Earticle

초록

영어

CRFR is involved in the pathophysiology of various disorders including depression, stress, anxiety, post-traumatic stress disorder, and addiction. The discovery of novel and structurally diverse CRF1 receptor inhibitors becomes essential. In this study, we have performed molecular docking of CRF1R with the derivatives of 8-substituted-2-aryl-5- alkylaminoquinolines as CRF1R inhibitors. The antagonist molecules were optimized and docked into the binding site of the receptor. On analysing the docked complexes we have identified that the residues HIS214, THR215, ARG227, ARG1008, LYS1060 and ASP1061 are important in forming hydrogen bond with the inhibitors. Further studies on these residues could reveal important structural features required for the formation of CRF1R-inhibitor complex and thus in the discovery of novel and potent inhibitors.

목차

Abstract
 1. Introduction
 2. Material and Methods
  2.1. Preparation of Protein Structure
  2.2. Preparation of Ligand Molecules
  2.3. Molecular Docking
 3. Results and Discussion
  3.1. Molecular Docking
 4. Conclusion
 References

키워드

저자

• Sathya Babu [ Molecular modeling lab, Department of Genetic Engineering, School of Bioengineering, SRM University, SRM Nagar, Kattankulathur, Chennai 603203, India ] Corresponding author

참고문헌

발행기관

간행물

표지보기 관심저널 등록

• 간행물명

  통합자연과학논문집(구 조선자연과학논문집) [Journal of Integrative Natural Science]

• 간기

  계간

• pISSN

  2005-1042

• 수록기간

  2008~2025

• 등재여부

  KCI 등재

• 십진분류

  KDC 405 DDC 505