Application of Residual Dipolar Couplings and Selective Quantitative NOE to Establish the Structures of Tetranortriterpenoids from Xylocarpus rumphii.

Waratchareeyakul, Watcharee; Hellemann, Erich; Gil, Roberto R; Chantrapromma, Kan; Langat, Moses K; Mulholland, Dulcie A

Waratchareeyakul, Watcharee; Hellemann, Erich; Gil, Roberto R; Chantrapromma, Kan; Langat, Moses K; Mulholland, Dulcie A.

Afiliación

Waratchareeyakul W; Natural Products Research Group, Department of Chemistry, Faculty of Engineering and Physical Sciences, University of Surrey , Guildford GU2 7XH, U.K.
Hellemann E; Department of Chemistry, Faculty of Science and Technology, Rambhai Barni Rajabhat University , Chanthaburi 22000, Thailand.
Gil RR; Department of Chemistry, Carnegie Mellon University , Pittsburgh, Pennsylvania 15213, United States.
Chantrapromma K; Department of Chemistry, Carnegie Mellon University , Pittsburgh, Pennsylvania 15213, United States.
Langat MK; Faculty of Science and Technology, Hatyai University , Songkhla 90110, Thailand.
Mulholland DA; Natural Products Research Group, Department of Chemistry, Faculty of Engineering and Physical Sciences, University of Surrey , Guildford GU2 7XH, U.K.

J Nat Prod ; 80(2): 391-402, 2017 02 24.

Article en En | MEDLINE | ID: mdl-28121439

Asunto(s)

Limoninas/aislamiento & purificación; Meliaceae/química; Triterpenos/aislamiento & purificación; Relación Dosis-Respuesta a Droga; Limoninas/química; Limoninas/farmacología; Estructura Molecular; Resonancia Magnética Nuclear Biomolecular/métodos; Estereoisomerismo; Triterpenos/química; Triterpenos/farmacología

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Triterpenos / Meliaceae / Limoninas Idioma: En Revista: J Nat Prod Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

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