| ²é¿´: 338 | »Ø¸´: 2 | ||
¿¨µ±Ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý£¬²»Éõ¸Ð¼¤£¡
|
|
19.9, 26.7, 27.0, 28.6, 30.3, 36.3, 38.2, 43.7, 51.2, 51.3, 52.1, 53.9, 69.9, 73.0, 73.7, 74.6, 81.3, 85.9, 111.6, 116.3, 156.6, 163.4, 168.2, 171.5, 172.2 12.0, 12.6, 18.7, 19.0, 19.8, 21.7, 23.0, 24.0, 26.0, 28.0, 29.1, 36.0, 37.0, 37.4, 38.0, 38.1, 39.4, 45.8, 46.6, 53.5, 56.0, 56.6, 57.5, 209.2, 211.3 |
» ²ÂÄãϲ»¶
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ11È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ14È˻ظ´
347²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó£¬³õÊÔ329£¬Çó»·¾³¿ÆÑ§Ó빤³Ìµ÷¼Á£¡
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ20È˻ظ´
0703»¯Ñ§
ÒѾÓÐ30È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ48È˻ظ´
Ò»Ö¾Ô¸»ª¶«Àí¹¤085601²ÄÁϹ¤³Ì303·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
Á½¸ö»¯ºÏÎï-----ÇóÖú¿ÉÒÔ²é΢Æ×Êý¾ÝµÄ³æ×Ó~
ÒѾÓÐ4È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
΢Æ×²é¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
±ÉÈËÊÖÉÏÓÐÈý¸ö»¯ºÏÎÇó¹ý·´óÏÀ¼ø¶¨ÓÐûÓÐ×ö¹ý¾§ÌåµÄÑо¿¡£¡£¡£¸Ð¼¤²»¾¡
ÒѾÓÐ13È˻ظ´
ÇóÖúÈýÝÆ»¯ºÏÎï½âÎö£¡²»Éõ¸Ð¼¤
ÒѾÓÐ38È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
tianhenlanqi
гæ (СÓÐÃûÆø)
- Ó¦Öú: 54 (³õÖÐÉú)
- ½ð±Ò: 1257
- ºì»¨: 5
- Ìû×Ó: 156
- ÔÚÏß: 11.3Сʱ
- ³æºÅ: 1280112
- ×¢²á: 2011-04-28
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:01
¿¨µ±: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-02-25 22:35:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:01
¿¨µ±: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-02-25 22:35:59
|
»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½40¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Bruceanic acid E methyl ester C26H34O12 ÏàËÆ¶È:57.6% Journal of Natural Products 2012 75 683-688 Bioactive Quassinoids from the Seeds of Brucea javanica Jun-Hong Liu, Nan Zhao, Gui-Jie Zhang, Shi-Shan Yu, Li-Jun Wu, Jing Qu, Shuang-Gang Ma, Xiao-Guang Chen, Tian-Qi Zhang, Jian Bai, Hui Chen, Zhen-Feng Fang, Fen Zhao, and Wei-Bin Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-Epi-GA 4 methyl ester 3-acetate C22H28O6 ÏàËÆ¶È:56% Phytochemistry 1995 38 1345-1348 3-epi-GA63, antheridiogen in Anemia phyllitidis Tadayuki Yamauchi, Naomi Oyama, Hisakazu Yamane, Noboru Murofushi, Helmut Schraudolf, David Owen, Lewis N. Mander Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 10 C26H44NO7S ÏàËÆ¶È:53.8% Journal of Asian Natural Products Research 2008 10 1063-1067 An effective O-demethylation of some C19-diterpenoid alkaloids with HBr-glacial acetic acid Chun-Lan Zou, Hong Ji, Guang-Bo Xie, Dong-Lin Chen and Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . virescenoside A6 C26H40O9 ÏàËÆ¶È:53.8% Natural Product Communications 2011 Vol. 6, No. 8 1063-1068 New Virescenosides from the Marine-derived Fungus Acremonium striatisporum Shamil Sh. Afiyatullov, Anatoly I. Kalinovsky and Alexandr S. Antonov Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . diacetylheteratisine C26H37NO7 ÏàËÆ¶È:53.8% Natural Product Research and Development 1997 9(1) 1-3 LACTONE-TYPE NORDITERPENOID ALKALOIDS FROM ACONITUM PULCHELLUM Chen Peiqin; He Lan; Ding Lisheng; Zhang Guolin; Li Bogong Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2¦Â,3¦Â,14¦Á,20S)-20-vinyl-14,20-dihydroxy-2,3-isopropylidenedioxy-5¦Â-pregn-7-ene-6-one ÏàËÆ¶È:53.8% Russian Journal of Organic Chemistry 2008 44 1590-1597 Synthesis of analogs of ecdysteroids containing an isoxaline ring in the side chain R. P. Litvinovskaya, S. V. Drach, G. A. Zhilitskaya and V. A. Khripach Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Penisimplicin B C28H38O8 ÏàËÆ¶È:53.5% Chemical & Pharmaceutical Bulletin 2005 53(9) 1114-1117 Two New Meroterpenoids, Penisimplicin A and B, Isolated from Penicillium simplicissimum Shin-ichirou KOMAI,Tomoo HOSOE, Takeshi ITABASHI,Koohei NOZAWA, Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Takashi YAGUCHI, Kayoko TAKIZAWA,Kazutaka FUKUSHIMA, and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 17¦Á-cerdollaside C30H46O9 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1987 35 2744-2749 Cardenolide Monoglycosides from the Leaves of Cerbera odollam and Cerbera manghas (Cerbera. III) TATSUO YAMAUCHI,FUMIKO ABE and ALFRED S.C. WAN Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 10 C23H32O8 ÏàËÆ¶È:52% Chemical & Pharmaceutical Bulletin 1989 37 1465-1469 Terpenoids. LI. : Structures of Antitumor Diterpenoids, Trichorabdals A-E, Isolated from Rabdosia trichocarpa Kaoru FUJI,Manabu NODE,Midori SAI,Eiichi FUJITA,Tetsuro SHINGU,William H. WATSON,David A. GROSSIE and Volker ZABEL Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-acetoxy-5¦Á-carda-8(14),20(22)-dienolide ÏàËÆ¶È:52% Chemical & Pharmaceutical Bulletin 1978 26 2894-2896 Carbon-13 NMR of 5¦Á-Cardenolides TATSUO YAMAUCHI,FUMIKO ABE and MASATOSHI NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-acetoxy-5¦Â-carda-8(14),20(22)-dienolide ÏàËÆ¶È:52% Chemical & Pharmaceutical Bulletin 1978 26 2894-2896 Carbon-13 NMR of 5¦Á-Cardenolides TATSUO YAMAUCHI,FUMIKO ABE and MASATOSHI NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 20 C25H41O6 ÏàËÆ¶È:52% Journal of Asian Natural Products Research 2006 8 545-554 An attempt to enlarge the B ring of maoecrystal B,an ent-kaurane-type diterpene L. XU and F.-P. WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ent-6¦Á,18-diacetoxy-11¦Â-hydroxymanoyl oxide ÏàËÆ¶È:52% Phytochemistry 1997 45 283-291 Biotransformation of ent-6¦Á-acetoxy- and ent-6-ketomanoyl oxides with rhizopus nigricans and curvularia lunata cultures Andr¨¦s Garc¨ªa-Granados, Juan J. Guti¨¦rrez, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦M. Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ajadelphine C25H39NO7 ÏàËÆ¶È:52% Journal of Natural Products 1992 Vol 55 736 Two New Norditerpenoid Alkaloids from the Roots of Delphinium ajacis S. William Pelletier, Sudhakar Bhandaru, Haridutt K. Desai, Samir A. Ross, Hanna M. Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (2S,4aR,6aR,7R,9S,10aS,10bR)-9-(Acetyloxy)-2-(5-bromo-2-oxo-2,5-dihydrofuran-3-yl)dodecahydro-6a,10b-dimethyl-4,10-dioxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester C23H27O9Br ÏàËÆ¶È:52% Journal of Natural Products 2006 69 107-112 Synthetic Studies of Neoclerodane Diterpenes from Salvia divinorum: Semisynthesis of Salvinicins A and B and Other Chemical Transformations of Salvinorin A Wayne W. Harding, Matthew Schmidt, Kevin Tidgewell, Pavitra Kannan, Kenneth G.Holden, Brian Gilmour, Hernan Navarro, Richard B. Rothman, and Thomas E. Prisinzano Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Epothilone A8 C25H38NO6S ÏàËÆ¶È:52% Journal of Natural Products 2001 64 847-856 New Natural Epothilones from Sorangium cellulosum, Strains So ce90/B2 and So ce90/D13: Isolation, Structure Elucidation, and SAR Studies Ingo H. Hardt, Heinrich Steinmetz, Klaus Gerth, F. Sasse, Hans Reichenbach, and Gerhard Höfle Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Guan-fu base X C22H29NO6 ÏàËÆ¶È:52% Phytochemistry Letters 2012 5 397-400 Three new hetisine-type diterpenoid alkaloids from Aconitum coreanum Qing-Fa Tang, Wen-Cai Ye, Jing-Han Liu, Chun-Hua Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . javanicin C22H26O11 ÏàËÆ¶È:52% Phytochemistry 1990 29 2720-2722 A quassinoid from Brucea javanica Long-Ze Lin,Geoffrey A. Cordell,Chao-Zhou Ni,Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1R,2R,3S,6R,8R,9R)-3-methoxy-1,8,12,12-tetramethyl-4-oxatricyclo[6.4.0.02,6]dodecan-9-yl 3-methylbut-2-enoate C21H34O4 ÏàËÆ¶È:52% Indian Journal of Chemistry 2010 49B 776-788 Enantiospecific total synthesis of ent-5-senecioyl-oxy-10,11-epoxythapsan-10-ol A Srikrishna* & K Anebouselvy Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Compound 4a C24H32NO9S ÏàËÆ¶È:52% Bioorganic & Medicinal Chemistry Letters 2006 16 3170-3174 Synthetic studies of neoclerodane diterpenes from Salvia divinorum: Selective modification of the furan ring Wayne W. Harding, Matthew Schmidt, Kevin Tidgewell, Pavitra Kannan, Kenneth G. Holden, Christina M. Dersch, Richard B. Rothman, Thomas E. Prisinzano Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-02-25 19:35:26
tianhenlanqi
гæ (СÓÐÃûÆø)
- Ó¦Öú: 54 (³õÖÐÉú)
- ½ð±Ò: 1257
- ºì»¨: 5
- Ìû×Ó: 156
- ÔÚÏß: 11.3Сʱ
- ³æºÅ: 1280112
- ×¢²á: 2011-04-28
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:07
¿¨µ±: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2013-02-25 22:36:18
xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:07
¿¨µ±: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2013-02-25 22:36:18
|
»¯ºÏÎï2 ²éѯ½á¹û£º¹²²éµ½3234¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 6b ÏàËÆ¶È:86.2% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . stigmasta-3,6-dione ÏàËÆ¶È:86.2% Acta Bot. Boreal. -Occident. Sin. 2009 29 1898-1903 Chemical Components of Glechoma biondiana XU Jing, WEI Ping-zhi, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5¦Á-stig-mastane-3,6-dione ÏàËÆ¶È:86.2% Acta Botanica Sinica 1996 38 161-166 Chemical Constituents from Roots of Jatropha curcas Kong Ling-yi, Min Zhi-da and Shi Jian-xia Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . stigmastan-3,6-dione C29H48O2 ÏàËÆ¶È:86.2% Acta Pharmaceutica Sinica 1993 28 684-689 STUDIDS ON THE CHEMICAL CONSTITUENTS OF EUONYMUS MUPINENSIS XL Yah; SX Liao; HQ Liang and P Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 24-ethylcholesta-3,6-dione C29H48O2 ÏàËÆ¶È:86.2% Steroids 2006 71 647-652 Ketosteroids and hydroxyketosteroids, minor metabolites of sugarcane wax Patricia Georges, Muriel Sylvestre, Heinz Ruegger, Paul Bourgeois Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 24R,5¦Á-stigmast-3,6-dione ÏàËÆ¶È:86.2% China Journal of Chinese Materia Medica 2005 30 270-272 Studies on chemical constituents in bark of Larix olgensis var. koreana YANG Baohua, ZHANG Weidong, GU Zhengbing, LI Tingzhao, ZHANG Chuang, ZHOU Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . stigmastan-3,6-dione ÏàËÆ¶È:86.2% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 4 ÏàËÆ¶È:86.2% Acta Pharmaceutica Sinica 1999 Vol 34 682-685 STUDIES ON THE CHEMICAL CONSTITUENTS FROM DESMOS DUMOSUS (ROXB.) SAFF Wu Jiuhong (Wu JH); Liao Shixuan (Liao SX); Mao Shilong (Mao SL); Yi Yanghua (Yi YH); Takeya K; Su Zhongwu (Su ZW) and Lan Chuanqing (Lan CQ) Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (24R)-5¦Á-stigmast-3,6-dione C29H48O2 ÏàËÆ¶È:86.2% Phytochemistry 1993 34 523-527 Steroidal constituents from mature wheat straw Elvira M.M. Gaspar, Higuinaldo J.C. das Neves Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Stigmastane-3,6-dione ÏàËÆ¶È:86.2% Korean Journal of Pharmacognosy 2008 39(3) 186-193 Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmastane-3,6-dione ÏàËÆ¶È:86.2% Magnetic Resonance in Chemistry 2004 42 355-359 Complete 1H and 13C NMR assignments of two phytosterols from roots of Piper nigrum Kun Wei, Wei Li, Kazuo Koike, Yuping Pei, Yingjie Chen and Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5¦Á-¶¹çÞ-3,6-¶þͪ ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2009 40 1554-1555 ÞµÀó»¯Ñ§³É·ÖÑо¿ ÕÅ·å;ÕÅ¿¡Çå;¿×ÁîÒå Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5¦Á-¶¹çÞ-3,6-¶þͪ ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2008 39 1138-1140 º£Ã¢¹û¾¥Æ¤»¯Ñ§³É·ÖµÄÑо¿ ÕÅСÆÂ;ÕÅ¿¡Çå;ÁõÃ÷Éú;ÅáÔºþ Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (24R)-5A-¶¹çÞÍé-3,6-¶þͪ ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2008 39 499-502 ¿ÕÐÄÁ«×Ӳݻ¯Ñ§³É·ÖÑо¿ Âí׿;ÀîÇíÛë;·¶ÎÄǬ;·½Äî²®;ÁõìÍÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (24R)-5¦Á-stigma-3,6-dione C29H48O2 ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2005 36 1466-1467 ľÃÞ¸ù»¯Ñ§³É·ÖµÄÑо¿(¢ó) ÆëһƼ,À賿¹â,ÀîС÷,¹ùË´Ãñ Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 5¦Á-stigmasta-3,6-dione ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2003 34 392-394 Stigmasterols from pericarp of Sphaerophysa salsula LI Guo-yu; WANG Jin-hui; LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (24R)-5¦Á-stigmast-3,6-dione ÏàËÆ¶È:86.2% Chinese Traditional and Herbal Drugs 2002 33 300-303 Studies on chemical constituents in seed of Litchi chinensis TU Peng fei; LUO Qing; ZHENG Jun hua Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5¦Á-stigmastane-3,6-dione ÏàËÆ¶È:86.2% Archives of Pharmacal Research 2005 28 1147-1151 Antimicrobial constituents from fruits of Ailanthus altissima SWINGLE Chun-Chao Zhao, Jian-Hua Shao, Xian Li, Jing Xu and Peng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 24(R)-5¦Á-stigmastane-3,6-dione ÏàËÆ¶È:86.2% Chinese Pharmaceutical Journal 2005 40 414-416 Chemical constituents of Pterocarya tonkinesis and their antitumor activity in vitro LIU Hong-bing, CUI Cheng-bin, GU Qian-qun, CAI Bing, ZHAO Qing-chun, GUAN Hua-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (24R)-5¦Á-stigmast-3,6-dione ÏàËÆ¶È:86.2% Chinese Pharmaceutical Journal 2008 43 897-899 Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook WANG Yuan, ZOU Zhong-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . stigmast-4-ene-3,6-dione ÏàËÆ¶È:86.2% Chinese Pharmaceutical Journal 2009 44 576-580 Studies on Antitumor Steroids and Flavonoids from Tamarix chinensis Lour. WANG Bin, REN Shu-wen, LI Guo-qiang, GUAN Hua-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (24R)-5¦Á-stigmast-3,6-dione ÏàËÆ¶È:86.2% Chinese Pharmaceutical Journal 2010 45 1460-1462 Chemical Components in Championella sarcorrhiza DONG Jian-yong, TIAN Li-li, LIN Chen, YUE Lei, ZHANG Yuan, LIN Guan-yang, CAI Jin-zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 24R-5-¶¹çÞÍé-3,6-¶þͪ ÏàËÆ¶È:86.2% Journal of Shenyang Pharmaceutical University 2009 26 196-197 Chemical constituents of Abutilon indicum (L.) Sweet LIU Na, JIA Ling-yun, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-02-25 19:38:19














»Ø¸´´ËÂ¥