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Bisindole Compounds—Synthesis and Medicinal Properties [PDF]

open access: yesAntibiotics
The indole nucleus stands out as a pharmacophore, among other aromatic heterocyclic compounds with remarkable therapeutic properties, such as benzimidazole, pyridine, quinoline, benzothiazole, and others.
Maria Marinescu
doaj   +4 more sources

One‐Pot Synthesis of Novel β‐Carboline‐{α‐Acylaminoamide}‐Bisindole Derivatives: Antibacterial Evaluation, Molecular Docking, and Density Functional Theory Studies [PDF]

open access: yesChemistryOpen
A new series of β‐carboline‐{α‐acylaminoamide}‐bisindole hybrids (12a–l) is designed and synthesized employing an atom‐economical one‐pot Ugi four‐component reaction (U‐4CR), affording the target compounds in good yields. All synthesized compounds (12a–l)
Ankit Kumar Atri   +8 more
doaj   +3 more sources

Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence [PDF]

open access: yesBMC Biology
Biofilms cling to surfaces to form complex architectures allowing their bacterial creators to acquire multidrug resistance and claiming countless lives worldwide.
Karina Golberg   +9 more
doaj   +2 more sources

Marine-Derived Bisindoles for Potent Selective Cancer Drug Discovery and Development [PDF]

open access: yesMolecules
Marine-derived bisindoles exhibit structural diversity and exert anti-cancer influence through multiple mechanisms. Comprehensive research has shown that the development success rate of drugs derived from marine natural products is four times higher than
Mengwei Xu   +9 more
doaj   +2 more sources

Exploring hydrophilic 2,2-di(indol-3-yl)ethanamine derivatives against Leishmania infantum. [PDF]

open access: yesPLoS ONE
Herein we report the design and the synthesis of a library of new and more hydrophilic bisindole analogues based on our previously identified antileishmanial compound URB1483 that failed the preliminary in vivo test.
Alessia Centanni   +10 more
doaj   +2 more sources

Synthesis and biological activity of bisindole derivatives as novel MARK4 inhibitors

open access: yesEuropean Journal of Medicinal Chemistry Reports, 2022
Bisindole alkaloids are well-known bioactive natural products presenting numerous pharmacological properties. Following the indolocarbazole biosynthetic pathway a series of bisindole derivatives were synthesized and their activity against MARK4 kinase ...
Maria Voura   +7 more
doaj   +1 more source

Dimethyl 3,3′-[(4-nitrophenyl)methylene]bis(1H-indole-2-carboxylate) ethanol hemisolvate

open access: yesIUCrData, 2021
There are two main molecules in asymmetric unit of the title compound, C27H21N3O6·0.5C2H5OH. In both, the indole ring systems are approximately perpendicular to each other, at dihedral angles of 69.3 (5) and 82.8(4)°. In the crystal, molecules are linked
Yu-Long Li   +6 more
doaj   +1 more source

Novel Small-Molecule Hybrid-Antibacterial Agents against S. aureus and MRSA Strains

open access: yesMolecules, 2021
Ongoing resistance developments against antibiotics that also affect last-resort antibiotics require novel antibacterial compounds. Strategies to discover such novel structures have been dimerization or hybridization of known antibacterial agents.
Robin Gehrmann   +5 more
doaj   +1 more source

Diethyl 3,3′-[(3-fluorophenyl)methylene]bis(1H-indole-2-carboxylate)

open access: yesIUCrData, 2020
In the title compound, C29H25FN2O4, the mean planes of the indole ring systems are approximately perpendicular to one another [dihedral angle = 88.3 (4)°]. The benzene ring is twisted with respect to the indole ring systems by 49.8 (5) and 77.6 (3)°.
Hong Jiang   +7 more
doaj   +1 more source

Catalyzed and uncatalyzed procedures for the syntheses of isomeric covalent multi-indolyl hetero non-metallides: an account

open access: yesBeilstein Journal of Organic Chemistry, 2021
Two or more indole molecules tailored to a single non-metal central atom, through any of their C2–7 positions are not only structurally engaging but also constitute a class of important pharmacophores.
Ranadeep Talukdar
doaj   +1 more source

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