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[ÇóÖú] ΢Æ×ÇóÖú-10

13C NMR (126 MHz, Pyr) ¦Ä12.57,12.62, 16.05, 18.84, 18.94, 19.61, 19.70, 20.45, 20.83, 21.65, 21.83, 21.98, 23.87, 27.66, 32.57, 33.10, 33.16, 34.88, 36.93, 38.11, 39.56, 41.19, 41.52, 43.20, 43.47, 46.54, 49.48, 50.58, 57.40, 68.01, 71.50, 73.32,130.52.
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huzuyan: ½ð±Ò+10 2013-10-24 09:46:35
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1 .     compound 3a
C31H52O4     ÏàËÆ¶È:66.6%
Phytochemistry          2004          65          2613-2618
Triterpenoidal glycosides from Justicia betonica
Tripetch Kanchanapoom, Pawadee Noiarsa, Somsak Ruchirawat,Ryoji Kasai, Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     ¦Â-Sitosterol
C29H50O     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2007          43          358-359
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXV. STEROLS AND TRITERPENOIDS FROM Astragalus orbiculatus
I. M. Isaev, R. P. Mamedova, M. A. Agzamova, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3 .     (22R,23R,24S)-[26-2H3]-2 -Bromo-3¦Á -hydroxy-22,23-diacetoxy-24-methyl-5 ¦Á-cholestan-6-one
C32H48D3BrO6     ÏàËÆ¶È:66.6%
Steroids          2002          67          587-595
Synthesis of [26-2H3]brassinosteroids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     compound 3
C30H50O5     ÏàËÆ¶È:66.6%
Phytochemistry          1992          31          3965-3968
Two oleanane triterpenes from Anagallis arvensis
Lorenzo de Napoli, Gennaro Piccialli, Vincenzo Piccialli, Ciro Santacroce, Rita Carolla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     ¦Â-sitosterol
    ÏàËÆ¶È:66.6%
Korean Journal of Pharmacognosy          1981          12(1)          12-24
Revision of 13C NMR Assignments of ¦Â-sitosterol and ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside Isolated from Plantago asiatica Seed
Chang, Il-Moo; YunChoi, Hye-Sook; Yamasaki, Kazuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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6 .     ¦Â-sitosterol
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          2005          17          125-127
Chemical Constituents of Tinospora craveniana
LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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7 .     24-methylcholesta-7,22(E)-diene-3¦Â-O-xylopyranoside
C33H54O5     ÏàËÆ¶È:66.6%
Indian Journal of Chemistry Section B          1993          32B          457-459
Chemical examination of a sea cucumber Holothuria spinifera(Holothurideae)
A S R Anjaneyulu, K V S Raju, U V Mallavadhani & C V S Prakash
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:66.6%
Journal of Beijing University of Chemical Technology (Natural Science Edition)          2012          39          40-45
Isolation of the triterpenes from Eriobotrya japonica leaves
CHEN Huan CHEN Guang REN HongMei YANG QuanHua YU ChangYuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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9 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:66.6%
Journal of Chinese Medicinal Materials          2006          29          21-23
Steroids Isolated from Fruit of Hovenia acerba
ZHANG Jing, CHEN Quan-cheng, Young Ho-kim, JONG Seong-kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     stigmasterol
C29H48O     ÏàËÆ¶È:66.6%
Journal of Chinese Medicinal Materials          2009          32          887-890
Studies on the Chemical Constituents of the Stems of Piper betle
YIN Yan, HUANG Xiang-zhong, WANG Jiong, DAI Jian-hui, LIANG Hui, DAI Yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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11 .     aglycone-I
    ÏàËÆ¶È:66.6%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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12 .     (32R,33R,34S)-12¦Á-methyl-32,33,34,35-bacteriohopanetetrol
C36H64O4     ÏàËÆ¶È:63.8%
Tetrahedron          2000          56          3781-3784
The First 12-Methylhopanoid: 12-Methylbacteriohopanetetrol from the Marine Sponge Plakortis simplex
Valeria Costantino, Ernesto Fattorusso, Concetta Imperatore, Alfonso Mangoni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-24 09:28:11
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