Development of novel triazolo-thiadiazoles from heterogeneous "green" catalysis as protein tyrosine phosphatase 1B inhibitors

10.1038/srep14195

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Main Authors: 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
Other Authors: DEPT OF PHARMACOLOGY
Format: Article
Published: Nature Publishing Group 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/175483
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spelling 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
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic 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
spellingShingle 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
description 10.1038/srep14195
author2 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