Search results for "Lactone"

showing 10 items of 335 documents

Diepoxyrollin and Diepomuricanin B:  Two New Diepoxyacetogenins from Rollinia membranacea Seeds

1997

Diepoxyrollin (1) and diepomuricanin B (2), two new Annonaceous acetogenins were isolated from the cytotoxic MeOH extract of the seeds of Colombian Rollinia membranacea. Five others known acetogenins were also isolated, dieporeticanin 1, dieporeticanin 2, diepomuricanin A, rollinone, and sylvaticin. Their structures were elucidated on the basis of spectral data. Compounds 1 and 2 belong to the rare type of diepoxyacetogenins, which are probably precursors of the mono-tetrahydrofuran acetogenins.

Pharmacologychemistry.chemical_classificationRollinia membranaceabiologyStereochemistrySylvaticinOrganic ChemistryPharmaceutical SciencePharmacognosybiology.organism_classificationAnalytical ChemistryComplementary and alternative medicinechemistryAnnonaceaeDrug DiscoveryMolecular MedicineAnnonaceous AcetogeninsSpectral dataLactoneJournal of Natural Products
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Preparation of 7-Alkoxylated Furanopyrones:  Semisynthesis of (−)-Etharvensin, a New Styryl-Lactone from Goniothalamus arvensis

1997

A new furanopyrone derivative, (−)-etharvensin (1), was isolated from the stem bark of Goniothalamus arvensis. Semisynthesis of the 7-ethoxyfuranopyrone 1 was achieved by addition of EtOH in concentrated acid medium to the unsaturated α-pyrone (+)-altholactone (2). This protocol constitutes a novel, direct (single-step), and efficient method to prepare this class of bioactive compounds.

Pharmacologychemistry.chemical_classificationStem barkbiologyStereochemistryOrganic ChemistryPharmaceutical Sciencebiology.organism_classificationSemisynthesisAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryMolecular MedicineDerivative (chemistry)EtharvensinGoniothalamusLactoneJournal of Natural Products
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Flavonoids and Others Constituents from Onopordon macracanthum.

1987

Pharmacologychemistry.chemical_classificationStereochemistryOrganic ChemistryFlavonoidPharmaceutical ScienceSesquiterpeneAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryMolecular MedicineOrganic chemistryLactonePlanta medica
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10-Oximeguanacone, the First Nitrogenated Acetogenin Derivative Found To Be a Potent Inhibitor of Mitochondrial Complex I

1998

A new 10-keto bis-tetrahydrofuran acetogenin, guanacone (1), has been isolated from a cytotoxic extract of Annona aff. spraguei seeds. The 10-oximeguanacone derivative 1f is the first bioactive nitrogenated acetogenin found to be a very potent inhibitor of complex I. In addition, a SAR study of guanacone analogues is reported based on the titration of the NADH oxidase and NADH:ubiquinone oxidoreductase activities.

Pharmacologychemistry.chemical_classificationStereochemistryOrganic ChemistryPharmaceutical ScienceBiological activityBiologyAnalytical Chemistrychemistry.chemical_compoundEnzymeComplementary and alternative medicinechemistryEnzyme inhibitorOxidoreductaseDrug DiscoveryAcetogeninbiology.proteinMolecular MedicineLactoneDerivative (chemistry)Heart metabolismJournal of Natural Products
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Neoclerodane Diterpenoids from Scutellaria polyodon

1997

Nine new neoclerodane diterpenoids, scupolins A−I, have been isolated from an Me2CO extract of the aerial parts of Scutellaria polyodon (3−11), together with the known neoclerodanes jodrellin B (1) and scutecolumnin A (2). Structures 3−11 were established by spectroscopic means and by comparison with closely related compounds.

Pharmacologychemistry.chemical_classificationbiologyStereochemistryOrganic ChemistryPharmaceutical ScienceEpoxidePharmacognosybiology.organism_classificationTerpenoidAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryScutellariaMolecular MedicineOrganic chemistryHemiacetalDiterpeneLactoneJournal of Natural Products
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Preparation and characterization of PCL/GO-g-PEG biocomposite nanofiber scaffolds

2016

Biocomposite nanofiber scaffolds of polycaprolactone (PCL) with different graphene oxide surface grafted with poly(ethylene glycol) (GO-g-PEG) concentrations were prepared by electrospinning. Morphological, mechanical as well as wettability characterization were carried out. Results showed that the average diameter of PLA/GO-g-PEG electrospun nanofibers increased by increasing the filler content. GO-g-PEG enhanced the electrospun PCL hydrophilicity as well as the Young modulus, in particular at low GO-g-PEG concentrations.

PolycaprolactonePolyethylene glycolElectrospinningTissue engineeringGraphene oxide
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1973

The thermal degradation of poly(oxycarbonylethylene) (poly-β-propiolactone) has been investigated within a temperature range of 180–220°C and under various pressures. The degradation begins with a considerable decrease in molecular weight, followed by an accelerating formation of acrylic acid. The reaction involves the following steps: 1 Random chain scission of polymer chains by typical ester pyrolysis with the formation of fragments one of which containing a carboxylic group the other one a CC-double bond at the chain end (Eq. (1)). 2 Formation of the volatile acrylic acid by scissions at the chain end, the amount of acrylic acid or the weight-loss increasing with the number of fragmentat…

Polyesterchemistry.chemical_classificationchemistry.chemical_compoundChain scissionChemistryCarboxylic groupPolymer chemistryDegradation (geology)β-propiolactonePolymerEster pyrolysisAcrylic acidDie Makromolekulare Chemie
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Core–shell-type multiarm star polyethylenimine-block-poly(ɛ-caprolactone): Synthesis and guest encapsulation potential

2006

Novel multiarm star copolymers with poly(e-caprolactone) (PCL) as the arms and hyperbranched polyethylenimine (HPEI) as the core have been successfully prepared by the tin(II) 2-ethylhexanoate catalyzed ring-opening polymerization of e-caprolactone (CL) with HPEI used directly as a macroinitiator. Not only primary but also secondary amine groups of HPEI participate in initiating the ring-opening polymerization of CL with almost 100% initiation efficiency. The average degree of polymerization of the PCL arms can be controlled by the feed ratio of the monomers to the initiating sites. Because of the polarity difference of the PCL arms and HPEI core, the obtained multiarm star polymers display…

PolyethyleniminePolymers and PlasticsOrganic ChemistryDegree of polymerizationRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerAmine gas treatingCaprolactoneJournal of Polymer Science Part A: Polymer Chemistry
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Covalently Binding of Bovine Serum Albumin to Unsaturated Poly(Globalide-Co-ε-Caprolactone) Nanoparticles by Thiol-Ene Reactions.

2019

When nanoparticles (NPs) are introduced to a biological fluid, different proteins (and other biomolecules) rapidly get adsorbed onto their surface, forming a protein corona capable of giving to the NPs a new "identity" and determine their biological fate. Protein-nanoparticle conjugation can be used in order to promote specific interactions between living systems and nanocarriers. Non-covalent conjugates are less stable and more susceptible to desorption in biological media, which makes the development of engineered nanoparticle surfaces by covalent attachment an interesting topic. In this work, the surface of poly(globalide-co-e-caprolactone) (PGlCL) nanoparticles containing double bonds i…

Polymers and PlasticsNanoparticleBioengineering02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundLactonesMaterials ChemistryAnimalsHumansBovine serum albuminParticle SizeCaproateschemistry.chemical_classificationbiologyThiol-ene reactionBiomoleculeSerum Albumin Bovine021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryCovalent bondbiology.proteinNanoparticlesCattleNanocarriers0210 nano-technologyCaprolactoneBiotechnologyConjugateHeLa CellsMacromolecular bioscience
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Lanthanides benzimidinates: initiators or real catalysts for theɛ-caprolactone polymerization

2000

Polymers and PlasticsOrganic ChemistryCationic polymerizationSolution polymerizationRing-opening polymerizationchemistry.chemical_compoundLiving free-radical polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationOrganic chemistryIonic polymerizationCaprolactoneMacromolecular Rapid Communications
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