Fitoterapia
ISSN: 0367-326X
Datasets associated with articles published in Fitoterapia
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- Anti-inflammatory kavalactones from Alpinia zerumbetNMR data of a new kavalactone derivative (aniba dimer C)
- Data for: 2-furyl(phenyl)methanol isolated from Atractilis gummifera rhizome exhibits anti-leishmanial activity Spectral Data of compounds isolated from the rhizome of Atractylis gummifera.
- Data for: Biotransformation of Huperzine A by Irpex lacteus-A Fungal Endophyte of Huperzia serrataIn this file, the HPLC profiles for the biotransformation and the spectroscopic data of the two new compounds were provided.
- Data for: Two new alkaloids isolated from Traditional Chinese Medicine Binglang the fruit of Areca catechu supplementary materials
- Data for: Estrogenic Phytochemical from Labisia pumila (Myrsinaceae) with Selectivity towards Estrogen Receptor Alpha and Beta SubtypesNMR spectra of alkyl resorcinols and a dimeric 1,4-benzoquinone from Labisia pumila. Inclusive of graphs of concentration-response curve for estrogen receptor alpha and beta binding assay and Cytotoxic HL60 assay.
- Data for: Discovery of Betulinaldehyde as a Natural RORγt AgonistHPLC and NMR of Compound 1, 2 and UA
- Data for: Secondary metabolites from the mangrove sediment-derived fungus Penicillium pinophilum SCAU037Summplementary data for the manuscirpt
- Data for: Cytotoxic, antimicrobial and antiviral secondary metabolites produced by the plant pathogenic fungus Cytospora sp. CCTU A309SI for our paper on new compounds from Cytospora
- Data for: Gambogenic Acid Triggers Apoptosis in Human Nasopharyngeal Carcinoma CNE-2Z Cells by Activating Volume-Sensitive Outwardly Rectifying Chloride ChannelSupplementary material for HPLC and MTT experiment.
- Data for: Target discovery of chlorogenic acid derivatives from the flower buds of Lonicera macranthoides and their MAO B inhibitory mechanismFig. S1-S10. HRESIMS, UV, IR and NMR spectra of compound 1 Fig. S11-S19. HRESIMS, UV, IR and NMR spectra of compound 2 Fig. S20-S29. HRESIMS, UV, IR and NMR spectra of compounds 3 Fig. S30-S32. HRESIMS and NMR spectra of compound 4 Fig. S33-S34. HRESIMS and NMR spectra of compound 1a Table 1S. All putative targets of CGAs Table 2S. Top 9 clusters associated with AD targets of CGAs according to the enrichment analysis based on GO and DAVID annotation Fig. S35 The residue contributions of MAO B to Compound 6 binding
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