citrusinine-i and lupalbigenin

citrusinine-i has been researched along with lupalbigenin* in 1 studies

Other Studies

1 other study(ies) available for citrusinine-i and lupalbigenin

Article	Year
A new flavonoid from the leaves of Atalantia monophylla (L.) DC. Natural product research, 2019, Volume: 33, Issue:8 A new flavonoid, atalantraflavone (1) as well as eight known compounds including atalantoflavone (2), racemoflavone (3), 5,4'-dihydroxy-(3″,4″-dihydro-3″,4″-dihydroxy)-2″,2″-dimethylpyrano-(5″,6″:7,8)-flavone (4), lupalbigenin (5), anabellamide (6), citrusinine I (7), p-hydroxybenzaldehyde (8), and frideline (9), were isolated from the leaves of Atalantia monophylla (L.) DC. Focusing on Alzheimer's disease, acetylcholine esterase (AChE) inhibition and antioxidant activity were evaluated using the modified Ellman's method and the ABTS scavenging assay, respectively. It was found that isoflavonoid 5, lupalbigenin, showed 79% inhibition to AChE and was 1.4-fold stronger than the tacrine standard. In addition, acridone 7, citrusinine I, displayed 90.68% antioxidant activity. Topics: Acridones; Alkaloids; Antioxidants; Cholinesterase Inhibitors; Drug Evaluation, Preclinical; Flavonoids; Isoflavones; Magnetic Resonance Spectroscopy; Molecular Structure; Plant Extracts; Plant Leaves; Rutaceae	2019

Article

Year

A new flavonoid from the leaves of Atalantia monophylla (L.) DC.

Natural product research, 2019, Volume: 33, Issue:8

A new flavonoid, atalantraflavone (1) as well as eight known compounds including atalantoflavone (2), racemoflavone (3), 5,4'-dihydroxy-(3″,4″-dihydro-3″,4″-dihydroxy)-2″,2″-dimethylpyrano-(5″,6″:7,8)-flavone (4), lupalbigenin (5), anabellamide (6), citrusinine I (7), p-hydroxybenzaldehyde (8), and frideline (9), were isolated from the leaves of Atalantia monophylla (L.) DC. Focusing on Alzheimer's disease, acetylcholine esterase (AChE) inhibition and antioxidant activity were evaluated using the modified Ellman's method and the ABTS scavenging assay, respectively. It was found that isoflavonoid 5, lupalbigenin, showed 79% inhibition to AChE and was 1.4-fold stronger than the tacrine standard. In addition, acridone 7, citrusinine I, displayed 90.68% antioxidant activity.

Topics: Acridones; Alkaloids; Antioxidants; Cholinesterase Inhibitors; Drug Evaluation, Preclinical; Flavonoids; Isoflavones; Magnetic Resonance Spectroscopy; Molecular Structure; Plant Extracts; Plant Leaves; Rutaceae

2019