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1.
Nat Prod Res ; 36(8): 1927-1933, 2022 Apr.
Article in English | MEDLINE | ID: mdl-33107346

ABSTRACT

A new diarylheptanoid, (1 R,2S,3S,5S)-2,3-dihydroxy-3',3''-dimethoxy-4'-de-O-methylcentrolobine (1) and a new bisabolane-type sesquiterpenoid, (1 R,7S)-1,12,13-trihydroxybisabola-3,10-diene (2), together with nineteen known compounds (3-21) were isolated from the EtOH extract of the stems and branches of Viscum coloratum (Kom.) Nakai. Their structures were elucidated by extensive analysis of 1 D and 2 D NMR spectra and from the HRESIMS. All the compounds were evaluated for their cytotoxic activity against eight human tumor cell lines.


Subject(s)
Antineoplastic Agents , Viscum , Diarylheptanoids , Humans , Magnetic Resonance Spectroscopy , Viscum/chemistry
2.
Phytochemistry ; 147: 1-8, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29257999

ABSTRACT

Under the guidance of anti-fungal bioassay, four previously undescribed oleanane-type and one lupane-type triterpenoid saponins, along with twelve known analogues, were isolated from the extract of Sapindus mukorossi pulps. Their structures were determined on the basis of spectroscopic analysis and chemical methods. In vitro biotests, oleanolic acid 3-O-ß-D-xylopyranosyl-(1 â†’ 3)-α-L-rhamnopyranosyl-(1 â†’ 2)-α-L-arabinopyranoside showed inhibitory activity against Trichophyton rubrum with MIC80 value of 8 µg/mL, while oleanolic acid 3-O-α-L-arabinopyranosyl-(1 â†’ 3)-α-L-rhamnopyranosyl-(1 â†’ 2)-α-L-arabinopyranoside exhibited inhibitory activity against both Trichophyton rubrum and Candida albicans with MIC80 values of 8 µg/mL.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Sapindus/chemistry , Saponins/pharmacology , Trichophyton/drug effects , Triterpenes/pharmacology , Antifungal Agents/chemistry , Antifungal Agents/isolation & purification , Candida albicans/cytology , Dose-Response Relationship, Drug , Fruit/chemistry , Microbial Sensitivity Tests , Molecular Conformation , Saponins/chemistry , Saponins/isolation & purification , Structure-Activity Relationship , Triterpenes/chemistry , Triterpenes/isolation & purification
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