1979
DOI: 10.1007/bf00566104
|View full text |Cite
|
Sign up to set email alerts
|

Lupinine alkaloids fromSophora alopecuroides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
4
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 1 publication
0
4
0
Order By: Relevance
“…Furthermore, several 7-(3-amino-2-hydroxypropoxy) flavonoid derivatives exhibited antihypertensive [5][6][7], antihyperglycemic [8], and antiproliferative [9] activity. Isoflavones containing an aminopropanol fragment showed anti-osteoporosis activity, an estrogen effect [10], and anticancer activity [11].In continuation of research on the synthesis of alkaloid-flavonoid conjugates, it seemed interesting to study the possibility of using a hydroxypropane linker to conjugate 7-hydroxyisoflavones and aloperine, which was isolated as a minor constituent from seeds and leaves of Sophora alopecuroides L. [12][13][14][15][16].Modification of this alkaloid was interesting because of its valuable biological properties. Aloperine exhibits antiinflammatory, anti-allergic [17,18], and antiviral activity [19]; inhibits proliferation of HCT116 cancer cells; initiates apoptosis; and interrupts the cell cycle [20].…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…Furthermore, several 7-(3-amino-2-hydroxypropoxy) flavonoid derivatives exhibited antihypertensive [5][6][7], antihyperglycemic [8], and antiproliferative [9] activity. Isoflavones containing an aminopropanol fragment showed anti-osteoporosis activity, an estrogen effect [10], and anticancer activity [11].In continuation of research on the synthesis of alkaloid-flavonoid conjugates, it seemed interesting to study the possibility of using a hydroxypropane linker to conjugate 7-hydroxyisoflavones and aloperine, which was isolated as a minor constituent from seeds and leaves of Sophora alopecuroides L. [12][13][14][15][16].Modification of this alkaloid was interesting because of its valuable biological properties. Aloperine exhibits antiinflammatory, anti-allergic [17,18], and antiviral activity [19]; inhibits proliferation of HCT116 cancer cells; initiates apoptosis; and interrupts the cell cycle [20].…”
mentioning
confidence: 99%
“…In continuation of research on the synthesis of alkaloid-flavonoid conjugates, it seemed interesting to study the possibility of using a hydroxypropane linker to conjugate 7-hydroxyisoflavones and aloperine, which was isolated as a minor constituent from seeds and leaves of Sophora alopecuroides L. [12][13][14][15][16].…”
mentioning
confidence: 99%
“…In continuation of research on the ability of quinolizidine alkaloids to undergo electrophilic substitution on a chromone ring of flavonoids [1-3], we studied the alkaloid aloperine (1) isolated as a minor constituent from seeds and leaves of Sophora alopecuroides L. [4][5][6][7][8] or synthesized by the published methods [9][10][11][12].…”
mentioning
confidence: 99%
“…A series of 8- (aloperin-12-yl)methyl-substituted isoflavone derivatives were synthesized.In continuation of research on the ability of quinolizidine alkaloids to undergo electrophilic substitution on a chromone ring of flavonoids [1-3], we studied the alkaloid aloperine (1) isolated as a minor constituent from seeds and leaves of Sophora alopecuroides L. [4][5][6][7][8] or synthesized by the published methods [9][10][11][12].Aloperine exhibits anti-inflammatory and antiallergic activity [13], which is responsible for its therapeutic effect in treating allergic contact dermatitis and eczema [14]. Furthermore, aloperine is a promising chemotherapy agent with significant antiproliferative activity against HCT116 cancer cells.…”
mentioning
confidence: 99%