TINGENONA
Espécie de Celastraceae de onde já foi isolado | Acanthathamnus aphyllus,
Austroplenckia populnea, Catha cassinoides, Cassine balae, Cassine pappillosa, Euonymus tingens, Glyptopetalum sclerocarpum, Gymnosporia emarginata, Kokoona ochracea, Maytenus canariensis, Maytenus laevis, Matytenus scutioides, Maytenus catingarum, Maytenus chuchuhuasca, Maytenus ilicifolia, Maytenus buchananii, Maytenus macrosperma, Maytenus obtusifolia, Maytenus horida, Maytenus blepharodes Peritassa campestris, Plenckia populnea, Reissantia indica, Schaefferia cuneifolia, Tripterigium wilfordii. |
Fórmula Molecular | C28H36O3 (420,59) |
PF (0C) | 147-149(CHCl3/éter de
petróleo) 200 (d) 203-204 |
Rotação ótica | [a]D -3410 (c 0,1; MeOH) |
Forma | Cristais vermelho-alaranjado |
IV (filme seco), n (máx; cm-1) | 3324, 2973-2872, 1706, 1595, 1514, 1437, 1289, 1217, 1184, 1084, 870, 756, 677 |
UV (nm, e ) | 210 (3,33); 242 (om 3.02); 288 (om 2,21); 421 (3,16) |
EM (%) | [M]+ 420(15), 406(4), 241(15), 202(100), 201(59), 187(6), 163(13), 135(14), 121(14), 95(29), 69(23), 41(45) |
Atividade biológica | Atividade antibicrobiana contra
bacteria gran positivas Antitumoral, citostático, citotóxica, tripanosomicida Inibidor da produção de IL-1b |
Tipo de derivado (PF)(oC) | Diacetil-dihidrotingenona
(208-210) Mono-O-acetiltingenona (185-186) Monoxido (262) 1,2,5-trimetil-6,7-di-O-acetil-naftaleno (118-119) Di-O-acetilisotingenona III (208-210) 1,2,5-trimetil-6,7-di-O-metil-naftaleno (95-97) |
J.Nat. Prod.
Vol.57 (1), 1-8, 1994 Journal Chemical Society Perkin I, 349-352,
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