionic liquid catalyst for preparation of new dimethyldihydropyrimido[4,5-b]quinolone derivatives
inferred← citeshttps://doi.org/10.1007/s11696-026-05605-8openalex-snapshot
In-vitro and in-silico evaluation of interactions between Camellia sinensis leaf extract and selected 4-aminoquinoline antimalarial drugs
inferred← citeshttps://doi.org/10.1007/s44371-025-00339-0openalex-snapshot
Deciphering the inhibitory activity of flavonoids against Plasmodium falciparum proteases through molecular docking, drug-likeness and pharmacokinetic studies
inferred← citeshttps://doi.org/10.1016/j.bmcl.2024.129992openalex-snapshot
Pyridine and Pyrimidine hybrids as privileged scaffolds in antimalarial drug discovery: A recent development
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114408openalex-snapshot
Design and synthesis of harmiquins, harmine and chloroquine hybrids as potent antiplasmodial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115458openalex-snapshot
Recent developments in antimalarial activities of 4-aminoquinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.119027openalex-snapshot
A critical review of quinoline hybrids as privileged scaffolds for anti-malarial therapy
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e25077openalex-snapshot
Biological evaluation of novel side chain containing CQTrICh-analogs as antimalarials and their development as PfCDPK1 kinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e26735openalex-snapshot
Synthesis, anticancer activity and molecular docking of new quinolines, quinazolines and 1,2,4-triazoles with pyrido[2,3-d] pyrimidines
inferred← citeshttps://doi.org/10.1016/j.jics.2024.101470openalex-snapshot
Synthesis of a novel 7-chloroquinoline-sulphocoumarin hybrid: Characterization, ADME profiling and elucidation of its antiproliferative and anti-EMT potential
inferred← citeshttps://doi.org/10.1016/j.jil.2025.100146openalex-snapshot
Ionic liquid-assisted approaches in the synthesis of nitrogen-containing heterocycles: A focus on 3- to 6-membered rings
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138882openalex-snapshot
Quinoline-1,2,3-triazole hybrids: Design, synthesis, antimalarial and antimicrobial evaluation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140814openalex-snapshot
Integration of In-vivo screening, molecular docking, and molecular dynamics simulations for studying the antiepileptic potential of newly synthesized 5-naphthalen-1-yl-5,10-dihydro-1H-pyrimido[4,5-b]quinoline-2,4-diones in optimized reaction conditions by utilizing -proline as green catalyst
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145705openalex-snapshot
Synthesis, anticancer and docking study of quinoline-linked pyrazine analogues
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101374openalex-snapshot
Novel styryl-heterocyclic hybrids: Synthesis, characterization and anticancer activity
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00393openalex-snapshot
Rh(III)-Catalyzed Regioselective C8-Alkylation of Quinoline N-Oxides with Maleimides and Acrylates
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.2c00531openalex-snapshot
Squaramide Tethered Clindamycin, Chloroquine, and Mortiamide Hybrids: Design, Synthesis, and Antimalarial Activity
inferred← citeshttps://doi.org/10.1039/d1gc02713aopenalex-snapshot
I 2 -induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines
inferred← citeshttps://doi.org/10.1039/d3md00083dopenalex-snapshot
Is structural hybridization invoking new dimensions for antimalarial drug discovery research?
inferred← citeshttps://doi.org/10.1039/d3sc06955aopenalex-snapshot
Rh( iii )-catalyzed sp 3 /sp 2 –C–H heteroarylations via cascade C–H activation and cyclization
inferred← citeshttps://doi.org/10.1039/d5cy00422eopenalex-snapshot
A passage from pincer complexes to rationally designed phosphine-free Co( iii ) catalysts supported by a pentadentate ligand for activation of alcohols: studies on sp 3 C–H alkylation of 9 H -fluorene and quinoline synthesis
inferred← citeshttps://doi.org/10.1039/d5cy01110hopenalex-snapshot
Metal–ligand cooperative strategy of a Zn-catalyst for multicomponent synthesis of highly substituted pyrazolines, pyrimidines, and quinolines: a combined experimental and DFT optimized study
inferred← citeshttps://doi.org/10.1039/d5cy01355kopenalex-snapshot
Mechanistic divergence in Rh( iii )-catalyzed cascades: how substrate identity switches between cyclization and migratory insertion
inferred← citeshttps://doi.org/10.1055/a-2122-8406openalex-snapshot
Photoredox Defluorinative Silylation of α-Trifluoromethyl Arylalkenes Using Silacarboxylic Acids as Silyl Radical Precursors
inferred← citeshttps://doi.org/10.1080/07391102.2025.2516143openalex-snapshot
Integrative computational and experimental approaches for identifying potent antimalarials by targeting falcipain-2 of Plasmodium falciparum
inferred← citeshttps://doi.org/10.1080/10406638.2021.1909082openalex-snapshot
Antitubercular, Antimalarial Activity and Molecular Docking Study of New Synthesized 7-Chloroquinoline Derivatives
inferred← citeshttps://doi.org/10.1080/13880209.2025.2547744openalex-snapshot
Design, evaluation, cytotoxic activity, molecular docking, ADMET analysis, and dynamic simulations and the preparation of new isoxazoles, thiazoles, 1,3-thiazines, and thiazolopyrimidines derived from quinoline-pyridopyrimidines
inferred← citeshttps://doi.org/10.1111/cbdd.70081openalex-snapshot
Targeting Blood‐Stage Malaria: Design, Synthesis, Characterization, In Vitro, and In Silico Evaluation of Pyrrolidinodiazenyl Chalcones
inferred← citeshttps://doi.org/10.1134/s0036024424702443openalex-snapshot
Studying the Electrochemical Behavior of a Smooth Gold Electrode in a Solution of Bridged 1,2,4-Trioxalane in Acetonitrile
inferred← citeshttps://doi.org/10.1134/s0036024425703133openalex-snapshot
Electrochemical Behavior of Tricyclic Monoperoxide in an Acetonitrile Solution on Smooth Gold
inferred← citeshttps://doi.org/10.2174/0109298673308069240815072244openalex-snapshot
Therapeutic Targeting and Role of Cysteine Proteases in the Life Cycle of Malaria Parasite
inferred← citeshttps://doi.org/10.2174/1570180820666230830125155openalex-snapshot
Quinoline-hydrazone Conjugates: Recent Insights into Synthetic Strategies, Structure-activity Relationship, and Biological Activities
inferred← citeshttps://doi.org/10.2174/1570193x20666230505152611openalex-snapshot
Quinoline and Analogs: Insight into the Synthesis, Biological Activity, Structure-Activity Relationship, and Interaction with Targets
inferred← citeshttps://doi.org/10.29356/jmcs.v66i1.1578openalex-snapshot
2-Oxoquinoline Arylaminothiazole Derivatives in Identifying Novel Potential Anticancer Agents by Applying 3D-QSAR, Docking, and Molecular Dynamics Simulation Studies
inferred← citeshttps://doi.org/10.33263/briac126.79577971openalex-snapshot
Synthesis and Antimalarial Activity of 7-Chloro-4-(4-(2-(Oxo, Hydroxyl & Fluoro-2-1 (4-Phenyl)Ethyl)Piperazin-1-yl)Quinoline Derivatives
inferred← citeshttps://doi.org/10.3389/fphar.2022.850176openalex-snapshot
Target-Based Virtual Screening of Natural Compounds Identifies a Potent Antimalarial With Selective Falcipain-2 Inhibitory Activity
inferred← citeshttps://doi.org/10.3390/antibiotics13020142openalex-snapshot
Synthesis of Novel Artemisinin, Ciprofloxacin, and Norfloxacin Hybrids with Potent Antiplasmodial Activity
inferred← citeshttps://doi.org/10.3390/ijms25179744openalex-snapshot
Synthesis of Ethyl Pyrimidine-Quinolincarboxylates Selected from Virtual Screening as Enhanced Lactate Dehydrogenase (LDH) Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules27134123openalex-snapshot
Domino Nitro Reduction-Friedländer Heterocyclization for the Preparation of Quinolines
inferred← citeshttps://doi.org/10.3390/molecules27175401openalex-snapshot
Synthesis, Structure and Antileishmanial Evaluation of Endoperoxide–Pyrazole Hybrids
inferred← citeshttps://doi.org/10.3390/ph17121632openalex-snapshot
Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Novel Thiazoles, Pyrazoles, 1,3-Thiazepinones, and 1,2,4-Triazolopyrimidines Derived from Quinoline-Pyrido[2,3-d] Pyrimidinones
inferred← citeshttps://doi.org/10.71267/mencom.7714openalex-snapshot
Electrochemical behavior of bridged 1,2,4-dioxazolidine derivative in acetonitrile medium on the smooth gold
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.