Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line
Synthetic benzophenone-bis-Schiff bases (1-17) were evaluated for PC3 cell line inhibition. Most of the compounds showed cytotoxic effects but compounds 4, 8, 14, 16, and 17 were found to be potent. The growth inhibition of PC3 cells was in a concentration-dependent manner when treated with compound...
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Chemical Society of Pakistan
2016
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2-s2.0-84995460997 Khan K.M.; Rasheed H.; Fatima B.; Hayat M.; Rahim F.; Ullah H.; Hameed A.; Taha M.; Tahir A.; Perveen S. Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line 2016 Journal of the Chemical Society of Pakistan 38 5 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995460997&partnerID=40&md5=57fae9b20ad7f8219576edc21143ce65 Synthetic benzophenone-bis-Schiff bases (1-17) were evaluated for PC3 cell line inhibition. Most of the compounds showed cytotoxic effects but compounds 4, 8, 14, 16, and 17 were found to be potent. The growth inhibition of PC3 cells was in a concentration-dependent manner when treated with compounds 4, 8, 14, 16 and 17 (Figure-2) after 24 h exposure time. The IC50 values of all five most active compounds were calculated as 4 (IC50 = 24 ± 1.4 μM), 8 (IC50 = 29 ± 1.3 μM), 14 (IC50 = 66 ± 2.8 μM), 16 (IC50 = 28 ± 1.4 μM) and 17 (IC50 = 18 ± 2.8 μM) when compared with standard cisplatin (IC50 = 20 ± 1.1 μM). This study has identified potent anticancer agents. © 2016, Chemical Society of Pakistan. All rights reserved. Chemical Society of Pakistan 2535106 English Article |
author |
Khan K.M.; Rasheed H.; Fatima B.; Hayat M.; Rahim F.; Ullah H.; Hameed A.; Taha M.; Tahir A.; Perveen S. |
spellingShingle |
Khan K.M.; Rasheed H.; Fatima B.; Hayat M.; Rahim F.; Ullah H.; Hameed A.; Taha M.; Tahir A.; Perveen S. Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
author_facet |
Khan K.M.; Rasheed H.; Fatima B.; Hayat M.; Rahim F.; Ullah H.; Hameed A.; Taha M.; Tahir A.; Perveen S. |
author_sort |
Khan K.M.; Rasheed H.; Fatima B.; Hayat M.; Rahim F.; Ullah H.; Hameed A.; Taha M.; Tahir A.; Perveen S. |
title |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
title_short |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
title_full |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
title_fullStr |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
title_full_unstemmed |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
title_sort |
Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line |
publishDate |
2016 |
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Journal of the Chemical Society of Pakistan |
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38 |
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5 |
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url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995460997&partnerID=40&md5=57fae9b20ad7f8219576edc21143ce65 |
description |
Synthetic benzophenone-bis-Schiff bases (1-17) were evaluated for PC3 cell line inhibition. Most of the compounds showed cytotoxic effects but compounds 4, 8, 14, 16, and 17 were found to be potent. The growth inhibition of PC3 cells was in a concentration-dependent manner when treated with compounds 4, 8, 14, 16 and 17 (Figure-2) after 24 h exposure time. The IC50 values of all five most active compounds were calculated as 4 (IC50 = 24 ± 1.4 μM), 8 (IC50 = 29 ± 1.3 μM), 14 (IC50 = 66 ± 2.8 μM), 16 (IC50 = 28 ± 1.4 μM) and 17 (IC50 = 18 ± 2.8 μM) when compared with standard cisplatin (IC50 = 20 ± 1.1 μM). This study has identified potent anticancer agents. © 2016, Chemical Society of Pakistan. All rights reserved. |
publisher |
Chemical Society of Pakistan |
issn |
2535106 |
language |
English |
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Article |
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scopus |
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Scopus |
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1809678487336779776 |