Direct and Indirect Drug Design Approaches for the Development of Novel Tricyclic Antipsychotics: Potential 5‐HT2A Antagonist
Author(s) -
Mahantesh Jadhav,
Ganesh R. Kokil,
Shilpa Sudhakar Harak,
Sanjay Baburao Wagh
Publication year - 2013
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/930354
Subject(s) - chemistry , tricyclic , antagonist , antipsychotic drug , pharmacology , drug , antipsychotic , stereochemistry , schizophrenia (object oriented programming) , receptor , psychiatry , psychology , biochemistry , medicine
Schizophrenia is a mental disorder manifested largely by disintegration of thought processes and emotional responsiveness. Given the therapeutic and toxic limitations of clinically available drugs, it is clear that there is still a need for the development of new generation antipsychotic agents with an improved clinical profile. Development of novel hybrid atypical tricyclic antipsychotic pharmacophore was achieved using direct (by measuring docking score of designed molecules on modelled 5- receptor) and indirect (current, clinically available therapeutic agents’ data) drug design approaches
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