| ²é¿´: 331 | »Ø¸´: 1 | ||
·çÉñzg121ľ³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖúÒÑÓÐ1È˲ÎÓë
|
|
CÆ×Êý¾Ý£º12.14,12.26,12.31,12.58,17.96,19.09,19.33,19.42,19.57,20.17,21.09,21.39,21.59,23.10,24.34,25.34,25.97,28.27,29.21,29.75,31.86,31.90,33.85,35.98, 36.69,37.32,38.81,42.34,45.65,50.10,51.09,55.94,56.67,61.58,70.57,73.94,77.21,77.26,77.45,101.32,121.64 |
» ²ÂÄãϲ»¶
¸ßÖ°µ¥Î»Í¶¼ÆËã»úÏà¹ØµÄ±±ºË»òSCIËÄÇøÆÚ¿¯ÍƼö£¬ÇóÖ§ÕУ¡
ÒѾÓÐ4È˻ظ´
²©Ê¿¶ÁÍêδÀ´Ò»¶¨»áºÃÂð
ÒѾÓÐ25È˻ظ´
µ¼Ê¦ÏëÈÃÎÒ´Ó¶ÀÁ¢Ò»×÷±ä³ÉÁ˹²Ò»µÚÒ»
ÒѾÓÐ9È˻ظ´
µ½Ðµ¥Î»ºó£¬»»ÁËеÄÑо¿·½Ïò£¬Ã»ÓÐÍŶӣ¬³ÖÐø»ýÀÛ2ÇøÒÔÉÏÂÛÎÄ£¬ÄÜÉêÇëµ½ÃæÉÏÂð
ÒѾÓÐ11È˻ظ´
¶Á²©
ÒѾÓÐ4È˻ظ´
JMPT ÆÚ¿¯Í¶¸åÁ÷³Ì
ÒѾÓÐ4È˻ظ´
ÐÄÂöÊÜËð
ÒѾÓÐ5È˻ظ´
SpringerÆÚ¿¯Í¶¸åÇóÖú
ÒѾÓÐ4È˻ظ´
СÂÛÎÄͶ¸å
ÒѾÓÐ3È˻ظ´
ÉêÇë2026Ä격ʿ
ÒѾÓÐ6È˻ظ´

ning-heng
Ìú³æ (ÕýʽдÊÖ)
- Ó¦Öú: 14 (СѧÉú)
- ½ð±Ò: 4676.4
- É¢½ð: 80
- Ìû×Ó: 337
- ÔÚÏß: 42.6Сʱ
- ³æºÅ: 2716254
- ×¢²á: 2013-10-11
- רҵ: Ò©Îﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 . ¦Â-sitosterol ÏàËÆ¶È:82.9% China Journal of Chinese Materia Medica 2002 27 752-754 Studies on the Chemical Constituents in Radix Astilbes Chinensis SUN Hongxiang, YE Yiping, YANG Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside C44H76O6 ÏàËÆ¶È:81.8% Journal of Ethnopharmacology 2011 135 78-87 Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:80.4% The Chinese Pharmaceutical Journal 2000 52 261-273 Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth ¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo) Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-sitosterol laminaribioside ÏàËÆ¶È:78.0% Natural Product Research and Development 2010 22 940-944 Chemical Constituents from Melastoma dodecandrum YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing; Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate C51H90O7 ÏàËÆ¶È:76.1% Natural Product Research and Development 2014 26 197-201 Chemical Constituents from the Roots of Nothapodytes pittosporoides BAI Yong-hua, SONG Qi-shi* Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . iyengaroside-B ÏàËÆ¶È:75.6% Natural Product Research 2002 16 407-413 Steroid and Antibacterial Steroidal Glycosides from Marine Green Alga Codium Iyengarii Borgesen Muhammad Shaiq Ali; Muhammad Saleem; Raghav Yamdagni; Muhammad Ashfaq Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosteroldiglucoside C41H70O11 ÏàËÆ¶È:75.6% Phytochemistry 1999 52 917-921 Two saponins from Pteleopsis hylodendron F.N. Ngounou, Atta-ur-Rahman, M. Iqbal Choudhary, Shahid Malik, Seema Zareen, Riaz Ali, D. Lontsi, B.L. Sondengam Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (6'-O-palmitoyl)-sitosterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:75.6% Journal of Natural Products 1987 Vol 50 881 Sterols and Steryl Glycosides from Urtica dioica Neera Chaurasia, Max Wichtl Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Sitosterol-3-O-¦Â-D-glucosl-6'-O-palmitate ÏàËÆ¶È:75.6% Phytochemical Analysis 1992 3 38-41 Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy Zhao Haoru and Zhao Shoushun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 24-Ethylcholesterol-acetate ÏàËÆ¶È:75.6% Steroids 1989 53 625-638 Sterols of some Clerodendrum species(verbenaceae): Occurrence of the 24¦Á- and 24¦Â-epimers of 24-ethylsterols lacking a ¦¤25-bond Toshihiro Akihisa, Yuzuru Matsubara, Parthasarathi Ghosh, Swapnadip Thakur, Toshitake Tamura, Taro Matsumoto Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-07-25 11:23:56












»Ø¸´´ËÂ¥