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2005112062

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13C NMR (MeOD)   12.36, 12.62, 17.33, 19.33, 19.44, 20.20, 22.32, 24.18, 25.23, 27.21, 29.38, 30.42, 31.62, 31.66, 33.48, 35.13, 35.27, 37.45, 39.33, 41.42, 41.50, 43.93, 46.59, 47.30, 57.46, 57.59, 68.35, 76.53, 76.88
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lifeliuyan

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À±±ÊvСÐÂ: ½ð±Ò+2, Gu li ying zhu 2014-02-09 06:27:10
²éѯ½á¹û£º¹²²éµ½11932¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     3,5,6-trihydroxysitostane
    ÏàËÆ¶È:100%
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
2 .     compound 3b
    ÏàËÆ¶È:93.1%
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
3 .     compound 5a
    ÏàËÆ¶È:93.1%
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 .     (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
C29H52O3     ÏàËÆ¶È:93.1%
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
5 .     (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:93.1%
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
6 .     (24S)-24-ethy lcholesta-3¦Â,5¦Á,6¦Â-triol
C29H52O3     ÏàËÆ¶È:93.1%
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
7 .     24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:89.6%
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
8 .     (24R)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol
C29H52O3     ÏàËÆ¶È:89.6%
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
9 .     5¦Á,6¦Â-Dihydroxysitosterol
    ÏàËÆ¶È:89.6%
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
10 .     5,6-epoxystigmastan-3-ol
C29H50O2     ÏàËÆ¶È:89.6%
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
11 .     (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol
    ÏàËÆ¶È:89.6%
Chinese Journal of Applied & Environmental Biology          2009          15          615-620
Chemical Constituents from Polygonum perfoliatum
LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé
    ÏàËÆ¶È:86.2%
Chinese Traditional and Herbal Drugs          2010          41          1782-1785
¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿
ÕÅΰ;ËÎÆôʾ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     stigmastane-3¦Â5,6¦Á-triol
    ÏàËÆ¶È:86.2%
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
14 .     ¦Á-Spinasterol
C29H52O3     ÏàËÆ¶È:86.2%
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
15 .     zahramycin A
C28H48O3     ÏàËÆ¶È:82.7%
Zeitschrift f¨¹r Naturforschung B          2013          68          939-945
Zahramycins A-B, Two New Steroids from the Coral Sarcophyton trocheliophorum
Mohamed Shaaban, Mohamed A. Ghani and Khaled A. Shaaban
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-02-08 13:06:27
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

2005112062

ľ³æ (ÕýʽдÊÖ)

Ê®·Ö¸Ðл ÍþÎäµÄ°æÖ÷
3Â¥2014-02-08 21:18:27
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

flowyang

Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

ÒýÓûØÌû:
2Â¥: Originally posted by lifeliuyan at 2014-02-08 13:06:27
²éѯ½á¹û£º¹²²éµ½11932¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     3,5,6-trihydroxysitostane
    ÏàËÆ¶È:100%
Phytochemistry          1998          47          789-797
On the cytotoxity of oxidized phytos ...

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4Â¥2014-02-09 00:43:13
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

ÒýÓûØÌû:
4Â¥: Originally posted by flowyang at 2014-02-09 00:43:13
°æÖ÷ÍþÎ䣬ÕâÊÇÓÃʲô²éµÄ£¿Ì«ÔÞÁË£¡...

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