Bioorganic chemistry

The Journal of Chemical Physics

Molecules (Basel, Switzerland)

International journal of biological macromolecules

acta crystallographica section c, structural chemistry

current medicinal chemistry

pakistan journal of pharmaceutical sciences

journal of materials chemistry b

[1] Synthesis of a New Series of Nitrogen/Sulfur Heterocycles by Linking Four Rings: Indole; 1,2,4-Triazole; Pyridazine; and Quinoxaline.

[2] Heterodimers made of metal-organic frameworks and upconversion nanoparticles for bioimaging and pH-responsive dual-drug delivery.

[3] Synthesis, anti-microbial and anti-mutagenic activities of some Schiff bases derivatives containing thiophene group.

[4] Synthesis, crystal structures, antiproliferative activities and reverse docking studies of eight novel Schiff bases derived from benzil.

[5] Effect of the chemical structure of an equatorial ligand on the spin crossover properties of the Fe(III) complex with 4-styrylpyridine axial ligands.

[6] Synthesis of N-substituted indole derivatives as potential antimicrobial and antileishmanial agents.

[7] indole-3-carbonitriles as dyrk1a inhibitors by fragment-based drug design

[8] indole derivatives from the egg masses of muricid molluscs

[9] crystal structure of rac-(3a'r,9a'r)-3a'-(indol-3-yl)-1′,2′,3′,3a',4′,9a'-hexahydrospiro[cyclopentane-1,9′-pentaleno[1,2-b]indole] p-xylene hemisolvate

[10] biomedical importance of indoles

[11] crystal structure of 14-methyl-11-(3-methylphenyl)-12-oxa-8,14-diazatetracyclo[8.3.3.01,10.02,7]hexadeca-2(7),3,5-triene-9,13-dione

[12] crystal structures of four indole derivatives with a phenyl substituent at the 2-position and a carbonyl group at the 3-position: the c(6) n—h...o chain remains the same, but the weak reinforcing interactions are different

[13] 5-(2-hydroxybenzoyl)-2-(1h-indol-3-yl)pyridine-3-carbonitrile

[14] dysbiosis of the vaginal microbiota and higher vaginal kynurenine/tryptophan ratio reveals an association with chlamydia trachomatis genital infections

[15] Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii

[16] [4 + 2] Annulation of 3-Nitroindoles with Alkylidene Malononitriles: Entry to Substituted Carbazol-4-amine Derivatives.

[17] Selective Synthesis of 3-(9 H-Carbazol-2-yl)indolin-2-ones and Spiro[tetrahydrocarbazole-3,3'-oxindoles] via a HOTf Catalyzed Three-Component Reaction.

[18] Phenanthroline- BuOK Promoted Intramolecular C-H Arylation of Indoles with ArI under Transition-Metal-Free Conditions.

[19] A trace alkaloid, oleraisoindole A from L. and its anticholinesterase effect.

[20] Indole-nitroimidazole conjugates as efficient manipulators to decrease the genes expression of methicillin-resistant Staphylococcus aureus.

[21] Lignans and indole alkaloids from the seeds of Centaurea vlachorum Hartvig (Asteraceae), growing wild in Albania and their biological activity.

[22] Isocoumarindole A, a Chlorinated Isocoumarin and Indole Alkaloid Hybrid Metabolite from an Endolichenic Fungus Aspergillus sp.

[23] Indole hybridized diazenyl derivatives: synthesis, antimicrobial activity, cytotoxicity evaluation and docking studies.

[24] Biomedical Importance of Indoles

[25] Indole-core-based novel antibacterial agent targeting FtsZ

[26] Plasma indoleamine 2,3-dioxygenase activity as a potential biomarker for early diagnosis of multidrug-resistant tuberculosis in tuberculosis patients

[27] Indole-core-based novel antibacterial agent targeting FtsZ

[28] Indole-core-based novel antibacterial agent targeting FtsZ

[29] Plasma indoleamine 2,3-dioxygenase activity as a potential biomarker for early diagnosis of multidrug-resistant tuberculosis in tuberculosis patients

[30] Indole-4-carboxaldehyde Isolated from Seaweed, , Attenuates Methylglyoxal-Induced Hepatic Inflammation.

[31] Discovery of certain benzyl/phenethyl thiazolidinone-indole hybrids as potential anti-proliferative agents: Synthesis, molecular modeling and tubulin polymerization inhibition study.

[32] Retracted: Bisindole-oxadiazole hybrids, T3P mediated -synthesis and appraisal of their apoptotic, antimetastatic and computational Bcl-2 binding potential.

[33] Dehydrative Transformation of Spirooxindoles to Pyrido[2,3-]indoles via POCl.

[34] Direct access to 2-difluoromethyl indoles via photoredox catalysis

[35] Indole Alkaloid Synthesis Facilitated by Photoredox Catalytic Radical Cascade Reactions

[36] Visible-Light-Induced Ring-Opening of Hydrogenolysis Spirocyclopropyl Oxindoles Through Photoredox Catalysis

[37] Three-Component One-Pot Synthesis of Highly Functionalized Bis-Indole Derivatives.

[38] Indole-3-carbinol protects against cisplatin-induced acute nephrotoxicity: role of calcitonin gene-related peptide and insulin-like growth factor-1

[39] Ammonia-Doped Polyaniline-Graphitic Carbon Nitride Nanocomposite as a Heterogeneous Green Catalyst for Synthesis of Indole-Substituted 4-Chromenes.

[40] Grignard addition to imines derived from isatine: a method for the asymmetric synthesis of quaternary 3-aminooxindoles.

[41] Grignard addition to imines derived from isatine: A method for the asymmetric synthesis of quaternary 3-aminooxindoles

[42] Therapeutic benefits of Indole-3-Carbinol in adjuvant-induced arthritis and its protective effect against methotrexate induced-hepatic toxicity.

[43] Cutaneous delivery of [1-(4-chloro-3-nitrobenzenesulfonyl)-1H-indol-3-yl]-methanol, an indole-3-carbinol derivative, mitigates psoriasiform lesion by blocking MAPK/NF-κB/AP-1 activation.

[44] UV Resonance Raman Characterization of a Substrate Bound to Human Indoleamine 2,3-Dioxygenase 1.

[45] The effect of π-π stacking interaction of the indole ring with the coordinated phenoxyl radical in a nickel(ii)-salen type complex. Comparison with the corresponding Cu(ii) complex.

[46] Indole-derived water-soluble N, O bi-dentate ligand-based mononuclear transition metal complexes: in silico and in vitro biological screening, molecular docking and macromolecule interaction studies.

[47] π-π Stacking Interaction in an Oxidized Cu -Salen Complex with a Side-Chain Indole Ring: An Approach to the Function of the Tryptophan in the Active Site of Galactose Oxidase.

[48] Bioactive and luminescent indole and isatin based gold(i) derivatives.

[49] Mechanism of the Alkylation of Indoles with Nitrostyrenes Catalyzed by Chiral-at-Metal Complexes

[50] New transition metal complexes with a pendent indole ring: Insights into the antifungal activity and mode of action

[51] New Acylhydrazones of Indole Series and Their Metal Complexes

[52] Synthesis, spectroscopic characterization, electrochemistry and biological activity evaluation of some metal (II) complexes with ONO donor ligands containing indole and coumarin moieties

[53] Reactivity of 3-Imino-Functionalized Indoles with Rare-Earth-Metal Amides: Unexpected Substituent Effects on C-H Activation Pathways and Assembly of Rare-Earth-Metal Complexes

[54] Synthesis and biological evaluation of metal complexes with pyrazoline derivative bearing indole and naphthyl moieties

[55] Poly(indole-6-carboxylic acid)/carbon composite as the matrix for the immobilization of the phenanthroline metal complexes, and the use of the composites as electrocatalyst for oxygen reduction reaction

[56] Synthesis, characterization, DNA cleavage and antimicrobial activities of schiff base ligand derived from 5-chloro-3-phenyl-1H-indole-2-carboxyhydrazide and O-vanillin and its metal (II) complexes

[57] Metal (II) complexes of ono donor schiff base ligand as a new class of bioactive compounds containing indole core: Synthesis and characterization

[58] Properties of the indole ring in metal complexes. A comparison with the phenol ring

[59] Isolation of ruthenium-indoline and -indole zwitterion complexes: Insight into the metal-induced cyclization of aniline-tethered alkynes and strategy to lower the activation barrier of metal-vinylidene formation

[60] Reactivity of functionalized indoles with rare-earth metal amides. Synthesis, characterization and catalytic activity of rare-earth metal complexes incorporating indolyl ligands

[61] A multiprotic indole-based thiocarbohydrazone in the formation of mono-, di- and hexa-nuclear metal complexes

[62] Metal complexes of indole-3-acetic acid: Synthesis, crystal structures, and Pb²⁺ chemosensing by cation-exchange reaction

[63] Chiral transition-metal complexes as Brønsted-acid catalysts for the asymmetric Friedel-Crafts hydroxyalkylation of indoles

[64] Synthesis characterization and DNA cleavage studies of some transition metal complexes derived from 5-chloro-3-phenyl-N'-(tetrazolo[1,5-a]quinolin-4-ylmethylene)-1H-indole-2-carbohydrazide

[65] Synthesis and characterization of novel transition metal complexes with indole acetic acid ligands: Evaluation of their catalytic activity for the oxidation of cyclohexane

[66] Synthesis, spectroscopic characterization, and biological screening of binuclear transition metal complexes of bicompartmental Schiff bases containing indole and resorcinol moieties

[67] Synthesis, characterization, antimicrobial, DNA cleavage, and antioxidant studies of some metal complexes derived from Schiff base containing indole and quinoline moieties

[68] Spectral characterization and biological activities of metal complexes of Cu(II), Ni(II) and Co(II) with tridentate a-amino-1-indole propionic acid based ligand

[69] Metal ion prompted macrocyclic complexes derived from indole-2,3-dione (isatin) and o-phenylenediamine with their spectroscopic and antibacterial studies

[70] Computational study on imidazole-2-carboxaldehyde-glycylglycine and indole-3-carboxaldehyde-glycylglycine Schiff base ligands and equilibrium studies on their metal complexes

[71] Group 6 metal carbonyl complexes of 3′H-spiro[indole-3,2′-[1,3]benzothiazole-2(1H)]-one

[72] Metal complexes involving indole rings: Structures and effects of metal-indole interactions

[73] Acute Toxicity and Gastroprotective Effect of the Schiff Base Ligand 1H-Indole-3-ethylene-5-nitrosalicylaldimine and Its Nickel (II) Complex on Ethanol Induced Gastric Lesions in Rats

[74] Synthesis, spectroscopic characterization, electrochemistry and biological activity evaluation of some metal (II) complexes with ONO donor ligands containing indole and coumarin moieties

[75] Subtle Modifications to the Indole-2-carboxamide Motif of the Negative Allosteric Modulator N-((trans)-4-(2-(7-Cyano-3,4-dihydroisoquinolin-2(1 H)-yl)ethyl)cyclohexyl)-1 H-indole-2-carboxamide (SB269652) Yield Dramatic Changes in Pharmacological Activity at the Dopamine D <inf>2</inf> Receptor

[76] Corrigendum to“An insight into the medicinal perspective of synthetic analogs of indole: A review” (European Journal of Medicinal Chemistry (2019) 180 (562–612), (S0223523419306403), (10.1016/j.ejmech.2019.07.019))

[77] Inhibition Mechanisms of Indoleamine 2,3-Dioxygenase 1 (IDO1).

[78] Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles

[79] 5-Fluoro-1-[(1-{[(1S,2R,6R,8S,9R)-4,4,11,11-tetramethyl-3,5,7,10,12-pentaoxatricyclo[7.3.0.02,6]dodecan-8-yl]methyl}-1H-1,2,3-triazol-4-yl)methyl]-2,3-dihydro-1H-indole-2,3-dione

[80] Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring

[81] Rhodium(II)-catalyzed intramolecular annulation of 1-sulfonyl-1,2,3-triazoles with pyrrole and indole rings: facile synthesis of N-bridgehead azepine skeletons.

[82] acute toxicity evaluation and molecular mechanism study of antiproliferative activity of a novel indole Schiff base -diiminato manganese complex in hormone-dependent and triple negative breast cancer cells.

[83] Angularly Prenylated Indole Alkaloids with Antimicrobial and Insecticidal Activities from an Endophytic Fungus Fusarium sambucinum TE-6L.

[84] Synthesis of Isoxazole and 1,2,3-Triazole Isoindole Derivatives via Silver- and Copper-Catalyzed 1,3-Dipolar Cycloaddition Reaction

[85] Melognine, a novel monoterpenoid indole alkaloid from that induce apoptosis in BT549 cells.

[86] Squaramide-catalyzed asymmetric Mannich reactions between 3-fluorooxindoles and pyrazolinone ketimines.

[87] Bifunctional Squaramide-Catalyzed Asymmetric [3 + 2] Cyclization of 2-(1-Methyl-2-oxoindolin-3-yl)malononitriles with Unsaturated Pyrazolones To Construct Spirooxindole-Fused Spiropyrazolones.

[88] Creation of bispiro[pyrazolone-3,3′-oxindoles]: Via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles

[89] Synthesis, biological evaluation, and docking study of indole aryl sulfonamides as aromatase inhibitors

[90] Indole-Based Hydrazones Containing A Sulfonamide Moiety as Selective Inhibitors of Tumor-Associated Human Carbonic Anhydrase Isoforms IX and XII

[91] Biosynthesis pathway of indole-3-acetyl-myo-inositol during development of maize (Zea mays L.) seeds.

[92] Biosynthesis pathway of indole-3-acetyl-myo-inositol during development of maize (Zea mays L.) seeds

[93] Synthesis, Antimicrobial Activity, Structure-Activity Relationship, and Molecular Docking Studies of Indole Diketopiperazine Alkaloids.

[94] A rhodium(ii) catalysed domino synthesis of azepino fused diindoles from isatin tethered N-sulfonyl-1,2,3-triazoles and indoles.

[95] Computational investigations and molecular dynamics simulations envisioned for potent antioxidant and anticancer drugs using indole-chalcone-triazole hybrids

[96] Discovery of dihydroxyindole-2-carboxylic acid derivatives as dual allosteric HIV-1 Integrase and Reverse Transcriptase associated Ribonuclease H inhibitors.

[97] The heat shock protein 40 LeDnaJ regulates stress resistance and indole-3-acetic acid biosynthesis in Lentinula edodes

[98] Synthesis of a New Series of Nitrogen/Sulfur Heterocycles by Linking Four Rings: Indole; 1,2,4-Triazole; Pyridazine; and Quinoxaline.

[99] Transition-Metal-Free Coupling Reaction of Dithiocarbamates with Indoles: C-S Bond Formation.

[100] Transition-Metal-Free Coupling Reaction of Dithiocarbamates with Indoles: C-S Bond Formation

[101] Versatile three component procedure for combinatorial synthesis of biologically relevant scaffold spiro[indole-thiazolidinones] under aqueous conditions