| ²é¿´: 910 | »Ø¸´: 4 | |||
ymr1гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï1 C13 NMR 11.97,12.15,14.20,16.90,18.72,19.02,19.83,21.08,21.17,23.04,24.14,26.07,28.24,29.11,30.19,30.83,32.37,33.89,34.52,36.18,38.29,39.92,40.70,42.73,45.80,45.88,55.92,56.13,60.42,67.65,118.83,171.20 |
» ²ÂÄãϲ»¶
Èç¹û´Ë¿ÌÄãÕýÔÚΪ¹ú»ù¸Ðµ½½¹ÂÇ£¬²»·ÁÀ´ÌýÌýÕâÊס¶»ù½ðÖ®Íâ¡·
ÒѾÓÐ4È˻ظ´
ÄÜ·ñÍ˳ö²ÎÓëµÄÃæÉÏÏîÄ¿½â³ýÏÞÏî
ÒѾÓÐ18È˻ظ´
½ñÈÕ²»·Å°ñ£¿Íø´«¹ú×ÔȻԤ¼Æ 8 Ô 27 Èտɲé½á¹û
ÒѾÓÐ21È˻ظ´
¹À¼ÆÊÇÖÜËÄ
ÒѾÓÐ4È˻ظ´
ÎÒÃæÉÏÍêµ°ÁË
ÒѾÓÐ9È˻ظ´
2026¹ú×ÔÈ»º¯ÆÀ·Ñµ½ÕË
ÒѾÓÐ18È˻ظ´
½¨Òé»ù½ð·¢²¼Ìáǰ¸ø³öÃ÷È·µÄʱ¼äµã
ÒѾÓÐ15È˻ظ´
·¶½øÖоÙÒ»ÎĵÄÖÐÐÄ˼Ïë
ÒѾÓÐ7È˻ظ´
ÅóÓÑȦ¿´µ½µÄ
ÒѾÓÐ9È˻ظ´
ÈÃÎÒÖÐÒ»¸öÃæÉϰɣ¡
ÒѾÓÐ16È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ70%£©
ÒѾÓÐ8È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48833.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ymr1: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-23 17:22:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ymr1: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-23 17:22:02
|
²éѯ½á¹û£º¹²²éµ½20545¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:81.2% 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 ̼Æ×Ä£Äâͼ 2 . (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:81.2% 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 ̼Æ×Ä£Äâͼ 3 . stigmastane-3¦Â5,6¦Á-triol ÏàËÆ¶È:81.2% 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 ̼Æ×Ä£Äâͼ 4 . ¦Á-Spinasterol C29H52O3 ÏàËÆ¶È:81.2% 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 ̼Æ×Ä£Äâͼ 5 . ¦Á-stigmastane-3¦Â-5,6¦Â-triol 3,6 diacetate ÏàËÆ¶È:78.7% Phytochemistry 1999 51 439-444 Steroids and a tetracyclic diterpene from Euphorbia boetica Maria-Jose U. Ferreira, Jose R. Ascenso Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5-diol ÏàËÆ¶È:78.1% Planta Medica 1993 59 572-573 Two New Sterols from the Marine Red Alga Gracilaria edulis B. Das and K. V. N. S. Srinivas Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 3b ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 8 . 5¦Á,6¦Â-dihydroxysitosterol C29H52O3 ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 9 . 24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 10 . 5-hydroxy,6-chloro-sitosterol ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 11 . (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 12 . 5¦Á,6¦Â-Dihydroxysitosterol ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 13 . Âó½ÇçÞ-3¦Â,5¦Á,6¦Â-Èý´¼ ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 14 . 5,6-epoxystigmastan-3-ol C29H50O2 ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 15 . 3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé ÏàËÆ¶È:78.1% Chinese Traditional and Herbal Drugs 2010 41 1782-1785 ¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿ ÕÅΰ;ËÎÆôʾ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 17 . (24S)-24-ethy lcholesta-3¦Â,5¦Á,6¦Â-triol C29H52O3 ÏàËÆ¶È:78.1% 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 ̼Æ×Ä£Äâͼ 18 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:78.1% Guihaia 2014 34 160-162 Chemical constituents of the stem and eaves of Baccaur earamiflora NING De-Sheng, WU Yun-Fei, L¨¹ Shi-Hong, PAN Zheng-Hong£± Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:78.1% Guihaia 2014 34 148-150 Chemical constituents from the root of Croton lachynocar pus PAN Zheng-Hong, WU Yun-Fei, NING De-Sheng, WEI Ying-Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 24(S)-24-enthyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:78.1% Journal of Hainan Normal University (Natural Science) 2004 27 153-156 Study on the Chemical Constituents From the Branches and Leaves of Pterospermum menglunense H MA Yan-fang, JIANG Jin-he, ZHAN Rui, LIU Ying, CHEN Ye-gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Â-triol C29H52O3 ÏàËÆ¶È:78.1% Journal of Northwest A & F University (Natural Science Edition) 2011 39 185-189 Studies on the chemical constituents 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 ̼Æ×Ä£Äâͼ |
2Â¥2015-01-23 16:49:09
ymr1
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 51.9
- Ìû×Ó: 29
- ÔÚÏß: 37Сʱ
- ³æºÅ: 3563263
- ×¢²á: 2014-11-27
- רҵ: ÖÐÒ©×ÊÔ´
3Â¥2015-01-23 17:27:10
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48833.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
4Â¥2015-01-23 17:31:32
ymr1
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 51.9
- Ìû×Ó: 29
- ÔÚÏß: 37Сʱ
- ³æºÅ: 3563263
- ×¢²á: 2014-11-27
- רҵ: ÖÐÒ©×ÊÔ´
5Â¥2015-01-23 17:35:13









»Ø¸´´ËÂ¥