On the public citation graph
Synthesis and Preliminary Characterization of a Novel Antiarrhythmic Compound (KB130015) with an Improved Toxicity Profile Compared with Amiodarone
0 signed · 132 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known work and none has been retracted — and get a dated CiteStamped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/10.1016/0024-3205(82)90293-4openalex-snapshot
The binding of [3H]nitrendipine to receptors for calcium channel antagonists in the heart, cerebral cortex, and ileum of rats
inferredcites →https://doi.org/10.1016/0378-1119(83)90223-8openalex-snapshot
Plasmid-encoded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0378-1119(88)90219-3openalex-snapshot
Secreted placental alkaline phosphatase: a powerful new quantitative indicator of gene expression in eukaryotic cells
inferredcites →https://doi.org/10.1016/0960-0760(91)90077-iopenalex-snapshot
High level expression of functional full length human thyroid hormone receptor β1 in insect cells using a recombinant baculovirus
inferredcites →https://doi.org/10.1016/s0002-9149(99)00700-6openalex-snapshot
Clinical organ toxicity of antiarrhythmic compounds: ocular and pulmonary manifestations
inferredcites →https://doi.org/10.1016/s0008-6363(97)00114-4openalex-snapshot
Cellular electropharmacology of amiodarone
inferredcites →https://doi.org/10.1016/s0021-9258(18)99192-1openalex-snapshot
High level expression of functional full length and truncated glucocorticoid receptor in Chinese hamster ovary cells. Demonstration of ligand-induced down-regulation of expressed receptor mRNA and protein
inferredcites →https://doi.org/10.1097/00005344-198609000-00025openalex-snapshot
Allosteric Modulation of [3H]Nitrendipine Binding to Cardiac and Cerebral Cortex Membranes by Amiodarone
inferredcites →https://doi.org/10.1111/j.1540-8167.1999.tb00674.xopenalex-snapshot
Current Antiarrhythmic Drugs
inferredcites →https://doi.org/10.1124/mol.54.1.105openalex-snapshot
Differential Response of Estrogen Receptor α and Estrogen Receptor β to Partial Estrogen Agonists/Antagonists
inferredcites →https://doi.org/10.1172/jci113874openalex-snapshot
Antagonism of thyroid hormone action by amiodarone in rat pituitary tumor cells.
inferredcites →https://doi.org/10.7326/0003-4819-121-7-199410010-00009openalex-snapshot
Amiodarone-associated Proarrhythmic Effects: A Review with Special Reference to Torsade de Pointes Tachycardia
inferredcites →https://doi.org/10.7326/0003-4819-68-1-269_2openalex-snapshot
Handbook of Experimental Pharmacology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471266949.bmc052.pub2openalex-snapshot
Thyroid Hormones and Thyromimetics
inferred← citeshttps://doi.org/10.1002/adsc.200900386openalex-snapshot
First Heterogeneous Ligand‐ and Salt‐Free Larock Indole Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.200900649openalex-snapshot
Phase‐Transfer‐Catalyzed Intramolecular Cyclization of ortho‐Alkynyl Phenyl Ether Derivatives for Synthesis of 2,3‐Disubstituted Benzo[b]furans
inferred← citeshttps://doi.org/10.1002/adsc.201500308openalex-snapshot
Palladium‐Catalyzed Synthesis of 2,3‐Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201800298openalex-snapshot
Cobalt(III)‐Catalyzed Construction of Benzofurans, Benzofuranones and One‐Pot Orthogonal C−H Functionalizations to Access Polysubstituted Benzofurans
inferred← citeshttps://doi.org/10.1002/ange.201411960openalex-snapshot
Cobalt‐katalysierte Negishi‐Kreuzkupplungen von (Hetero)Arylzinkreagentien mit primären und sekundären Alkylbromiden und ‐iodiden
inferred← citeshttps://doi.org/10.1002/anie.201305326openalex-snapshot
Palladium‐Catalyzed Synthesis of Benzofurans and Coumarins from Phenols and Olefins
inferred← citeshttps://doi.org/10.1002/anie.201411960openalex-snapshot
Cobalt‐Catalyzed Negishi Cross‐Coupling Reactions of (Hetero)Arylzinc Reagents with Primary and Secondary Alkyl Bromides and Iodides
inferred← citeshttps://doi.org/10.1002/ejoc.201200708openalex-snapshot
Access to 2,3‐Disubstituted Benzofurans through One‐Pot Acid‐Catalyzed Nucleophilic Substitution/TBAF‐Mediated Oxacycloisomerization
inferred← citeshttps://doi.org/10.1002/hc.20162openalex-snapshot
Synthesis and antimicrobial evaluation of some 1,2,4‐triazole, 1,3,4‐oxa(thia)diazole, and 1,2,4‐triazolo[3,4‐b]‐1,3,4‐thiadiazine derivatives
inferred← citeshttps://doi.org/10.1002/jhet.2083openalex-snapshot
Synthesis of Arylated Benzofurans by RegioselectiveSuzuki–Miyaura Cross‐Coupling Reactions of 2,3‐Dibromobenzofurans‐ and 2,3,5‐Tribromobenzofurans
inferred← citeshttps://doi.org/10.1002/ps.5528openalex-snapshot
Benzofuran‐2‐acetic esters as a new class of natural‐like herbicides
inferred← citeshttps://doi.org/10.1002/ps.6159openalex-snapshot
Discovery of novel benzofuran scaffold as 4‐hydroxyphenylpyruvate dioxygenase inhibitors
inferred← citeshttps://doi.org/10.1007/s00063-005-1096-zopenalex-snapshot
Inhibition des muskarinergen Kaliumionenstroms durch das neue Klasse-III-Antiarrhythmikum KB130015 im Vergleich zu Ibutilide
inferred← citeshttps://doi.org/10.1007/s00210-016-1232-8openalex-snapshot
The class III anti-arrhythmic agent, amiodarone, inhibits voltage-dependent K+ channels in rabbit coronary arterial smooth muscle cells
inferred← citeshttps://doi.org/10.1007/s11164-014-1544-6openalex-snapshot
Solution-phase photochemical transformation of 2-aroylbenzofurans: addition–elimination mechanism
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00306-0openalex-snapshot
Furans and their Benzo Derivatives: Reactivity
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.01.028openalex-snapshot
Synthesis and evaluation of the permeability transition inhibitory characteristics of paramagnetic and diamagnetic amiodarone derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.02.053openalex-snapshot
Novel thyroid hormone receptor antagonists with an N-alkylated diphenylamine skeleton
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118397openalex-snapshot
Structure-based design of novel THR-β agonists and mechanism of activation research by molecular dynamics simulations
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.04.032openalex-snapshot
Thyroid receptor ligands. Part 2: Thyromimetics with improved selectivity for the thyroid hormone receptor beta
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.06.093openalex-snapshot
A new class of high affinity thyromimetics containing a phenyl-naphthylene core
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.11.077openalex-snapshot
Thyroid receptor ligands. Part 5: Novel bicyclic agonist ligands selective for the thyroid hormone receptor β
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.01.009openalex-snapshot
Thyroid receptor ligands. Part 7: Indirect antagonists of the thyroid hormone receptor with improved affinity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.05.049openalex-snapshot
Thyroid receptor ligands. Part 8: Thyromimetics derived from N-acylated-α-amino acid derivatives displaying modulated pharmacological selectivity compared with KB-141
inferred← citeshttps://doi.org/10.1016/j.ddstr.2005.05.016openalex-snapshot
Selective thyroid hormone agonists: A strategy for treating metabolic syndrome
inferred← citeshttps://doi.org/10.1016/j.ejmech.2006.12.031openalex-snapshot
Synthesis and cytotoxicity properties of amiodarone analogues
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.02.020openalex-snapshot
Convenient synthesis and antimicrobial evaluation of some novel 2-substituted-3-methylbenzofuran derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.09.002openalex-snapshot
Stereoselective synthesis and antimicrobial activity of benzofuran-based (1E)-1-(piperidin-1-yl)-N2-arylamidrazones
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.12.061openalex-snapshot
Synthesis, structure–activity relationship of iodinated-4-aryloxymethyl-coumarins as potential anti-cancer and anti-mycobacterial agents
inferred← citeshttps://doi.org/10.1016/j.ejphar.2006.10.053openalex-snapshot
The amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015) opens large-conductance Ca2+-activated K+ channels and relaxes vascular smooth muscle
inferred← citeshttps://doi.org/10.1016/j.ejphar.2010.01.010openalex-snapshot
The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115351openalex-snapshot
Copper-catalyzed regioselective C−H alkylation of phenol derivatives with unactivated alkyl chlorides: Manifesting a Cu(I)/Cu(III) pathway
inferred← citeshttps://doi.org/10.1016/j.taap.2014.07.009openalex-snapshot
Prediction of binding affinity and efficacy of thyroid hormone receptor ligands using QSAR and structure-based modeling methods
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.046openalex-snapshot
Recent advances in the chemistry of 2-(2-oxoalkylidene)tetrahydrofurans
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.112openalex-snapshot
Regioselective synthesis of ω-bromo-3-ketosulfones, ω-bromo-3-ketonitriles and 2-(ω-bromoalkyl)benzofurans based on a ‘ring-closing/ring-opening’ strategy
inferred← citeshttps://doi.org/10.1016/j.tet.2009.06.049openalex-snapshot
Expeditious synthesis of 2,3-dihydro-2-alkoxy-3-methylenebenzofurans from N-benzofuran-3-ylmethyl N,N,N-trialkylammonium bromides: a new approach to access the natural product, 2-hydroxy-3-methylene-6-methyl-2, 3-dihydrobenzofuran
inferred← citeshttps://doi.org/10.1016/j.tet.2016.03.099openalex-snapshot
Synthesis and optical properties of π-conjugated push–pull dyes incorporating a functionalized benzo[1,2-b:3,4-b′]difuran spacer
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.150openalex-snapshot
A simple approach to highly functionalized benzo[b]furans from phenols and aryl iodides via aryl propargyl ethers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.069openalex-snapshot
Efficient synthesis of functionalized dibenzofurans by domino ‘twofold Heck/6π-electrocyclization’ reactions of 2,3-di- and 2,3,5-tribromobenzofuran
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.141openalex-snapshot
Site-selective Suzuki cross-coupling reactions of 2,3-dibromobenzofuran
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.10.045openalex-snapshot
Metal-free synthesis of 3-chalcogen benzo[b]furans via an iodine-mediated electrophilic cyclisation of 2-alkynylanisoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.12.108openalex-snapshot
One pot rhodium catalyzed, base and solvent-free synthesis of 2-(bromomethyl)furan derivatives and synthesis of Hashmi phenol through platinum catalyzed cascade cyclization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.089openalex-snapshot
Target cum flexibility: simple access to benzofuran conjugated sugar and nucleoside derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.040openalex-snapshot
One-pot synthesis of 2,2′-bisbenzofurans using cuprous chloride as a catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.002openalex-snapshot
Fluorescent 2-(2′-hydroxybenzofuran)benzoxazole (HBBO) borate complexes: synthesis, optical properties, and theoretical calculations
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.076openalex-snapshot
Synthesis of substituted benzofurans and indoles by Zn-catalyzed tandem Sonogashira-cyclization strategy
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.054openalex-snapshot
Pd-catalyzed intramolecular Heck reaction for the synthesis of 2-methylbenzofurans
inferred← citeshttps://doi.org/10.1016/j.theochem.2007.02.042openalex-snapshot
ONIOM study of the 4′-hydroxyl hydrogen bond acceptor/donor group nature in thyromimetics
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c01083openalex-snapshot
Copper and Silver Complexes of o-Ph2PC6H4C(O)N(H)C9H6N: Synthesis and Catalytic Applications of CuI Complexes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01992openalex-snapshot
Visible-Light-Promoted Oxidative Annulation of Naphthols and Alkynes: Synthesis of Functionalized Naphthofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01680openalex-snapshot
Copper-Catalyzed Three-Component Tandem Cyclization for One-Pot Synthesis of Indole-Benzofuran Bis-Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00146openalex-snapshot
Synthesis of 2-Aryl and 3-Aryl Benzo[b]furan Thioethers Using Aryl Sulfonyl Hydrazides as Sulfenylation Reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03036openalex-snapshot
Synthesis of 3-Chalcogenylated Benzo[ b ]furans Enabled by a Multicomponent Reagent System
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04134openalex-snapshot
Rhodium-Catalyzed Twofold Unsymmetrical C–H Alkenylation–Annulation/Thiolation Reaction To Access Thiobenzofurans
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02388openalex-snapshot
Synthesis of Benzofuran Derivates via a Gold-Catalyzed Claisen Rearrangement Cascade
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01352openalex-snapshot
Metal-Free Oxidative Annulation of 2-Naphthols with Terminal Alkynes Affording 2-Arylnaphtho[2,1-b]furans
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00980openalex-snapshot
Ag-Catalyzed Oxidative Cyclization Reaction of 1,6-Enynes and Sodium Sulfinate: Access to Sulfonylated Benzofurans
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c05156openalex-snapshot
Brønsted Acid Ionic Liquid-Catalyzed Ring Opening of 3,3-Disubstituted Oxetanes in Water: Efficient Access to Furans and Benzofurans
inferred← citeshttps://doi.org/10.1021/jacsau.5c00908openalex-snapshot
Unprecedented Copper/Iron-Cocatalyzed Homocoupling of Propargyl Ethers to Conjugated Benzofurans
inferred← citeshttps://doi.org/10.1021/jm021080fopenalex-snapshot
Thyroid Receptor Ligands. 1. Agonist Ligands Selective for the Thyroid Receptor β1
inferred← citeshttps://doi.org/10.1021/jm050004kopenalex-snapshot
Thyroid Receptor Ligands. 3. Design and Synthesis of 3,5-Dihalo-4-alkoxyphenylalkanoic Acids as Indirect Antagonists of the Thyroid Hormone Receptor
inferred← citeshttps://doi.org/10.1021/jm060521iopenalex-snapshot
Thyroid Receptor Ligands. 6. A High Affinity “Direct Antagonist” Selective for the Thyroid Hormone Receptor
inferred← citeshttps://doi.org/10.1021/jo051079zopenalex-snapshot
Synthesis of Benzofurans with Remote Bromide Functionality by Domino “Ring-Cleavage-Deprotection-Cyclization” Reactions of 2-Alkylidenetetrahydrofurans with Boron Tribromide
inferred← citeshttps://doi.org/10.1021/jo051767iopenalex-snapshot
Efficient Synthesis of Furan-2-ylacetates, 7-(Alkoxycarbonyl)benzofurans, and 7-(Alkoxycarbonyl)-2,3-dihydrobenzofurans Based on Cyclization Reactions of Free and Masked Dianions: A “Cyclization/Dehydrogenation” Strategy
inferred← citeshttps://doi.org/10.1021/jo301162xopenalex-snapshot
Iodine(III)-Mediated Tandem Oxidative Cyclization for Construction of 2-Nitrobenzo[b]furans
inferred← citeshttps://doi.org/10.1021/jo701656zopenalex-snapshot
An Efficient Synthesis and Substitution of 3-Aroyl-2-bromobenzo[b]furans
inferred← citeshttps://doi.org/10.1021/ol8028687openalex-snapshot
Palladium-Catalyzed Sequential Oxidative Cyclization/Coupling of 2-Alkynylphenols and Alkenes: A Direct Entry into 3-Alkenylbenzofurans
inferred← citeshttps://doi.org/10.1021/ol902157copenalex-snapshot
Oxidative Aromatic C−O Bond Formation: Synthesis of 3-Functionalized Benzo[ b ]furans by FeCl 3 -Mediated Ring Closure of α-Aryl Ketones
inferred← citeshttps://doi.org/10.1038/sj.bjp.0705379openalex-snapshot
Action potential changes associated with a slowed inactivation of cardiac voltage‐gated sodium channels by KB130015
inferred← citeshttps://doi.org/10.1039/c3sc51489gopenalex-snapshot
Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes
inferred← citeshttps://doi.org/10.1039/c4cc07026gopenalex-snapshot
Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C–H olefination of phenols
inferred← citeshttps://doi.org/10.1039/c4ob00575aopenalex-snapshot
Palladium-catalyzed tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates: one-pot synthesis of 2-arylbenzofurans
inferred← citeshttps://doi.org/10.1039/c4ob02691hopenalex-snapshot
Fluorination of 2-substituted benzo[b]furans with Selectfluor™
inferred← citeshttps://doi.org/10.1039/c4qo00196fopenalex-snapshot
Synthesis of benzofurans via ruthenium-catalyzed redox-neutral C–H functionalization and reaction with alkynes under mild conditions
inferred← citeshttps://doi.org/10.1039/c5ob00577aopenalex-snapshot
Intramolecular oxidative coupling: I 2 /TBHP/NaN 3 -mediated synthesis of benzofuran derivatives
inferred← citeshttps://doi.org/10.1039/c6cc09080jopenalex-snapshot
Palladium-catalyzed synthesis of [60]fullerene-fused benzofurans via heteroannulation of phenols
inferred← citeshttps://doi.org/10.1039/c6qo00112bopenalex-snapshot
Hydrazone–palladium catalyzed annulation of 1-cinnamyloxy-2-ethynylbenzene derivatives
inferred← citeshttps://doi.org/10.1039/c7cc02053hopenalex-snapshot
Palladium-catalyzed benzofuran and indole synthesis by multiple C–H functionalizations
inferred← citeshttps://doi.org/10.1039/c7ob02873copenalex-snapshot
Hydrazone–Pd-catalyzed direct intermolecular reaction of o -alkynylphenols with allylic acetates
inferred← citeshttps://doi.org/10.1039/d0ra03071fopenalex-snapshot
Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans
inferred← citeshttps://doi.org/10.1039/d4ob01223bopenalex-snapshot
Switching the regioselectivity of acid-catalyzed reactions of arylnaphtho[2,1- b ]furans via a [1,2]-aryl shift
inferred← citeshttps://doi.org/10.1039/d5ra05084gopenalex-snapshot
7-Methoxybenzofuran-triazole tethered N -phenylacetamides as a promising class of tyrosinase inhibitors: synthesis, biological evaluation and computational analyses against fungal and human tyrosinases
inferred← citeshttps://doi.org/10.1046/j.1540-8167.2003.03064.xopenalex-snapshot
Effects of Amiodarone and Dronedarone on Voltage‐Dependent Sodium Current in Human Cardiomyocytes
inferred← citeshttps://doi.org/10.1055/a-2642-9128openalex-snapshot
Visible-Light-Induced I2-Mediated Cyclization of ortho-Biarylchalcones of Naphthofuran Series toward Oxa[5]helicenes
inferred← citeshttps://doi.org/10.1055/sos-sd-110-00529openalex-snapshot
10.1 Product Class 1: Benzo[b]furans
inferred← citeshttps://doi.org/10.1080/00397911.2014.907425openalex-snapshot
Reactivity of Benzofuran Derivatives
inferred← citeshttps://doi.org/10.1080/00397911.2019.1611856openalex-snapshot
Facile synthesis of 3-aryl benzofurans, 3-aryl benzothiophenes, 2-aryl indoles and their dimers
inferred← citeshttps://doi.org/10.1097/fjc.0b013e31816c4325openalex-snapshot
Inward Rectifier Potassium Currents as a Target for Atrial Fibrillation Therapy
inferred← citeshttps://doi.org/10.1097/fjc.0b013e31818914b6openalex-snapshot
Amiodarone as Paradigm for Developing New Drugs for Atrial Fibrillation
inferred← citeshttps://doi.org/10.1111/j.1527-3466.2003.tb00117.xopenalex-snapshot
KB130015, A New Amiodarone Derivative with Multiple Effects on Cardiac Ion Channels
inferred← citeshttps://doi.org/10.1111/j.1527-3466.2005.tb00161.xopenalex-snapshot
Development of the Thyroid Hormone Receptor β-Subtype Agonist KB-141 : A Strategy for Body Weight Reduction and Lipid Lowering with Minimal Cardiac Side Effects
inferred← citeshttps://doi.org/10.1124/jpet.102.042218openalex-snapshot
Slowing of the Inactivation of Cardiac Voltage-Dependent Sodium Channels by the Amiodarone Derivative 2-Methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015)
inferred← citeshttps://doi.org/10.1124/jpet.103.057646openalex-snapshot
Inhibition of G Protein-Coupled and ATP-Sensitive Potassium Currents by 2-Methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015), an Amiodarone Derivative
inferred← citeshttps://doi.org/10.1124/jpet.105.092221openalex-snapshot
The Amiodarone Derivative KB130015 [2-Methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran] Induces an Na+-Dependent Increase of [Ca2+] in Ventricular Myocytes
inferred← citeshttps://doi.org/10.1124/jpet.106.108993openalex-snapshot
Hepatocellular Toxicity and Pharmacological Effect of Amiodarone and Amiodarone Derivatives
inferred← citeshttps://doi.org/10.1124/jpet.106.116152openalex-snapshot
Pharmacological Profile of the Thyroid Hormone Receptor Antagonist NH3 in Rats
inferred← citeshttps://doi.org/10.1128/aac.01184-06openalex-snapshot
Amiodarone and Bepridil Inhibit Anthrax Toxin Entry into Host Cells
inferred← citeshttps://doi.org/10.1134/s1070428023120059openalex-snapshot
Design, Synthesis, and Antiarrhythmic Activity of New Indole-3-carboxamide Derivatives
inferred← citeshttps://doi.org/10.1152/ajplung.00434.2003openalex-snapshot
Effects of metabolites and analogs of amiodarone on alveolar macrophages: structure-activity relationship
inferred← citeshttps://doi.org/10.1210/me.2006-0035openalex-snapshot
Thyroid Hormones Signaling Is Getting More Complex: STORMs Are Coming
inferred← citeshttps://doi.org/10.1517/13543770903567069openalex-snapshot
Thyromimetics: a review of recent reports and patents (2004 – 2009)
inferred← citeshttps://doi.org/10.1517/13543776.14.8.1169openalex-snapshot
Therapeutic thyroid hormone ligand patents 1998 – 2003
inferred← citeshttps://doi.org/10.1517/13543776.2013.801455openalex-snapshot
Benzofuran derivatives: a patent review
inferred← citeshttps://doi.org/10.1517/13543784.13.4.415openalex-snapshot
Dronedarone: an amiodarone analogue
inferred← citeshttps://doi.org/10.1517/13543784.16.2.169openalex-snapshot
Pharmacological therapy of atrial fibrillation
inferred← citeshttps://doi.org/10.1517/14728222.11.9.1161openalex-snapshot
Pharmacologic targets for atrial fibrillation
inferred← citeshttps://doi.org/10.22159/ijpps.2017v9i11.21413openalex-snapshot
IN VITRO ANTIOXIDANT, ANTIMICROBIAL AND ADMET STUDY OF NOVEL FURAN/BENZOFURAN C-2 COUPLED QUINOLINE HYBRIDS
inferred← citeshttps://doi.org/10.24820/ark.5550190.p010.609openalex-snapshot
Microwave promoted Heck and Suzuki coupling reactions of new 3-(5-bromobenzofuranyl)pyrazole in aqueous media
inferred← citeshttps://doi.org/10.25258/ijpqa.14.3.34openalex-snapshot
In-silico and In-vitro Studies on Targeting Tumor Apoptosis by Activating Caspase-3
inferred← citeshttps://doi.org/10.3184/174751917x14839766277170openalex-snapshot
One-pot Synthesis of Novel 2-(Benzofuran-2-yl)-4-Phenylquinoline-3-Carboxylates
inferred← citeshttps://doi.org/10.31857/s0514749223120054openalex-snapshot
Design, synthesis and antiarrhythmic activity of new amide derivatives of indole-3-carboxylic acid
inferred← citeshttps://doi.org/10.32725/jab.2003.027openalex-snapshot
Amiodarone - excellent antiarrhythmic drug? (Happy end after 40 years of problems)
inferred← citeshttps://doi.org/10.3389/fphys.2022.974160openalex-snapshot
Multitargeting nature of muscarinic orthosteric agonists and antagonists
inferred← citeshttps://doi.org/10.3390/molecules22111820openalex-snapshot
Synthesis and 2D-QSAR Study of Active Benzofuran-Based Vasodilators
inferred← citeshttps://doi.org/10.4236/gsc.2011.14025openalex-snapshot
Phase-Transfer-Catalyzed Intramolecular Hydroaryloxylation and Hydroamination of C≡C Triple Bonds: An Efficient Synthesis of Benzo[b]furan and 3-Methyleneisoindoline-1-one Derivatives
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.