Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors
10.1038/srep14195
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sg-nus-scholar.10635-1754832023-08-30T22:32:04Z Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors Baburajeev, C.P Dhananjaya Mohan, C Ananda, H Rangappa, S Fuchs, J.E Jagadish, S Sivaraman Siveen, K Chinnathambi, A Ali Alharbi, S Zayed, M.E Zhang, J Li, F Sethi, G Girish, K.S Bender, A Basappa Rangappa, K.S DEPT OF PHARMACOLOGY CANCER SCIENCE INSTITUTE OF SINGAPORE 6-(2-benzylphenyl)-3-phenyl-(1,2,4)triazolo(3)(1,3,4)thiadiazole antineoplastic agent benzofuran derivative BIRC5 protein, human caspase 3 chromone derivative cyclin D1 inhibitor of apoptosis protein nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase protein bcl 2 protein tyrosine phosphatase 1B PTPN1 protein, human sanggenone C STAT3 protein STAT3 protein, human thiadiazole derivative triazole derivative animal antagonists and inhibitors biosynthesis Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular cell motion disease model dose response drug effects female G1 phase cell cycle checkpoint Hep-G2 cell line human Liver Neoplasms metabolism molecular model mouse Neovascularization, Pathologic pathology rat Sprague Dawley rat structure activity relation synthesis tumor cell line tumor invasion umbilical vein endothelial cell Animals Antineoplastic Agents Benzofurans Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular Caspase 3 Cell Line, Tumor Cell Movement Chromones Cyclin D1 Disease Models, Animal Dose-Response Relationship, Drug Female G1 Phase Cell Cycle Checkpoints Hep G2 Cells Human Umbilical Vein Endothelial Cells Humans Inhibitor of Apoptosis Proteins Liver Neoplasms Mice Models, Molecular Neoplasm Invasiveness Neovascularization, Pathologic Poly(ADP-ribose) Polymerases Protein Tyrosine Phosphatase, Non-Receptor Type 1 Proto-Oncogene Proteins c-bcl-2 Rats Rats, Sprague-Dawley STAT3 Transcription Factor Structure-Activity Relationship Thiadiazoles Triazoles 10.1038/srep14195 Scientific Reports 5 14195 2020-09-10T01:51:10Z 2020-09-10T01:51:10Z 2015 Article Baburajeev, C.P, Dhananjaya Mohan, C, Ananda, H, Rangappa, S, Fuchs, J.E, Jagadish, S, Sivaraman Siveen, K, Chinnathambi, A, Ali Alharbi, S, Zayed, M.E, Zhang, J, Li, F, Sethi, G, Girish, K.S, Bender, A, Basappa, Rangappa, K.S (2015). Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors. Scientific Reports 5 : 14195. ScholarBank@NUS Repository. https://doi.org/10.1038/srep14195 20452322 https://scholarbank.nus.edu.sg/handle/10635/175483 Nature Publishing Group Unpaywall 20200831 |
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6-(2-benzylphenyl)-3-phenyl-(1,2,4)triazolo(3)(1,3,4)thiadiazole antineoplastic agent benzofuran derivative BIRC5 protein, human caspase 3 chromone derivative cyclin D1 inhibitor of apoptosis protein nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase protein bcl 2 protein tyrosine phosphatase 1B PTPN1 protein, human sanggenone C STAT3 protein STAT3 protein, human thiadiazole derivative triazole derivative animal antagonists and inhibitors biosynthesis Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular cell motion disease model dose response drug effects female G1 phase cell cycle checkpoint Hep-G2 cell line human Liver Neoplasms metabolism molecular model mouse Neovascularization, Pathologic pathology rat Sprague Dawley rat structure activity relation synthesis tumor cell line tumor invasion umbilical vein endothelial cell Animals Antineoplastic Agents Benzofurans Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular Caspase 3 Cell Line, Tumor Cell Movement Chromones Cyclin D1 Disease Models, Animal Dose-Response Relationship, Drug Female G1 Phase Cell Cycle Checkpoints Hep G2 Cells Human Umbilical Vein Endothelial Cells Humans Inhibitor of Apoptosis Proteins Liver Neoplasms Mice Models, Molecular Neoplasm Invasiveness Neovascularization, Pathologic Poly(ADP-ribose) Polymerases Protein Tyrosine Phosphatase, Non-Receptor Type 1 Proto-Oncogene Proteins c-bcl-2 Rats Rats, Sprague-Dawley STAT3 Transcription Factor Structure-Activity Relationship Thiadiazoles Triazoles |
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6-(2-benzylphenyl)-3-phenyl-(1,2,4)triazolo(3)(1,3,4)thiadiazole antineoplastic agent benzofuran derivative BIRC5 protein, human caspase 3 chromone derivative cyclin D1 inhibitor of apoptosis protein nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase protein bcl 2 protein tyrosine phosphatase 1B PTPN1 protein, human sanggenone C STAT3 protein STAT3 protein, human thiadiazole derivative triazole derivative animal antagonists and inhibitors biosynthesis Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular cell motion disease model dose response drug effects female G1 phase cell cycle checkpoint Hep-G2 cell line human Liver Neoplasms metabolism molecular model mouse Neovascularization, Pathologic pathology rat Sprague Dawley rat structure activity relation synthesis tumor cell line tumor invasion umbilical vein endothelial cell Animals Antineoplastic Agents Benzofurans Carcinoma, Ehrlich Tumor Carcinoma, Hepatocellular Caspase 3 Cell Line, Tumor Cell Movement Chromones Cyclin D1 Disease Models, Animal Dose-Response Relationship, Drug Female G1 Phase Cell Cycle Checkpoints Hep G2 Cells Human Umbilical Vein Endothelial Cells Humans Inhibitor of Apoptosis Proteins Liver Neoplasms Mice Models, Molecular Neoplasm Invasiveness Neovascularization, Pathologic Poly(ADP-ribose) Polymerases Protein Tyrosine Phosphatase, Non-Receptor Type 1 Proto-Oncogene Proteins c-bcl-2 Rats Rats, Sprague-Dawley STAT3 Transcription Factor Structure-Activity Relationship Thiadiazoles Triazoles Baburajeev, C.P Dhananjaya Mohan, C Ananda, H Rangappa, S Fuchs, J.E Jagadish, S Sivaraman Siveen, K Chinnathambi, A Ali Alharbi, S Zayed, M.E Zhang, J Li, F Sethi, G Girish, K.S Bender, A Basappa Rangappa, K.S Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
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10.1038/srep14195 |
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DEPT OF PHARMACOLOGY |
author_facet |
DEPT OF PHARMACOLOGY Baburajeev, C.P Dhananjaya Mohan, C Ananda, H Rangappa, S Fuchs, J.E Jagadish, S Sivaraman Siveen, K Chinnathambi, A Ali Alharbi, S Zayed, M.E Zhang, J Li, F Sethi, G Girish, K.S Bender, A Basappa Rangappa, K.S |
format |
Article |
author |
Baburajeev, C.P Dhananjaya Mohan, C Ananda, H Rangappa, S Fuchs, J.E Jagadish, S Sivaraman Siveen, K Chinnathambi, A Ali Alharbi, S Zayed, M.E Zhang, J Li, F Sethi, G Girish, K.S Bender, A Basappa Rangappa, K.S |
author_sort |
Baburajeev, C.P |
title |
Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
title_short |
Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
title_full |
Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
title_fullStr |
Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
title_full_unstemmed |
Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors |
title_sort |
development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1b inhibitors |
publisher |
Nature Publishing Group |
publishDate |
2020 |
url |
https://scholarbank.nus.edu.sg/handle/10635/175483 |
_version_ |
1778169928568799232 |