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1 . (8E)-n¨¹zhenide
ÏàËÆ¶È:96.8%
Chemical & Pharmaceutical Bulletin 2002 50(4) 493-497
Studies on the Constituents of Syringa Species. X. Five New Iridoid Glycosides from the Leaves of Syringa reticulata (BLUME) HARA
Koichi MACHIDA, Atsuko KANEKO, Tomokazu HOSOGAI, Rie KAKUDA, Yasunori YAOITA, and Masao KIKUCHI
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
2 . nuezhenide
ÏàËÆ¶È:93.7%
Chinese Pharmaceutical Journal 2011 46 259-262
Chemical Constituents from the Fruits of Ligustrum lucidum
FENG Zhi-yi, FENG Jing, CUI Ying
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
3 . oleonuezhenide
ÏàËÆ¶È:90.6%
Chinese Pharmaceutical Journal 2011 46 259-262
Chemical Constituents from the Fruits of Ligustrum lucidum
FENG Zhi-yi, FENG Jing, CUI Ying
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
4 . (8E)-Å®Õê×ÓÜÕ
C31H42O17 ÏàËÆ¶È:90.6%
Chinese Journal of Medicinal Chemistry 2007 17 173-177
Isolation and identification of iridoid glycosides from Ilex pubescens
YANG Xin, DING Yi, ZHANG Dong-ming
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
5 . Safghanoside F
C38H48O18 ÏàËÆ¶È:88.2%
Chemical & Pharmaceutical Bulletin 2007 55 689-728
Naturally Occurring Secoiridoids and Bioactivity of Naturally Occurring Iridoids and Secoiridoids. A Review, Part 2
Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
6 . 2'-(3',4'-¶þôÇ»ù±½»ù) ÒÒ»ù-(6''-O-ľϬéÜÕ-11-¼×õ¥)-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ
C31H42O18 ÏàËÆ¶È:87.5%
Chinese Journal of Medicinal Chemistry 2007 17 173-177
Isolation and identification of iridoid glycosides from Ilex pubescens
YANG Xin, DING Yi, ZHANG Dong-ming
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
7 . excelside B
C31H42O17 ÏàËÆ¶È:84.3%
Journal of Natural Products 2010 73 2-6
Iridoids from Fraxinus excelsior with Adipocyte Differentiation-Inhibitory and PPAR¦Á Activation Activity
Naisheng Bai, Kan He, Alvin Ibarra, Antoine Bily, Marc Roller, Xiaozhuo Chen and Ralph Rhl
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
8 . 3¡ä-O-¦Â-D-glucopyranosyl ligustroside
C31H42O17 ÏàËÆ¶È:81.2%
Heterocycles 2009 77 557-563
Secoiridoid Di-glycosides from Osmanthus ilicifolius
Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
9 . G 13
ÏàËÆ¶È:81.2%
Chinese Pharmaceutical Journal 2011 46 259-262
Chemical Constituents from the Fruits of Ligustrum lucidum
FENG Zhi-yi, FENG Jing, CUI Ying
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
10 . (8E)-nuezhenide
ÏàËÆ¶È:81.2%
Chemistry & Biodiversity 2013 10 96-128
Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum
Bei-Bei Gao, Gai-Mei She and Dong-Mei She
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
11 . (8E)-Å®Õê×ÓÜÕ
ÏàËÆ¶È:81.2%
Chinese Traditional and Herbal Drugs 2011 42 1894-1899
Chemical constituents from seeds of Syringa oblata
ZHANG, Shu-jun, GUO, Hua-qiang, HAN, Jing, ZHAO, Ming, WANG, Jin-lan
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
12 . angustifolioside B
C31H42O17 ÏàËÆ¶È:78.1%
Phytochemistry 1993 33 1453-1456
Secoiridoids from Fraxinus angustifolia
Ihsan Cäliş, Mohammed Hosny, Taha Khalifa, Sansei Nishibe
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
13 . Excelside B
C31H42O17 ÏàËÆ¶È:78.1%
Chemical & Pharmaceutical Bulletin 2011 59 803-833
Naturally Occurring Iridoids and Secoiridoids. An Updated Review, Part 4
Biswanath DINDA, Sudhan DEBNATH, and Rajarshi BANIK
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
14 . 1'''-O-¦Â-D-glucosylfraxiformoside
C38H48O18 ÏàËÆ¶È:76.4%
Phytochemistry 1994 35 177-181
Secoiridoid glucosides from Fraxinus malacophylla
He Zheng-Dan, Shinichi Ueda, Kenichiro Inoue, Masako Akaji, Tetsuro Fujita, Yang Chong-Ren
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
15 . (8Z)-n¨¹zhenide
C31H42O17 ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin 2002 50(4) 493-497
Studies on the Constituents of Syringa Species. X. Five New Iridoid Glycosides from the Leaves of Syringa reticulata (BLUME) HARA
Koichi MACHIDA, Atsuko KANEKO, Tomokazu HOSOGAI, Rie KAKUDA, Yasunori YAOITA, and Masao KIKUCHI
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
16 . 1'''-O-¦Â-D-glucosylformoside
C38H48O17 ÏàËÆ¶È:75%
Phytochemistry 1993 32 133-136
Five secoiridoid glucosides from Fraxinus formosana
Takao Tanahashi, Hiroko Watanabe, Atsuko Itoh, Naotaka Nagakura, Kenichiro Inoue, Masami Ono, Tetsuro Fujita, Masanori Morita, Cheng-chang Chen
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
17 . 3¡ä-O-¦Â-D-glucopyranosyl oleuropein
C31H42O18 ÏàËÆ¶È:75%
Heterocycles 2009 77 557-563
Secoiridoid Di-glycosides from Osmanthus ilicifolius
Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
18 . 3¡ä-O-¦Â-D-glucopyranosyl 10-hydroxyligustroside
C31H42O18 ÏàËÆ¶È:75%
Heterocycles 2009 77 557-563
Secoiridoid Di-glycosides from Osmanthus ilicifolius
Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
19 . (8Z)-nuezhenide
ÏàËÆ¶È:75%
Chemistry & Biodiversity 2013 10 96-128
Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum
Bei-Bei Gao, Gai-Mei She and Dong-Mei She
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
20 . 3¡ä-O-¦Â-D-glucopyranosyl 10-acetoxyligustroside
C33H44O19 ÏàËÆ¶È:72.7%
Heterocycles 2009 77 557-563
Secoiridoid Di-glycosides from Osmanthus ilicifolius
Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
21 . jasnudifloside K
C33H52O18 ÏàËÆ¶È:71.8%
Chemical & Pharmaceutical Bulletin 2002 50(3) 384-389
Nine New Secoiridoid Glucosides from Jasminum nudiflorum
Yukiko TAKENAKA,Takao TANAHASHI, Hiromi TAGUCHI,Naotaka NAGAKURA, and Toyoyuki NISHI
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
22 . safghanoside B
C32H40O17 ÏàËÆ¶È:71.8%
Phytochemistry 2002 59 779-787
Secoiridoid and iridoid glucosides from Syringa afghanica
Yukiko Takenaka, Naoaki Okazaki, Takao Tanahashi,Naotaka Nagakura, Toyoyuki Nishi
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
23 . escuside
C32H38O19 ÏàËÆ¶È:71.8%
Fitoterapia 2002 73 386-389
Escuside, a new coumarin-secoiridoid from Fraxinus ornus bark
T. Iossifova, B. Vogler, I. Kostova
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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