| ²é¿´: 233 | »Ø¸´: 1 | ||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾ÝÈçÏ£º13.6,13.6,13.7,17.8,20.6,22.6,28.4,31.8,34.2,36.1,37.5,38.3,38.6,42.2,50.6,50.8,54.5,65.4,75.5,76.5,219.9 |
» ²ÂÄãϲ»¶
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ4È˻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´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
283·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
0703»¯Ñ§
ÒѾÓÐ23È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÃÌËáï®XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúάÆ×Êý¾Ý¿â
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻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 ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 19:43:26
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 19:43:26
|
²éѯ½á¹û£º¹²²éµ½1093¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3¦Â,4¦Á-dihydroxypregnan-16-one C21H34O3 ÏàËÆ¶È:100% Canadian Journal of Chemistry 2003 81 253-257 A pentanortriterpenoid with a novel carbon skeleton and a new pregnane from Trichilia connaroides Hua-Ping Zhang, Shao-Hua Wu, Yue-Mao Shen, Yun-Bao Ma, Da-Gang Wu, Shu-Hua Qi, Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Toonasterone A C21H34O4 ÏàËÆ¶È:85.7% Steroids 2011 76 571-576 Structural and stereochemical studies of five new pregnane steroids from the stem bark of Toona ciliata var. pubescens Jian-Rong Wang, Qiang Shen, Li Fang, Shu-Ying Peng, Yi-Ming Yang, Jia Li, Hai-Li Liu, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . meliavosin C21H34O3 ÏàËÆ¶È:85.7% The Journal of Organic Chemistry 1998 63 3781-3785 New Bioactive Steroids from Melia volkensii Lingling L. Rogers, Lu Zeng, and Jerry L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 6¦Á,7¦Â-dihydroxy-17(20)-cis-5¦Á-pregna-16-one C21H32O3 ÏàËÆ¶È:80.9% Chinese Journal of Chemistry 2003 21 200-203 Chemical Constituents of Ailanthus triphysa Qi Shu-Hua, Wu Da-Gang, Ma Yun-Bao and Luo Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . aglatomin A C22H36O3 ÏàËÆ¶È:77.2% Phytochemistry 1999 51 1031-1037 Dammarane triterpenes and pregnane steroids from Aglaia lawii and A. tomentosa Khalit Mohamad, Thierry Sevenet, Vincent Dumontet, Mary Pais, Mai Van Tri, Hamid Hadi, Khalijah Awang, Marie-There se Martin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2¦Â,3¦Â-dihydroxy-5¦Á-pregnane-16-one C21H34O3 ÏàËÆ¶È:76.1% Phytochemistry 1997 45 1225-1228 Pregnanes and triterpenoid hydroperoxides from the leaves of Aglaia grandis Akira Inada, Hiroko Murata, Yuka Inatomi, Tsutomu Nakanishi, Dedy Darnaedi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Toonasterone B C21H34O3 ÏàËÆ¶È:76.1% Steroids 2011 76 571-576 Structural and stereochemical studies of five new pregnane steroids from the stem bark of Toona ciliata var. pubescens Jian-Rong Wang, Qiang Shen, Li Fang, Shu-Ying Peng, Yi-Ming Yang, Jia Li, Hai-Li Liu, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (E)-Toonasterone C C21H32O3 ÏàËÆ¶È:76.1% Steroids 2011 76 571-576 Structural and stereochemical studies of five new pregnane steroids from the stem bark of Toona ciliata var. pubescens Jian-Rong Wang, Qiang Shen, Li Fang, Shu-Ying Peng, Yi-Ming Yang, Jia Li, Hai-Li Liu, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3¦Â-hydroxypregnan-16-one ÏàËÆ¶È:76.1% Canadian Journal of Chemistry 2001 79 1747-1753 Synthesis of trichiliasterones A and B 16-Ketosteroids isolated from Trichilia hirta and Trichilia americana Susanne M Hantos, Sasmita Tripathy, Najma Alibhai, Tony Durst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (Z)-Toonasterone C C21H32O3 ÏàËÆ¶È:71.4% Steroids 2011 76 571-576 Structural and stereochemical studies of five new pregnane steroids from the stem bark of Toona ciliata var. pubescens Jian-Rong Wang, Qiang Shen, Li Fang, Shu-Ying Peng, Yi-Ming Yang, Jia Li, Hai-Li Liu, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 2¦Á,3¦Â,4¦Â-Trihydroxypregnan-16-one C21H34O4 ÏàËÆ¶È:71.4% Turkish Journal of Chemistry 2009 33 501-506 Pregnane steroids from the heartwood of Azadirachta indica BINA SHAHEEN SIDDIQUI, SYED KASHIF ALI, SYED TARIQ ALI, FAYYAZ AHMED Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2¦Á-hydroxypregnan-3,16-dione C21H32O3 ÏàËÆ¶È:71.4% Canadian Journal of Chemistry 2001 79 1747-1753 Synthesis of trichiliasterones A and B 16-Ketosteroids isolated from Trichilia hirta and Trichilia americana Susanne M Hantos, Sasmita Tripathy, Najma Alibhai, Tony Durst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Â,4¦Â-dihydroxypregnan-16-one ÏàËÆ¶È:71.4% Natural Product Communications 2010 5 179-184 Two New Terpenoids from Trichilia quadrijuga (Meliaceae) Virginia F. Rodriguesa*, Hadria M. Carmo, Raimundo Braz Filho, Leda Mathias andIvo J. Curcino Vieira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3¦Â,4¦Á-dihydroxypregnan-21-one C21H34O3 ÏàËÆ¶È:66.6% Phytochemistry 2008 69 1319-1327 Structural elucidation of limonoids and steroids from Trichilia connaroides Xiao-Ning Wang, Cheng-Qi Fan, Sheng Yin, Li-She Gan, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ekeberin B C21H32O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2008 71(2) 167-174 Antiplasmodial Triterpenoids from Ekebergia capensis Toshihiro Murata, Toshio Miyase, Francis Wamakima Muregi, Yasuko Naoshima-Ishibashi, Kaoru Umehara, Tsutomu Warashina, Shigeyuki Kanou, Gerald M. Mkoji, Mamoru Terada, and Akira Ishih Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . toosendansterol A C21H34O3 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1988 36 609-612 Phytochemical Studies on Meliaceous Plants. III. : Structures of Two New Pregnane Steroids, Toosendansterols A and B, from Leaves of Melia toosendan SIEB. et ZUCC. AKIRA INADA,MARI KOBAYASHI and TSUTOMU NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 2¦Á,3¦Â-Dihydro-5-pregnen-16-one C21H32O3 ÏàËÆ¶È:66.6% Steroids 2009 74 761-765 Steroids from the leaves of Chinese Melia azedarach and their cytotoxic effects on human cancer cell lines Shi-Biao Wu, Yan-Ping Ji, Jing-Jing Zhu, Yun Zhao, Gang Xia, Ying-He Hu, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 2¦Â,3¦Â,4¦Â-Trihydroxypregnan-16-one ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2003 5 215-221 THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-12 11:57:16














»Ø¸´´ËÂ¥