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Results 1 - 20 of 83  for All Library Resources

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1
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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2
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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3
Novel steroidal components from the underground parts of Ruscus aculeatus L
Novel steroidal components from the underground parts of Ruscus aculeatus L
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Novel steroidal components from the underground parts of Ruscus aculeatus L

Molecules (Basel, Switzerland), 2012-11, Vol.17 (12), p.14002-14014 [Peer Reviewed Journal]

Copyright MDPI AG 2012 ;2012 by the authors; licensee MDPI, Basel, Switzerland. 2012 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules171214002 ;PMID: 23183890

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4
Identification of minor secondary metabolites from the latex of Croton lechleri (Muell-Arg) and evaluation of their antioxidant activity
Identification of minor secondary metabolites from the latex of Croton lechleri (Muell-Arg) and evaluation of their antioxidant activity
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Identification of minor secondary metabolites from the latex of Croton lechleri (Muell-Arg) and evaluation of their antioxidant activity

Molecules (Basel, Switzerland), 2008-06, Vol.13 (6), p.1219-1229 [Peer Reviewed Journal]

Copyright MDPI AG 2008 ;2008 by the authors. 2008 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules13061219 ;PMID: 18596648

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5
Marine and semi-synthetic hydroxysteroids as new scaffolds for pregnane X receptor modulation
Marine and semi-synthetic hydroxysteroids as new scaffolds for pregnane X receptor modulation
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Marine and semi-synthetic hydroxysteroids as new scaffolds for pregnane X receptor modulation

Marine drugs, 2014-05, Vol.12 (6), p.3091-3115 [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/md12063091 ;PMID: 24871460

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6
Swinholide J, a potent cytotoxin from the marine sponge Theonella swinhoei
Swinholide J, a potent cytotoxin from the marine sponge Theonella swinhoei
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Swinholide J, a potent cytotoxin from the marine sponge Theonella swinhoei

Marine drugs, 2011-06, Vol.9 (6), p.1133-1141 [Peer Reviewed Journal]

Copyright MDPI AG 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;2011 by the authors; licensee MDPI, Basel, Switzerland. 2011 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md9061133 ;PMID: 21747751

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7
Differential in gel electrophoresis (DIGE) comparative proteomic analysis of macrophages cell cultures in response to perthamide C treatment
Differential in gel electrophoresis (DIGE) comparative proteomic analysis of macrophages cell cultures in response to perthamide C treatment
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Differential in gel electrophoresis (DIGE) comparative proteomic analysis of macrophages cell cultures in response to perthamide C treatment

Marine drugs, 2013-04, Vol.11 (4), p.1288-1299 [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/md11041288 ;PMID: 23595056

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8
Anti-inflammatory and analgesic activities with gastroprotective effect of semi-purified fractions and isolation of pure compounds from Mediterranean gorgonian Eunicella singularis
Anti-inflammatory and analgesic activities with gastroprotective effect of semi-purified fractions and isolation of pure compounds from Mediterranean gorgonian Eunicella singularis
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Anti-inflammatory and analgesic activities with gastroprotective effect of semi-purified fractions and isolation of pure compounds from Mediterranean gorgonian Eunicella singularis

Asian Pacific journal of tropical medicine, 2015-08, Vol.8 (8), p.598-603 [Peer Reviewed Journal]

2015 Hainan Medical College ;Copyright © 2015 Hainan Medical College. Production and hosting by Elsevier B.V. All rights reserved. ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;ISSN: 1995-7645 ;EISSN: 2352-4146 ;DOI: 10.1016/j.apjtm.2015.07.019 ;PMID: 26321512

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9
Preliminary structure-activity relationship on theonellasterol, a new chemotype of FXR antagonist, from the marine sponge Theonella swinhoei
Preliminary structure-activity relationship on theonellasterol, a new chemotype of FXR antagonist, from the marine sponge Theonella swinhoei
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Preliminary structure-activity relationship on theonellasterol, a new chemotype of FXR antagonist, from the marine sponge Theonella swinhoei

Marine drugs, 2012-11, Vol.10 (11), p.2448-2466 [Peer Reviewed Journal]

Copyright MDPI AG 2012 ;2012 by the authors; licensee MDPI, Basel, Switzerland. 2012 ;ISSN: 1660-3397 ;EISSN: 1660-3397 ;DOI: 10.3390/md10112448 ;PMID: 23203270

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10
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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11
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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12
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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13
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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14
Discovery of ((1,2,4-oxadiazol-5-yl)pyrrolidin-3-yl)ureidyl derivatives as selective non-steroidal agonists of the G-protein coupled bile acid receptor-1
Discovery of ((1,2,4-oxadiazol-5-yl)pyrrolidin-3-yl)ureidyl derivatives as selective non-steroidal agonists of the G-protein coupled bile acid receptor-1
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Discovery of ((1,2,4-oxadiazol-5-yl)pyrrolidin-3-yl)ureidyl derivatives as selective non-steroidal agonists of the G-protein coupled bile acid receptor-1

Scientific reports, 2019-02, Vol.9 (1), p.2504-2504, Article 2504 [Peer Reviewed Journal]

This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-019-38840-z ;PMID: 30792450

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15
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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16
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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17
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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18
Theonellasterols and conicasterols from Theonella swinhoei. Novel marine natural ligands for human nuclear receptors
Theonellasterols and conicasterols from Theonella swinhoei. Novel marine natural ligands for human nuclear receptors
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Theonellasterols and conicasterols from Theonella swinhoei. Novel marine natural ligands for human nuclear receptors

Journal of medicinal chemistry, 2011-04, Vol.54 (8), p.3065 [Peer Reviewed Journal]

EISSN: 1520-4804 ;DOI: 10.1021/jm200169t ;PMID: 21428459

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19
GPBAR1 Activation by C6-Substituted Hyodeoxycholane Analogues Protect against Colitis
GPBAR1 Activation by C6-Substituted Hyodeoxycholane Analogues Protect against Colitis
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GPBAR1 Activation by C6-Substituted Hyodeoxycholane Analogues Protect against Colitis

ACS medicinal chemistry letters, 2020-05, Vol.11 (5), p.818-824 [Peer Reviewed Journal]

Copyright © 2020 American Chemical Society. ;Copyright © 2020 American Chemical Society 2020 American Chemical Society ;ISSN: 1948-5875 ;EISSN: 1948-5875 ;DOI: 10.1021/acsmedchemlett.9b00636 ;PMID: 32435390

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20
Phytochemical Analysis of the Methanolic Extract and Essential Oil from Leaves of Industrial Hemp Futura 75 Cultivar: Isolation of a New Cannabinoid Derivative and Biological Profile Using Computational Approaches
Phytochemical Analysis of the Methanolic Extract and Essential Oil from Leaves of Industrial Hemp Futura 75 Cultivar: Isolation of a New Cannabinoid Derivative and Biological Profile Using Computational Approaches
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Phytochemical Analysis of the Methanolic Extract and Essential Oil from Leaves of Industrial Hemp Futura 75 Cultivar: Isolation of a New Cannabinoid Derivative and Biological Profile Using Computational Approaches

Plants (Basel), 2022-06, Vol.11 (13), p.1671 [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: 2223-7747 ;EISSN: 2223-7747 ;DOI: 10.3390/plants11131671 ;PMID: 35807623

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