0000000001304698

AUTHOR

Michael Eitel

showing 9 related works from this author

Selective mono-de-O-acetylation of the per-O-acetylated brasilicardin carbohydrate side chain

2021

Abstract Methanol dried over powdered 4 A molecular sieves can be used for a selective mono-de-O-acetylation of the phenolic acetyl group of the per-O-acetyl protected brasilicardin A carbohydrate side chain. This reaction opens a practical procedure for a synthetic access to derivates of the immunosuppressive and cytotoxic natural product brasilicardin A.

Natural product010405 organic chemistryChemistryOrganic ChemistryCarbohydratesAcetylationGeneral MedicineCarbohydrate010402 general chemistryMolecular sieve01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundAcetylationSide chainOrganic chemistryMethanolProtein Processing Post-TranslationalCarbohydrate Research
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Deep metazoan phylogeny: When different genes tell different stories

2013

11 páginas, 4 figuras, 1 tabla.

GenomicsBiologyCnidariaPhylogeneticsGeneticsAnimalsSupermatrixPlacozoaMolecular BiologyGeneEcology Evolution Behavior and SystematicsPhylogenyLong branch attractionGeneticsLikelihood FunctionsModels GeneticPhylogenetic treeCtenophoraBayes TheoremGenomicsRibosomal RNAPoriferaTaxonAnimal evolutionEvolutionary biologyRibosomes
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Structural Optimization of a Pyridinylimidazole Scaffold: Shifting the Selectivity from p38α Mitogen-Activated Protein Kinase to c-Jun N-Terminal Kin…

2018

Starting from known p38α mitogen-activated protein kinase (MAPK) inhibitors, a series of inhibitors of the c-Jun N-terminal kinase (JNK) 3 was obtained. Altering the substitution pattern of the pyridinylimidazole scaffold proved to be effective in shifting the inhibitory activity from the original target p38α MAPK to the closely related JNK3. In particular, a significant improvement for JNK3 selectivity could be achieved by addressing the hydrophobic region I with a small methyl group. Furthermore, additional structural modifications permitted to explore structure–activity relationships. The most potent inhibitor 4-(4-methyl-2-(methylthio)-1H-imidazol-5-yl)-N-(4-morpholinophenyl)pyridin-2-a…

MAPK/ERK pathwaybiology010405 organic chemistryKinaseChemistryStereochemistryGeneral Chemical Engineeringc-junGeneral Chemistry01 natural sciencesArticle0104 chemical scienceslcsh:Chemistry010404 medicinal & biomolecular chemistrylcsh:QD1-999Mitogen-activated protein kinasebiology.proteinTransferaseSelectivityProtein kinase AIC50ACS Omega
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(2S,3S)-2-Azaniumyl-4-[(1S,4aS,4bS,6S,7S,8aS,10aS)-6,7-dihydroxy-2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]-…

2018

The title compound, which crystallized as a methanol and water solvate, C24H41NO5·CH4O·H2O, was obtained by heterologous expression of the brasilicardin gene cluster in the bacterium Amycolatopsis japonicum. In the crystal, the components are linked by numerous hydrogen bonds, generating a three-dimensional network.

crystal structureperhydrophenanthrenelcsh:QD901-999heterologous expressionlcsh:CrystallographyBrasilicardin AIUCrData
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(2S,3S)-2-Azaniumyl-4-[(1S,4aS,4bS,6S,7S,8aS,10aS)-6,7-dihydroxy-2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]-…

2018

The title compound, which crystallized as a methanol and water solvate, C24H41NO5·CH4O·H2O, was obtained by heterologous expression of the brasilicardin gene cluster in the bacterium Amycolatopsis japonicum. In the crystal, the components are linked by numerous hydrogen bonds, generating a three-dimensional network.

010405 organic chemistryHydrogen bondStereochemistryGeneral MedicineMeth-Crystal structure010402 general chemistry01 natural sciences0104 chemical sciencesCrystalchemistry.chemical_compoundchemistryGene clusterHeterologous expressionMethanolMethanol waterIUCrData
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(E)-1-(Pyridin-4-yl)propan-1-one O-tosyl oxime

2017

The title compound, C15H16N2O3S, was obtained by the reaction of (E)-1-(pyridin-4-yl)propan-1-one oxime andpara-toluenesulfonic acid. The pyridine ring makes a dihedral angle of 54.70 (10)° with the benzene ring. In the crystal, molecules are linked by C—H...O hydrogen bonds, forming a chain along thec-axis direction.

pyridinecrystal structureHydrogen bondCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)Oximehydrogen bonding01 natural sciences0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographytosyl oximechemistryTosylPyridinelcsh:QD901-999lcsh:CrystallographyIUCrData
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(E)-1-(Pyridin-4-yl)propan-1-one oxime

2016

The asymmetric unit of the title compound, C8H10N2O, contains two crystallographically independent molecules of slightly different conformation, which are linkedviaan intermolecular O—H...N hydrogen bond. The dihedral angle between the pyridine ring and the oxime plane of moleculeA[2.09 (19)°] is smaller than in moleculeB[16.50 (18)°].

pyridinecrystal structure010405 organic chemistryChemistryStereochemistryHydrogen bondGeneral MedicineCrystal structureDihedral angle010402 general chemistryOximeRing (chemistry)01 natural sciencesoxime0104 chemical sciencesCrystallographychemistry.chemical_compoundPyridinelcsh:QD901-999lcsh:CrystallographyIUCrData
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CCDC 2058115: Experimental Crystal Structure Determination

2021

Related Article: Michael Eitel, Dhafer S. Zinad, Dieter Schollmeyer, Harald Gross, Pierre Koch|2021|Carbohydr.Res.|504|108312|doi:10.1016/j.carres.2021.108312

Space GroupCrystallographyCrystal System4-({3-acetamido-45-bis(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl}oxy)-5-(acetyloxy)-2-methyl-6-[(prop-2-en-1-yl)oxy]oxan-3-yl 3-hydroxybenzoate monohydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1824231: Experimental Crystal Structure Determination

2018

Related Article: Francesco Ansideri, Joana T. Macedo, Michael Eitel, Ahmed El-Gokha, Dhafer S. Zinad, Camilla Scarpellini, Mark Kudolo, Dieter Schollmeyer, Frank M. Boeckler, Bärbel S. Blaum, Stefan A. Laufer, and Pierre Koch|2018|ACS Omega|3|7809|doi:10.1021/acsomega.8b00668

Space GroupCrystallography2-chloro-4-[15-dimethyl-2-(methylsulfanyl)-1H-imidazol-4-yl]pyridineCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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