Literature DB >> 15072436

Pharmacophore and receptor models for neurokinin receptors.

Anders Poulsen1, Berith Bjørnholm, Klaus Gundertofte, Irina D Pogozheva, Tommy Liljefors.   

Abstract

Three neurokinin (NK) antagonist pharmacophore models (Models 1-3) accounting for hydrogen bonding groups in the 'head' and 'tail' of NK receptor ligands have been developed by use of a new procedure for treatment of hydrogen bonds during superimposition. Instead of modelling the hydrogen bond acceptor vector in the strict direction of the lone pair, an angle is allowed between the hydrogen bond acceptor direction and the ideal lone pair direction. This approach adds flexibility to hydrogen bond directions and produces more realistic RMS values. By using this approach, two novel pharmacophore models were derived (Models 2 and 3) and a hydrogen bond acceptor was added to a previously published NK2 pharmacophore model [Poulsen et al., J. Comput.-Aided Mol. Design, 16 (2002) 273] (Model 1). Model 2 as well as Model 3 are described by seven pharmacophore elements: three hydrophobic groups, three hydrogen bond acceptors and a hydrogen bond donor. Model 1 contains the same hydrophobic groups and hydrogen bond donor as Models 2 and 3, but only one hydrogen bond acceptor. The hydrogen bond acceptors and donor are represented as vectors. Two of the hydrophobic groups are always aromatic rings whereas the other hydrophobic group can be either aromatic or aliphatic. In Model 1 the antagonists bind in an extended conformation with two aromatic rings in a parallel displaced and tilted conformation. Model 2 has the same two aromatic rings in a parallel displaced conformation whereas Model 3 has the rings in an edge to face conformation. The pharmacophore models were evaluated using both a structure (NK receptor homology models) and a ligand based approach. By use of exhaustive conformational analysis (MMFFs force field and the GB/SA hydration model) and least-squares molecular superimposition studies, 21 non-peptide antagonists from several structurally diverse classes were fitted to the pharmacophore models. More antagonists could be fitted to Model 2 with a low RMS and a low conformational energy penalty than to Models 1 and 3. Pharmacophore Model 2 was also able to explain the NK1, NK2 and NK3 subtype selectivity of the compounds fitted to the model. Three NK 7TM receptor models were constructed, one for each receptor subtype. The location of the antagonist binding site in the three NK receptor models is identical. Compounds fitted to pharmacophore Model 2 could be docked into the NK1, NK2 and NK3 receptor models after adjustment of the conformation of the flexible linker connecting the head and tail. Models I and 3 are not compatible with the receptor models.

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Year:  2003        PMID: 15072436     DOI: 10.1023/b:jcam.0000017497.58165.d8

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  29 in total

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Authors:  D Donnelly; S Maudsley; J P Gent; R N Moser; C R Hurrell; J B Findlay
Journal:  Biochem J       Date:  1999-04-01       Impact factor: 3.857

2.  Combined NK1 and NK2 tachykinin receptor antagonists: synthesis and structure-activity relationships of novel oxazolidine analogues.

Authors:  T Nishi; T Fukazawa; K Ishibashi; K Nakajima; Y Sugioka; Y Iio; H Kurata; K Itoh; O Mukaiyama; Y Satoh; T Yamaguchi
Journal:  Bioorg Med Chem Lett       Date:  1999-03-22       Impact factor: 2.823

3.  Efficient computation of three-dimensional protein structures in solution from nuclear magnetic resonance data using the program DIANA and the supporting programs CALIBA, HABAS and GLOMSA.

Authors:  P Güntert; W Braun; K Wüthrich
Journal:  J Mol Biol       Date:  1991-02-05       Impact factor: 5.469

4.  Conformational energy penalties of protein-bound ligands.

Authors:  J Boström; P O Norrby; T Liljefors
Journal:  J Comput Aided Mol Des       Date:  1998-07       Impact factor: 3.686

5.  High affinity, selective neurokinin 2 and neurokinin 3 receptor antagonists from a common structural template.

Authors:  T Harrison; M P Korsgaard; C J Swain; M A Cascieri; S Sadowski; G R Seabrook
Journal:  Bioorg Med Chem Lett       Date:  1998-06-02       Impact factor: 2.823

6.  Parallel-compound synthesis: methodology for accelerating drug discovery.

Authors:  C N Selway; N K Terrett
Journal:  Bioorg Med Chem       Date:  1996-05       Impact factor: 3.641

7.  An alpha-carbon template for the transmembrane helices in the rhodopsin family of G-protein-coupled receptors.

Authors:  J M Baldwin; G F Schertler; V M Unger
Journal:  J Mol Biol       Date:  1997-09-12       Impact factor: 5.469

8.  Interaction of glutamine 165 in the fourth transmembrane segment of the human neurokinin-1 receptor with quinuclidine antagonists.

Authors:  T M Fong; H Yu; M A Cascieri; D Underwood; C J Swain; C D Strader
Journal:  J Biol Chem       Date:  1994-05-27       Impact factor: 5.157

9.  Spiro-substituted piperidines as neurokinin receptor antagonists. III. Synthesis of (+/-)-N-[2-(3,4-dichlorophenyl)-4-(spiro-substituted piperidin-1'-yl)butyl]-N-methylbenzamides and evaluation of NK1-NK2 dual antagonistic activities.

Authors:  H Kubota; A Kakefuda; Y Okamoto; M Fujii; O Yamamoto; Y Yamagiwa; M Orita; K Ikeda; M Takeuchi; T Shibanuma; Y Isomura
Journal:  Chem Pharm Bull (Tokyo)       Date:  1998-10       Impact factor: 1.645

10.  New spiropiperidines as potent and selective non-peptide tachykinin NK2 receptor antagonists.

Authors:  P W Smith; A W Cooper; R Bell; I J Beresford; P M Gore; A B McElroy; J M Pritchard; V Saez; N R Taylor; R L Sheldrick
Journal:  J Med Chem       Date:  1995-09-15       Impact factor: 7.446

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  1 in total

Review 1.  Current progress in Structure-Based Rational Drug Design marks a new mindset in drug discovery.

Authors:  Valère Lounnas; Tina Ritschel; Jan Kelder; Ross McGuire; Robert P Bywater; Nicolas Foloppe
Journal:  Comput Struct Biotechnol J       Date:  2013-04-02       Impact factor: 7.271

  1 in total

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