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Pharmacophore and Virtual Screening of JAK3 inhibitors

Janus kinase 3 (JAK3) is a non-receptor tyrosine kinases family of protein which is comprised of JAK1, JAK2, JAK3 and TYK2. It plays an important role in immune function and lymphoid development and it only resides in the hematopoietic system. Therefore, selective targeting JAK3 is a rational approa...

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Detalles Bibliográficos
Autores principales: Rajeswari, Murugesan, Santhi, Natchimuthu, Bhuvaneswari, Vembu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974243/
https://www.ncbi.nlm.nih.gov/pubmed/24748756
http://dx.doi.org/10.6026/97320630010157
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author Rajeswari, Murugesan
Santhi, Natchimuthu
Bhuvaneswari, Vembu
author_facet Rajeswari, Murugesan
Santhi, Natchimuthu
Bhuvaneswari, Vembu
author_sort Rajeswari, Murugesan
collection PubMed
description Janus kinase 3 (JAK3) is a non-receptor tyrosine kinases family of protein which is comprised of JAK1, JAK2, JAK3 and TYK2. It plays an important role in immune function and lymphoid development and it only resides in the hematopoietic system. Therefore, selective targeting JAK3 is a rational approach in developing new therapeutic molecule. In this study, about 116 JAK3 inhibitors were collected from the literature and were used to build four-point pharmacophore model using Phase (Schrodinger module). The statistically significant pharmacophore hypothesis of AAHR.92 with r2 value of 0.942 was used as 3D query to search against 3D database namely Zincpharmer. A total of 2, 27,483 compounds obtained as hit were subjected to high throughput virtual screening (HTVS module of Schrodinger). Among the hits, ten compounds with good G-score ranging from -12.96 to -11.18 with good binding energy to JAK3 were identified.
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spelling pubmed-39742432014-04-18 Pharmacophore and Virtual Screening of JAK3 inhibitors Rajeswari, Murugesan Santhi, Natchimuthu Bhuvaneswari, Vembu Bioinformation Hypothesis Janus kinase 3 (JAK3) is a non-receptor tyrosine kinases family of protein which is comprised of JAK1, JAK2, JAK3 and TYK2. It plays an important role in immune function and lymphoid development and it only resides in the hematopoietic system. Therefore, selective targeting JAK3 is a rational approach in developing new therapeutic molecule. In this study, about 116 JAK3 inhibitors were collected from the literature and were used to build four-point pharmacophore model using Phase (Schrodinger module). The statistically significant pharmacophore hypothesis of AAHR.92 with r2 value of 0.942 was used as 3D query to search against 3D database namely Zincpharmer. A total of 2, 27,483 compounds obtained as hit were subjected to high throughput virtual screening (HTVS module of Schrodinger). Among the hits, ten compounds with good G-score ranging from -12.96 to -11.18 with good binding energy to JAK3 were identified. Biomedical Informatics 2014-03-19 /pmc/articles/PMC3974243/ /pubmed/24748756 http://dx.doi.org/10.6026/97320630010157 Text en © 2014 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Rajeswari, Murugesan
Santhi, Natchimuthu
Bhuvaneswari, Vembu
Pharmacophore and Virtual Screening of JAK3 inhibitors
title Pharmacophore and Virtual Screening of JAK3 inhibitors
title_full Pharmacophore and Virtual Screening of JAK3 inhibitors
title_fullStr Pharmacophore and Virtual Screening of JAK3 inhibitors
title_full_unstemmed Pharmacophore and Virtual Screening of JAK3 inhibitors
title_short Pharmacophore and Virtual Screening of JAK3 inhibitors
title_sort pharmacophore and virtual screening of jak3 inhibitors
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974243/
https://www.ncbi.nlm.nih.gov/pubmed/24748756
http://dx.doi.org/10.6026/97320630010157
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