Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors
Thiourea analogs 1-20 were synthesized and evaluated for their in vitro β-glucuronidase inhibitory potential. The compounds 9 (0.86 ± 0.01 μM), 6 (1.24 ± 0.01 μM), 16 (1.64 ± 0.02 μM) and 15 (2.12 ± 0.02 μM) showed potent activity. Other analogs 1-5, 7, 8, 10, 11, 13, 17, 20 showed better activity t...
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Birkhauser Boston
2015
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2-s2.0-84937730306 Taha M.; Ismail N.H.; Jamil W.; Khan K.M.; Salar U.; Kashif S.M.; Rahim F.; Latif Y. Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors 2015 Medicinal Chemistry Research 24 8 10.1007/s00044-015-1369-x https://www.scopus.com/inward/record.uri?eid=2-s2.0-84937730306&doi=10.1007%2fs00044-015-1369-x&partnerID=40&md5=ffd0582f288ac79483ed2b6ce61d2930 Thiourea analogs 1-20 were synthesized and evaluated for their in vitro β-glucuronidase inhibitory potential. The compounds 9 (0.86 ± 0.01 μM), 6 (1.24 ± 0.01 μM), 16 (1.64 ± 0.02 μM) and 15 (2.12 ± 0.02 μM) showed potent activity. Other analogs 1-5, 7, 8, 10, 11, 13, 17, 20 showed better activity than standard drug d-saccharic acid 1,4-lactone (47.34 ± 0.21 μM) ranging 4.36-34.4 μM. All synthetic compounds were characterized by different spectroscopic methods. This study has identified a new class of potent inhibitors β-glucuronidase. © 2015 Springer Science+Business Media New York. Birkhauser Boston 10542523 English Article |
author |
Taha M.; Ismail N.H.; Jamil W.; Khan K.M.; Salar U.; Kashif S.M.; Rahim F.; Latif Y. |
spellingShingle |
Taha M.; Ismail N.H.; Jamil W.; Khan K.M.; Salar U.; Kashif S.M.; Rahim F.; Latif Y. Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
author_facet |
Taha M.; Ismail N.H.; Jamil W.; Khan K.M.; Salar U.; Kashif S.M.; Rahim F.; Latif Y. |
author_sort |
Taha M.; Ismail N.H.; Jamil W.; Khan K.M.; Salar U.; Kashif S.M.; Rahim F.; Latif Y. |
title |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
title_short |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
title_full |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
title_fullStr |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
title_full_unstemmed |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
title_sort |
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors |
publishDate |
2015 |
container_title |
Medicinal Chemistry Research |
container_volume |
24 |
container_issue |
8 |
doi_str_mv |
10.1007/s00044-015-1369-x |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84937730306&doi=10.1007%2fs00044-015-1369-x&partnerID=40&md5=ffd0582f288ac79483ed2b6ce61d2930 |
description |
Thiourea analogs 1-20 were synthesized and evaluated for their in vitro β-glucuronidase inhibitory potential. The compounds 9 (0.86 ± 0.01 μM), 6 (1.24 ± 0.01 μM), 16 (1.64 ± 0.02 μM) and 15 (2.12 ± 0.02 μM) showed potent activity. Other analogs 1-5, 7, 8, 10, 11, 13, 17, 20 showed better activity than standard drug d-saccharic acid 1,4-lactone (47.34 ± 0.21 μM) ranging 4.36-34.4 μM. All synthetic compounds were characterized by different spectroscopic methods. This study has identified a new class of potent inhibitors β-glucuronidase. © 2015 Springer Science+Business Media New York. |
publisher |
Birkhauser Boston |
issn |
10542523 |
language |
English |
format |
Article |
accesstype |
|
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678486791520256 |