東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

Phytoceuticals from Hemerocallis flo...

Cichewicz, Robert Henry.

Linked to FindBook

Google Book

Amazon

博客來

Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities./
Author:	Cichewicz, Robert Henry.
Description:	116 p.
Notes:	Source: Dissertation Abstracts International, Volume: 63-09, Section: B, page: 4183.
Contained By:	Dissertation Abstracts International63-09B.
Subject:	Chemistry, Pharmaceutical. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3064210
ISBN:	0493830006

Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities.
Cichewicz, Robert Henry.

Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities. - 116 p.

Source: Dissertation Abstracts International, Volume: 63-09, Section: B, page: 4183.

Thesis (Ph.D.)--Michigan State University, 2002.

Daylilies (Hemerocallis spp., Hemerocailidaceae) are widely consumed in eastern Asian as both a traditional food and medicine. In this study, Hemerocallis flowers and roots were examined in order to identify bioactive constituents that may exhibit antioxidant, anticancer, mosquitocidal, and schistosome inhibitory properties. An investigation of Hemerocallis cv. Stella de Oro flowers lead to the isolation of nine kaempferol, quercetin, and isorhamnetin 3-O-glycosides (1--9), phenethyl beta-D-glucopyranoside (10), orcinol beta-D-glucopyranoside ( 11), phloretin 2'-O-beta- D-glucopyranoside (12), phloretin 2'- O-beta-D-xylopyranosyl-(1 → 6)-beta- D-glucopyranoside (13), a new napthalene-glycoside, stelladerol (14), and an amino acid (longitubanine A) (15). An examination of Hemerocallis fulva 'Kwanzo' Kaempfer roots lead to the isolation of seven new anthraquinones, kwanzoquinones A (16), B (17), C (19), D (20 ), E (21), F (22), and G (24), two known anthraquinones, 2-hydroxychrysophanol (18) and rhein (23), one new naphthalene glycoside, 5-hydroxydianellin ( 26), one known naphthalene glycoside, dianellin (25), one known flavone, 6-methylluteolin (27), and alpha-tocopherol.

ISBN: 0493830006Subjects--Topical Terms:

550957
Chemistry, Pharmaceutical.

Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities.
LDR:03298nmm 2200301 4500 001 1851767
005 20051216102527.5
008 130614s2002 eng d
020 $a 0493830006
035 $a (UnM)AAI3064210
035 $a AAI3064210
040 $a UnM $c UnM
100 1 $a Cichewicz, Robert Henry. $3 1939649
245 1 0 $a Phytoceuticals from Hemerocallis flowers and roots with antioxidant, anticancer, mosquitocidal, and schistosome inhibitory activities.
300 $a 116 p.
500 $a Source: Dissertation Abstracts International, Volume: 63-09, Section: B, page: 4183.
500 $a Adviser: Muraleedharan G. Nair.
502 $a Thesis (Ph.D.)--Michigan State University, 2002.
520 $a Daylilies (Hemerocallis spp., Hemerocailidaceae) are widely consumed in eastern Asian as both a traditional food and medicine. In this study, Hemerocallis flowers and roots were examined in order to identify bioactive constituents that may exhibit antioxidant, anticancer, mosquitocidal, and schistosome inhibitory properties. An investigation of Hemerocallis cv. Stella de Oro flowers lead to the isolation of nine kaempferol, quercetin, and isorhamnetin 3-O-glycosides (1--9), phenethyl beta-D-glucopyranoside (10), orcinol beta-D-glucopyranoside ( 11), phloretin 2'-O-beta- D-glucopyranoside (12), phloretin 2'- O-beta-D-xylopyranosyl-(1 → 6)-beta- D-glucopyranoside (13), a new napthalene-glycoside, stelladerol (14), and an amino acid (longitubanine A) (15). An examination of Hemerocallis fulva 'Kwanzo' Kaempfer roots lead to the isolation of seven new anthraquinones, kwanzoquinones A (16), B (17), C (19), D (20 ), E (21), F (22), and G (24), two known anthraquinones, 2-hydroxychrysophanol (18) and rhein (23), one new naphthalene glycoside, 5-hydroxydianellin ( 26), one known naphthalene glycoside, dianellin (25), one known flavone, 6-methylluteolin (27), and alpha-tocopherol.
520 $a Several new compounds such as kwanzoquinones A (16), B ( 17), C (19), E (21), and kwanzoquinone A and B monoacetates (16a and 17a, respectively) exhibited promising cancer cell growth inhibitory activity. In addition, the known compounds 2-hydroxychrysophanol (18) and rhein (23) inhibited cancer cell growth. Three compounds, kwanzoquinone D (20), stelladerol (14), and 5-hydroxydianellin (26), demonstrated remarkable antioxidant activity by inhibiting lipid oxidation more than 90% in an in vitro assay system. Three compounds, 2-hydroxychrysophanol ( 18) and kwanzoquinones C (19) and E (21), exhibited mosquitocidal properties against fourth instar Ades aegyptii larvae. Two compounds, 2-hydroxychrysophanol (18) and kwanzoquinone E (21), were discovered as novel agents for the prevention and treatment of schistosomiasis. These compounds were found to inhibit the motility and induce mortality in Schistosoma mansoni cercariae and adults. The bioactive constituents from daylilies are being further investigated in order to determine their modes of action and for development as new phytoceuticals.
590 $a School code: 0128.
650 4 $a Chemistry, Pharmaceutical. $3 550957
650 4 $a Health Sciences, Pharmacy. $3 1017737
650 4 $a Health Sciences, Oncology. $3 1018566
690 $a 0491
690 $a 0572
690 $a 0992
710 2 0 $a Michigan State University. $3 676168
773 0 $t Dissertation Abstracts International $g 63-09B.
790 1 0 $a Nair, Muraleedharan G., $e advisor
790 $a 0128
791 $a Ph.D.
792 $a 2002
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3064210