| ²é¿´: 394 | »Ø¸´: 1 | ||||
²»¿ÞÌú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»´ó¼ÒÁË£¡ ÒÑÓÐ1È˲ÎÓë
|
|
ÎÒµÄÊý¾ÝÈçÏ£º 13C NMR (CDCl3) ¦Ä 16.0,16.3,16.9,17.2,18.8,21.0,21.8,22.1,24.3,26.7,28.9,31.0,33.4,33.6,34.5,37.5,40.4,41.4,42.0,42.0,42.2,44.2,50.0,50.5,51.2,54.1,56.2,74.1 ÔÚ33.4ºÍ18.8¿ÉÄÜÓÐÐźŵÄÖØµþ¡£ лл´ó¼ÒÁË£¡ |
» ²ÂÄãϲ»¶
0703»¯Ñ§µ÷¼Á £¬Áù¼¶Òѹý£¬ÓпÆÑоÀú
ÒѾÓÐ8È˻ظ´
268Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁÏ£¬·ÄÖ¯£¬ÉúÎ0856¡¢0710£©£¬»¯Ñ§ÕÐÉúÀ²
ÒѾÓÐ7È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
281Çóµ÷¼Á£¨0805£©
ÒѾÓÐ7È˻ظ´
²ÄÁÏÓ뻯¹¤Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
299Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
277µ÷¼Á
ÒѾÓÐ6È˻ظ´
341Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
328Çóµ÷¼Á£¬Ó¢ÓïÁù¼¶551£¬ÓпÆÑоÀú
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»´óÉñ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬ÀàËÆéÎÆ¤ËصĶà¶à¸ø
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬ky7......
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡2551
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¶àл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
½¨ÒéȺÖ÷¿ªÒ»¸ö΢Æ×ÇóÖúרÀ¸°É
ÒѾÓÐ14È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
²ËÄñÇóÖúCVÇúÏß·ÖÎö
ÒѾÓÐ10È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²»¿Þ: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄ㣡 2014-05-01 12:51:30
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²»¿Þ: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄ㣡 2014-05-01 12:51:30
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½14653¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 10 ÏàËÆ¶È:96.5% Phytochemistry 1993 32 1235-1237 Sesqui- and triterpenoids of the liverwort Conocephalum japonicum Masao Toyota, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . hydroxyhopane ÏàËÆ¶È:96.5% Chinese Journal of Medicinal Chemistry 2008 18 291-293 Chemical constituents from the root of Lygodium japonicum(Thunb.) Sw. ZHU Lin-xia, ZHANG Guo-gang, WANG Sheng-chao, ZUO Tian-tian Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 22-hydroxyhopane ÏàËÆ¶È:93.3% Chemical & Pharmaceutical Bulletin 1993 41 1939-1943 NMR Spectra of Triterpenoids. I. Conformation of the Side Chain of Hopane and Isohopane, and Their Derivatives Hiroyuki AGETA,Kenji SHIOJIMA,Hideki SUZUKI and Sachiko NAKAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 22-hydroxyhopane ÏàËÆ¶È:93.3% Chinese Pharmaceutical Journal 2008 43 18-20 Studies on Chemical Constituents of Marchantia polymorpha L. FANG Lei, NIU Chong, LOU Hong-xiang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 22-hydroxyhopane C30H52O ÏàËÆ¶È:93.3% Phytotherapy Research 1998 12 S21-S24 Three triterpenoids and one flavonoid from the liverwort Asterella blumeana grown in vitro M. Neves, R. Morais, S. Gafner and K. Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . hopan-22-ol ÏàËÆ¶È:93.3% Qu¨ªmica Nova 2007 30 292-297 Chemical composition and evaluation of allelopathic potentials of Adiantum tetraphyllum Humb. & Bonpl. Ex. Willd (Pteridaceae) Melos, Jorge L. R.; Silva, Luciana B.; Peres, Marize T. L. P.; Mapeli, Ana M.; Faccenda, Odival; Anjos, H¨¢tino H.; Torres, Thais G.; Tiviroli, Soraia C.; Batista, Ana L.; Almeida, Felipe G. N.; Flauzino, Natasha S.; Tibana, Let¨ªcia A.; Hess, Sônia C.; Hon Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Hopan-22-ol ÏàËÆ¶È:93.3% Australian Journal of Chemistry 1987 40 1713-1721 A 13C N.M.R. Study of Some Oxygenated Hopane Triterpenes AL Wilkins, KJ Ronaldson, PM Jager and PW Bird Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . hydroxyhopane ÏàËÆ¶È:90% Chemical & Pharmaceutical Bulletin 1990 38 2130-2132 Fern Constituents : Triterpenoids Isolated from the Leaves of Cheiropleuria bicuspis Rumiko KAMAYA,Yoshiko TANAKA,Rie HIYAMA and Hiroyuki AGETA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . hydroxyhopane ÏàËÆ¶È:90% Journal of Natural Products 1990 Vol 53 325 Chemotaxonomy of Ferns, 3. Triterpenoids from Polypodium polypodioides Hiroyuki Ageta, Yoko Arai Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . diplopterol ÏàËÆ¶È:90% Phytochemistry 1994 35 1293-1296 Triterpenes from Fossombronia liverworts Carola Grammes, Gunther Burkhardt, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 4 ÏàËÆ¶È:90% Chemical & Pharmaceutical Bulletin 1987 35 4016-4021 Chemical and Chemotaxonomical Studies of Filices. LXXI. Chemical Studies on the Constituents of Cheiropleuria bicuspis (BL.) PR. NOBUTOSHI TANAKA,HIROSHI WADA,MASAAKI KOJIMA,TAKAO MURAKAMI,YASUHISA SAIKI,CHIU-MING CHEN and YOICHI IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . hydroxyhopanone ÏàËÆ¶È:86.6% Chemical & Pharmaceutical Bulletin 1996 44 1033-1038 Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica Hiroyuki FUCHINO,Soh KONISHI,Tetsuya SATOH,Akiko YAGI,Kohei SAITSU,Tatsuya TATSUMI and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . diploterol ÏàËÆ¶È:86.6% Acta Botanica Boreali-Occidentalia Sinica 2008 28 1246-1249 Chemical Constituents in the Leaves of Alsophila spinulosa CHEN Feng-zheng, XIANG Qing-xiang, LI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . diploterol ÏàËÆ¶È:86.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-05-01 09:02:27













»Ø¸´´ËÂ¥