known α-amyrin triterpenoids, ursolic acid (1), 2α,3α-dihydro xyurs-12-ene-28-oic acid (2) andeuscaphic acid (3), and β-amyrin triterpenoid, 3β-hydroxyolean-5,12-diene (4), and α-spinasterol (5) have beenisolated from the fractionated n-butanol ...
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https://www.riss.kr/link?id=A104469626
우미희 (대구가톨릭대학교) ; Soon Jung Byun (Catholic University of Daegu) ; Zhe Fang (Catholic University of Daegu) ; Su Yang Jeong (Catholic University of Daegu) ; Chong Soon Lee (Yeungnam University) ; 손종근 (영남대학교)
2007
English
KCI등재,SCOPUS
학술저널
359-364(6쪽)
0
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
known α-amyrin triterpenoids, ursolic acid (1), 2α,3α-dihydro xyurs-12-ene-28-oic acid (2) andeuscaphic acid (3), and β-amyrin triterpenoid, 3β-hydroxyolean-5,12-diene (4), and α-spinasterol (5) have beenisolated from the fractionated n-butanol ...
known α-amyrin triterpenoids, ursolic acid (1), 2α,3α-dihydro xyurs-12-ene-28-oic acid (2) andeuscaphic acid (3), and β-amyrin triterpenoid, 3β-hydroxyolean-5,12-diene (4), and α-spinasterol (5) have beenisolated from the fractionated n-butanol extracts of the spikes of Prunella vulgaris var. lilacina, guided by DNAtopoisomerases I and II inhibitory activities and cytotoxic activity against human cancer cells. Their structureswere elucidated on the basis of spectroscopic and chemical methods. Compound 4 exhibited significant cytotoxicactivity against human colon adenoblastoma (HT-29), and 5 showed DNA topoisomerase I and II inhibitions.Key words - Prunella vulgaris var. lilacina, DNA topoisomerases I and II inhibitory activities, cytotoxic activity,ursolic acid, 2α,3α-dihydroxyurs-12-ene-28-oic acid, euscaphic acid
참고문헌 (Reference)
1 Bodley, "Topoisomerases as novel targets for cancerchemotherapy" 1315-1319, 1988
2 Grover, "Thestereochemical dependence of d-substituent effect in 13C-NMRspectra" 227-230, 1973
3 Kang, "Synthesis of epaleuritolic acid" 153-156, 1986
4 Fukuda, M, "Synergism between cisplatin and topoisomerase I inhibitors, NB-506 and SN-38" 56 : 789-793, 1996
5 "Mas spectrometry in structural and stereochemicalproblems" 3688-3699, 1963
6 "Configurational studies on hydroxyl groups atC-2 3 and 23 or 24 of oleanane and ursane-type triterpenes by NMRspectroscopy" 1703-1710, 1989
7 "13C NMR Spectroscopy of Amyrins" 151-167, 1987
1 Bodley, "Topoisomerases as novel targets for cancerchemotherapy" 1315-1319, 1988
2 Grover, "Thestereochemical dependence of d-substituent effect in 13C-NMRspectra" 227-230, 1973
3 Kang, "Synthesis of epaleuritolic acid" 153-156, 1986
4 Fukuda, M, "Synergism between cisplatin and topoisomerase I inhibitors, NB-506 and SN-38" 56 : 789-793, 1996
5 "Mas spectrometry in structural and stereochemicalproblems" 3688-3699, 1963
6 "Configurational studies on hydroxyl groups atC-2 3 and 23 or 24 of oleanane and ursane-type triterpenes by NMRspectroscopy" 1703-1710, 1989
7 "13C NMR Spectroscopy of Amyrins" 151-167, 1987
Cytotoxic and Antibacterial Activities of Gossypin
Farnesyl Protein Transferase Inhibitory Componentsof Lithospermum erythrorhizon
Antipruritic Effect of Black Colored Rice
Pharmacognostical Identification of Stem and Root of Ipomoea quamoclit (Linn.)
학술지 이력
연월일 | 이력구분 | 이력상세 | 등재구분 |
---|---|---|---|
2023 | 평가예정 | 해외DB학술지평가 신청대상 (해외등재 학술지 평가) | |
2020-01-01 | 평가 | 등재학술지 유지 (해외등재 학술지 평가) | |
2011-01-01 | 평가 | 등재학술지 유지 (등재유지) | |
2009-01-01 | 평가 | 등재학술지 유지 (등재유지) | |
2006-01-01 | 평가 | 등재학술지 선정 (등재후보2차) | |
2005-01-01 | 평가 | 등재후보 1차 PASS (등재후보1차) | |
2003-07-01 | 평가 | 등재후보학술지 선정 (신규평가) |
학술지 인용정보
기준연도 | WOS-KCI 통합IF(2년) | KCIF(2년) | KCIF(3년) |
---|---|---|---|
2016 | 0.18 | 0.18 | 0.16 |
KCIF(4년) | KCIF(5년) | 중심성지수(3년) | 즉시성지수 |
0.15 | 0.15 | 0.359 | 0.02 |