Results 31 to 40 of about 11,524 (228)

The Structure of Adamantane Clusters: Atomistic vs. Coarse-Grained Predictions From Global Optimization

open access: yesFrontiers in Chemistry, 2019
Candidate structures for the global minima of adamantane clusters, (C10H16)N, are presented. Based on a rigid model for individual molecules with atom-atom pairwise interactions that include Lennard-Jones and Coulomb contributions, low-energy structures ...
Javier Hernández-Rojas, Florent Calvo
doaj   +1 more source

Bioactive Molecules – Polycyclic Guanidine Derivatives [PDF]

open access: yesKemija u Industriji, 2015
Biological activity of different adamantane derivatives and their application has been described in various reviews. Similarly, many reviews deal with biological activity and application of guanidine compounds.
M. Šekutor , K. Mlinarić-Majerski
doaj   +1 more source

4-Aminoquinoline-Based Adamantanes as Potential Anticholinesterase Agents in Symptomatic Treatment of Alzheimer’s Disease

open access: yesPharmaceutics, 2022
Considering that acetylcholinesterase (AChE) inhibition is the most important mode of action expected of a potential drug used for the treatment of symptoms of Alzheimer’s disease (AD), our previous pilot study of 4-aminoquinolines as potential human ...
Katarina Komatović   +8 more
doaj   +1 more source

Adamantane ionic liquids [PDF]

open access: yes, 2014
Accepted 11 Jun 2014.We report the synthesis and characteristic thermal properties of the adamantane-based ionic salts. The ionic salts with adamantane carboxylates and imidazolium cations were prepared via neutralization.
Hiraoka, Tatsuhiro   +4 more
core   +1 more source

Lipidation of NOD2 Agonists with Adamantane and Stearoyl Moieties Differentially Regulates Their In Vivo Adjuvant Activity

open access: yesPharmaceutics, 2022
NOD2 is an innate immune receptor that constitutes an important target for the development of small molecule immunopotentiators with great potential to be used as vaccine adjuvants.
Samo Guzelj   +5 more
doaj   +1 more source

Mannose-decorated cyclodextrin vesicles: The interplay of multivalency and surface density in lectin–carbohydrate recognition

open access: yesBeilstein Journal of Organic Chemistry, 2012
Cyclodextrin vesicles are versatile models for biological cell membranes since they provide a bilayer membrane that can easily be modified by host–guest interactions with functional guest molecules.
Ulrike Kauscher, Bart Jan Ravoo
doaj   +1 more source

Synthesis of Adamantane Derivatives. III. Synthesis of Adamantane Heterocycles [PDF]

open access: yesBulletin of the Chemical Society of Japan, 1969
Abstract Preparation of 1-adamantyl and adamantane-1-carbonyl derivatives having benzimidazole, 1,3,5-oxadiazole, oxazoline-2, quinoxaline, 2-aminothiazole, thiazolone, 2-methylthiazole, 1,2,3-thiadiazole, pyrazole or pyrazoline ring is described.
Tadashi Sasaki   +2 more
openaire   +1 more source

Novel Biphenyl Amines Inhibit Oestrogen Receptor (ER)-α in ER-Positive Mammary Carcinoma Cells

open access: yesMolecules, 2021
Herein, the activity of adamantanyl-tethered-biphenyl amines (ATBAs) as oestrogen receptor alpha (ERα) modulating ligands is reported. Using an ERα competitor assay it was demonstrated that ATBA compound 3-(adamantan-1-yl)-4-methoxy-N-(4-(trifluoromethyl)
Basappa Basappa   +5 more
doaj   +1 more source

Synthesis of Norabietyl and Nordehydroabietyl Imidazolidine-2,4,5-Triones and Their Activity against Tyrosyl-DNA Phosphodiesterase 1

open access: yesMolbank, 2023
New imidazolidine-2,4,5-triones with norabietic, nordehydroabietic, and adamantane substituents were synthesized by reacting oxalyl chloride and the corresponding ureas, providing good yields. Bioisosteric replacement of the ureide group with a parabanic
Kseniya S. Kovaleva   +8 more
doaj   +1 more source

1-(2-Phenylethyl)adamantane [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
In the title compound, C(18)H(24), the adamantane cage consists of three fused cyclo-hexane rings in almost ideal chair conformations, with C-C-C angles in the range 108.0 (14)-111.1 (15)°. The phenyl and 1-adamantyl substituents adopt anti orientations with a C-C-C-C torsion angle of 177.10 (16)°.
Rouchal, Michal   +2 more
openaire   +4 more sources

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