Two new triterpenoids from the roots of Pinus densiflora

被引：6
作者：
Otaka, Junnosuke [1 ]
Komatsu, Masabumi [2 ]
Miyazaki, Yasumasa [2 ]
Futamura, Yushi [1 ]
Osada, Hiroyuki [1 ]
机构：
[1] RIKEN Ctr Sustainable Res Sci, Chem Biol Res Grp, Wako, Saitama, Japan
[2] Forestry & Forest Prod Res Inst, Dept Appl Microbiol, Tsukuba, Ibaraki, Japan
来源：
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY | 2017年 / 81卷 / 03期
关键词：
Pinus densiflora; Pinaceae; roots; triterpenoid; ACID-DERIVATIVES; ABIETIC ACID; STEM BARK; CONSTITUENTS; TERPENOIDS;
D O I：
10.1080/09168451.2016.1263149
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Chemical investigation of the roots of Pinus densiflora led to the isolation of two new triterpenoids, (24S)-3-methoxy-24,25-epoxy-lanost-9(11)-ene (1) and 29-acetoxy-3-methoxyserrat-14-en-21-ol (2), together with three known serratene-type triterpenoids (3-5) and four known diterpenoids (6-9). Their structures were determined by spectroscopic analyses.
引用
收藏
页码：449 / 452
页数：4
相关论文
共 24 条
  • [1] ENDOPEROXIDE DITERPENOIDS AND OTHER CONSTITUENTS FROM ABIES-MAROCANA
    BARRERO, AF
    SANCHEZ, JF
    ALVAREZMANZANEDA, EJ
    DORADO, RMM
    HAIDOUR, A
    [J]. PHYTOCHEMISTRY, 1991, 30 (02) : 593 - 597
  • [2] EMMONS GT, 1989, J LIPID RES, V30, P133
  • [3] Catechols from abietic acid:: Synthesis and evaluation as bioactive compounds
    Gigante, B
    Santos, C
    Silva, AM
    Curto, MJM
    Nascimento, MSJ
    Pinto, E
    Pedro, M
    Cerqueira, F
    Pinto, MM
    Duarte, MP
    Laires, A
    Rueff, J
    Gonçalves, J
    Pegado, MI
    Valdeira, ML
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (08) : 1631 - 1638
  • [4] Synthesis and biological evaluation of dehydroabietic acid derivatives
    Gonzalez, Miguel A.
    Perez-Guaita, David
    Correa-Royero, Julieth
    Zapata, Bibiana
    Agudelo, Lee
    Mesa-Arango, Ana
    Betancur-Galvis, Liliana
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (02) : 811 - 816
  • [5] Inhibition of malaria parasite growth by quinomycin A and its derivatives through DNA-intercalating activity
    Hayase, Hiroki
    Watanabe, Nobumoto
    Lim, Chung Liang
    Nogawa, Toshihiko
    Komatsuya, Keisuke
    Kita, Kiyoshi
    Osada, Hiroyuki
    [J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2015, 79 (04) : 633 - 635
  • [6] RESIN ACIDS .4. 12-HYDROXYABIETIC ACID AND ITS REDUCTION
    HERZ, W
    WAHLBORG, HJ
    LLOYD, WD
    SCHULLER, WH
    HEDRICK, GW
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (09) : 3190 - &
  • [7] RK-270A-C, new oxindole derivatives isolated from a microbial metabolites fraction library of Streptomyces sp RK85-270
    Jang, Jun-Pil
    Nogawa, Toshihiko
    Uramoto, Masakazu
    Okano, Akiko
    Futamura, Yushi
    Shimizu, Takeshi
    Takahashi, Shunji
    Jang, Jae-Hyuk
    Ahn, Jong Seog
    Osada, Hiroyuki
    [J]. JOURNAL OF ANTIBIOTICS, 2015, 68 (04) : 293 - 295
  • [8] Antioxidative activities and composition analysis of Pinus densiflora root by ultra high pressure extraction
    Joo, Chul Gue
    Lee, Keun Ha
    Park, Chung
    Lee, Bum Chun
    [J]. JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, 2011, 17 (04) : 712 - 716
  • [9] A New Abietic Acid-Type Diterpene Glucoside from the Needles of Pinus densiflora
    Jung, Mee Jung
    Jung, Hyun Ah
    Kang, Sam Sik
    Hwang, Geum-Sook
    Choi, Jae Sue
    [J]. ARCHIVES OF PHARMACAL RESEARCH, 2009, 32 (12) : 1699 - 1704
  • [10] SOME REACTIONS OF LEVOPIMARIC ACID DIOXIDE
    KANNO, H
    SCHULLER, WH
    LAWRENCE, RV
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1966, 31 (12) : 4138 - &
123