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1
Theonella : A Treasure Trove of Structurally Unique and Biologically Active Sterols
Theonella : A Treasure Trove of Structurally Unique and Biologically Active Sterols
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Theonella : A Treasure Trove of Structurally Unique and Biologically Active Sterols

Marine drugs, 2023-05, Vol.21 (5), p.291 [Peer Reviewed Journal]

2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md21050291 ;PMID: 37233485

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Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists
Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists
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Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists

Molecules (Basel, Switzerland), 2023-03, Vol.28 (6), p.2840 [Peer Reviewed Journal]

2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules28062840 ;PMID: 36985811

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3
Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction
Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction
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Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1092 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms23031092 ;PMID: 35163018

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4
Chemoproteomics Reveals USP5 (Ubiquitin Carboxyl-Terminal Hydrolase 5) as Promising Target of the Marine Polyketide Gracilioether A
Chemoproteomics Reveals USP5 (Ubiquitin Carboxyl-Terminal Hydrolase 5) as Promising Target of the Marine Polyketide Gracilioether A
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Chemoproteomics Reveals USP5 (Ubiquitin Carboxyl-Terminal Hydrolase 5) as Promising Target of the Marine Polyketide Gracilioether A

Marine drugs, 2024-01, Vol.22 (1), p.41 [Peer Reviewed Journal]

COPYRIGHT 2024 MDPI AG ;2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md22010041 ;PMID: 38248666

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5
Discovering the Biological Target of 5-epi-Sinuleptolide Using a Combination of Proteomic Approaches
Discovering the Biological Target of 5-epi-Sinuleptolide Using a Combination of Proteomic Approaches
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Discovering the Biological Target of 5-epi-Sinuleptolide Using a Combination of Proteomic Approaches

Marine drugs, 2017-10, Vol.15 (10), p.312 [Peer Reviewed Journal]

Copyright MDPI AG 2017 ;2017 by the authors. 2017 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md15100312 ;PMID: 29027931

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6
Molecular Network and Culture Media Variation Reveal a Complex Metabolic Profile in Pantoea cf. eucrina D2 Associated with an Acidified Marine Sponge
Molecular Network and Culture Media Variation Reveal a Complex Metabolic Profile in Pantoea cf. eucrina D2 Associated with an Acidified Marine Sponge
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Molecular Network and Culture Media Variation Reveal a Complex Metabolic Profile in Pantoea cf. eucrina D2 Associated with an Acidified Marine Sponge

International journal of molecular sciences, 2020-08, Vol.21 (17), p.6307 [Peer Reviewed Journal]

2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 by the authors. 2020 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms21176307 ;PMID: 32878176

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7
Phytochemical and Biological Studies of Nepeta asterotricha Rech. f. (Lamiaceae): Isolation of Nepetamoside
Phytochemical and Biological Studies of Nepeta asterotricha Rech. f. (Lamiaceae): Isolation of Nepetamoside
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Phytochemical and Biological Studies of Nepeta asterotricha Rech. f. (Lamiaceae): Isolation of Nepetamoside

Molecules (Basel, Switzerland), 2019-04, Vol.24 (9), p.1684 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules24091684 ;PMID: 31052163

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8
Insights on FXR selective modulation. Speculation on bile acid chemical space in the discovery of potent and selective agonists
Insights on FXR selective modulation. Speculation on bile acid chemical space in the discovery of potent and selective agonists
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Insights on FXR selective modulation. Speculation on bile acid chemical space in the discovery of potent and selective agonists

Scientific reports, 2016-01, Vol.6 (1), p.19008-19008, Article 19008 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jan 2016 ;Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep19008 ;PMID: 26740187

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9
Investigation around the Oxadiazole Core in the Discovery of a New Chemotype of Potent and Selective FXR Antagonists
Investigation around the Oxadiazole Core in the Discovery of a New Chemotype of Potent and Selective FXR Antagonists
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Investigation around the Oxadiazole Core in the Discovery of a New Chemotype of Potent and Selective FXR Antagonists

ACS medicinal chemistry letters, 2019-04, Vol.10 (4), p.504-510 [Peer Reviewed Journal]

Copyright © 2019 American Chemical Society 2019 American Chemical Society ;ISSN: 1948-5875 ;EISSN: 1948-5875 ;DOI: 10.1021/acsmedchemlett.8b00534 ;PMID: 30996787

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10
Binding mechanism of the farnesoid X receptor marine antagonist suvanine reveals a strategy to forestall drug modulation on nuclear receptors. Design, synthesis, and biological evaluation of novel ligands
Binding mechanism of the farnesoid X receptor marine antagonist suvanine reveals a strategy to forestall drug modulation on nuclear receptors. Design, synthesis, and biological evaluation of novel ligands
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Binding mechanism of the farnesoid X receptor marine antagonist suvanine reveals a strategy to forestall drug modulation on nuclear receptors. Design, synthesis, and biological evaluation of novel ligands

Journal of medicinal chemistry, 2013-06, Vol.56 (11), p.4701 [Peer Reviewed Journal]

EISSN: 1520-4804 ;DOI: 10.1021/jm400419e ;PMID: 23656455

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11
Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonism
Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonism
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Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonism

Scientific reports, 2015-11, Vol.5 (1), p.16605-16605, Article 16605 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2015 ;Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep16605 ;PMID: 26567894

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12
Antioxidant Activity and Chemical Components as Potential Anticancer Agents in the Olive Leaf (Olea europaea L. cv Leccino.) Decoction
Antioxidant Activity and Chemical Components as Potential Anticancer Agents in the Olive Leaf (Olea europaea L. cv Leccino.) Decoction
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Antioxidant Activity and Chemical Components as Potential Anticancer Agents in the Olive Leaf (Olea europaea L. cv Leccino.) Decoction

Anti-cancer agents in medicinal chemistry, 2014-01, Vol.14 (10), p.1376-1385 [Peer Reviewed Journal]

ISSN: 1871-5206 ;EISSN: 1875-5992 ;DOI: 10.2174/1871520614666140804153936 ;PMID: 25102361

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13
Navigation in bile acid chemical space: discovery of novel FXR and GPBAR1 ligands
Navigation in bile acid chemical space: discovery of novel FXR and GPBAR1 ligands
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Navigation in bile acid chemical space: discovery of novel FXR and GPBAR1 ligands

Scientific reports, 2016-07, Vol.6 (1), p.29320-29320, Article 29320 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2016 ;Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep29320 ;PMID: 27381677

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14
Synergism of a Novel 1,2,4-oxadiazole-containing Derivative with Oxacillin against Methicillin-Resistant Staphylococcus aureus
Synergism of a Novel 1,2,4-oxadiazole-containing Derivative with Oxacillin against Methicillin-Resistant Staphylococcus aureus
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Synergism of a Novel 1,2,4-oxadiazole-containing Derivative with Oxacillin against Methicillin-Resistant Staphylococcus aureus

Antibiotics (Basel), 2021-10, Vol.10 (10), p.1258 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2079-6382 ;EISSN: 2079-6382 ;DOI: 10.3390/antibiotics10101258 ;PMID: 34680838

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15
Molecular decodification of gymnemic acids from Gymnema sylvestre. Discovery of a new class of liver X receptor antagonists
Molecular decodification of gymnemic acids from Gymnema sylvestre. Discovery of a new class of liver X receptor antagonists
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Molecular decodification of gymnemic acids from Gymnema sylvestre. Discovery of a new class of liver X receptor antagonists

Steroids, 2015-04, Vol.96, p.121 [Peer Reviewed Journal]

Copyright © 2015 Elsevier Inc. All rights reserved. ;EISSN: 1878-5867 ;DOI: 10.1016/j.steroids.2015.01.024 ;PMID: 25668616

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16
Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases
Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases
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Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases

Frontiers in pharmacology, 2017-03, Vol.8, p.162-162 [Peer Reviewed Journal]

COPYRIGHT 2017 Frontiers Research Foundation ;Copyright © 2017 Festa, De Marino, Carino, Sepe, Marchianò, Cipriani, Di Leva, Limongelli, Monti, Capolupo, Distrutti, Fiorucci and Zampella. 2017 Festa, De Marino, Carino, Sepe, Marchianò, Cipriani, Di Leva, Limongelli, Monti, Capolupo, Distrutti, Fiorucci and Zampella ;ISSN: 1663-9812 ;EISSN: 1663-9812 ;DOI: 10.3389/fphar.2017.00162 ;PMID: 28424617

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17
Biological Profile of Two Gentiana lutea L. Metabolites Using Computational Approaches and In Vitro Tests
Biological Profile of Two Gentiana lutea L. Metabolites Using Computational Approaches and In Vitro Tests
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Biological Profile of Two Gentiana lutea L. Metabolites Using Computational Approaches and In Vitro Tests

Biomolecules (Basel, Switzerland), 2021-10, Vol.11 (10), p.1490 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2218-273X ;EISSN: 2218-273X ;DOI: 10.3390/biom11101490 ;PMID: 34680124

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18
Bioactive cembrane derivatives from the Indian Ocean soft coral, Sinularia kavarattiensis
Bioactive cembrane derivatives from the Indian Ocean soft coral, Sinularia kavarattiensis
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Bioactive cembrane derivatives from the Indian Ocean soft coral, Sinularia kavarattiensis

Marine drugs, 2014-07, Vol.12 (7), p.4045-4068 [Peer Reviewed Journal]

Copyright MDPI AG 2014 ;2014 by the authors; licensee MDPI, Basel, Switzerland. 2014 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md12074045 ;PMID: 25056629

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19
Oxygenated polyketides from Plakinastrella mamillaris as a new chemotype of PXR agonists
Oxygenated polyketides from Plakinastrella mamillaris as a new chemotype of PXR agonists
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Oxygenated polyketides from Plakinastrella mamillaris as a new chemotype of PXR agonists

Marine drugs, 2013-07, Vol.11 (7), p.2314-2327 [Peer Reviewed Journal]

Copyright MDPI AG 2013 ;2013 by the authors; licensee MDPI, Basel, Switzerland. 2013 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md11072314 ;PMID: 23820629

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20
L-Cysteine (3-Nitrophenyl)methyl Ester Hydrochloride: A New Chiral Reagent in the Sugar Analysis
L-Cysteine (3-Nitrophenyl)methyl Ester Hydrochloride: A New Chiral Reagent in the Sugar Analysis
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L-Cysteine (3-Nitrophenyl)methyl Ester Hydrochloride: A New Chiral Reagent in the Sugar Analysis

Letters in organic chemistry, 2017-02, Vol.14 (2), p.69-73 [Peer Reviewed Journal]

ISSN: 1570-1786 ;EISSN: 1875-6255 ;DOI: 10.2174/1570178614666170123122831

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