| ²é¿´: 252 | »Ø¸´: 1 | ||
dylhdaר¼Ò¹ËÎÊ (ÖøÃûдÊÖ)
|
[ÇóÖú]
άÆ×ÇóÖú£¬¼±Çó ÒÑÓÐ1È˲ÎÓë
|
|
13.1,13.9,14.3,17.8,18.4,19.4,19.9,20.2,20.9,21.1,22.9,23.6,28.8,29.6,30.3,30.8,32.1,33.3,34.9,37.1,37.2,39.6,39.9,43.0,44.8,51.3,51.9,56.4,65.8,66.7,79.6,82.4,129.1,131.0,131.1,132.5,135.4,135.6. ¼±Çó£¬Ð»Ð» |
» ²ÂÄãϲ»¶
£¨µ÷¼Á£©Ò»Ö¾Ô¸±¨¿¼¹þ¶û±õ¹¤Òµ´óѧ0857×ÊÔ´Óë»·¾³×¨Òµ378·Ö¿¼Éú
ÒѾÓÐ4È˻ظ´
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ8È˻ظ´
²ÄÁÏÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸ ½ÄÏ´óѧ 085602 »¯¹¤×¨Ë¶ 338·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ085600Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÁ½¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
άÆ×Êý¾Ý²éѯÇóÖú£¬¡µ70%
ÒѾÓÐ4È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúάÆ×Êý¾Ý£¬¿ÉÄÜÊǽṹºÜ¶Ô³ÆµÄ»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
½¨ÒéȺÖ÷¿ªÒ»¸ö΢Æ×ÇóÖúרÀ¸°É
ÒѾÓÐ14È˻ظ´
ÇóÖúESR¸ßÊÖ½âÆ×
ÒѾÓÐ14È˻ظ´
50½ð±ÒÇóÖúºË´ÅÁׯ×
ÒѾÓÐ8È˻ظ´
ÇóÖú HÆ×ºÍCÆ×
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú¸ßÊÖ½âÇâÆ×
ÒѾÓÐ16È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÎöÁׯ×
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿¿Ç¾ÛÌÇÊÇ·ñÓж¾ÐÔ
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿¼±ÇóÌմɽéµçÎÂÆ×²âÁ¿
ÒѾÓÐ14È˻ظ´
¡¾ÇóÖú¡¿ATRºìÍâÆ×ͼ³öÏÖ·´Ïà·å
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿H NMRͼÆ×·ÖÎö£¨Òѽâ¾ö£©
ÒѾÓÐ37È˻ظ´
¡¾ÇóÖú¡¿¼±ÇóºË´ÅÆ×ͼ½âÎö
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿¼±Çó½âÊÍÒ»ÏÂESI-MSÆ×
ÒѾÓÐ3È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-10 18:23:15
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-10 18:23:15
|
²éѯ½á¹û£º¹²²éµ½2111¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5¦Á,8¦Á-epidioxyergosta-6,22-dien-3¦Â-yl stearate C46H78O4 ÏàËÆ¶È:78.9% Planta Medica 2003 69 628-631 Inhibitory Effect of Sterols from Ruprechtia triflora and Diterpenes from Calceolaria pinnifolia on the Growth of Mycobacterium tuberculosis Girma M.Woldemichael,Scott G.Franzblau,Fangqiu Zhang,Yuehong Wang,Barbara N.Timmermann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-¦Â-D-Glucopyranosyl-22E,24R-5¦Á,8¦Á-epidioxyergosta-6,22-diene ÏàËÆ¶È:73.6% Chinese Pharmaceutical Journal 2012 47 1285-1288 Chemical constituents of Ramaria flava LIU Kun; WANG Jun-li; ZHAO Le; XU Dong-ting; LI Jian-fei; ZHANG Lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5¦Á,8¦Á-epidioxy-24(R)-methylcholesta-6,22-dien-3¦Â-D-glucopyranoside C34H54O8 ÏàËÆ¶È:71.0% Phytochemistry 1999 51 891-898 Antitumor sterols from the mycelia of Cordyceps sinensis Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-O-glucopyranosyl-5,8-epidioxyergosta-6,22-diene C34H54O8 ÏàËÆ¶È:68.4% Phytochemistry 1991 30 4117-4120 Glycosides of ergosterol derivatives from Hericum erinacens Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . axinysasterol p-bromobenzoate ÏàËÆ¶È:68.4% Chinese Journal of Marine Drugs 1994 4 1-5 STUDIES ON THE CONSTITUENTS OF MARINE SPONGE AXINYSSA SP. Yang Zhi, Iguchi Kazuo, Yamada Yasuji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . axinysterol p-bromobenzoate ÏàËÆ¶È:68.4% Steroids 1993 58 410-413 A new 5¦Á,8¦Á-epidioxy sterol from the okinawan marine sponge of the Axinyssa genus Kazuo Iguchi, Hiromi Shimura, Zhi Yang, Yasuji Yamada Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Ergosterol peroxide 3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:68.4% European Journal of Plant Pathology 2012 134 239-247 Toxins from a symbiotic fungus, Leptographium qinlingensis associated with Dendroctonus armandi and their in vitro toxicities to Pinus armandi seedlings Xiao-Jun Li, Jin-Ming Gao, Hui Chen, An-Ling Zhang, Ming Tang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Stigmastanol-3¦Â-p-butanoxydihydrocoumaroate C42H68O3 ÏàËÆ¶È:66.6% Phytochemical Analysis 2006 17 36-45 Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381) Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 10-acetoxy-9-hydroxy-and 9-acetoxy-10-hydroxy-amphilecta-8,10,12,14-tetraenes C22H30O3 ÏàËÆ¶È:65.8% Tetrahedron 2006 62 4205-4213 Further studies on the constituents of the gorgonian octocoral Pseudopterogorgia elisabethae collected in San Andr¨¦s and Providencia islands, Colombian Caribbean: isolation of a putative biosynthetic intermediate leading to erogorgiaene Carmenza Duque, M¨®nica Puyana, Leonardo Castellanos, Andrea Arias, Hebelin Correa, Oscar Osorno, Teigo Asai, Noriyuki Hara, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . mixture of 10-acetoxy-9-hydroxy-and 9-acetoxy-10-hydroxy-amphilecta-8,10,12,14-tetraenes C22H30O3 ÏàËÆ¶È:65.8% Tetrahedron 2006 62 4205-4213 Further studies on the constituents of the gorgonian octocoral Pseudopterogorgia elisabethae collected in San Andr¨¦s and Providencia islands, Colombian Caribbean: isolation of a putative biosynthetic intermediate leading to erogorgiaene Carmenza Duque, M¨®nica Puyana, Leonardo Castellanos, Andrea Arias, Hebelin Correa, Oscar Osorno, Teigo Asai, Noriyuki Hara, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 29 C36H56N2O6 ÏàËÆ¶È:65.7% Journal of Natural Products 1998 61 1491-1496 Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Á-(3'-butylcarboxyacetoxy)oxepanoquercinic acid C C38H60O8 ÏàËÆ¶È:65.7% Fitoterapia 2009 80 263-266 Antibacterial triterpenes from the threatened wood-decay fungus Fomitopsis rosea Milena Popova, Boryana Trusheva, Melania Gyosheva, Iva Tsvetkova, Vassya Bankova Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . euphol 3-O-cinnamate C39H56O2 ÏàËÆ¶È:65.7% Phytochemistry 1990 29 1625-1628 Constituents of the latex of Euphorbia antiquorum Mohan B. Gewali,Masao Hattori,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Methyl (3¦Â)-3-(Benzoyloxy)-12-oxo-8,14-secoursa-8,13-dien-28-oate C38H50O5 ÏàËÆ¶È:65.7% Helvetica Chimica Acta 2012 95 1026-1032 Synthesis of Novel 8,14-Secoursane Derivatives: Key Intermediates for the Preparation of Chiral Decalin Synthons from Ursolic Acid Chongnan Zhang, Haijun Yang, Guangying L¨¹, Cailin Liu, Yun Tang and Laibao Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[¦Á]phenanthren-3-yloxy)-3,6-dihydro-2H-pyran-2-yl)methyl acetate ÏàËÆ¶È:64.1% Archives of Pharmacal Research 2012 35 455-460 Novel Human Umbilical Vein Endothelial Cells (HUVEC)-Apoptosis Inhibitory Phytosterol Analogues: Insight into Their Structure-Activity Relationships Sujin Lee,Sony Marharjan,Jong-Wha Jung,Nam-Jung Kim,Kyeojin Kim,Young Taek Han,Changjin Lim,Hyun-Jung Choi,Young-Geun Kwon,and Young-Ger Suh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-04-10 17:52:50














»Ø¸´´ËÂ¥