Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Three-dimensional activity relationship

I and C L Waller 1997. Theoretical and Practical Aspects of Three-Dimensional Quantitative icture-Activity Relationships. In Lipkowitz K B and D B Boyd (Editors) Reviews in iputational Chemistry Volume 11. New York, VCH Publishers, pp. 127-182. [Pg.736]

K and G M Crippen 1986. Atomic Physicochemical Parameters for Three-dimensional Struc-directed Quantitative Structure-Activity Relationships. I. Partition Coefficients as a Measure ydrophobicity. Journal of Computational Chemistry 7 565-577. [Pg.738]

Ekins S, De Groot MJ, Jones JP. Pharmacophore and three-dimensional quantitative structure activity relationship methods for modeling cytochrome P450 active sites. Drug Metab Dispos 2001 29 936-44. [Pg.348]

Ekins S, Bravi G, Ring BJ, Gillespie TA, Gillespie JS, VandenBranden M, et al. Three dimensional-quantitative structure activity relationship (3D-QSAR) analyses of substrates for CYP2B6. J Pharmacol Exp Ther 1999 288 21-9. [Pg.460]

Snyder R, Sangar R, Wang J, Ekins S. Three dimensional quantitative structure activity relationship for CYP2D6 substrates. Quant Struct Act Relationship 2002 21 357-68. [Pg.460]

Afzelins L, Zamora I, RidderstromM, AnderssonTB, Karlen A, Masimirembwa CM. Competitive CYP2C9 inhibitors enzyme inhibition stndies, protein homology modeling, and three dimensional qnantitative strnctnre activity relationship analysis. Mol Pharmacol 2001 59 909-19. [Pg.462]

Wang Q, Halpert JR. Combined three-dimensional qnantitative strnctnre-activity relationship analysis of cytochrome P450 2B6 snbstrates and protein homology modeling. Drug Metab Dispos 2002 30 86-95. [Pg.462]

Liu XH, Yang ZF, Wang LS. Three-dimensional quantitative structure-activity relationship study for phenylsulfonyl carboxylates using CoMFA and CoMSI A. Chemosphere 2003 53 945-52. [Pg.491]

Ekins S, Kim RB, Leake BE, Dantzig AH, Schuetz E, Lan LB, et al. Application of three dimensional quantitative structure-activity relationships of P-glycoprotein inhibitors and substrates. Mol Pharmacol 2002 61 974-981. [Pg.510]

Viswanadhan, V. N., Chose, A. K., Revankar, G. R., Robins, R. K. Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. [Pg.377]

Ghose, A. K., Pritchett, A., Crippen, G. M. Atomic physicochemical parameters for three-dimensional strucmre direded quantitative stmcmre-activity relationships III modeling hydrophobic interactions./ Comp. Chem. 1988, 9, 80-90. [Pg.378]

Three-dimensional quantitative structure-activity relationships of inhibitors of P-glycoprotein, Molec. Pharmacol. 2002, 61, 964-973. [Pg.130]

In this section, the structure, function, and reactivity of amino acids, peptides, and proteins will be discussed with the goal of providing a foundation for successful derivatization. The interplay of amino acid functionality and the three-dimensional folding of polypeptide chains will be seen as forming the basis for protein activity. Understanding how the attachment of foreign molecules can affect this tenuous relationship, and thus alter protein function, ultimately will create a rational approach to protein chemistry and modification. [Pg.4]

Although structurally-diverse as evidenced above, the insecticidal pyrethroids still conform to a unique, operationally-defined, structure-activity relationship based on the physical characteristics and three-dimensional shape of the entire molecule conforming to those originally evidenced in the natural pyrethrins [13]. From this relationship, it becomes apparent that there is no single molecular aspect or reactive moiety that serves as a true toxophore for the pyrethroids and that their actions at target sites are dependent upon the entire stereospecific structure of these insecticides [1]. [Pg.53]


See other pages where Three-dimensional activity relationship is mentioned: [Pg.326]    [Pg.252]    [Pg.72]    [Pg.664]    [Pg.219]    [Pg.351]    [Pg.267]    [Pg.46]    [Pg.157]    [Pg.44]    [Pg.302]    [Pg.144]    [Pg.35]    [Pg.112]    [Pg.128]    [Pg.411]    [Pg.4]    [Pg.94]    [Pg.463]    [Pg.115]    [Pg.193]    [Pg.114]   
See also in sourсe #XX -- [ Pg.267 ]




SEARCH



Approaches to Three-Dimensional Quantitative Structure—Activity Relationships

Lipophilicity Fields An Enhancement of Three-Dimensional Quantitative Structure-Activity Relationships

Quantitative structure-activity relationship three-dimensional descriptors

Quantitative structure-activity relationships three-dimensional

Structure-activity relationships three-dimensional-ligand-based

Structure-activity relationships three-dimensional-protein-based

Theoretical and Practical Aspects of Three-Dimensional Quantitative Structure-Activity Relationships

Three-dimensional ligand-based models structure-activity relationships

Three-dimensional quantitative structure activity relationships conformation

Three-dimensional quantitative structure activity relationships superposition

Three-dimensional quantitative structure-activity relationship drug design

Three-dimensional quantitative structure-activity relationship example

Three-dimensional quantitative structure-activity relationship methods

Three-dimensional quantitative structure-activity relationship models

Three-dimensional structure, relationship biological activity

© 2024 chempedia.info