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Book
Marine Natural Products and Obesity
Authors: ---
ISBN: 3039211927 3039211919 Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Obesity and related co-morbidities are increasing worldwide and pose a serious health problem. Changes in lifestyle and diet would be the best remedies to fight obesity; however, many people will still rely on medical aid. Marine organisms have been prolific in the production of bioactive compounds for many diseases, e.g., cancer, and promise to be an excellent source for natural-derived molecules and novel nutraceuticals. Bioactive compounds with beneficial activities towards obesity have been described from diverse marine organism including marine algae, bacteria, sponges, fungi, crustaceans or fish. This Special Issue will highlight the progress in the following topics: Bioactive compounds for the treatment of obesity and obesity-related co-morbidities (diabetes, fatty liver, hyperlipidemia) from marine organisms; the isolation of novel compounds, the bioactivity screening of marine organisms and the elucidation of molecular mode of action of marine bioactive compounds.


Book
Advances in Plant Alkaloid Research
Author:
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Plant alkaloids are critical components of modern medicine and pharmaceuticals. These compounds are also becoming increasingly important for industrial uses as part of the green chemistry revolution. This Special Issue will focus on the molecular advances being made in understanding how such a large and diverse class of compounds are made by plants and how metabolic engineering advances are increasing the overall yield of crucial precursors.

Keywords

Research & information: general --- Biology, life sciences --- canthin-6-one --- Picrolemma huberi --- Simaroubaceae --- antiplasmodial activity --- Sarcococca hookeriana --- sarchookloides A–C --- steroidal alkaloid --- cytotoxicity --- Rhodophiala --- alkaloids --- molecular docking --- AChE --- BuChE --- GC-MS --- Mahonia imbricata --- Berberidaceae --- isoquinoline alkaloid --- mahimbrine A --- hedgehog signaling --- Veratrum californicum --- cyclopamine --- HPLC-MS --- Shh-Light II cells --- halogencyclopropane --- dichlorocarbene --- epoxidation --- vindoline --- catharanthine --- dimer alkaloids --- vindoline trimer --- Ruta graveolens --- photosystem II --- Chl a fluorescence --- Hill reaction inhibitors --- acridone alkaloids --- benzylisoquinoline alkaloids --- cytochrome P450 monooxygenase --- medicinal properties --- methyltransferase --- Nelumbo nucifera --- norcoclaurine synthase --- sacred lotus --- stereochemistry --- Aristotelia chilensis Molina Stuntz --- vascular activity --- endothelium-independent --- indole alkaloid --- 8-oxo-9-dihydromakomakine --- voltage-dependent calcium channels --- Catharanthus roseus --- cambial meristematic cells --- Aspergillus flavus --- terpenoid indole alkaloids --- biosynthesis --- Buxaceae --- Borago officinalis --- Crassocephalum --- Copper-dependent diamine oxidase --- Gynura bicolor --- Homospermidine synthase --- Lolium perenne --- Necic acids --- Necine bases --- Pyrrolizidine alkaloid biosynthesis --- Senecionine --- tropane alkaloids --- scopolamine --- cocaine --- calystegine --- chemistry --- pharmacology --- biotechnological production --- Erythroxylaceae --- Erythroxylum coca --- next generation sequencing --- traditional medicine --- bioprospecting --- tropane --- late-stage functionalization --- sulfinate --- DiversinateTM --- natural product --- medicinal chemistry --- papaverine --- scaffold --- library --- biodiscovery --- Swinglea glutinosa --- dereplication --- acridones --- phenylacrylamides --- canthin-6-one --- Picrolemma huberi --- Simaroubaceae --- antiplasmodial activity --- Sarcococca hookeriana --- sarchookloides A–C --- steroidal alkaloid --- cytotoxicity --- Rhodophiala --- alkaloids --- molecular docking --- AChE --- BuChE --- GC-MS --- Mahonia imbricata --- Berberidaceae --- isoquinoline alkaloid --- mahimbrine A --- hedgehog signaling --- Veratrum californicum --- cyclopamine --- HPLC-MS --- Shh-Light II cells --- halogencyclopropane --- dichlorocarbene --- epoxidation --- vindoline --- catharanthine --- dimer alkaloids --- vindoline trimer --- Ruta graveolens --- photosystem II --- Chl a fluorescence --- Hill reaction inhibitors --- acridone alkaloids --- benzylisoquinoline alkaloids --- cytochrome P450 monooxygenase --- medicinal properties --- methyltransferase --- Nelumbo nucifera --- norcoclaurine synthase --- sacred lotus --- stereochemistry --- Aristotelia chilensis Molina Stuntz --- vascular activity --- endothelium-independent --- indole alkaloid --- 8-oxo-9-dihydromakomakine --- voltage-dependent calcium channels --- Catharanthus roseus --- cambial meristematic cells --- Aspergillus flavus --- terpenoid indole alkaloids --- biosynthesis --- Buxaceae --- Borago officinalis --- Crassocephalum --- Copper-dependent diamine oxidase --- Gynura bicolor --- Homospermidine synthase --- Lolium perenne --- Necic acids --- Necine bases --- Pyrrolizidine alkaloid biosynthesis --- Senecionine --- tropane alkaloids --- scopolamine --- cocaine --- calystegine --- chemistry --- pharmacology --- biotechnological production --- Erythroxylaceae --- Erythroxylum coca --- next generation sequencing --- traditional medicine --- bioprospecting --- tropane --- late-stage functionalization --- sulfinate --- DiversinateTM --- natural product --- medicinal chemistry --- papaverine --- scaffold --- library --- biodiscovery --- Swinglea glutinosa --- dereplication --- acridones --- phenylacrylamides


Book
Advances in Plant Alkaloid Research
Author:
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Plant alkaloids are critical components of modern medicine and pharmaceuticals. These compounds are also becoming increasingly important for industrial uses as part of the green chemistry revolution. This Special Issue will focus on the molecular advances being made in understanding how such a large and diverse class of compounds are made by plants and how metabolic engineering advances are increasing the overall yield of crucial precursors.

Keywords

canthin-6-one --- Picrolemma huberi --- Simaroubaceae --- antiplasmodial activity --- Sarcococca hookeriana --- sarchookloides A–C --- steroidal alkaloid --- cytotoxicity --- Rhodophiala --- alkaloids --- molecular docking --- AChE --- BuChE --- GC-MS --- Mahonia imbricata --- Berberidaceae --- isoquinoline alkaloid --- mahimbrine A --- hedgehog signaling --- Veratrum californicum --- cyclopamine --- HPLC-MS --- Shh-Light II cells --- halogencyclopropane --- dichlorocarbene --- epoxidation --- vindoline --- catharanthine --- dimer alkaloids --- vindoline trimer --- Ruta graveolens --- photosystem II --- Chl a fluorescence --- Hill reaction inhibitors --- acridone alkaloids --- benzylisoquinoline alkaloids --- cytochrome P450 monooxygenase --- medicinal properties --- methyltransferase --- Nelumbo nucifera --- norcoclaurine synthase --- sacred lotus --- stereochemistry --- Aristotelia chilensis Molina Stuntz --- vascular activity --- endothelium-independent --- indole alkaloid --- 8-oxo-9-dihydromakomakine --- voltage-dependent calcium channels --- Catharanthus roseus --- cambial meristematic cells --- Aspergillus flavus --- terpenoid indole alkaloids --- biosynthesis --- Buxaceae --- Borago officinalis --- Crassocephalum --- Copper-dependent diamine oxidase --- Gynura bicolor --- Homospermidine synthase --- Lolium perenne --- Necic acids --- Necine bases --- Pyrrolizidine alkaloid biosynthesis --- Senecionine --- tropane alkaloids --- scopolamine --- cocaine --- calystegine --- chemistry --- pharmacology --- biotechnological production --- Erythroxylaceae --- Erythroxylum coca --- next generation sequencing --- traditional medicine --- bioprospecting --- tropane --- late-stage functionalization --- sulfinate --- DiversinateTM --- natural product --- medicinal chemistry --- papaverine --- scaffold --- library --- biodiscovery --- Swinglea glutinosa --- dereplication --- acridones --- phenylacrylamides

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