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Active Ligands sentence examples within 4 hydroxy 1



Relationship between solid state structure and solution stability of copper(II)–hydroxypyridinecarboxylate complexes


Active Ligands sentence examples within Optically Active Ligands



Synthesis of 2-Amino-apopinan-3-ol and Applications of Its Derivatives in Asymmetric Reduction of Ketones



Хиральные комплексы переходных металлов с хелатными азотными лигандами в асимметрическом гидрировании с переносом водорода


Active Ligands sentence examples within Biologically Active Ligands



Radiosynthesis and evaluation of a novel monoacylglycerol lipase radiotracer: 1,1,1,3,3,3-hexafluoropropan-2-yl-3-(1-benzyl-1H-pyrazol-3-yl)azetidine-1-[11C]carboxylate.



Role of fatty acid binding proteins (FABPs) in cancer development and progression.



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Active Ligands sentence examples within Identify Active Ligands



Prediction of Orthosteric and Allosteric Regulations on Cannabinoid Receptors Using Supervised Machine Learning Classifiers.



A novel G protein-biased and subtype selective agonist for a G protein-coupled receptor discovered from screening herbal extracts


Active Ligands sentence examples within active ligands could



Insulin-like growth factor type I selectively binds to G-quadruplex structures.



Mapping the Azolog Space Enables the Optical Control of New Biological Targets


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10.1016/j.jpba.2019.03.029

Identification of eupatilin and ginkgolide B as p38 ligands from medicinal herbs by surface plasmon resonance biosensor-based active ingredients recognition system.


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10.1016/BS.MIE.2019.04.027

Identifying and validating small molecules interacting with RNA (SMIRNAs).


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10.2174/1389557517666171101104024

Antimicrobial Potential of Benzimidazole Derived Molecules.


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10.1016/j.aca.2018.10.022

Highly stable Ni-MOF comprising triphenylamine moieties as a high-performance redox indicator for sensitive aptasensor construction.



Photochromic diarylethene ligands featuring 2-(imidazol-2-yl)pyridine coordination site and their iron(II) complexes


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10.1002/chem.201802691

Ligand Design to Acquire Specificity to Intended G-Quadruplex Structures.



Investigating targets for neuropharmacological intervention by molecular dynamics simulations.


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10.1016/J.JAGP.2019.01.038

THE USE OF COGNITIVE AND ERP BIOMARKERS OF CHOLINERGIC FUNCTION IN NOVEL TESTS OF MUSCARINIC POSITIVE ALLOSTERIC MODULATORS


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10.1021/acs.inorgchem.9b02796

Synthesis and Cytotoxicity of Water-Soluble Dual- and Triple-Action Satraplatin Derivatives: Replacement of Equatorial Chlorides of Satraplatin by Acetates.



New heterobimetallic ferrocenyl derivatives are promising antitrypanosomal agents.


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10.1016/j.molliq.2019.111887

Comparative solution equilibria studies of complex formation between Ir(III) ion and antituberculosis drug analogues: Spectroscopic, potentiometric and conductometric approach


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10.2174/0929867326666190417143533

Metal Complexes As Promising Agents For Biomedical Applications.


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10.1016/j.bioorg.2019.103332

Towards breast cancer targeting: Synthesis of tetrahydroindolocarbazoles, antibreast cancer evaluation, uPA inhibition, molecular genetic and molecular modelling studies.


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10.22270/jddt.v9i1-s.2331

Peptide Conjugated Lipid Nanoparticles for Anti-Cancer Drug Delivery


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10.1080/00958972.2019.1624728

Tunable intramolecular multicenter H-bonding interactions in first-row metal complexes bearing bidentate redox-active ligands



Emerging platinum(iv) prodrugs to combat cisplatin resistance: from isolated cancer cells to tumor microenvironment.



Efficient ligand discovery from natural herbs by integrating virtual screening, affinity mass spectrometry and targeted metabolomics.


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10.2174/0929867326666190517114450

Immunoliposomes in acute myeloid leukaemia therapy. An overview of possible targets and obstacles.


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10.1016/j.bios.2019.111743

Electroactive metal-organic framework composites: Design and biosensing application.


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10.1016/j.bmc.2019.115185

Synthesis, in-vitro antiprotozoal activity and molecular docking study of isothiocyanate derivatives.


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10.33612/diss.107969043

Redox-behavior and reactivity of formazanate ligands : Boron and aluminum chemistry


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10.1021/acsami.9b03029

Stretchable and Bioadhesive Supramolecular Hydrogels Activated by a One-Stone-Two-Bird Postgelation Functionalization Method.



Hydrogenase biomimics containing redox-active ligands: Fe2(CO)4(μ-edt)(κ2-bpcd) with electron-acceptor 4,5-bis(diphenylphosphino)-4-cyclopenten-1,3-dione (bpcd) as a potential [Fe4-S4]H surrogate.


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10.1007/978-3-030-06115-9_19

Polydopamine-Based Simple and Versatile Surface Modification of Polymeric Nano Drug Carriers


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10.1080/07391102.2019.1574603

QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives


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10.1002/cctc.201900953

Electrocatalytic H2 Evolution by the Co‐Mabiq Complex Requires Tempering of the Redox‐Active Ligand


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10.1016/j.jinorgbio.2018.11.008

Multi-action Pt(IV) anticancer agents; do we understand how they work?


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10.1002/anie.201910014

Expanding the Arsenal of PtIV Anticancer Agents; Multi-action PtIV Anticancer Agents with Bioactive Ligands Possessing Hydroxyl Functional Group.


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10.1016/j.jinorgbio.2019.110768

Hydroxyquinoline-derived anticancer organometallics: Introduction of amphiphilic PTA as an ancillary ligand increases their aqueous solubility.


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10.1016/j.sbi.2019.02.011

Automated discovery of GPCR bioactive ligands.


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10.1002/chem.201901962

Alkali Metal Aminotroponiminates: Selectivities and Equilibria in Reversible Radical Coupling of Delocalized π-Electron Systems.


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10.1016/J.ICA.2019.118960

Stabilizing a NiII-aqua complex via intramolecular hydrogen bonds: synthesis, structure, and redox properties.



A coordinatively unsaturated iridium complex with an unsymmetrical redox-active ligand: (spectro)electrochemical and reactivity studies.


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10.1016/j.jinorgbio.2019.110779

Pt-Fe ferrocenyl compounds with hydroxyquinoline ligands show selective cytotoxicity on highly proliferative cells.


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10.1021/acs.inorgchem.9b00652

Effect of Redox Active Ligands on the Electrochemical Properties of Manganese Tricarbonyl Complexes.



Discovery of high in vitro and in vivo antitumor activities of organometallic ruthenium(ii)-arene complexes with 5,7-dihalogenated-2-methyl-8-quinolinol.



The anatomy of concussion and chronic traumatic encephalopathy: A comprehensive review


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10.1021/acs.biomac.8b01496

Enzymatic Activity in Fractal Networks of Self-Assembling Peptides.


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10.1007/s10965-019-1728-2

Surface-attached dual-functional hydrogel for controlled cell adhesion based on poly(N,N-dimethylacrylamide)


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10.1002/ADMI.201900572

Controlling Cell Behavior through the Design of Biomaterial Surfaces: A Focus on Surface Modification Techniques


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10.1016/j.bbagen.2018.09.022

Insulin-like growth factor type I selectively binds to G-quadruplex structures.



[Current situation of researches on a sensor organelle, primary cilium, to understand the pathogenesis of ciliopathy].


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10.1007/978-3-030-32656-2_11

Canonical and Noncanonical Androgen Metabolism and Activity.


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10.1016/J.BIOORG.2019.03.003

Synthesis, biological activity and multiscale molecular modeling studies of bis-coumarins as selective carbonic anhydrase IX and XII inhibitors with effective cytotoxicity against hepatocellular carcinoma.


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10.1002/chem.201900002

Multi-electron Reduction Capacity and Multiple Binding Pockets in Metal-Organic Redox Assembly at Surfaces.


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10.3389/fchem.2019.00602

Structural, Thermodynamic, and Kinetic Traits of Antiestrogen-Compounds Selectively Targeting the Y537S Mutant Estrogen Receptor α Transcriptional Activity in Breast Cancer Cell Lines


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10.1007/s11356-019-04348-2

Photogeneration of hydroxyl radical in Fe(III)-citrate-oxalate system for the degradation of fluconazole: mechanism and products


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10.1007/s12282-019-01011-z

Comparative anti-proliferative effects of potential HER2 inhibitors on a panel of breast cancer cell lines


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10.1021/acscentsci.8b00881

Mapping the Azolog Space Enables the Optical Control of New Biological Targets


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10.1109/JSEN.2019.2927283

Development of Sensor Based on Copper(II) Thiocyanate Pyridine Polymeric Complex for Detection of Catechol


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10.1021/acs.inorgchem.9b01675

The Influence of Redox-Innocent Donor Groups in Tetradentate Ligands Derived from o-Phenylenediamine: Electronic Structure Investigations with Nickel.


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10.1016/j.biomaterials.2019.119310

Remote and reversible control of in vivo bacteria clustering by NIR-driven multivalent upconverting nanosystems.


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10.1016/j.bmc.2019.115234

Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening.


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10.2174/1568026620666191226101543

Integrated Protocol to Design Potential Inhibitors of Dipeptidyl Peptidase-4 (DPP-4).


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10.1007/s11934-019-0938-9

Renal Cell Carcinoma: the Oncologist Asks, Can PSMA PET/CT Answer?


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10.1016/J.APSUSC.2018.11.056

Fabrication of stable biomimetic coating on PDMS surface: Cooperativity of multivalent interactions


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10.1021/acs.accounts.8b00604

Dynamic Synthetic Biointerfaces: From Reversible Chemical Interactions to Tunable Biological Effects.


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10.1021/ACSOMEGA.8B03041

Orthogonally “Clickable” Biodegradable Nanofibers: Tailoring Biomaterials for Specific Protein Immobilization


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10.1021/ACSCATAL.9B00708

Robust and SelectiveCobalt Catalysts Bearing Redox-ActiveBipyridyl‑ N ‑heterocyclic Carbene Frameworksfor Electrochemical CO 2 Reduction in Aqueous Solutions



Stable Cyclopropenium-Based Radicals


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10.1016/j.jpba.2018.12.009

Recent advances in bio‐affinity chromatography for screening bioactive compounds from natural products


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10.1038/s41589-019-0329-z

Publisher Correction: BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design


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10.2174/1381612825666190304123414

Molecular Dynamics Simulations of Adenosine Receptors: Advances, Applications and Trends.


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10.1021/acsami.9b08537

Thermosensitive display of carbohydrate ligands on microgels for switchable binding of proteins and bacteria.


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10.1007/s13205-019-1718-4

Potential anticancer applications of the novel naringin-based ruthenium (II) complex


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10.1021/acs.jcim.9b00032

Template-Based Method for Conformation Generation and Scoring for Congeneric Series of Ligands



Influence of structure–activity relationships on through-space intervalence charge transfer in metal–organic frameworks with cofacial redox-active units† †Electronic supplementary information (ESI) available. CCDC 1585897 and 1585898. For ESI and crystallographic data in CIF or other electronic form


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10.1016/j.biocel.2019.04.010

Chalcone derivatives as non-canonical ligands of TRPV1.


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10.1002/anie.201905790

Sign Inversion in Photopharmacology: Incorporation of Cyclic Azobenzenes in Photoswitchable Potassium Channel Blockers and Openers.


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10.1016/j.acax.2019.100017

Evaluation of the selectivity of G-quadruplex ligands in living cells with a small molecule fluorescent probe


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