Phytochemical Name : Mammea A/AA

Properties Information
PhytoCAT-ID PhytoCAT-2024
Phytochemical name or plant extracts Mammea A/AA
PMID 15787438
Literature evidence Author information: (1)Departamento de Química Farmacéutica, Facultad de Farmacia, Universidad de Salamanca, Campus Unamuno, E-37007, Salamanca, Spain. lopez@usal.es Bioassay-guided fractionation of the CH(2)Cl(2) extract of the leaves of Marila pluricostata led to the isolation of 17 naturally occurring 4-phenylcoumarins, three of them, 5-hydroxy-8,8-dimethyl-4-phenyl-9,10-dihydro-8H-pyrano-[2,3-f]chromen-2-one (1), 5-hydroxy-8,8-dimethyl-4-phenyl-6-propionyl-9,10-dihydro-8H-pyrano-[2,3-f]chromen-2-one (2), and 5,7-dihydroxy-8-(3-methylbut-2-enyl)-4-phenylchromen-2-one (3), are new natural compounds; the remaining (4-17) are known mammea-type coumarins.
IUPAC name 5,7-dihydroxy-6-(3-methylbutanoyl)-8-(3-methylbut-2-enyl)-4-phenylchromen-2-one
Phytochemicals’ class or type of plant extracts Flavonoid
Source of phytochemicals or plant Extracts Marila pluricostata
Geographical availability Colombia, Costa Rica, Ecuador, Nicaragua, Panamá
Plant parts Leaves
Other cancers Breast cancer, Lung cancer, Glioma
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 NA
Potency GI50 = 0.2 μg/mL for MCF-7
Cell line/ mice model MCF-7, H-460, SF-268
Additional information  Cytotoxic potency of the crude CH2 Cl2 extract was mainly due to the 4-phenylcoumarins, of which, mammesin (4), mammea A/AB (10), mesuol (11), and mammea A/AB (12) were the most cytotoxic.
PubChem ID 5281419
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:153156-2
Safety NA