| ²é¿´: 293 | »Ø¸´: 1 | ||
ФºÕгæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú bb-48µÄ½á¹¹ ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 11.87,12.00,18.80,19.06,19.40,19.84,21.09,23.07,24.32,26.07,28.27,29.15,31.45,31.90,33.94,36.16,36.49,37.25,39.78,42.09,42.32,45.82,50.13,56.06,56.77,71.79,121.72,127.15,128.56,129.35,140.69,173.58,173.85,175.84 |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú³¬¾§¸ñÌåϵµÄÄÜ´ø½á¹¹¼ÆËã
ÒѾÓÐ7È˻ظ´
ÇóÖúb-¹ÈçÞ´¼µÄ½á¹¹Ê½
ÒѾÓÐ4È˻ظ´
ÇóÖú¹¦ÄܲÄÁÏÓë½á¹¹²ÄÁϵĵÄ׼ȷ¶¨ÒåÓë·ÖÀà
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿laronidaseµÄ»¯Ñ§½á¹¹Ê½ÊÇʲôѽ£¿»òÕß´ÓÄÄÄܲ鵽½á¹¹Ê½
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿Çå³þµÄµ°°×Öʶþ¼¶½á¹¹Í¼
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿¡¾ÇóÖú¡¿Õâ¿ÉÄÜÊÇʲô½á¹¹µÄ¸ß·Ö×Ó
ÒѾÓÐ4È˻ظ´
ÇóÖú½âÎö¾§Ìå½á¹¹µÄһЩÊý¾Ýº¬Òå
ÒѾÓÐ2È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ¸ù¾Ý½á¹¹Ê½ÕÒÌìÈ»²úÎïµÄÀàËÆ½á¹¹
ÒѾÓÐ17È˻ظ´
¡¾ÇóÖú¡¿¿ËÀ³¶÷ϵÁÐÑÕÁϵĴóÖ½ṹ
ÒѾÓÐ25È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿²ËÄñÇóÖú£¬ÈçºÎÓɵ°°×ÖʵÄÒ»¼¶½á¹¹µÃµ½Èý¼¶½á¹¹£¿
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿Ê¯Ä¥Ï©Æ½ÃæÄÜ´ø½á¹¹¼°¼ò²¢¶ÈµÄÎÊÌâ
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿ÇóÖúÒ»¸öÒ©ÎïµÄ¾§Ìå½á¹¹Êý¾Ý£¡
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú-½âÎöHMBC È·¶¨½á¹¹
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿Çó¶àÌǵĸ߼¶½á¹¹Í¼
ÒѾÓÐ16È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ФºÕ: ½ð±Ò+6, ¡ïÓаïÖú 2014-11-28 16:35:08
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ФºÕ: ½ð±Ò+6, ¡ïÓаïÖú 2014-11-28 16:35:08
|
²éѯ½á¹û£º¹²²éµ½7079¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . mixture of ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:82.8% Food Chemistry 2011 127 394-403 Chemical composition and biological activity of Citrus jambhiri Lush Dalia Hamdan, Mahmoud Zaki El-Readi, Ahmad Tahrani, Florian Herrmann, Dorothea Kaufmann, Nawal Farrag, Assem El-Shazly, Michael Wink Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 5 ÏàËÆ¶È:82.8% Molecules 2014 19 4046-4057 Chemical Composition and Biological Activities of Gerbera anandria Fa He, Miao Wang, Minghuan Gao, Min Zhao, Yuhua Bai and Chunjie Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Phytochemistry 2004 65 2463-2470 Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae) Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Stigmasterol ÏàËÆ¶È:82.3% Acta Botanica Yunnanica 1995 17(1) 103-108 CHEMICAL CONSTITUENTS FROM CLERODENDRUM JAPONICUM TIAN Jun, SUN Han-Dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . sitosterol ÏàËÆ¶È:82.3% Chemical & Pharmaceutical Bulletin 1979 27 38-42 Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Chemistry of Natural Compounds 2000 36 595-598 13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Chemistry of Natural Compounds 1999 35 642-645 I3C NMR SPECTRA OF STEROL DERIVATIVES,INTERMEDIATES IN THE SYNTHESIS OF ECDY- AND BRASSINOSTEROIDS N. V. Kovganko, Zh. N. Kashkan,and E. V. Borisov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:82.3% Acta Botanica Boreali-Occidentalia Sinica 2004 24 1292-1294 Chemical constituents from Saussurea polycolea LI Yu-lin, WANG Hong-lun, SUO You-rui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Acta Botanica Sinica 1999 41 107-110 Chemical constituents of the Anemone tomentosa Root Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Journal of Chinese Pharmaceutical Sciences 1999 8 237-240 Chemical Constituents of Stelmatocrypton khasianum Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Journal of Chinese Pharmaceutical Sciences 2005 14 75-78 Chemical Constituents of Hedysarum gmelinii LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Journal of Asian Natural Products Research 2002 4 73-79 A NEW COMPOUND FROM GASTRODIA ELATA BLUME YONG-QING XIAO, LI LI, XIAO-LIN YOU, BAO-LIN BIAN, XIN-MIAO LIANG and YI-TAO WANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . lawsaritol A C29H50O2 ÏàËÆ¶È:82.3% Natural Product Research 1994 4 195-201 Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Natural Product Research 1994 4 195-201 Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Natural Product Research 2006 20 860-865 A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:82.3% Natural Product Research 2008 22 1085-1093 Isolation of antibacterial diterpenoids from Cryptomeria japonica bark Wen-Hsin Li; Shang-Tzen Chang; Shan-Chwen Chang; Hui-Ting Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . stigmasterol ÏàËÆ¶È:82.3% Chemical & Pharmaceutical Bulletin 1998 46 1408-1411 New Sterols and Triterpenoids of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-sitosterol ÏàËÆ¶È:82.3% China Journal of Chinese Materia Medica 2002 27 843-845 Studies on Chemical Constituents in the Root of Hedysarum polybotrys HAI Liqian, LIANG Hong, ZHAO Yuying, DU Niansheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Acta Pharmaceutica Sinica 2002 Vol 37 196-198 STUDIES ON FLAVONIOD CONSTITUENTS OF HEDYSARUM MULTIJUGUM WANG Wei; CHEN Hu-biao; WANG Wen-ming; ZHAO Yu-ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-sitosterol ÏàËÆ¶È:82.3% Natural Product Sciences 2000 6 135-138 Antioxidative Constituents from the Seeds of Cuscuta chinensis Kwon, Yong-Soo; Chang, Bok-Sim; Kim, Chang-Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-11-28 11:05:13














»Ø¸´´ËÂ¥
120