A method for determination of the structure of the intramolecular hydrogen bond in the cations of unsymmetrically substituted 1,8-bis(dimethylamino)naphthalenes in solution

2006 ◽  
Vol 55 (1) ◽  
pp. 164-167 ◽  
Author(s):  
V. A. Ozeryanskii ◽  
A. F. Pozharskii
Keyword(s):  
Hydrogen Bond ◽  
Intramolecular Hydrogen Bond ◽  
Intramolecular Hydrogen

Spectrophotometric Determination of the pK Values for Dissociation of the Sugar Hydroxyls in Pyrimidine Arabinonucleosides

1975 ◽  
Vol 30 (9-10) ◽  
pp. 565-570 ◽  
Author(s):  
Edward Darżynkiewicz ◽  
Henryk Sierakowski ◽  
David Shugar
Keyword(s):  
Hydrogen Bond ◽  
Intramolecular Hydrogen Bond ◽  
Spectrophotometric Determination ◽  
Spectrophotometric Titration ◽  
Factors Affecting ◽  
Alkyl Derivatives ◽  
Intramolecular Hydrogen

Arabinonucleosides, Spectrophotometric Titration, Sugar Hydroxyl Dissociation Spectrophotometric titration in the ultraviolet has been employed to determine the pK values for dissociation of the sugar hydroxyls in pyrimidine arabinonucleosides and some of their O′-methyl and O′-ethyl derivatives. The order of dissociation of the sugar hydroxyls in the arabinofuranose ring was 2′-OH > 3′-OH > 5′-OH. The higher acidity (lower pK) of the 2′-OH was interpreted in terms of formation of an intramolecular hydrogen bond of the form 5′-OH···2′-O(-) and the accompanying changes in conformation of the arabinose ring. The various factors affecting the dissociation of specific hydroxyls in some of the O′-alkyl derivatives are discussed in relation to steric, conformational and other effects.

Effect of the intramolecular hydrogen bond in the active metabolite analogs of leflunomide for blocking the Plasmodium falciparum dihydroorotate dehydrogenase enzyme: QTAIM, NBO, and docking study

2020 ◽  
Vol 16 ◽  
Author(s):  
Reihaneh Heidarian ◽  
Mansoureh Zahedi-Tabrizi
Keyword(s):  
Hydrogen Bond ◽  
Plasmodium Falciparum ◽  
Molecular Orbital ◽  
Intramolecular Hydrogen Bond ◽  
Active Metabolite ◽  
Chemical Hardness ◽  
Dihydroorotate Dehydrogenase ◽  
Molecular Orbital Analysis ◽  
Intramolecular Hydrogen ◽  
Orbital Analysis

: Leflunomide (LFM) and its active metabolite, teriflunomide (TFM), have drawn a lot of attention for their anticancer activities, treatment of rheumatoid arthritis and malaria due to their capability to inhibit dihydroorotate dehydrogenase (DHODH) and Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) enzyme. In this investigation, the strength of intramolecular hydrogen bond (IHB) in five analogs of TFM (ATFM) has been analyzed employing density functional theory (DFT) using B3LYP/6-311++G (d, p) level and molecular orbital analysis in the gas phase and water solution. A detailed electronic structure study has been performed using the quantum theory of atoms in molecules (QTAIM) and the hydrogen bond energies (EHB) of stable conformer obtained in the range of 76-97 kJ/mol, as a medium hydrogen bond. The effect of substitution on the IHB nature has been studied by natural bond orbital analysis (NBO). 1H NMR calculations show an upward trend in the proton chemical shift of the enolic proton in the chelated ring (14.5 to 15.7ppm) by increasing the IHB strength. All the calculations confirmed the strongest IHB in 5-F-ATFM and the weakest IHB in 2-F-ATFM. Molecular orbital analysis, including the HOMO-LUMO gap and chemical hardness, was performed to compare the reactivity of inhibitors. Finally, molecular docking analysis was carried out to identify the potency of inhibition of these compounds against PfDHODH enzyme.

scholarly journals CP/MASS 13C NMR Spectra of Cellulose Solids: An Explanation by the Intramolecular Hydrogen Bond Concept

1985 ◽  
Vol 17 (5) ◽  
pp. 701-706 ◽  
Author(s):  
Kenji Kamide ◽  
Kunihiko Okajima ◽  
Keisuke Kowsaka ◽  
Toshihiko Matsui
Keyword(s):  
Hydrogen Bond ◽  
Intramolecular Hydrogen Bond ◽  
13C Nmr ◽  
Nmr Spectra ◽  
13C Nmr Spectra ◽  
Intramolecular Hydrogen

(1′R,3S)-2-Oxo-1-(1′-phenylethyl)piperidine-3-carboxylic acid: a case of a very strong intramolecular hydrogen bond

2004 ◽  
Vol 60 (11) ◽  
pp. o2110-o2112
Author(s):  
Ana-María Lumbreras-García ◽  
Alberto Galindo-Guzmán ◽  
Dino Gnecco ◽  
Joel-Luis Terán ◽  
Sylvain Bernès
Keyword(s):  
Hydrogen Bond ◽  
Carboxylic Acid ◽  
Intramolecular Hydrogen Bond ◽  
Intramolecular Hydrogen ◽  
Strong Intramolecular Hydrogen Bond
Sign in / Sign up

Export Citation Format

Share Document