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2005112062

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»¯ºÏÎï1    13C NMR (100 MHz, CDCl3) ¦Ä 15.78, 17.88, 19.87, 20.28, 20.70, 21.13, 21.65, 24.31, 25.88, 27.62, 28.18, 29.11, 35.38, 37.4, 38.06, 38.20, 38.63, 38.76, 39.09, 41.87, 43.43, 44.90, 66.36, 66.65, 70.15, 78.30, 78.60, 83.82, 123.36, 123.85, 127.61, 130.23, 135.09, 136.05, 142.79, 152.38, 199.39
»¯ºÏÎï2     13C NMR (100 MHz, CDCl3) ¦Ä 11.98, 12.17, 16.87, 18.74, 19.06, 19.80, 21.20, 23.12, 24.16, 26.24, 28.23, 29.23, 29.70, 30.24, 30.90, 32.41, 33.98, 34.60, 36.18, 38.35, 39.98, 40.80, 42.78, 45.90, 45.94, 55.99, 56.21, 67.64, 76.11, 76.13, 77.20
»¯ºÏÎï3    13C NMR (100 MHz, CDCl3) ¦Ä 11.93, 11.96, 14.07, 17.37, 18.69, 19.03, 19.78, 21.04, 22.66, 23.09, 24.17, 26.14, 28.17, 29.20, 29.34, 29.68, 31.91, 32.06, 32.93, 33.90, 33.95, 35.64, 35.70, 36.10, 38.59, 39.64, 42.39, 45.86, 53.84, 55.89, 56.04, 123.74, 123.75, 171.56, 199.51
»¯ºÏÎï4  13C NMR (101 MHz, CDCl3) ¦Ä 11.84, 11.96, 18.76, 19.03, 19.27, 19.79, 21.02, 23.07, 24.27, 26.10, 27.76, 28.22, 29.16, 29.68, 31.84, 31.88, 33.94, 36.14, 36.56, 36.92, 38.06, 39.70, 42.31, 45.84, 50.02, 56.04, 56.68, 73.96, 122.97, 139.30, 160.61
»¯ºÏÎï5   13C NMR (100 MHz, DMSO) ¦Ä 11.65, 11.76, 18.59, 18.91, 19.07, 19.68, 20.56, 22.58, 23.84, 25.43, 27.76, 28.69, 29.25, 31.35, 31.40, 33.33, 35.45, 36.19, 36.81, 38.29, 41.83, 45.12, 49.58, 55.41, 56.15, 61.07, 70.09, 73.45, 76.73, 76.76, 76.89, 100.77, 121.17, 140.43
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1 .     quadranoside V
C36H56O11     ÏàËÆ¶È:59.4%
Journal of Natural Products          2000          63          496-500
Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     kakisaponin C
C36H58O10     ÏàËÆ¶È:59.4%
Chemical & Pharmaceutical Bulletin          2009          57          532-535
Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki
Guang Chen, Zong-Quan Wang and Ji-Ming Jia
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     adociasulfate 3
C36H54O10S2Na2     ÏàËÆ¶È:59.4%
The Journal of Organic Chemistry          1999          64          5565-5570
Adociasulfates 1−6, Inhibitors of Kinesin Motor Proteins from the Sponge Haliclona (aka Adocia) sp.
Christine L. Blackburn, Cordula Hopmann, Roman Sakowicz, Michael S. Berdelis, Lawrence S. B. Goldstein, and D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     adociasulfate 6
C36H53O6SNa     ÏàËÆ¶È:59.4%
The Journal of Organic Chemistry          1999          64          5565-5570
Adociasulfates 1−6, Inhibitors of Kinesin Motor Proteins from the Sponge Haliclona (aka Adocia) sp.
Christine L. Blackburn, Cordula Hopmann, Roman Sakowicz, Michael S. Berdelis, Lawrence S. B. Goldstein, and D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     Feroniellide E
C35H56O6     ÏàËÆ¶È:59.4%
Natural Product Research          2013          27          753-760
Feroniellides C-E, new apotirucallane triterpenoids from the stem bark of Feroniella lucida
Preecha Phuwapraisirisan, Sitthidesch Sombund, Santi Tip-pyang & Pongpun Siripong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     cumingianoside B
C38H64O11     ÏàËÆ¶È:57.8%
The Journal of Organic Chemistry          1992          57          6946-6953
Anti-tumor agents. 136. Cumingianosides A-F, potent antileukemic new triterpene glucosides, and cumindysosides A and B, trisnor- and tetranortriterpene glucosides with a 14,18-cycloapoeuphane-type skeleton from Dysoxylum cumingianum
Yoshiki Kashiwada, Toshihiro Fujioka, Jer Jang Chang, Ih Sheng Chen, Kunihide Mihashi, Kuo Hsiung Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     pittoviridagenin
C40H62O8     ÏàËÆ¶È:57.5%
Journal of Natural Products          2002          65          65-68
A New Triterpene Saponin from Pittosporum viridiflorum from the Madagascar Rainforest1
Youngwan Seo,John M. Berger, Jeannine Hoch, Kim M. Neddermann, Isia Bursuker,Steven W. Mamber, and David G. I. Kingston
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3-epi-29-acetoxystelliferin E
C36H52O7     ÏàËÆ¶È:56.7%
Journal of Natural Products          2006          69(3)          373-376
Bioactive Isomalabaricane Triterpenoids from Rhabdastrella globostellata that Stabilize the Binding of DNA Polymerase ¦Â to DNA
Jason A. Clement, Mei Li, Sidney M. Hecht, and David G. I. Kingston
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     stelliferin G
C32H48O5     ÏàËÆ¶È:56.7%
Journal of Natural Products          2001          64          389-392
New Cytotoxic Isomalabaricane Triterpenes from the Sponge Jaspis Species
Karina M. Meragelman, Tawnya C. McKee, and Michael R. Boyd
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     3-epi-29-hydroxystelliferin E
C34H50O6     ÏàËÆ¶È:56.7%
Journal of Natural Products          2000          63          205-209
New Isomalabaricane Triterpenes from the Marine Sponge Stelletta globostellata That Induce Morphological Changes in Rat Fibroblasts1
Naoya Oku, Shigeki Matsunaga, Shun-ichi Wada, Shugo Watabe, and Nobuhiro Fusetani
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     compound 1b
    ÏàËÆ¶È:56.7%
Chinese Chemical Letters          2005          16          867-870
Synthesis of Boswellic Acid Derivatives and Primary Research on their Activities
Yan Qiu MENG, Lin Xiang ZHAO, Zan WANG, Dan LIU, Yong Kui JING
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     3-O-¦Â-D-glucopyranosylpyrocincholate
C35H56O8     ÏàËÆ¶È:56.7%
Journal of Asian Natural Products Research          2007          9          505-510
27-Nor-triterpenoid glycosides from the barks of Zygophyllum fabago L
YU-LIN FENG, HE-RAN LI, LI-ZHEN XU and SHI-LIN YANG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     22-O-angeloyltheasapogenol B
C35H58O6     ÏàËÆ¶È:56.7%
China Journal of Chinese Materia Medica          1997          22          228-230
Studies on the Chemical Constituents of Seeds of Camellia sinensis var. Assamica
Wei J unxian , Zuo Qunying and Zhu Yan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     l¦Á,7¦Á-diacetoxyapotirucall-14-ene-3¦Á,21,22,24,25-pentaol
C34H56O9     ÏàËÆ¶È:56.7%
Fitoterapia          2000          71          668-672
A new triterpenoid from Azadirachta indica
Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma,Da-Gang Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     24-ethyllanosta-8,24(24')-diene-3¦Â,22-diol
C32H54O2     ÏàËÆ¶È:56.7%
Phytochemistry          1997          45          499-504
Triterpenoids from Pisolithus tinctorius isolates and ectomycorrhizas
Alfred Baumert, Brigitte Schumann, Andrea Porzel, J¨¹rgen Schmidt, Dieter Strack
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     sigmoside C
C36H60O8     ÏàËÆ¶È:56.7%
Phytochemistry          1997          44          1151-1155
Triterpenoid saponins from Erythrina sigmoidea
J. Tanyi Mbafor, Jean-Claude Ndom, Z. Tanee Fomum
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     isomultiflorenyl acetate
    ÏàËÆ¶È:56.7%
Journal of Natural Products          1991          Vol 54          1564
Application of Inverse-Detected Two-Dimensional Heteronuclear-Correlated Nmr Spectroscopy to the Complete Carbon- 13 Assignment of Isomultiflorenyl Acetate
Robert Faure, Emile M. Gaydou, Eckhard Wollenweber
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     Carpesterol
C37H54O4     ÏàËÆ¶È:56.7%
Phytochemistry          1996          41          935-939
A neolignan and sterols in fruits of Solanum sisymbrifolium
Ajit Kumar Chakravarty, Sibabrata Mukhopadhyay, Subrata Saha, Satyesh Chandra Pakrashi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     cis-karenin
C39H54O6     ÏàËÆ¶È:56.7%
Phytochemistry          1995          39          171-174
Two cytotoxic pentacyclic triterpenoids from Nerium oleander
Bina Shaheen Siddiqui, Sabira Begum, Salimuzzaman Siddiqui, Wolf Lichter
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     trans-karenin
C39H54O6     ÏàËÆ¶È:56.7%
Phytochemistry          1995          39          171-174
Two cytotoxic pentacyclic triterpenoids from Nerium oleander
Bina Shaheen Siddiqui, Sabira Begum, Salimuzzaman Siddiqui, Wolf Lichter
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-02-08 08:07:57
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1 .     stigmastane-3¦Â5,6¦Á-triol
    ÏàËÆ¶È:90.3%
Natural Product Research and Development          2000          12(5)          14-16
STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS
Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¦Á-Spinasterol
C29H52O3     ÏàËÆ¶È:90.3%
Natural Product Research and Development          2011          23          1002-1005
Chemical Constituents from Hypoxis aurea Lour.
CHENG, Zhong-quan, YANG, Dan, MA, Qing-yun, LIU, Yu-qing, ZHOU, Jun, ZHAO, You-xing,
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 3b
    ÏàËÆ¶È:87.0%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:87.0%
China Journal of Chinese Materia Medica          2008          33          1035-1038
Study on Steroids of Cacalia tangutica
LIU Qing, LIU Zhenling, TIAN Xuan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
C29H52O3     ÏàËÆ¶È:87.0%
Journal of Natural Products          1991          Vol 54          1570
3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa
Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     5¦Á,6¦Â-Dihydroxysitosterol
    ÏàËÆ¶È:87.0%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     5,6-epoxystigmastan-3-ol
C29H50O2     ÏàËÆ¶È:87.0%
Chinese Traditional and Herbal Drugs          2005          36          1142-1144
ÇåÏãľ½ª×ӵĻ¯Ñ§³É·ÖÑо¿
ФÓÂ,Öܺ콿,ÑòÏþ¶«,ÕÔ¾²·å,»ÆÈÙ,ÀîÁ¼
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé
    ÏàËÆ¶È:87.0%
Chinese Traditional and Herbal Drugs          2010          41          1782-1785
¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿
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Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:87.0%
Chinese Pharmaceutical Journal          2008          43          897-899
Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook
WANG Yuan, ZOU Zhong-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (24S)-24-ethy lcholesta-3¦Â,5¦Á,6¦Â-triol
C29H52O3     ÏàËÆ¶È:87.0%
Journal of Northwest A&F University (Natural Science)          2011          39          187-189
Studies on the chemical consitituents in Streptocaulon griffithii Hook
XI Peng-zhou, QIN Ya-li, WANG Yue-hu, YAN Yong-ming, ZHANG Yue-jin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     24-methylene-27-methylcholestane-3¦Â,5R,6¦Â-triol
C29H50O3     ÏàËÆ¶È:83.8%
Journal of Natural Products          2007          70          1114-1117
Stellettins L and M, Cytotoxic Isomalabaricane-Type Triterpenes, and Sterols from the Marine Sponge Stelletta tenuis
Hou-wen Lin,Zeng-lei Wang,Jiu-hong Wu, Ning Shi, Hong-jun Zhang,Wan-sheng Chen,Susan L. Morris-Natschke, and An-Shen Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:83.8%
Chemistry of Natural Compounds          2001          37          351-355
13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES
N. V. Kovganko and Yu. G. Chernov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:83.8%
Chemistry of Natural Compounds          2000          36          189-191
NOVEL SYNTHESIS OF (24R,6E)-24-ETHYLCHOLEST-6-HYDROXYIMINO-4-EN-3-ONE, A STEROIDAL OXIME FROM Cinachyrella spp. SPONGES
N. B. Kovganko and Yu. G. Chernov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     5¦Á,6¦Â-dihydroxysitosterol
C29H52O3     ÏàËÆ¶È:83.8%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     stigmastanol glucoside
    ÏàËÆ¶È:83.8%
Fitoterapia          2000          71          722-724
New constituents from Gliricidia sepium
H.M.T.B. Herath, Susila deSilva
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     5-hydroxy,6-chloro-sitosterol
    ÏàËÆ¶È:83.8%
Phytochemistry          1998          47          789-797
On the cytotoxity of oxidized phytosterols isolated from photoautotrophic cell cultures of Chenopodium rubrum tested on meal-worms Tenebrio molitor
Werner Meyer, Harald Jungnickel, Markus Jandke, Konrad Dettner, Gerhard Spiteller
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     (24R)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
C29H52O3     ÏàËÆ¶È:83.8%
Journal of Natural Products          1991          Vol 54          1570
3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa
Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     Âó½ÇçÞ-3¦Â,5¦Á,6¦Â-Èý´¼
    ÏàËÆ¶È:83.8%
Chinese Journal of Marine Drugs          2010          29(2)          6-9
Secondary metabolites from marine actinomycete Strep tomyces sp. ( No. 172221)
MA Jing-jing, T ANG Jin-shan, GAO Hao, HONG Kui, ZHOU Guang-xiong, YAO Xin-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.8%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     (24R)-stigmastan-3¦Â,5¦Á,6¦Â-triol 3-O-¦Â-D-glucopyranoside
C32H62O8     ÏàËÆ¶È:82.8%
Journal of China Pharmaceutical University          2006          37          491-493
A new steroidal glycoside from Lygodium japonicum
ZHANG Lei-hong; FAN Chun-lin; ZHANG Xian-tao; YIN Zhiqi; YE Wen-cai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3Â¥2014-02-08 08:10:47
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1 .     stigmastane-3¦Â,6¦Á-diyl
C33H56O4     ÏàËÆ¶È:77.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     poriferastane-3¦Â,6¦Á-diyl diacetates
C33H56O4     ÏàËÆ¶È:77.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     24-Hydroxy-5¦Á-cholestan-3-one
C29H46O2     ÏàËÆ¶È:75%
Steroids          2002          67          291-304
The synthesis of spermine analogs of the shark aminosterol squalamine
Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Dispiro[cyclohexan-2'-oxiran-3',3''-(2¦Â,3¦Â-dihydro-cyclopropa[3,4]cholestan)]
C34H56O     ÏàËÆ¶È:74.2%
Helvetica Chimica Acta          1976          59          2821-2829
¦Ã-Lakton-cis-anellierung an ¦¤2-und ¦¤3-Cholesten
Reinhard Dammann, Manfred Braun and Dieter Seebach
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ethyl (24R)-24-methylcholestan-3¦Â-ol-26-oate
    ÏàËÆ¶È:72.2%
Chemistry of Natural Compounds          2012          48          606-609
Synthesis of [26-2H3]-campesterin and [26-2H3]-campestanol, deuterated analogs of biosynthetic precursors of 28C-brassinosteroids
V. A. Khripach, V. N. Zhabinskii, Yu. V. Ermolovich and O. V. Gulyakevich
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     vignasterol A
C38H56O4     ÏàËÆ¶È:72.2%
International Journal of Molecular Sciences          2012          13          9754-9768
Constituents from Vigna vexillata and Their Anti-Inflammatory Activity
Yann-Lii Leu, Tsong-Long Hwang, Ping-Chung Kuo, Kun-Pei Liou, Bow-Shin Huang and Guo-Feng Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Vignasterol A
C38H56O4     ÏàËÆ¶È:72.2%
International Journal of Molecular Sciences          2012          13          9754-9768
Constituents from Vigna vexillata and Their Anti-Inflammatory Activity
Yann-Lii Leu, Tsong-Long Hwang, Ping-Chung Kuo, Kun-Pei Liou, Bow-Shin Huang and Guo-Feng Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     24-methylenecholesterol palmitate
C44H76O2     ÏàËÆ¶È:71.4%
Phytochemistry          2008          69          2061-2066
Antioxidant constituents of Nymphaea caerulea flowers
Vijai K. Agnihotri, Hala N. ElSohly, Shabana I. Khan, Troy J. Smillie, Ikhlas A. Khan, Larry A. Walker
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     riisein B
C36H60O10     ÏàËÆ¶È:71.4%
Journal of Natural Products          2000          63          1427-1430
New Cytotoxic Sterol Glycosides from the Octocoral Carijoa (Telesto) riisei
Lenize F. Maia, Rosangela de A. Epifanio, and William Fenical
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     24-Amino-5¦Á-cholestan-3-one
    ÏàËÆ¶È:71.4%
Steroids          2002          67          291-304
The synthesis of spermine analogs of the shark aminosterol squalamine
Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     Di-tert-butyl 4-(2-tert-butoxycarbonylethyl)-4-[3-(5¦Á-cholestan-3¦Á-yl)ureido]heptanedioate
C50H88N2O7     ÏàËÆ¶È:71.4%
Steroids          2007          72          615-626
Synthesis and antimicrobial evaluation of water-soluble, dendritic derivatives of epimeric 5¦Á-cholestan-3-amines and 5¦Á-cholestan-3-yl aminoethanoates
Eko W. Sugandhi, Carla Slebodnick, Joseph O. Falkinham III, Richard D. Gandour
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     ethylpavlovol
    ÏàËÆ¶È:71.4%
Fitoterapia          2005          76          433-438
A new dihydroxysterol from the marine phytoplankton Diacronema sp.
Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 2b
C56H62O5     ÏàËÆ¶È:71.4%
Phytochemistry          1997          46          729-734
Diterpenes of Bahia glandulosa
Ana-L. P¨¦rez-Castorena, Mariano Mart¨ªnez-V¨¢squez, Alfonso Romo de Vivar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (22S,25R)-16¦Â-acetoxy-22,26-N-Cbz-epiminocholest-4-en-3-one
C37H51NO5     ÏàËÆ¶È:71.4%
Journal of Natural Products          1992          Vol 55          1178
On the Synthesis of 4-Keto-Steroidal Alkaloids
Elizabeth Viloria, Gina Meccia, Alfredo N. Usubillaga
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Dispiro[cyclohexan-2'-oxiran-3',3''-(2¦Â,3¦Â-dihydro-cyclopropa[2,3]cholestan)]
C34H56O     ÏàËÆ¶È:71.4%
Helvetica Chimica Acta          1976          59          2821-2829
¦Ã-Lakton-cis-anellierung an ¦¤2-und ¦¤3-Cholesten
Reinhard Dammann, Manfred Braun and Dieter Seebach
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     Cordinoic acid
C30H44O5     ÏàËÆ¶È:71.4%
Chemistry & Biodiversity          2011          Vol.8          850-861
Chemical Constituents of Cordia latifolia and Their Nematicidal Activity
Sabira Begum, Sobiya Perwaiz, Bina S. Siddiqui, Shazia Khan, Shahina Fayyaz, and Musarrat Ramzan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound 1a
C31H32O2     ÏàËÆ¶È:71.4%
Phytochemistry          1987          26          753-754
Iridoid glycosides from Penstemon richardsonii
Birgit Gering,Peter Junior,Max Wichtl
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     Stigmast-5-en-3-O-¦Â-D-glucoside
C35H60O6     ÏàËÆ¶È:71.4%
Magnetic Resonance in Chemistry          2001          39          399-405
Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative
Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     24 ¦Î-n-propyl-cholestan-3-one
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          2010          41          195-197
ºÚÀÏ»¢¸ù»¯Ñ§³É·ÖµÄÑо¿
Íõéª;ÀîÕ¼ÁÖ;»ª»áÃ÷
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ethylpavlovol
    ÏàËÆ¶È:71.4%
Lipids          1993          28          771-773
Identification of two novel dihydroxysterols fromPavlova
Gleen W. Patterson, Patricia K. Gladu, Gary H. Wikfors, Edward J. Parish and Peter D. Livant, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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²éѯ½á¹û£º¹²²éµ½12891¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Sitost-5-en-3¦Â-ol acetate
C31H52O2     ÏàËÆ¶È:93.5%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¡÷5'-3¦Â-OAc (Sitosterol )
    ÏàËÆ¶È:93.5%
Phytochemistry          1989          28          1721-1724
Acylglucosyl sterols from Momordica charantia
Amelia P. Guevara,Clara Y. Lim-Sylianco,Fabian M. Dayrit,Paul Finch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     stigmast-5-ene-3¦Â-yl formate
C30H50O2     ÏàËÆ¶È:93.5%
Journal of Asian Natural products Research          2010          12          424-428
New cytotoxic steroids from the fruits of Syzygium siamense
Parinuch Chumkaew; Shigeru Kato; Kan Chantrapromma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-sitosteryl acetate
    ÏàËÆ¶È:93.5%
Chemical Communications          1978                   319-320
Biosynthesis of ¦Â-sitosterol from [4-13C]mevalonic acid and sodium [1, 2-13C]acetate in tissue cultures of Isodon japonicus hara
Shujiro Seo, Yutaka Tomita and Kazuo Tori
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-Sitosteryl acetate
    ÏàËÆ¶È:93.5%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-Sitosterol acetate
C31H52O2     ÏàËÆ¶È:93.5%
Journal of Chinese Pharmaceutical Sciences          2012          21          428-434
Chemical constituents of Pseudolarix kaempferi Gord
Tianzhi Cai; Wen Qi; Lianmei Yang; Guangzhong Tu; Rong Yang; Kehui Xie; Hongzheng Fu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-(acetyloxy)stigmast-5-ene
    ÏàËÆ¶È:93.5%
Yakugaku Zasshi          1991          111          299-305
Studies on the Anticomplementary Activity of Jozann. Antlcomplementary Activity of Steroid Derivatives
Tsuyoshi EBIHARA, Tomoko KAWAI, Masanori KUROYANAGI, Seigo FUKUSHIMA, Akira UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 2
    ÏàËÆ¶È:90.3%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     compound 1a
C31H32O2     ÏàËÆ¶È:90.3%
Phytochemistry          1987          26          753-754
Iridoid glycosides from Penstemon richardsonii
Birgit Gering,Peter Junior,Max Wichtl
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-Sitosterol acetate
    ÏàËÆ¶È:90.3%
Archives of Pharmacal Research          2005          28          1135-1141
Inhibitory effect on TNF-¦Á-induced IL-8 production in the HT29 cell of constituents from the leaf and stem ofWeigela subsessilis
Phuong Thien Thuong, WenYi Jin, JongPill Lee, RackSeon Seong and Young-Mi Lee, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     4-methoxy1,2-dihydrocyclobutabenzene
C9H10O     ÏàËÆ¶È:90.3%
Journal of Plant Resources and Environment          2011          20          94-96
ÒæÖÇÈʵĻ¯Ñ§³É·Ö
Û¡, ÀÚ, ÍõÖÎÔª, Íõ, Ö¾, Àî, Äþ, Íõ¿ª½ð
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     compound 3
    ÏàËÆ¶È:90.3%
Chinese Journal of Antibiotics          1998          23          401-463
¶¾Á¦³æÃ¹EB-82 ÃðÑÁ¾ú·¢½Í²úÎïµÄÓÐЧ³É·ÖÑо¿¢ñ. ÃðÑÁ¾úËØA µÄ·ÖÀëºÍ½á¹¹¼ø¶¨
Íõº£Ñà, ÐíºèÕÂ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosterol acetate
    ÏàËÆ¶È:87.0%
Chinese Pharmaceutical Journal          2008          43          897-899
Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook
WANG Yuan, ZOU Zhong-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     [(13)C,24,28-(2)H2]clionasteryl acetate
    ÏàËÆ¶È:87.0%
Journal of the Chemical Society, Perkin Transactions 1          1990                   105-109
Biosynthesis of isofucosterol from [2-13C2H3]acetate and [1,2-13C2]acetate in tissue cultures of Physalis peruviana−the stereochemistry of the hydride shift from C-24 to C-25
Shujiro Seo, Atsuko Uomori, Yohko Yoshimura, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi, Ushio Sankawa and Ken'ichi Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     compound Ia
C29H50O     ÏàËÆ¶È:87.0%
Journal of Chemical Sciences          2005          117          263-266
¦Â-Sitosterol-3-O-¦Â-D-xylopyranoside from the flowers of Tridax procumbens Linn.
V K SAXENA and SOSANNA ALBERT
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol benzoate
    ÏàËÆ¶È:84.8%
Planta Medica          1988          54          223-224
Antihepatotoxic Principles of Sambucus formosana
Chun-Nan Lin and Whey-Pin Tome
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-sitosterol-3-O-¦Â-D-xylopyranoside
C34H58O5     ÏàËÆ¶È:84.8%
Chinese Pharmaceutical Journal          1997          32          8-11
Chemical constituents from the seeds of Cuscuta australis
Guo Cheng(Guo C), Han Gongyu(Han GY), Su Zhongwu(Su ZW)
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-sitosterol
    ÏàËÆ¶È:83.8%
Natural Product Sciences          1996          2          19-23
Sterols and Sterol Glycosides from the Leaves of Gynura procumbens
Sadikun, A.; Aminah, I.; Ismail, N.; Ibrahim, P.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     ¦Â-sitosterol
    ÏàËÆ¶È:83.8%
Chinese Traditional and Herbal Drugs          2009          40          1015-1018
Chemical constituents in Tridax procumbens
XU Run-sheng; YUAN Ke; YIN Ming-wen; FANG Lei-jie; MAO Nong-nong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-sitosterol
    ÏàËÆ¶È:83.8%
Journal of Shenyang Pharmaceutical University          2010          27          615-617
Isolation and identification of chemical constituents from stems of Smilax glabra Roxb.
WU Bo, MA Yue-ping, YUAN Jiu-zhi, SUN Qi-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5Â¥2014-02-08 08:14:11
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²éѯ½á¹û£º¹²²éµ½6608¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:100%
Korean Journal of Pharmacognosy          1996          27(1)          75-79
Phytochemical Constituents from Aconitum pseudolaeve Var. erectum
Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-Sitosterol-3-O-¦Â-D-glycoside
    ÏàËÆ¶È:100%
Archives of Pharmacal Research          2004          27          1016-1019
A new sesquiterpene lactone from Artemisia rubripes nakai
Kyu Ha Lee, Yong Deuk Min, Sang Zin Choi, Hak Cheol Kwon and Ock Ryun Cho, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     ¦Â-Sitosterol-3-O-glucoside
    ÏàËÆ¶È:100%
Archives of Pharmacal Research          2005          28          39-43
Antitumor and antiinflammatory constituents from celtis sinensis
Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Stigmast-5-en-3-O-¦Â-D-glucoside
C35H60O6     ÏàËÆ¶È:97.1%
Magnetic Resonance in Chemistry          2001          39          399-405
Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative
Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     daucosterol
C35H60O4     ÏàËÆ¶È:97.1%
Chinese Journal of Natural Medicines          2006          4          257-259
Chemical Constituents of Sibiraea angustata
TAO Ting-Ting; SEI Yasuo; WANG Tian-Zhi; BAI Chuan; CHANG Yan-Bo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:97.1%
Archives of Pharmacal Research          2002          25          628-635
Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines
Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-daucosterol
    ÏàËÆ¶È:97.1%
Chinese Pharmaceutical Journal          2011          46          341-343
Chemical Constituents of Lysimachia clethroides Duby
YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     daucosterol
    ÏàËÆ¶È:97.1%
Chinese Journal of Medicinal Chemistry          2006          16          303-305
The constituents of Veratrum japonicum Loes. f.
ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
Journal of Shenyang Pharmaceutical University          2008          25          630-632
Chemical constituents from the fruits of Xanthium sibiricum
DAI Ying-hui, CUI Zheng, WANG Dong, LI Jian-lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     daucosterol
    ÏàËÆ¶È:97.1%
Natural Product Research and Development          2009          21          784-786
Study on the Chemical Constituents of Fruits of Cannabis Sativa L.
SHEN Qian;CAI Guang-ming; HE Gui-xia; DU Fang-lu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     daucosterol
    ÏàËÆ¶È:97.1%
Natural Product Research and Development          2008          20          60-62
Chemical Constituents from the Defatted Seeds of Linum usitatissimum L.
SHI Gao-feng; SUN Hao-ran;ZHAO Yan-fang; CHEN Xue-fu; QI Zhi-guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
Natural Product Research and Development          1998          10(3)          15-19
CHEMICAL STUDY OF RABDOSIA COETSA
Wang Jianzhong; Wang Fengpeng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
Chinese Traditional and Herbal Drugs          2013          44          133-136
Chemical constituents in roots of Phyllanthus emblica
ZHAO Qin, LIANG Rui-jun, ZHANG Yu-jie, HONG Ai-hua, WANG Yi-fei, CEN Ying-zhou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     ¦Â-Sitosterol Glucoside
    ÏàËÆ¶È:97.1%
Journal of Agricultural and Food Chemistry          2010          58          180-186
Bioactive Compounds from Sour Orange Inhibit Colon Cancer Cell Proliferation and Induce Cell Cycle Arrest
G. K. Jayaprakasha, Y. Jadegoud, G. A. Nagana Gowda and Bhimanagouda S. Patil
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     daucosterol
    ÏàËÆ¶È:97.1%
Chinese Traditional and Herbal Drugs          2012          43          1905-1909
Resource chemical constituents from sarcocarp of Ziziphus jujuba var. spinosa
GUO Sheng; DUAN Jin-ao; ZHAO Jin-long; QIAN Ye-fei; TANG Yu-ping; QIAN Da-wei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-ºúÂܲ·ÜÕ
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2012          37          1408-1411
¦Á-glucosidase inhibitory active constituents contained in nutshell of Trapa acornis
CHEN Baiquan; ZHANG Qian; WANG Wei; HUANG Huan; KANG Wenyi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     7¦Â-hydroxysitosterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:97.1%
Lishizhen Medicine and Materia Medica Research          2012          23          1-2
Chemical Constituents from Angiopteris Fokiensis
WEN Xiao-qiong; HU Ying; ZENG Xiao-jun; ZHANG Lei; CEN Ying-zhou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
Natural Product Research and Development          2011          23          404-409
Chemical Constituents from Acorus tatarinowii
TONG, Xiao-gang, CHENG, Yong-xian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     daucosterol
    ÏàËÆ¶È:97.1%
Marine Sciences          2009          33          81-86
Chemical constituents of EN-22, an endophytic fungus derived from the marine red alga Polysiphonia urceolata
ZHAO Ting-ting, LI Xiao-ming, LI Jing-mei, LI Ke, CUI Chuan-ming, LI Chun-shun, WANG Bin-gui
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-Sitosterol ¦Â-D-glucopyranoside
    ÏàËÆ¶È:97.0%
Korean Journal of Pharmacognosy          2007          38(4)          354-357
Isolation of Two Steroids and a Triterpenoid from the Roots of Potentilla discolor
Park, Hee-Juhn; Lee, Kyung-Tae; Park, Jong-Hee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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1 .     Sitost-5-en-3¦Â-ol acetate
C31H52O2     ÏàËÆ¶È:93.5%
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