» Articles » PMID: 1818090

HINT: a New Method of Empirical Hydrophobic Field Calculation for CoMFA

Overview
Publisher Springer
Date 1991 Dec 1
PMID 1818090
Citations 58
Authors
Affiliations
Soon will be listed here.
Abstract

An empirical hydrophobic field-like 3D function has been calculated with the program HINT (hydrophobic interactions) and imported into the SYBYL implementation of CoMFA (Comparative Molecular Field Analysis). The addition of hydrophobicity appears to offer increased chemical interpretability of CoMFA models. An example is given using the steroid model reported by Cramer et al. (J. Am. Chem. Soc., 110 (1988) 5959). While addition of the HINT field did not improve statistical parameters in this model, the CoMFA coefficient contours from the hydrophobic field unambiguously define the most active steroid molecules in the chemical terms of hydrophobic and polar substituents.

Citing Articles

The Potential of Molecular Docking for Predictive Toxicology.

Cozzini P, Agosta F Methods Mol Biol. 2024; 2834:171-180.

PMID: 39312165 DOI: 10.1007/978-1-0716-4003-6_8.


Molecular Interaction Fields Describing Halogen Bond Formable Areas on Protein Surfaces.

Hayakawa D, Watanabe Y, Gouda H J Chem Inf Model. 2024; 64(15):6003-6013.

PMID: 39012240 PMC: 11323840. DOI: 10.1021/acs.jcim.4c00896.


A Combined Molecular Dynamics and Hydropathic INTeraction (HINT) Approach to Investigate Protein Flexibility: The PPARγ Case Study.

Agosta F, Cozzini P Molecules. 2024; 29(10).

PMID: 38792097 PMC: 11124508. DOI: 10.3390/molecules29102234.


A Computational Workflow to Predict Biological Target Mutations: The Spike Glycoprotein Case Study.

Cozzini P, Agosta F, Dolcetti G, Dal Palu A Molecules. 2023; 28(20).

PMID: 37894561 PMC: 10609230. DOI: 10.3390/molecules28207082.


Screening and Biological Evaluation of Soluble Epoxide Hydrolase Inhibitors: Assessing the Role of Hydrophobicity in the Pharmacophore-Guided Search of Novel Hits.

Vazquez J, Ginex T, Herrero A, Morisseau C, Hammock B, Luque F J Chem Inf Model. 2023; 63(10):3209-3225.

PMID: 37141492 PMC: 10207366. DOI: 10.1021/acs.jcim.3c00301.


References
1.
Abraham D, Leo A . Extension of the fragment method to calculate amino acid zwitterion and side chain partition coefficients. Proteins. 1987; 2(2):130-52. DOI: 10.1002/prot.340020207. View

2.
Cramer R, Patterson D, Bunce J . Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins. J Am Chem Soc. 2011; 110(18):5959-67. DOI: 10.1021/ja00226a005. View

3.
Allen M, Tan Y, Trudell M, Narayanan K, Schindler L, Martin M . Synthetic and computer-assisted analyses of the pharmacophore for the benzodiazepine receptor inverse agonist site. J Med Chem. 1990; 33(9):2343-57. DOI: 10.1021/jm00171a007. View

4.
Wireko F, Kellogg G, Abraham D . Allosteric modifiers of hemoglobin. 2. Crystallographically determined binding sites and hydrophobic binding/interaction analysis of novel hemoglobin oxygen effectors. J Med Chem. 1991; 34(2):758-67. DOI: 10.1021/jm00106a042. View

5.
Norinder U . Experimental design based 3-D QSAR analysis of steroid-protein interactions: application to human CBG complexes. J Comput Aided Mol Des. 1990; 4(4):381-9. DOI: 10.1007/BF00117403. View