PubMed:22360797 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/22360797","sourcedb":"PubMed","sourceid":"22360797","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/22360797","text":"Chemical constituents of the hemiparasitic plant Phoradendron brachystachyum DC Nutt (Viscaceae).\nPhoradendron brachystachyum is a hemiparasitic plant widely distributed in México that belongs to the Viscaceae family. It has been commonly used in folk medicine as a substitute for the European mistletoe. In this chemical study, morolic acid was isolated as the major component (47.54% of the total composition of acetone extract) of this plant. In addition, 19 known compounds were identified: β-sitosteryl and stigmasteryl linoleates, β-sitosterol, stigmasterol, triacontanol, squalene, α- and β-amyrin, lupeol, lupenone, betulin aldehyde, betulon aldehyde, oleanolic aldehyde, betulinic acid, betulonic acid, moronic acid, morolic acid, oleanolic acid, flavonoids acacetin and acacetin 7-methyl ether. There have been no previous reports in the literature on the chemical composition of this potential natural source of hypoglycaemic and antihypertensive compounds.","tracks":[{"project":"CHEMDNER-training-test","denotations":[{"id":"T1","span":{"begin":329,"end":341},"obj":"TRIVIAL"},{"id":"T2","span":{"begin":414,"end":421},"obj":"SYSTEMATIC"},{"id":"T3","span":{"begin":495,"end":535},"obj":"MULTIPLE"},{"id":"T4","span":{"begin":537,"end":549},"obj":"TRIVIAL"},{"id":"T5","span":{"begin":551,"end":563},"obj":"TRIVIAL"},{"id":"T6","span":{"begin":565,"end":577},"obj":"TRIVIAL"},{"id":"T7","span":{"begin":579,"end":604},"obj":"MULTIPLE"},{"id":"T8","span":{"begin":606,"end":612},"obj":"TRIVIAL"},{"id":"T9","span":{"begin":614,"end":622},"obj":"TRIVIAL"},{"id":"T10","span":{"begin":624,"end":640},"obj":"TRIVIAL"},{"id":"T11","span":{"begin":642,"end":658},"obj":"TRIVIAL"},{"id":"T12","span":{"begin":660,"end":678},"obj":"TRIVIAL"},{"id":"T13","span":{"begin":680,"end":694},"obj":"TRIVIAL"},{"id":"T14","span":{"begin":696,"end":710},"obj":"TRIVIAL"},{"id":"T15","span":{"begin":712,"end":724},"obj":"TRIVIAL"},{"id":"T16","span":{"begin":726,"end":738},"obj":"TRIVIAL"},{"id":"T17","span":{"begin":740,"end":754},"obj":"TRIVIAL"},{"id":"T18","span":{"begin":756,"end":766},"obj":"FAMILY"},{"id":"T19","span":{"begin":767,"end":775},"obj":"TRIVIAL"},{"id":"T20","span":{"begin":780,"end":803},"obj":"SYSTEMATIC"}],"attributes":[{"subj":"T1","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T2","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T3","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T4","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T5","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T6","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T7","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T8","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T9","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T10","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T11","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T12","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T13","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T14","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T15","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T16","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T17","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T18","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T19","pred":"source","obj":"CHEMDNER-training-test"},{"subj":"T20","pred":"source","obj":"CHEMDNER-training-test"}]},{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":923,"end":936},"obj":"HP_0001943"}],"attributes":[{"subj":"T1","pred":"source","obj":"PubmedHPO"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"CHEMDNER-training-test","color":"#ecd193","default":true},{"id":"PubmedHPO","color":"#b793ec"}]}]}}