Ligand binding to I2 imidazoline receptor: the role of lipophilicity in quantitative structure-activity relationship models. (Q48296707)

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9 December 2019

title

Ligand binding to I2 imidazoline receptor: the role of lipophilicity in quantitative structure-activity relationship models (English)

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9 December 2019

0 references

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quantitative structure-activity relationship

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4

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Livio Brasili

3

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Francesco Leonetti

9

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author name string

M Pigini

1

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P Bousquet

2

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R Cavagna

5

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M Dontenwill

6

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F Gentili

7

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M Giannella

8

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A Piergentili

10

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W Quaglia

11

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A Carotti

12

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9 December 2019

language of work or name

English

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publication date

1 December 1998

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Bioorganic & Medicinal Chemistry

9 December 2019

published in

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volume

6

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issue

12

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9 December 2019

page(s)

2245-2260

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9 December 2019

cites work

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Central imidazoline (I1) receptors as targets of centrally acting antihypertensives: moxonidine and rilmenidine

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The effects of chronic imidazoline drug treatment on glial fibrillary acidic protein concentrations in rat brain

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Stimulation of insulin release from the MIN6 cell line by a new imidazoline compound, S-21663: evidence for the existence of a novel imidazoline site in beta cells.

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The I1-imidazoline receptor: from binding site to therapeutic target in cardiovascular disease

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Imidazoline receptors: qualitative structure-activity relationships and discovery of tracizoline and benazoline. Two ligands with high affinity and unprecedented selectivity.

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2-D and 3-D modeling of imidazoline receptor ligands: insights into pharmacophore

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Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins

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Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs

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Enantiomeric resolution of sulfoxides on a DACH-DNB chiral stationary phase: A quantitative structure-enantioselective retention relationship (QSERR) study

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Study of Benzodiazepines Receptor Sites Using a Combined QSAR-CoMFA Approach

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Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis

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7 January 2021

Molecular lipophilicity potential, a tool in 3D QSAR: method and applications.

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Binding of arylpiperazines, (aryloxy)propanolamines, and tetrahydropyridylindoles to the 5-HT1A receptor: contribution of the molecular lipophilicity potential to three-dimensional quantitative structure-affinity relationship models

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7 January 2021

Lipophilicity in molecular modeling

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MOPAC: a semiempirical molecular orbital program

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Novel anthelmintic agents. 6. Pyrantel analogs with activity against whipworm

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Novel anthelmintic agents. II. Pyrantel and other cyclic amidines

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Validation of the general purpose Tripos 5.2 force field

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7 January 2021

10.1016/S0968-0896(98)80005-9

Identifiers

DOI

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9 December 2019

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