FN Archimer Export Format
PT J
TI Cytotoxic and Anti-Inflammatory Effects of Ent-Kaurane Derivatives Isolated from the Alpine Plant Sideritis hyssopifolia
BT 
AF Aimond, Axelle
   Calabro, Kevin
   Audoin, Coralie
   Olivier, Elodie
   Dutot, Mélody
   Buron, Pauline
   Rat, Patrice
   Laprévote, Olivier
   Prado, Soizic
   Roulland, Emmanuel
   Thomas, Olivier P.
   Genta-Jouve, Grégory
AS 1:1,2;2:3;3:2;4:1;5:1;6:1;7:1;8:1;9:4;10:4;11:3;12:1,5;
FF 1:;2:;3:;4:;5:;6:;7:;8:;9:;10:;11:;12:;
C1 Laboratoire de Chimie-Toxicologie Analytique et Cellulaire (C-TAC) UMR CNRS 8038 CiTCoM Université Paris-Descartes, 4, Avenue de l’Observatoire, 75006 Paris, France
   Laboratoires Clarins, 5 Rue Ampère, 95300 Pontoise, France
   Marine Biodiscovery, School of Chemistry and Ryan Institute, National University of Ireland Galway (NUI Galway), University Road, H91 TK33 Galway, Ireland
   Muséum National d’Histoire Naturelle, Unité Molécules de Communication et Adaptation des Micro-Organismes, UMR 7245, CP 54, 57 rue Cuvier, 75005 Paris, France
   Laboratoire Ecologie, Evolution, Interactions des Systèmes Amazoniens (LEEISA), USR 3456, Université De Guyane, CNRS Guyane, 275 Route de Montabo, 97334 Cayenne, French Guiana
C2 UNIV PARIS 04, FRANCE
   LAB CLARINS, FRANCE
   UNIV NATL IRELAND, IRELAND
   MNHN, FRANCE
   CNRS, FRANCE
UM LEEISA
IN WOS Cotutelle UMR
   DOAJ
   copubli-france
   copubli-europe
IF 0.182
TC 5
UR https://archimer.ifremer.fr/doc/00610/72214/71012.pdf
   https://archimer.ifremer.fr/doc/00610/72214/71013.pdf
LA English
DT Article
DE ;Sideritis hyssopifolia;ent-kaurane;anti-inflammatory;NMR
AB This paper reports the isolation and structural characterization of four new ent-kaurane derivatives from the Lamiaceae plant Sideritis hyssopifolia. Planar structures and relative configurations were determined using both mass spectrometry and nuclear magnetic resonance (1D and 2D). Absolute configurations were determined by comparing experimental and theoretical electronic circular dichroism spectra. The cytotoxic and microbial activities of all new compounds were tested. Compounds that were non-cytotoxic were further evaluated for anti-inflammatory activity. 
PY 2020
PD FEB
SO Molecules
SN 1420-3049
PU MDPI AG
VL 25
IS 3
UT 000515384800159
DI 10.3390/molecules25030589
ID 72214
ER

EF