Synthesis, spectroscopic and theoretical studies of new quasi-podands from bile acid derivatives linked by 1,2,3-triazole rings

scientific article published on 24 February 2014

Synthesis, spectroscopic and theoretical studies of new quasi-podands from bile acid derivatives linked by 1,2,3-triazole rings is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3390/MOLECULES19022557
P932PMC publication ID6270822
P698PubMed publication ID24566321

P50authorIwona KowalczykQ63861458
Bogumił BryckiQ65168901
Tomasz PospiesznyQ80505150
Hanna KoenigQ83372695
P2093author name stringTomasz Pospieszny
Hanna Koenig
Iwona Kowalczyk
P2860cites workClick Chemistry: Diverse Chemical Function from a Few Good ReactionsQ28204398
How to acquire new biological activities in old compounds by computer prediction.Q30952705
Bile acid amidoalcohols: simple organogelators.Q30976823
Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azidesQ33958790
A new family of "clicked" estradiol-based low-molecular-weight gelators having highly symmetry-dependent gelation abilityQ34000878
Ruthenium-catalyzed cycloaddition of alkynes and organic azidesQ34467516
Robustness of biological activity spectra predicting by computer program PASS for noncongeneric sets of chemical compounds.Q34512569
"On water": unique reactivity of organic compounds in aqueous suspensionQ34556981
Prediction of biological activity spectra for substances: evaluation on the diverse sets of drug-like structures.Q35060982
Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes.Q36925684
Bioconjugate-based molecular umbrellasQ37171368
Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-beta-lactamQ39931047
Influence of the amino acid moiety on deconjugation of bile acid amidates by cholylglycine hydrolase or human fecal culturesQ42201746
Substrate specificity of cholylglycine hydrolase for the hydrolysis of bile acid conjugatesQ42240635
1,2,3-Triazole-containing molecular pockets derived from cholic acid: the influence of structure on host-guest coordination propertiesQ42942779
Molecular pockets derived from cholic acid as chemosensors for metal ionsQ43273101
Invertible amphiphilic molecular pockets made of cholic acidQ43280077
Molecular umbrella-assisted transport of an oligonucleotide across cholesterol-rich phospholipid bilayersQ46796448
Optimization of parameters for semiempirical methods I. MethodQ56429661
An improved procedure for the synthesis of glycine and taurine conjugates of bile acidsQ67577441
Hydrophobic Pockets in a Nonpolymeric Aqueous Gel: Observation of such a Gelation Process by Color Change We thank the Jawaharlal Nehru Center for Advanced Scientific Research (Bangalore), and Mitokor, Inc. (San Diego) for supporting this work throuQ74122976
Synthesis of conjugated bile acids by means of a peptide coupling reagentQ77090778
Dimeric and Oligomeric SteroidsQ77646517
Steroids in Molecular RecognitionQ77651450
Anion recognition by 1,2,3-triazolium receptors: application of click chemistry in anion recognitionQ80202354
A straightforward synthesis of tetrameric estrone-based macrocyclesQ81683809
Synthesis of click bile acid polymers and their application in stabilization of silver nanoparticles showing iodide sensing propertyQ84963694
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)2557-2570
P577publication date2014-02-24
P1433published inMoleculesQ151332
P1476titleSynthesis, spectroscopic and theoretical studies of new quasi-podands from bile acid derivatives linked by 1,2,3-triazole rings
P478volume19

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cites work (P2860)
Q39228385Designing, synthesis, and antimicrobial action of oxazoline and thiazoline derivatives of fatty acid esters.
Q42293318Pd- and Cu-catalyzed approaches in the syntheses of new cholane aminoanthraquinone pincer-like ligands.
Q50080735Synthesis, Structure, Surface and Antimicrobial Properties of New Oligomeric Quaternary Ammonium Salts with Aromatic Spacers.