Search results for "Stilbene"

showing 10 items of 159 documents

Blue Fluorescent Exciplexes Consisting oftrans-Stilbene and Antibodies

2001

biologyChemistrybiology.proteinTrans stilbeneGeneral ChemistryAntibodyPhotochemistryFluorescenceCatalysisAngewandte Chemie International Edition
researchProduct

ChemInform Abstract: Blue Fluorescent Exciplexes Consisting of trans-Stilbene and Antibodies.

2010

biologyStereochemistryChemistrybiology.proteinTrans stilbeneGeneral MedicineAntibodyFluorescenceChemInform
researchProduct

Classification of stilbenoid compounds by entropy of artificial intelligence

2013

A set of 66 stilbenoid compounds is classified into a system of periodic properties by using a procedure based on artificial intelligence, information entropy theory. Eight characteristics in hierarchical order are used to classify structurally the stilbenoids. The former five features mark the group or column while the latter three are used to indicate the row or period in the table of periodic classification. Those stilbenoids in the same group are suggested to present similar properties. Furthermore, compounds also in the same period will show maximum resemblance. In this report, the stilbenoids in the table are related to experimental data of bioactivity and antioxidant properties avail…

business.industryChemistryEntropyPlant ScienceGeneral MedicineHorticultureStilbenoidBiochemistryTechnical literatureAntioxidantsMolecular classificationArtificial IntelligenceStilbenesEntropy (information theory)Extreme rightArtificial intelligencebusinessMolecular BiologyPhytochemistry
researchProduct

Abstract 1390: A combination of natural polyphenols, a NAD+ booster, and a Toll-like receptor 2/6 agonist exerts high radioprotection in normal tissu…

2021

Abstract Ionizing radiation damages cells via direct ionization of DNA and other cellular targets as well as by indirect effects through reactive oxygen species. The response to radiation exposure depends on the cell type and dose of radiation, inherent tissue sensitivity and repair, and modulating intracellular factors that include cell cycle status, O2 pressure, and levels of thiols and other antioxidants. Potentially protective agents against exposure to harmful radiation have been investigated for decades. However, no ideal radioprotector is currently available. A wide range of phytochemicals are antioxidants and, thus, potentially radioprotective. Topical administration of Pterostilben…

chemistry.chemical_classificationAgonistCancer ResearchReactive oxygen speciesPterostilbeneNicotinamidemedicine.drug_classSilibininPharmacologychemistry.chemical_compoundOncologychemistryIn vivoNicotinamide ribosidemedicineNAD+ kinaseCancer Research
researchProduct

Abstract 1605: Pterostilbene, a natural phytoalexin, effectively protects against UVB-induced skin carcinogenesis by increasing antioxidant cellular …

2014

Abstract Clinical and laboratory studies have demonstrated that skin exposure to ultraviolet radiation (UV) is the main cause of non-melanoma skin cancer (NMSC) (≈ 99%) and melanoma (≈ 95%) development. The procarcinogenic effects of solar exposure are mainly due to UVB radiation (290-320 nm range), the same tight range that produces burning in human skin (erythema), inflammation, oxidative stress, DNA damage, etc. The number of skin cancers around the world keeps increasing and, thus, it is an urgent need to find effective protection remedies. Phytoalexins of polyphenolic structure are naturally occurring compounds involved in the defense against pathogens and environmental stresses in pla…

chemistry.chemical_classificationCancer ResearchAntioxidantPterostilbeneintegumentary systemChemistrymedicine.medical_treatmentPhytoalexinMelanomaHuman skinPharmacologyResveratrolmedicine.disease_causemedicine.diseaseToxicologychemistry.chemical_compoundOncologymedicineSkin cancerOxidative stressCancer Research
researchProduct

Biological activity of resveratrol, a stilbenic compound from grapevines, against Botrytis cinerea, the causal agent for gray mold

1997

The biological activity of resveratrol, a stilbenic compound synthesized by grapevines in response to various stresses, was reevaluated against Botrytis cinerea using a novel in vitro system that enabled direct observation of the fungus with an inverted microscope. We determined that 90 μg resveratrol/ml reduced germination of B. cinerea conidia by ca. 50%. Moreover, resveratrol was shown to significantly reduce mycelial growth of B. cinerea at concentrations ranging from 60 to 140 μg/ml. Exposure to resveratrol at concentrations ranging from 60 to 140 μg/ml resulted in cytological changes in B. cinerea, such as production of secondary or tertiary germ tubes by conidia, cytoplasmic granulat…

chemistry.chemical_classificationPterostilbenePhytoalexinfungiHyphal tipfood and beveragesGerm tubeGeneral MedicineBiologyResveratrolbiology.organism_classificationBiochemistryMicrobiologyConidiumchemistry.chemical_compoundchemistryBotanyskin and connective tissue diseasesEcology Evolution Behavior and SystematicsMyceliumBotrytis cinerea
researchProduct

Degradation of stilbene-type phytoalexins in relation to the pathogenicity of Botrytis cinerea to grapevines

1996

The ability of eight isolates of Botrytis cinerea to degrade the stilbene phytoalexins, resveratrol and pterostilbene, was compared with their pathogenicity to grapevines. All strains which degraded resveratrol and pterostilbene were highly or moderately pathogenic to in vitro cultures of grapevines (Vitis rupestris) after inoculation with agar disks containing mycelium, while those which were unable to degrade phytoalexins were non-pathogenic. In all cases, the hydroxystilbene-degrading activity was related to the presence of laccase activity in the culture filtrates, as shown by using syringaldazine as substrate. The role of laccase-mediated degradation of phytoalexins in relation to path…

chemistry.chemical_classificationPterostilbenebiologyInoculationPhytoalexinfungifood and beveragesPlant ScienceFungi imperfectiHorticultureResveratrolbiology.organism_classificationMicrobiologychemistry.chemical_compoundchemistryBotanyGeneticsRootstockAgronomy and Crop ScienceMyceliumBotrytis cinereaPlant Pathology
researchProduct

Stilbene Content of MatureVitis viniferaBerries in Response to UV-C Elicitation

2001

A method using HPLC analysis has been used to compare the level of resveratrol and its derivatives, piceid, pterostilbene and epsilon-viniferin, in grapevine berries of three Vitis vinifera varieties. The concentration of these compounds has been evaluated in healthy and Botrytis cinerea infected grape clusters, both in natural vineyard conditions and in response to UV elicitation.

chemistry.chemical_classificationPterostilbenebiologyPlant ExtractsUltraviolet RaysPhytoalexinGeneral ChemistryFungi imperfectiResveratrolPlant disease resistancebiology.organism_classificationVineyardHorticulturechemistry.chemical_compoundchemistryFruitStilbenesBotanyGeneral Agricultural and Biological SciencesChromatography High Pressure LiquidBotrytis cinereaPiceidJournal of Agricultural and Food Chemistry
researchProduct

The Significance of Stilbene-Type Phytoalexin Degradation by Culture Filtrates of Botrytis Cinerea in the Vine-Botrytis Interaction

1993

Phytoalexins, antimicrobial compounds, synthesized by a plant in response to infection or a variety of stresses are known to be the most efficient way by which grapevines withstand an attack by Botrytis cinerea Pers., the causal organism for grey mould. In that plant, such responses include the production of a simple stilbene, resveratrol, and the biosynthetically related compounds, viniferins and pterostilbene. If stilbene-type phytoalexins represent a contributory factor in the resistance of grapevines to B.cinerea, the capacity of the pathogen to metabolize antifungal compounds released by the host could also play a significant role in the outcome of the interaction between grapevines an…

chemistry.chemical_classificationPterostilbenefood.ingredientbiologyHost (biology)Phytoalexinfungifood and beveragesFungusResveratrolbiology.organism_classificationMicrobiologychemistry.chemical_compoundfoodchemistryPathogenBotrytis cinereaBotrytis
researchProduct

5,10-Dihydroindeno[2,1-a]indene

2019

The title compound, C16H12, crystallizes with four half molecules in the asymmetric unit, each of which is located on a crystallographic centre of inversion. The molecules are essentially planar. The crystal studied was a non-merohedral twin.

crystal structurepolycyclic hydrocarbonplanarized stilbeneCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesInversion (discrete mathematics)0104 chemical sciencesCrystalCrystallographychemistry.chemical_compoundPlanarchemistrylcsh:QD901-999lcsh:CrystallographyIndeneIUCrData
researchProduct