Triterpene Saponins from the Roots of Ilex asprella. Issue 5 (May 2014)
- Record Type:
- Journal Article
- Title:
- Triterpene Saponins from the Roots of Ilex asprella. Issue 5 (May 2014)
- Main Title:
- Triterpene Saponins from the Roots of Ilex asprella
- Authors:
- Lei, Yu
Shi, She‐Po
Song, Yue‐Lin
Bi, Dan
Tu, Peng‐Fei - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Six new triterpene saponins, ilexasprellanosides A–F (<bold>1</bold>–<bold>6</bold>, resp.), together with eleven known compounds were isolated from the roots of <italic>Ilex asprella.</italic> The new saponins were characterized as ursa‐12, 18‐dien‐28‐oic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐xylopyranoside (<bold>1</bold>), 19<italic>α</italic>‐hydroxyursolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐(2′‐<italic>O</italic>‐acetylxylopyranoside) (<bold>2</bold>), 19<italic>α</italic>‐hydroxyursolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside (<bold>3</bold>), 3<italic>β</italic>, 19<italic>α</italic>‐dihydroxyolean‐12‐en‐23, 28‐dioic acid 28‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucopyranoside (<bold>4</bold>), 19<italic>α‐</italic>hydroxyoleanolic acid 3‐<italic>O‐β</italic>‐<sc>D</sc>‐(2′‐<italic>O</italic>‐acetylxylopyranoside) (<bold>5</bold>), 19<italic>α</italic>‐hydroxyoleanolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside (<bold>6</bold>). The structures of the new compounds were elucidated by analysis of their spectroscopic data and chemical degradation. Compounds <bold>2, 4</bold>, oleanolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside, 3‐<italic>β</italic>‐acetoxy‐28‐hydroxyurs‐12‐ene, and pomolic acid showed significant cytotoxic activities against human<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Six new triterpene saponins, ilexasprellanosides A–F (<bold>1</bold>–<bold>6</bold>, resp.), together with eleven known compounds were isolated from the roots of <italic>Ilex asprella.</italic> The new saponins were characterized as ursa‐12, 18‐dien‐28‐oic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐xylopyranoside (<bold>1</bold>), 19<italic>α</italic>‐hydroxyursolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐(2′‐<italic>O</italic>‐acetylxylopyranoside) (<bold>2</bold>), 19<italic>α</italic>‐hydroxyursolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside (<bold>3</bold>), 3<italic>β</italic>, 19<italic>α</italic>‐dihydroxyolean‐12‐en‐23, 28‐dioic acid 28‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucopyranoside (<bold>4</bold>), 19<italic>α‐</italic>hydroxyoleanolic acid 3‐<italic>O‐β</italic>‐<sc>D</sc>‐(2′‐<italic>O</italic>‐acetylxylopyranoside) (<bold>5</bold>), 19<italic>α</italic>‐hydroxyoleanolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside (<bold>6</bold>). The structures of the new compounds were elucidated by analysis of their spectroscopic data and chemical degradation. Compounds <bold>2, 4</bold>, oleanolic acid 3‐<italic>O</italic>‐<italic>β</italic>‐<sc>D</sc>‐glucuronopyranoside, 3‐<italic>β</italic>‐acetoxy‐28‐hydroxyurs‐12‐ene, and pomolic acid showed significant cytotoxic activities against human tumor cell line A549 (<italic>IC</italic><sub>50</sub> values of 1.87, 2.51, 1.41, 3.24, and 5.63 μ<sc>M</sc>, resp.).</p> </abstract> … (more)
- Is Part Of:
- Chemistry & biodiversity. Volume 11:Issue 5(2014:May)
- Journal:
- Chemistry & biodiversity
- Issue:
- Volume 11:Issue 5(2014:May)
- Issue Display:
- Volume 11, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 11
- Issue:
- 5
- Issue Sort Value:
- 2014-0011-0005-0000
- Page Start:
- 767
- Page End:
- 775
- Publication Date:
- 2014-05
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Biodiversity -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1612-1880 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cbdv.201300155 ↗
- Languages:
- English
- ISSNs:
- 1612-1872
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.887500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3541.xml