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Therapeutic Potential of Boron-Containing Compounds
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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In Vitro Penetration of a Novel Oxaborole Antifungal (AN2690) Into the Human Nail Plate
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Boronic acid compounds as potential pharmaceutical agents
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Molecular Diversity of Cyclic AMP Signalling
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A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-ACP reductase
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Cytochemistry of membrane proteases
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Tissue Uptake of BSH in Patients with Glioblastoma in the EORTC 11961 Phase I BNCT Trial
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Mechanism of proline-specific proteinases: (I) substrate specificity of dipeptidyl peptidase IV from pig kidney and proline-specific endopeptidase from Flavobacterium meningosepticum
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Structure-based optimization of cephalothin-analogue boronic acids as β-lactamase inhibitors
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Synthesis and in vitro biological evaluation of aryl boronic acids as potential inhibitors of factor XIa
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Identification of a novel boron-containing antibacterial agent (AN0128) with anti-inflammatory activity, for the potential treatment of cutaneous diseases
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Potent inhibitors of HCV-NS3 protease derived from boronic acids
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Discovery and structure–activity study of a novel benzoxaborole anti-inflammatory agent (AN2728) for the potential topical treatment of psoriasis and atopic dermatitis
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Pharmacokinetic and Pharmacodynamic Assessments of the Dipeptidyl Peptidase-4 Inhibitor PHX1149: Double-Blind, Placebo-Controlled, Single- and Multiple-Dose Studies in Healthy Subjects
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Boron neutron capture therapy (BNCT) for glioblastoma multiforme: A phase II study evaluating a prolonged high-dose of boronophenylalanine (BPA)
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Daily Boron Intake from the American Diet
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Inhibition of IgA1 proteinases from Neisseria gonorrhoeae and Hemophilus influenzae by peptide prolyl boronic acids.
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Recent Developments in β-Lactamases and Inhibitors
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P1 Phenethyl peptide boronic acid inhibitors of HCV NS3 protease
inferredcites →https://doi.org/10.1016/s0960-894x(98)00126-7openalex-snapshot
Syntheses and evaluation of benzodiazaborine compounds against M. tuberculosis H37Rv in vitro
inferredcites →https://doi.org/10.1016/s1471-4892(01)00079-0openalex-snapshot
β-Lactamase-inhibitor combinations in the 21st century: current agents and new developments
inferredcites →https://doi.org/10.1021/ja00096a017openalex-snapshot
Boron Heterocycles Bearing a Peripheral Resemblance to Naturally-Occurring Purines: Design, Syntheses, Structures, and Properties
inferredcites →https://doi.org/10.1021/ja042850aopenalex-snapshot
Structure, Function, and Inhibition along the Reaction Coordinate of CTX-M β-Lactamases
inferredcites →https://doi.org/10.1021/ja963784iopenalex-snapshot
Planar Boron Heterocycles with Nucleic Acid-Like Hydrogen-Bonding Motifs
inferredcites →https://doi.org/10.1021/jm00374a003openalex-snapshot
Preparation and antibacterial activities of new 1,2,3-diazaborine derivatives and analogs
inferredcites →https://doi.org/10.1021/jm0342414openalex-snapshot
Structure−Activity Study on a Novel Series of Macrocyclic Inhibitors of the Hepatitis C Virus NS3 Protease Leading to the Discovery of BILN 2061
inferredcites →https://doi.org/10.1021/jm0603724openalex-snapshot
Discovery of a New Boron-Containing Antifungal Agent, 5-Fluoro-1,3-dihydro-1-hydroxy-2,1- benzoxaborole (AN2690), for the Potential Treatment of Onychomycosis
inferredcites →https://doi.org/10.1021/jm800390nopenalex-snapshot
Dipeptide Boronic Acid Inhibitors of Dipeptidyl Peptidase IV: Determinants of Potency and in Vivo Efficacy and Safety
inferredcites →https://doi.org/10.1021/jm950732fopenalex-snapshot
Structure−Activity Relationships of Boronic Acid Inhibitors of Dipeptidyl Peptidase IV. 1. Variation of the P2Position of Xaa-boroPro Dipeptides
inferredcites →https://doi.org/10.1038/293662a0openalex-snapshot
A diazaborine derivative inhibits lipopolysaccharide biosynthesis
inferredcites →https://doi.org/10.1073/pnas.88.4.1556openalex-snapshot
Inhibition of dipeptidyl aminopeptidase IV (DP-IV) by Xaa-boroPro dipeptides and use of these inhibitors to examine the role of DP-IV in T-cell function.
inferredcites →https://doi.org/10.1074/jbc.271.38.23222openalex-snapshot
Investigation of Glucose-dependent Insulinotropic Polypeptide(1-42) and Glucagon-like Peptide-1-(7-36) Degradation by Dipeptidyl Peptidase IV Using Matrix-assisted Laser Desorption/Ionization-Time of Flight Mass Spectrometry
inferredcites →https://doi.org/10.1093/jac/41.suppl_4.25openalex-snapshot
Beta-lactamase-mediated resistance and opportunities for its control
inferredcites →https://doi.org/10.1097/00045391-200109000-00005openalex-snapshot
Boron Therapeutics on the Horizon
inferredcites →https://doi.org/10.1107/s0108270197012432openalex-snapshot
A 2-Alkyl Substituted 2,3,1-Benzodiazaborine
inferredcites →https://doi.org/10.1107/s0108270199007520openalex-snapshot
A boron-containing estrogen mimic
inferredcites →https://doi.org/10.1107/s0108767398008125openalex-snapshot
X-ray Crystallography of Surfaces and Interfaces
inferredcites →https://doi.org/10.1107/s0907444996005458openalex-snapshot
Crystallization of Escherichia coli enoyl reductase and its complex with diazaborine
inferredcites →https://doi.org/10.1111/j.1463-1326.2008.00868.xopenalex-snapshot
The dipeptidyl peptidase‐4 inhibitor PHX1149 improves blood glucose control in patients with type 2 diabetes mellitus
inferredcites →https://doi.org/10.1111/j.1600-0749.1989.tb00207.xopenalex-snapshot
Acute and Subacute Toxicity of 10B‐Paraboronophenylalanine
inferredcites →https://doi.org/10.1124/dmd.104.002956openalex-snapshot
HUMAN METABOLISM OF THE PROTEASOME INHIBITOR BORTEZOMIB: IDENTIFICATION OF CIRCULATING METABOLITES
inferredcites →https://doi.org/10.1124/pr.58.3.5openalex-snapshot
Cyclic Nucleotide Phosphodiesterases: Molecular Regulation to Clinical Use
inferredcites →https://doi.org/10.1126/science.1142189openalex-snapshot
An Antifungal Agent Inhibits an Aminoacyl-tRNA Synthetase by Trapping tRNA in the Editing Site
inferredcites →https://doi.org/10.1126/science.2523562openalex-snapshot
Isolation of a cDNA cLone Derived from a Blood-Borne Non-A, Non-B Viral Hepatitis Genome
inferredcites →https://doi.org/10.1126/science.257.5073.1064openalex-snapshot
The Crisis in Antibiotic Resistance
inferredcites →https://doi.org/10.1126/science.274.5295.2107openalex-snapshot
A Mechanism of Drug Action Revealed by Structural Studies of Enoyl Reductase
inferredcites →https://doi.org/10.1128/aac.39.6.1211openalex-snapshot
A functional classification scheme for beta-lactamases and its correlation with molecular structure
inferredcites →https://doi.org/10.1128/mmbr.62.4.1079-1093.1998openalex-snapshot
Multimodular Penicillin-Binding Proteins: An Enigmatic Family of Orthologs and Paralogs
inferredcites →https://doi.org/10.1136/thx.46.7.512openalex-snapshot
Phosphodiesterase inhibitors: new opportunities for the treatment of asthma.
inferredcites →https://doi.org/10.1152/physrev.1995.75.4.725openalex-snapshot
Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms
inferredcites →https://doi.org/10.1158/1078-0432.ccr-05-0035openalex-snapshot
Boron Neutron Capture Therapy of Cancer: Current Status and Future Prospects
inferredcites →https://doi.org/10.1182/blood.v106.11.1863.1863openalex-snapshot
A Phase I Double-Blind, Ascending Dose Study of an Oral Synthetic Direct Thrombin Inhibitor, TGN167.
inferredcites →https://doi.org/10.1210/en.136.8.3585openalex-snapshot
Degradation of glucose-dependent insulinotropic polypeptide and truncated glucagon-like peptide 1 in vitro and in vivo by dipeptidyl peptidase IV
inferredcites →https://doi.org/10.1242/jcs.01096openalex-snapshot
PDE4-regulated cAMP degradation controls the assembly of integrin-dependent actin adhesion structures and REF52 cell migration
inferredcites →https://doi.org/10.1358/dot.2007.43.11.1157620openalex-snapshot
Sitagliptin: Profile of a novel DPP-4 inhibitor for the treatment of type 2 diabetes (update)
inferredcites →https://doi.org/10.1517/13543784.17.3.285openalex-snapshot
Novel β-lactam antibiotics and inhibitor combinations
inferredcites →https://doi.org/10.2174/138945009787122860openalex-snapshot
Emerging Drug Candidates of Dipeptidyl Peptidase IV (DPP IV) Inhibitor Class for the Treatment of Type 2 Diabetes
inferredcites →https://doi.org/10.2337/diabetes.47.5.764openalex-snapshot
Dipeptidyl peptidase IV inhibition potentiates the insulinotropic effect of glucagon-like peptide 1 in the anesthetized pig.
inferredcites →https://doi.org/10.4161/cbt.6.11.4874openalex-snapshot
Phase II trial of single agent Val-boroPro (talabostat) inhibiting fibroblast activation protein in patients with metastatic colorectal cancer
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Principles of Drug Metabolism
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Solid‐state Nuclear Magnetic Resonance of Polymorphic Materials
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Iridium‐Catalyzed Chemoselective and Enantioselective Hydrogenation of (1‐Chloro‐1‐Alkenyl) Boronic Esters
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Copper‐Catalyzed Enantioselective 1,6‐Boration of para‐Quinone Methides and Efficient Transformation of gem‐Diarylmethine Boronates to Triarylmethanes
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Modular Assembly of Reversible Multivalent Cancer‐Cell‐Targeting Drug Conjugates
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Highly Enantiospecific Borylation for Chiral α‐Amino Tertiary Boronic Esters
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Stereoselective Unsymmetrical 1,1‐Diborylation of Alkynes with a Neutral sp2−sp3 Diboron Reagent
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N‐Heterocycle‐Editing to Access Fused‐BN‐Heterocycles via Ring‐Opening/C−H Borylation/Reductive C−B Bond Formation
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Zero‐Valent Copper Catalysis Enables Regio‐ and Stereoselective Difunctionalization of Alkynes
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Direct Conversion of Aromatic Lactones into Bioisosteres by Carbonyl‐to‐Boranol Exchange
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Bench‐Stable Boryl Thianthrenium Dication Enables Aziridinyl Boronate Synthesis via Metal‐Free Late‐Stage Aziridination with Diverse Nitrogen Nucleophiles
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Direct Molecular Editing of Complex Molecules for Drug Discovery
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Iridium‐Catalyzed Chemoselective and Enantioselective Hydrogenation of (1‐Chloro‐1‐Alkenyl) Boronic Esters
inferred← citeshttps://doi.org/10.1002/anie.201505926openalex-snapshot
Copper‐Catalyzed Enantioselective 1,6‐Boration of para‐Quinone Methides and Efficient Transformation of gem‐Diarylmethine Boronates to Triarylmethanes
inferred← citeshttps://doi.org/10.1002/anie.201703492openalex-snapshot
Modular Assembly of Reversible Multivalent Cancer‐Cell‐Targeting Drug Conjugates
inferred← citeshttps://doi.org/10.1002/anie.201809389openalex-snapshot
Highly Enantiospecific Borylation for Chiral α‐Amino Tertiary Boronic Esters
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Stereoselective Unsymmetrical 1,1‐Diborylation of Alkynes with a Neutral sp 2 −sp 3 Diboron Reagent
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N‐Heterocycle‐Editing to Access Fused‐BN‐Heterocycles via Ring‐Opening/C−H Borylation/Reductive C−B Bond Formation
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Zero‐Valent Copper Catalysis Enables Regio‐ and Stereoselective Difunctionalization of Alkynes
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Direct Conversion of Aromatic Lactones into Bioisosteres by Carbonyl‐to‐Boranol Exchange
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Bench‐Stable Boryl Thianthrenium Dication Enables Aziridinyl Boronate Synthesis via Metal‐Free Late‐Stage Aziridination with Diverse Nitrogen Nucleophiles
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Boric Acid and Borax Protect Human Lymphocytes from Oxidative Stress and Genotoxicity Induced by 3-Monochloropropane-1,2-diol
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Investigating the Mechanisms of Anti-tumoral Effect of Combination Therapy of Calcitriol and Sodium Pentaborate Pentahydrate on HepG2 Hepatocellular Carcinoma Cells
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Effects of curcumin-/boron-based compound complexation on antioxidant and antiproliferation activity
inferred← citeshttps://doi.org/10.1007/s40121-020-00350-1openalex-snapshot
Microbiology of Meropenem-Vaborbactam: A Novel Carbapenem Beta-Lactamase Inhibitor Combination for Carbapenem-Resistant Enterobacterales Infections
inferred← citeshttps://doi.org/10.1007/s42250-022-00562-7openalex-snapshot
Synthesis and Antimicrobial Activities of Boron-Containing Isoniazid Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12406-0openalex-snapshot
Direct-Acting Antiviral Agents for the Treatment of Hepatitis C Virus Infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00098-6openalex-snapshot
Six-Membered Rings With Two or More Heteroatoms With at Least One Boron
inferred← citeshttps://doi.org/10.1016/b978-0-12-822127-3.00001-6openalex-snapshot
Boron-containing small molecules as antiparasitic agents
inferred← citeshttps://doi.org/10.1016/b978-0-323-85730-7.00026-6openalex-snapshot
Antimicrobial (viral, bacterial, fungal, and parasitic) mechanisms of action of boron-containing compounds
inferred← citeshttps://doi.org/10.1016/b978-0-323-95388-7.00005-xopenalex-snapshot
Challenges in the development of novel antibiotics
inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00003-7openalex-snapshot
Visible light–driven organic synthesis under other miscellaneous photocatalysis
inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00004-9openalex-snapshot
Visible light–driven organic synthesis under iridium (IrIII)-complex photocatalysis
inferred← citeshttps://doi.org/10.1016/b978-0-443-44593-4.00002-xopenalex-snapshot
Boron-based optical probes for biological applications
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00819-1openalex-snapshot
Six-membered Rings with Two or More Heteroatoms with at least One Boron
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.10.002openalex-snapshot
Recent Developments in the Chemistry of Boron Heterocycles
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.01.010openalex-snapshot
Recent developments in the medicinal chemistry of single boron atom-containing compounds
inferred← citeshttps://doi.org/10.1016/j.apsusc.2018.09.157openalex-snapshot
Microstructure, chemical and biological performance of boron-modified TiCaPCON films
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2014.01.009openalex-snapshot
Effects of S-PRG eluate on oral biofilm and oral malodor
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103081openalex-snapshot
Antifungal activity and tautomeric cyclization equilibria of formylphenylboronic acids
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103158openalex-snapshot
Arylboronate prodrugs of doxorubicin as promising chemotherapy for pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106976openalex-snapshot
Boron-containing carbonic anhydrases inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.06.014openalex-snapshot
Synthesis, reactivity and biological activity of N(4)-boronated derivatives of 2′-deoxycytidine
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116748openalex-snapshot
Boron-Containing heterocycles as promising pharmacological agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2024.117999openalex-snapshot
Synthesis and structure-activity relationship of boronic acid bioisosteres of combretastatin A-4 as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.12.045openalex-snapshot
Synthesis and antibacterial evaluation of a novel tricyclic oxaborole-fused fluoroquinolone
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.03.067openalex-snapshot
Recent advances in malaria drug discovery
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.06.049openalex-snapshot
Synthesis, characterization and antimicrobial activity of novel Schiff base tethered boronate esters of 1,2-O-isopropylidene-α-d-xylofuranose
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128089openalex-snapshot
Exploring boron applications in modern agriculture: A structure-activity relationship study of a novel series of multi-substitution benzoxaboroles for identification of potential fungicides
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128864openalex-snapshot
Design, development, synthesis, and crystal structure of the prototype of a new class of deep blue-fluorescing boron heterocycle estrogen mimics
inferred← citeshttps://doi.org/10.1016/j.ccr.2024.215892openalex-snapshot
Synthesis, properties and emerging applications of multi-boron coordinated chromophores
inferred← citeshttps://doi.org/10.1016/j.comptc.2026.116042openalex-snapshot
Assessment of borole as an electron-withdrawing group
inferred← citeshttps://doi.org/10.1016/j.ddtec.2018.08.002openalex-snapshot
Borylated reagents for multicomponent reactions
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.01.040openalex-snapshot
Novel oleanolic vinyl boronates: Synthesis and antitumor activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.02.056openalex-snapshot
Boronic species as promising inhibitors of the Staphylococcus aureus NorA efflux pump: Study of 6-substituted pyridine-3-boronic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.06.092openalex-snapshot
Boron in drug design: Recent advances in the development of new therapeutic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112670openalex-snapshot
Anticancer boron-containing prodrugs responsive to oxidative stress from the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115761openalex-snapshot
Elemental exchange: Bioisosteric replacement of phosphorus by boron in drug design
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118224openalex-snapshot
Benzoxaboroles in medicinal chemistry: A structure-guided perspective on next-generation therapeutics
inferred← citeshttps://doi.org/10.1016/j.ejphar.2019.04.020openalex-snapshot
In vitro anti-glioblastoma activity of L-valine derived boroxazolidones
inferred← citeshttps://doi.org/10.1016/j.etap.2019.103208openalex-snapshot
Responses of Chlorella vulgaris exposed to boron: Mechanisms of toxicity assessed by multiple endpoints
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e27215openalex-snapshot
The efficacy of topical sodium pentaborate formulation on hemorrhoid disease: A randomized, double-blind, placebo-controlled trial
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131268openalex-snapshot
Identification, crystallization, and first X-ray structure analyses of phenyl boronic acid-based inhibitors of human carbonic anhydrase-II
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2022.122070openalex-snapshot
Rheological analysis of a novel phenylboronic acid-closomer gel
inferred← citeshttps://doi.org/10.1016/j.jas.2015.01.020openalex-snapshot
Testing Dioscorides' medicinal clays for their antibacterial properties: the case of Samian Earth
inferred← citeshttps://doi.org/10.1016/j.jddst.2018.05.027openalex-snapshot
Synthesis of nucleoside-boronic esters hydrophobic pro-drugs: A possible route to improve hydrophilic nucleoside drug loading into polymer nanoparticles
inferred← citeshttps://doi.org/10.1016/j.jma.2023.09.018openalex-snapshot
Electrochemical synthesis of boron-containing coatings on Mg alloy for thermal neutron shielding
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.03.017openalex-snapshot
Benzoboroxoles: Synthesis and applications in medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.07.019openalex-snapshot
An original one-pot approach to boronic esters using the titanium-catalyzed reaction of cyclic olefins with alkyldichloroboranes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.120958openalex-snapshot
Efficient and chemoselective hydroboration of organic nitriles promoted by TiIV catalyst supported by unsymmetrical acenaphthenequinonediimine ligand
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2026.124089openalex-snapshot
Synthesis and evaluation of boron-containing heterocycles as drug candidates: Benzoxazaborinins as PARP inhibitors
inferred← citeshttps://doi.org/10.1016/j.jtemb.2020.126573openalex-snapshot
In vitro effects of boric acid on human liver hepatoma cell line (HepG2) at the half-maximal inhibitory concentration
inferred← citeshttps://doi.org/10.1016/j.jtemb.2021.126714openalex-snapshot
Effects of boron-containing compounds in the fungal kingdom
inferred← citeshttps://doi.org/10.1016/j.jtemb.2023.127139openalex-snapshot
In silico and biological activity evaluation of quercetin-boron hybrid compounds, anti-quorum sensing effect as alternative potential against microbial resistance
inferred← citeshttps://doi.org/10.1016/j.jtemb.2025.127594openalex-snapshot
Exploring the role of boron-containing compounds in biological systems: Potential applications and key challenges
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.117116openalex-snapshot
Inhibition of the transcriptional repressor LexA: Withstanding drug resistance by inhibiting the bacterial mechanisms of adaptation to antimicrobials
inferred← citeshttps://doi.org/10.1016/j.mencom.2018.11.003openalex-snapshot
An original catalytic synthesis of boriran-1-ols
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.132057openalex-snapshot
Benzoxaboroles: New emerging and versatile scaffold with a plethora of pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144690openalex-snapshot
Design, synthesis, and evaluation of anticancer activities of 1,2-diborolane derivatives for hepatocellular carcinoma: An in vitro and in silico study
inferred← citeshttps://doi.org/10.1016/j.neuro.2013.10.005openalex-snapshot
Boron-containing acids: Preliminary evaluation of acute toxicity and access to the brain determined by Raman scattering spectroscopy
inferred← citeshttps://doi.org/10.1016/j.pep.2017.10.009openalex-snapshot
Soluble expression and purification of a full-length asparaginyl tRNA synthetase from Fasciola gigantica
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2023.108548openalex-snapshot
Boron in cancer therapeutics: An overview
inferred← citeshttps://doi.org/10.1016/j.taap.2016.08.002openalex-snapshot
Disruption of motor behavior and injury to the CNS induced by 3-thienylboronic acid in mice
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.065openalex-snapshot
Study of chemoselective asymmetric hydrogenation of (1-bromo-1-alkenyl)boronic esters with iridium–PˆN complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.097openalex-snapshot
Synthesis of novel dehydroacetic acid N -aroylhydrazone-derived boron heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132578openalex-snapshot
Amide directed iridium C(sp3)–H borylation catalysis with high N-methyl selectivity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.08.012openalex-snapshot
Potassium haloalkyltrifluoroborate salts: synthesis, application, and reversible ligand replacement with MIDA
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153657openalex-snapshot
Synthesis of a boron-containing amidoxime reagent and its application to synthesize functionalized oxadiazole and quinazolinone derivatives
inferred← citeshttps://doi.org/10.1016/j.toxlet.2016.06.018openalex-snapshot
Current data regarding the structure-toxicity relationship of boron-containing compounds
inferred← citeshttps://doi.org/10.1016/j.vibspec.2020.103131openalex-snapshot
Accessible approaches for vibrational zero point energy calculation of organoboron compounds
inferred← citeshttps://doi.org/10.1016/j.xphs.2016.06.002openalex-snapshot
Antibiotic Resistance: The Need For a Global Strategy
inferred← citeshttps://doi.org/10.1021/acs.accounts.6c00094openalex-snapshot
BX 3 -Mediated Directed Electrophilic Borylation: Advances, Applications, and Mechanistic Insights
inferred← citeshttps://doi.org/10.1021/acs.biochem.5c00655openalex-snapshot
Inhibition of Mandelate Racemase by Boron-Based Inhibitors: Different Binding Modes for Benzoxaboroles Versus Boronic Acids
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00663openalex-snapshot
The Rise of Boron-Containing Compounds: Advancements in Synthesis, Medicinal Chemistry, and Emerging Pharmacology
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c01194openalex-snapshot
Expanding the Role of Boron in New Drug Chemotypes: Properties, Chemistry, Pharmaceutical Potential of Hemiboronic Naphthoids
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00341openalex-snapshot
Click Chemistry in Lead Optimization of Boronic Acids as β-Lactamase Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01932openalex-snapshot
Challenges and Opportunities for the Application of Boron Clusters in Drug Design
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c01766openalex-snapshot
Rediscovering Diazaborines: Synthesis and Bioactivity Profiling of Boron-Containing FabI Inhibitors against Gram-Negative Bacteria
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b00878openalex-snapshot
De Novo Design of Boron-Based Peptidomimetics as Potent Inhibitors of Human ClpP in the Presence of Human ClpX
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00246openalex-snapshot
o-Boronato- and o-Trifluoroborato–Phosphonium Salts Supported by l -α-Amino Acid Side Chain
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00747openalex-snapshot
Azaborininones: Synthesis and Structural Analysis of a Carbonyl-Containing Class of Azaborines
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00325openalex-snapshot
Modular Synthesis of β-Amino Boronate Peptidomimetics
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01493openalex-snapshot
Transition Metal-Free Trans Hydroboration of Alkynoic Acid Derivatives: Experimental and Theoretical Studies
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02887openalex-snapshot
Tunable Synthesis of α-Amino Boronic Esters from Available Aldehydes and Amines through Sequential One-Pot Dehydration and Copper-Catalyzed Borylacylation
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.8b00873openalex-snapshot
Direct and Real-Time Quantification Of Bortezomib Release From Alginate Microparticles Using Boron (11B) Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00485openalex-snapshot
Flash Communication: Copper-Catalyzed Borylation of Imines for the Synthesis of Four-Coordinate α-Aminoboranes Using sp 2 -sp 3 Diboron Reagents
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00468openalex-snapshot
Ring Contraction of a Pinacolatoboryl Group To Form a 1,2-Oxaboretane Ring: Reaction of Unsymmetrical Diborane(4) with 2,6-Dimethylphenyl Isocyanide
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03033openalex-snapshot
Palladium-Catalyzed Borylative Cyclizations of α-(2-Bromoaryl) Ketones to Form 1,2-Benzoxaborinines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03812openalex-snapshot
Gold-Catalyzed Cyclization/Hydroboration of 1,6-Enynes: Synthesis of Bicyclo[3.1.0]hexane Boranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00857openalex-snapshot
Cope-Type Hydroamination of Vinylboronates
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02260openalex-snapshot
Synthesis of Highly Substituted Oxaboroles from Oxaboranes via a Selective Petasis Borono–Mannich Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00934openalex-snapshot
Copper(I)-Catalyzed Asymmetric Pinacolboryl Addition of N -Boc-imines Using a Chiral Sulfoxide–Phosphine Ligand
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01382openalex-snapshot
Base Mediated 1,2-Carboboration: Direct Access to Multisubstituted Alkenyl and Alkylboronates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01934openalex-snapshot
Diastereoselective [3 + 2] Cycloaddition of Lewis Acidic Alkenylboranes and Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00466openalex-snapshot
Accessing Elaborated 2,1-Borazaronaphthalene Cores Using Photoredox/Nickel Dual-Catalytic Functionalization
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03326openalex-snapshot
Regioselective Copper-Catalyzed Boracarboxylation of Vinyl Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02947openalex-snapshot
Copper-Mediated SN2′ Allyl–Alkyl and Allyl–Boryl Couplings of Vinyl Cyclic Carbonates
inferred← citeshttps://doi.org/10.1021/acsanm.0c00762openalex-snapshot
Self-Therapeutic Nanomaterials for Cancer Therapy: A Review
inferred← citeshttps://doi.org/10.1021/acsanm.3c03259openalex-snapshot
Meta-Isobutoxy Phenylboronic Acid for Nanoscale Multi-Stimuli-Responsive Low-Molecular-Weight Hydrogelator
inferred← citeshttps://doi.org/10.1021/acscatal.1c01689openalex-snapshot
Synthesis of Chiral α-Amino Tertiary Boronates via the Catalytic Enantioselective Nucleophilic Borylation of Dialkyl Ketimines
inferred← citeshttps://doi.org/10.1021/acscatal.2c00614openalex-snapshot
(CAAC)Copper Catalysis Enables Regioselective Three-Component Carboboration of Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acscatal.5c01288openalex-snapshot
Modular Synthesis of Chiral 1,3-Diboronates with Differentiable Boryl Groups via Cu-Catalyzed Borylalkylation of Styrenes
inferred← citeshttps://doi.org/10.1021/acsomega.9b01774openalex-snapshot
Synthesis and Antimicrobial Evaluation of γ-Borono Phosphonate Compounds in Escherichia coli and Mycobacterium smegmatis
inferred← citeshttps://doi.org/10.1021/acsptsci.5c00238openalex-snapshot
Recent Development of Boron-Containing Small-Molecule Anticancer Agents
inferred← citeshttps://doi.org/10.1021/acssensors.6b00522openalex-snapshot
Visualization of Boronic Acid Containing Pharmaceuticals in Live Tumor Cells Using a Fluorescent Boronic Acid Sensor
inferred← citeshttps://doi.org/10.1021/cb400345hopenalex-snapshot
Rational Design of a Transition State Analogue with Picomolar Affinity for Pseudomonas aeruginosa PvdQ, a Siderophore Biosynthetic Enzyme
inferred← citeshttps://doi.org/10.1021/ci300461aopenalex-snapshot
Broad Coverage of Commercially Available Lead-like Screening Space with Fewer than 350,000 Compounds
inferred← citeshttps://doi.org/10.1021/cr2000866openalex-snapshot
Boron in Drug Discovery: Carboranes as Unique Pharmacophores in Biologically Active Compounds
inferred← citeshttps://doi.org/10.1021/cr500642dopenalex-snapshot
Recent Developments in the Chemistry and Biological Applications of Benzoxaboroles
inferred← citeshttps://doi.org/10.1021/cr608202mopenalex-snapshot
Boron Containing Compounds as Protease Inhibitors
inferred← citeshttps://doi.org/10.1021/ja304173dopenalex-snapshot
Boroalkyl Group Migration Provides a Versatile Entry into α-Aminoboronic Acid Derivatives
inferred← citeshttps://doi.org/10.1021/ja5036754openalex-snapshot
Trans -Diborylation of Alkynes: Pseudo -Intramolecular Strategy Utilizing a Propargylic Alcohol Unit
inferred← citeshttps://doi.org/10.1021/jacs.1c02462openalex-snapshot
Lewis or Brønsted? A Rectification of the Acidic and Aromatic Nature of Boranol-Containing Naphthoid Heterocycles
inferred← citeshttps://doi.org/10.1021/jacs.2c03429openalex-snapshot
Unraveling the Silent Hydrolysis of Cyclic B–X/C═C Isosteres: The Striking Impact of a Single Heteroatom on the Aromatic, Acidic, and Dynamic Properties of Hemiboronic Phenanthroids
inferred← citeshttps://doi.org/10.1021/jacs.4c14890openalex-snapshot
Enantioselective α-C(sp 3 )–H Borylation of Masked Primary Alcohols Enabled by Iridium Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.5b03760openalex-snapshot
Synthesis of Chiral α-Amino Tertiary Boronic Esters by Enantioselective Hydroboration of α-Arylenamides
inferred← citeshttps://doi.org/10.1021/jacs.5c00974openalex-snapshot
Copper-Catalyzed C–B(sp3) Bond Formation through the Intermediacy of Cu–B(sp3) Complex
inferred← citeshttps://doi.org/10.1021/jacs.5c22151openalex-snapshot
Copper(I)–NHC-Catalyzed Enantioselective Borylation and Silylation of Ketimines
inferred← citeshttps://doi.org/10.1021/jacs.6c13223openalex-snapshot
Enantioenriched Alkylboron Synthesis Via a Chiral Diborylalkane Platform
inferred← citeshttps://doi.org/10.1021/jacs.7b06212openalex-snapshot
Transition Metal-Free trans-Selective Alkynylboration of Alkynes
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