| ²é¿´: 205 | »Ø¸´: 1 | ||
aydchp½ð³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
| 12.03, 18.14, 20.03, 20.41, 21.48, 21.99, 30.67, 33.88, 36.04, 36.13, 41.10, 43.80, 49.31, 51.04, 56.13, 105.71, 112.68, 133.23, 136.22, 171.35 |
» ²ÂÄãϲ»¶
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
277Çóµ÷¼Á ÊýÒ»104·Ö
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
ÓÐËù²»Îª
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 304 (´óѧÉú)
- ½ð±Ò: 9684.2
- É¢½ð: 16
- ºì»¨: 14
- Ìû×Ó: 1106
- ÔÚÏß: 814.3Сʱ
- ³æºÅ: 481441
- ×¢²á: 2007-12-17
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
aydchp: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-29 23:39:05
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
aydchp: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-29 23:39:05
|
²éѯ½á¹û£º¹²²éµ½769¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 4-hydroxy-17R-methylincisterol ÏàËÆ¶È:85.7% Chinese Journal of Marine Drugs 2012 31 8-13 Secondary metabolites from a fungus Peniophora sp.isolated from a gorgonian Echinogorgia sp. ZHOU Jing; CHEN Min; LI Yun; LIU Yun-zhang; WANG Chang-yun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 9¦Á-hydroxy-1,2,3,4,5,10,19-heptanorergosta-7,22-diene-6,9-lactone C21H32O3 ÏàËÆ¶È:85% Natural Medicines 1996 50 179-181 Sterol Constituents from the Sclerotium of Polyporus umbellatus Fries OHTA KOJI,YAOITA YASUNORI,MATSUDA NORIKO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (17R)-4-hydroxy-17-methylincisterol ÏàËÆ¶È:80.9% Heterocycles 2006 69 253-258 Chaxine A, an Osteoclast-Forming Suppressing Substance, from the Mushroom Agrocybe chaxingu Hirokazu Kawagishi,* Takuto Akachi, Tetsuhiro Ogawa, Kikuko Masuda, Kohji Yamaguchi, Kazunaga Yazawa, and Mamoru Takahashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Demethylincisterol A3 C21H32O3 ÏàËÆ¶È:76.1% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . demethylincisterol A2 C21H32O3 ÏàËÆ¶È:71.4% Journal of Natural Products 2005 68 331-336 Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp. Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . volemolide C22H36O3 ÏàËÆ¶È:68.1% Natural Product Research and Development 2010 22 786-788 Chemical Constituents of Culture Broth of Hebeloma westraliense SHAO Hong-jun;FANG Li-zhen; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . chaxine A C21H34O3 ÏàËÆ¶È:66.6% Heterocycles 2006 69 253-258 Chaxine A, an Osteoclast-Forming Suppressing Substance, from the Mushroom Agrocybe chaxingu Hirokazu Kawagishi,* Takuto Akachi, Tetsuhiro Ogawa, Kikuko Masuda, Kohji Yamaguchi, Kazunaga Yazawa, and Mamoru Takahashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Chaxine A C21H34O3 ÏàËÆ¶È:66.6% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . demethylincisterol A1 C20H30O3 ÏàËÆ¶È:65% Journal of Natural Products 2005 68 331-336 Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp. Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Â,17¦Â-dihydroxyandrost-4-ene ÏàËÆ¶È:65% Steroids 1999 64 770-779 Steroid transformations with Exophiala jeanselmei var. lecanii-corni and Ceratocystis paradoxa Roy B. R. Porter, Winklet A. Gallimore, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 12 C21H34O2 ÏàËÆ¶È:65% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . sarcophytin ÏàËÆ¶È:65% Tetrahedron Letters 2012 53 5759-5762 Pavidolides A¨CE, new cembranoids from the soft coral Sinularia pavida Shi Shen, Huajie Zhu, Dawei Chen, Dong Liu, Leen van Ofwegen, Peter Proksch, Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . volemolide C22H34O3 ÏàËÆ¶È:63.6% Bioscience, Biotechnology, and Biochemistry 1994 58 1542-1544 Volemolide, a Novel Norsterol from the Fungus Lactarius volemus Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . incisterol C21H32O3 ÏàËÆ¶È:61.9% Journal of Natural Products 2005 68 331-336 Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp. Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 16-Methyl-17-acetoxy-5¦Á-androstan-3¦Â-ol 7c C22H36O3 ÏàËÆ¶È:61.9% Steroids 2001 66 833-843 Configurational analysis and relative binding affinities of 16-methyl-5¦Á-androstane derivatives P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, P¨¦ter Forg¨®, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (1R,3aR,4Z,5R,7aR,10R,20E,40R)-5,6,7,7a-Tetrahydro-4-(2-hydroxyethylidene)-7a-methyl-1-(10,40,50-trimethyl-20-hexenyl)-3aHindan-5-ol C21H36O2 ÏàËÆ¶È:61.9% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 15-Azidoimbricatolic acid methyl ester C21H35N3O2 ÏàËÆ¶È:61.9% Molecules 2013 18 5936-5953 Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . agallochin H C20H30O3 ÏàËÆ¶È:60% Journal of Natural Products 2002 65 382-385 ent-Kaurane and Beyerane Diterpenoids from Excoecaria agallocha1 Ammanamanchi S. R. Anjaneyulu, Vadali Lakshmana Rao, and Karanam Sreedhar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 10 C18H30O4 ÏàËÆ¶È:60% Journal of Natural Products 1997 60 1115-1120 Sesquiterpenoids of the Drimane Class from a Sponge of the Genus Dysidea Valerie J. Paul, Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, and Patricia R. Bergquist Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 12-hydroxy-8,13e-labdadien-15-oic acid ÏàËÆ¶È:60% Journal of Integrative Plant Biology 2006 48 478-482 Labdane doterpenoids from Coleus forskohlii Briq. Ling-ling XU and Ling-yi KONG Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-11-29 22:02:09














»Ø¸´´ËÂ¥