Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands

Design and synthesis of a novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives are reported and their in vitro thyroid hormone receptor selectivity has been evaluated in the thyroid luciferase receptor assay. The 3-[3,5-dichloro-4-(4-hydroxy-3-isopropylphenoxy)-phenylamino]-4-hydroxy- cyclobut-3-ene...

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Main Authors: Raval, S., Raval, P., Bandyopadhyay, D., Soni, K., Yevale, D., Jogiya, D., Modi, H., Joharapurkar, A., Gandhi, Neha, Jain, M., Patel, P.
Format: Journal Article
Published: Pergamon 2008
Online Access:http://hdl.handle.net/20.500.11937/25636
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author Raval, S.
Raval, P.
Bandyopadhyay, D.
Soni, K.
Yevale, D.
Jogiya, D.
Modi, H.
Joharapurkar, A.
Gandhi, Neha
Jain, M.
Patel, P.
author_facet Raval, S.
Raval, P.
Bandyopadhyay, D.
Soni, K.
Yevale, D.
Jogiya, D.
Modi, H.
Joharapurkar, A.
Gandhi, Neha
Jain, M.
Patel, P.
author_sort Raval, S.
building Curtin Institutional Repository
collection Online Access
description Design and synthesis of a novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives are reported and their in vitro thyroid hormone receptor selectivity has been evaluated in the thyroid luciferase receptor assay. The 3-[3,5-dichloro-4-(4-hydroxy-3-isopropylphenoxy)-phenylamino]-4-hydroxy- cyclobut-3-ene-1,2-dione 21 has shown selectivity towards thyroid hormone receptor ß. © 2008 Elsevier Ltd. All rights reserved.
first_indexed 2025-11-14T07:57:54Z
format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:57:54Z
publishDate 2008
publisher Pergamon
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-256362017-09-13T15:15:34Z Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands Raval, S. Raval, P. Bandyopadhyay, D. Soni, K. Yevale, D. Jogiya, D. Modi, H. Joharapurkar, A. Gandhi, Neha Jain, M. Patel, P. Design and synthesis of a novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives are reported and their in vitro thyroid hormone receptor selectivity has been evaluated in the thyroid luciferase receptor assay. The 3-[3,5-dichloro-4-(4-hydroxy-3-isopropylphenoxy)-phenylamino]-4-hydroxy- cyclobut-3-ene-1,2-dione 21 has shown selectivity towards thyroid hormone receptor ß. © 2008 Elsevier Ltd. All rights reserved. 2008 Journal Article http://hdl.handle.net/20.500.11937/25636 10.1016/j.bmcl.2008.06.038 Pergamon restricted
spellingShingle Raval, S.
Raval, P.
Bandyopadhyay, D.
Soni, K.
Yevale, D.
Jogiya, D.
Modi, H.
Joharapurkar, A.
Gandhi, Neha
Jain, M.
Patel, P.
Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title_full Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title_fullStr Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title_full_unstemmed Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title_short Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (TR-ß) selective ligands
title_sort design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor ß (tr-ß) selective ligands
url http://hdl.handle.net/20.500.11937/25636