Search results for "isomerisation"

showing 6 items of 6 documents

α,β-Dehydroamino acids in naturally occurring peptides

2014

α,β-Dehydroamino acids are naturally occurring non-coded amino acids, found primarily in peptides. The review focuses on the type of α,β-dehydroamino acids, the structure of dehydropeptides, the source of their origin and bioactivity. Dehydropeptides are isolated primarily from bacteria and less often from fungi, marine invertebrates or even higher plants. They reveal mainly antibiotic, antifungal, antitumour, and phytotoxic activity. More than 60 different structures were classified, which often cover broad families of peptides. 37 different structural units containing the α,β-dehydroamino acid residues were shown including various side chains, Z and E isomers, and main modifications: meth…

Dehydroamino acidsStereochemistryClinical BiochemistryPeptideReview ArticleHeterocyclesBiochemistryMethylationResidue (chemistry)IsomerismDepsipeptidesSide chainPeptide bondAmino AcidsDepsipeptidechemistry.chemical_classificationNatural productsbiologyChemistryDehydropeptidesOrganic ChemistryBiological activitybiology.organism_classificationAmino acidBiochemistryZ/E isomerisationPeptidesBacteriaAmino Acids
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Solvent effects on the conformational preferences of model peptoids. MP2 study.

2014

The influence of aqueous environment on the main-chain conformation (ω0, ϕ, and ψ dihedral angles) of two model peptoids: N-acetyl-N-methylglycine N’-methylamide (Ac-N(Me)-Gly-NHMe) (1) and N-acetyl-N-methylglycine N’,N’-dimethylamide (Ac-N(Me)-Gly-NMe2) (2) was investigated by MP2/6-311++G(d,p) method. The Ramachandran maps of both studied molecules with cis and trans configuration of the N-terminal amide bond in the gas phase and in water environment were obtained and all energy minima localized. The polarizable continuum model was applied to estimate the solvation effect on conformation. Energy minima of the Ac-N(Me)-Gly-NHMe and Ac-N(Me)-Gly-NMe2 have been analyzed in terms of the possi…

Models MolecularStereochemistryMolecular ConformationDihedral angleBiochemistryPolarizable continuum modelPeptoidsStructural BiologyDrug DiscoveryWater environmentMolecular BiologyPharmacologysolvent effectMP2ChemistryHydrogen bondOrganic Chemistryconformational analysiscis - trans isomerisationSolvationHydrogen BondingGeneral MedicineN-methylationCrystallographyPCMSolventsMolecular MedicineSolvent effectsCis–trans isomerismRamachandran plotJournal of peptide science : an official publication of the European Peptide Society
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Ab initio study on the low-lying excited states of retinal

1997

Ab initio results for the electronic spectrum of all-trans-retinal and its truncated model 3-methyl-all-trans (10-s-cis)-2,4,6,8,10-undecapentaen-1-al are presented. The study includes geometry determination of the ground state. Vertical excitation energies have been computed using multiconfigurational second-order perturbation theory through the CASPT2 formalism. The lowest singlet excited state in gas phase is predicted to be of nπ∗ character. The lowest triplet state corresponds, however, to a ππ∗ state. The most intense feature of the spectrum is due to the strongly dipole-allowed ππ∗ transition, in accordance with the observed maximum in the one-photon spectra. The vertical excitation …

PhotochemistryChemistryExcited statesAb initioGeneral Physics and AstronomyPerturbation theoryTriplet stateSpectral lineGround statesUNESCO::FÍSICA::Química físicaAb initio quantum chemistry methodsExcited stateOrganic compoundsSolvent effectsTwo-photon spectraIsomerisationAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]Ground stateExcitationOrganic compounds ; Excited states ; Ab initio calculations ; Perturbation theory ; Triplet state ; Solvent effects ; Isomerisation ; Ground states ; Two-photon spectra ; Photochemistry
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The conformation cis of N-acetyl-N-methyl-α,β-dehydroalanine N′-methylamide and saturated analogues

2007

A series of three homologous amino acids derivatives: N-acetyl-N-methyl-α,β–dehydroalanine N′-methylamide (1), N-acetyl-N-methyl-L-alanine N′-methylamide (2), and N-acetyl-N-methyl-DL-alanine N′-methylamide have been synthesised. The racemic species undergoes spontaneous separation into L and D-enantiomers. From these two chiral forms, the structure of L-enantiomer (3) was analysed. The molecules of 1 – 3 adopt the cis arrangement of the N-terminal amide bond. The molecular conformations are similar for 1 (φ, ψ = 94.6(1)°, −1.7(1)°) and 3 (φ, ψ = 111.5(1)°, −23.8(1)°), and also 2 (φ, ψ = −114.8(2)°, 29.5(2)°), if inversion through the chiral C2 carbon is considered. They are stabilised by i…

chemistry.chemical_classificationDouble bondDehydroamino acidsHydrogen bondStereochemistryMethylamidetrans-cis IsomerisationN-methylationSingle crystal structure analysisCondensed Matter PhysicsX-ray diffractionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAmideIntramolecular forceMoleculePeptide bondGeneral Materials ScienceIsomerizationZeitschrift Fur Kristallographie
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N-Methyldehydroamino acids promote a configuration cis of N-methylamide bond

2008

Abstract Dehydroamino acids with a methylated N-terminal tertiary amide bond occur in natural small cyclic peptide toxins. To investigate their conformational preferences a systematic theoretical analysis was performed on N ′-methylamides of N -acetyl- N -methyldehydroamino acids (Ac-Δ(Me)Xaa-NHMe, where Xaa = ( Z )-Abu, ( E )-Abu, Val, ( Z )-Phe, and ( E )-Phe) considering the configuration trans and cis of the tertiary amide bond. The ϕ , ψ potential energy surfaces were calculated at the B3LYP/6-31+G ∗∗ //HF/3-21G level with inclusion of the solvent (water) effect (SCRF method). The conformers localised were fully optimised at the B3LYP/6-31+G ∗∗ in vacuo. The accessible areas of the pot…

chemistry.chemical_classificationN-MethylationNodularinDehydroamino acidsDouble bondStereochemistryHydrogen bondMicrocystinMethylamidePotential energy surfaceCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundchemistryAmidePeptide bondTentoxinPhysical and Theoretical Chemistrytrans–cis isomerisationConformational isomerismIsomerizationCis–trans isomerismJournal of Molecular Structure: THEOCHEM
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Functional molecular materials: supramolecular networks and coordination polymers with optical and/or magnetic properties

2020

El camp dels materials moleculars atrau l’atenció de molts científics degut al gran potencial de la química molecular en el disseny de materials amb un ajust precís de les seues propietats. Els dos projectes tractats en aquesta tesi representen dos temes que destaquen en aquesta àrea, materials de transició d’espín i polímers de coordinació amb propietats òptiques i/o magnètiques, gràcies al seu significant progrés i ràpid desenvolupament en els últims anys. La primera part d’aquesta tesi es basa en l’ús d’enllaços d’hidrogen en el disseny de xarxes multifuncionals de ferro(II) amb transicions d’espín abruptes. El capítol 1 és una introducció a aquest tema des de la perspectiva dels complex…

sonogashira reactionpicolinatespin crossoverUNESCO::QUÍMICAhydrogen bondsferroelectricsiron(II) complexesproton migrationisomerisationsensing experiments:QUÍMICA [UNESCO]
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