Search results for "RPE"

showing 10 items of 2566 documents

New Acylated Presenegenin Saponins from Two Species ofMuraltia

2004

Six new acylated bisdesmosidic triterpene glycosides 1–6 were isolated from the roots of Muraltia heisteria (L.) DC., as three inseparable mixtures 1/2, 3/4, and 5/6 of the (E)- and (Z)-3,4,5-trimethoxycinnamoyl derivatives. The compound pair 1/2 along with four known saponins were also isolated from the roots of Muraltia satureioides DC. Their structures were elucidated mainly by spectroscopic experiments including 2D-NMR techniques as 3-O-(β-D-glucopyranosyl)presenegenin 28-{O-β-D-apiofuranosyl-(13)-O-[β-D-xylopyranosyl-(14)]-O-α-L-rhamnopyranosyl-(12)-O-[6-O-acetyl-β-D-galactopyranosyl-(13)]-4-O-[(E)-3,4,5-trimethoxycinnamoyl]-β-D-fucopyranosyl} ester (1) and its (Z)-isomer 2, 3-O-(β-D-g…

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryMuraltia heisteriaGlycosideBiochemistryPresenegeninCatalysisMuraltia satureioidesInorganic ChemistryTriterpeneDrug DiscoveryPhysical and Theoretical ChemistryHelvetica Chimica Acta
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Oplopanone derivatives monoterpene glycosides from Artemisia sieberi

1993

Abstract The aerial parts of Artemisia sieberi yielded three new oplopanone derivatives, three new monoterpene glycosides, a new germacrane alcohol and a monoterpene acid related to nerolidol.

chemistry.chemical_classificationStereochemistryMonoterpeneGlycosidePlant ScienceGeneral MedicineHorticultureBiochemistrychemistry.chemical_compoundchemistryArtemisia sieberiOrganic chemistryMolecular BiologyNerolidolPhytochemistry
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New Triterpene Saponins fromAcanthophyllum pachystegium

2004

Four new triterpenoid saponins, pachystegiosides A (1), B (2), C (3), and D (4), were isolated from the roots of Acanthophyllum pachystegium K. H. Their structures were elucidated by means of a combination of homo- and heteronuclear 2D-NMR techniques (COSY, TOCSY, NOESY, HSQC, and HMBC) and by FAB-MS. The new compounds were characterized as 3-O-{O-β-D-galactopyranosyl-(12)-O-[β-D-xylopyranosyl-(13)]-β-D-glucuronopyranosyl}quillaic acid 28-{O-β-D-xylopyranosyl-(13)-O-β-D-xylopyranosyl-(14)-O-α-L-rhamnopyranosyl-(12)-O-[3,4-di-O-acetyl-β-D-quinovopyranosyl-(14)]-β-D-fucopyranosyl}ester (1), 3-O-{O-β-D-galactopyranosyl-(12)-O-[β-D-xylopyranosyl-(13)]-β-D-glucuronopyranosyl}quillaic acid 28-{O-…

chemistry.chemical_classificationStereochemistryOrganic ChemistryBiochemistryCatalysisInorganic ChemistryQuillaic acidTriterpenoidTriterpenechemistryHeteronuclear moleculeAcanthophyllum pachystegiumDrug DiscoveryPhysical and Theoretical ChemistryTwo-dimensional nuclear magnetic resonance spectroscopyHeteronuclear single quantum coherence spectroscopyHelvetica Chimica Acta
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Acylated Triterpene Saponins from Atroxima libericaStapf

2011

The four new acylated triterpene saponins 1–4, isolated as two pairs of isomers and named libericosides A1/A2 and B1/B2, one pair of isomers 5/6, the (Z)-isomer libericoside C2 (5) being new, one new sucrose ester, atroximoside (7), and eight known compounds were isolated from the roots of Atroxima liberica by repeated MPLC and VLC on normal and reversed-phase silica gel. Their structures were elucidated on the basis of extensive 1D- and 2D-NMR studies (1H- and 13C-NMR, DEPT, COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3-O-β-D-glucopyranosylpresenegenin 28-{O-α-L-arabinopyranosyl-(13)-O-β-D-xylopyranosyl-(14)-O-α-L-rhamnopyranosyl-(12)-4-O-[(E)-3,4-dimethoxycinnamoyl]-β-D-f…

chemistry.chemical_classificationStereochemistryOrganic ChemistryDEPTMass spectrometryBiochemistryCatalysisInorganic ChemistryHuman colon cancerTriterpenechemistryDrug DiscoveryPhysical and Theoretical ChemistryAtroxima libericaTwo-dimensional nuclear magnetic resonance spectroscopyHelvetica Chimica Acta
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Transformation of artemisin into artapshin and 8α-hydroxy-11β,13-dihydrobalchanin

1987

Abstract Partial syntheses of the sesquiterpene lactones artapshin ( 1 ) and 8α-hydroxy-11β, 13-dihydrobalchanin ( 2 ) from artemisin ( 3 ) are described.

chemistry.chemical_classificationStereochemistryOrganic ChemistryDiolEpoxideAlcoholSesquiterpeneBiochemistrychemistry.chemical_compoundTransformation (genetics)ArtemisinechemistryDrug DiscoveryOrganic chemistryLactoneTetrahedron
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Synthesis and evaluation of tritium labelled 10-methylgalanthamine iodide: a novel compound to examine the mechanism of interaction of galanthamine d…

2003

Summary A new promising galanthamine derivative, 10-[ 3 H]methylgalanthamine iodide, was synthesized for binding studies to nicotinic acetylcholine receptors expressed in Torpedo electric ray electroplaques. Galanthamine was reacted with [ 3 H]methyl iodide to yield 10-[ 3 H]methylgalanthamine iodide with a radiochemical yield of >70% and a specific activity of 32 Ci/mmol after purification via solid phase extraction. To test the ligand properties of the radioligand, calcium imaging and electrophysiology of the non-radioactive analogue were performed to obtain an EC50 of 270 nM, a Hill coefficient of 1.9 and the induced cell current. Copyright # 2003 John Wiley & Sons, Ltd.

chemistry.chemical_classificationStereochemistryOrganic ChemistryIodideLigand (biochemistry)BiochemistryMedicinal chemistryChemical synthesisAnalytical Chemistrylaw.inventionchemistry.chemical_compoundNicotinic agonistchemistrylawDrug DiscoveryRadioligandRadiology Nuclear Medicine and imagingSpectroscopyTorpedoAcetylcholine receptorMethyl iodideJournal of Labelled Compounds and Radiopharmaceuticals
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Synthesis of (+)-Isoalantolactone and (+)-Isoalloalantolactone from (−)-Santonin

1992

Abstract This paper reports on the chemical conversion of (−)-santonin into (+)-isoalantolactone and (+)-isoalloalantolactone involving functionality transfer from C 6 to C 8 , refunctionalization of the ring A and the formation of the α-methylene-8 β,12-olide moiety.

chemistry.chemical_classificationStereochemistryOrganic ChemistryRing (chemistry)SesquiterpeneBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryChemical conversionMoietyEnantiomerEnoneLactoneSantoninTetrahedron
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Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides.

2014

The Michael addition of dibenzylamine to (+)-tert-butyl perillate (3) and to (+)-tert-butyl phellandrate (6), derived from (S)-(−)-perillaldehyde (1), resulted in diastereomeric β-amino esters 7A–D in a moderately stereospecific reaction in a ratio of 76:17:6:1. After separation of the diastereoisomers, the major product, cis isomer 7A, was quantitatively isomerized to the minor component, trans-amino ester 7D. All four isomers were transformed to the corresponding β-amino acids 10A–D, which are promising building blocks for the synthesis of β-peptides and 1,3-heterocycles in three steps. The steric effects of the isopropyl group at position 4 and of the α-methyl substituent of (R)-N-benzyl…

chemistry.chemical_classificationStereochemistryOrganic Chemistryasymmetric synthesisDiastereomerSubstituentEnantioselective synthesisFull Research PaperAmino acidlcsh:QD241-441chiralchemistry.chemical_compoundChemistryStereospecificitylcsh:Organic chemistrychemistryMichael additionβ-amino acidMichael reactionlcsh:QStereoselectivitylcsh:Scienceta116IsopropylmonoterpeneBeilstein journal of organic chemistry
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Omphalocarpoidone, a new lanostane-type furano-spiro-γ-lactone from the wood of Tridesmostemon omphalocarpoides Engl. (Sapotaceae)

2013

Abstract Phytochemical studies of the wood and the stem bark of Tridesmostemon omphalocarpoides Engl. (Sapotaceae) led to the isolation of omphalocarpoidone (1), a new lanostane-type furano-spiro-γ-lactone together with β-amyrin acetate (2), taraxerol (3), spinasterol (4), lichexanthone (5), epi-catechin (6), spinasterol 3-O-β- d -glucopyranoside (7), tormentic acid (8), and 1,2,3,4-tetrahydronorharman-1-one (9). Their structures were established on the basis of extensive NMR studies, mass spectrometry, and by comparison of the data with those previously reported in the literature. The structure of the new secondary metabolite was later confirmed by X-ray crystallography. Except for spinast…

chemistry.chemical_classificationStereochemistryTormentic acidPlant ScienceSecondary metaboliteBiologybiology.organism_classificationBiochemistryLanostaneSapotaceaeTaraxerolchemistry.chemical_compoundSpinasterolchemistryTriterpenemedicineOrganic chemistryAgronomy and Crop ScienceLactoneBiotechnologymedicine.drugPhytochemistry Letters
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Flavones, sesquiterpene lactones and glycosides isolated from Centaurea aspera var. Stenophylla

1984

Abstract From the alcoholic extract of Centaurea aspera var. stenophylla benzoic acid, p-hydroxybenzoic acid, apigenin, 6-methoxyluteolin, 11,13-dehydromelitensin, melitensin, stenophyliolide, ethyl-7-O-apigenin-glucuronate and the glucosides of sitosterol and stigmasterol were isolated and characterized. Stenophyllolide was shown to be 9,15-dihydroxygermacra-1(10),4,11-trien-12,6-olide.

chemistry.chemical_classificationStigmasterolFlavonoidGlycosidePlant ScienceGeneral MedicineHorticultureSesquiterpeneBiochemistryFlavoneschemistry.chemical_compoundchemistryCentaurea asperaBotanyApigeninMolecular BiologyBenzoic acidPhytochemistry
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