| ²é¿´: 656 | »Ø¸´: 1 | |||
¿¼ÑÐÅ®º¢GOÌú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
ǰ±²£¬Î¬ÆÕÇóÖú лл
|
| 13.0,13.1,20.1,20.3,42.9,61.3,70.1,73.8,76.6,76.7,78.1,79.4,104.3,124.0,132.4,140.8,168.7,206.4. |
» ²ÂÄãϲ»¶
285Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
325 µ÷¼Á
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸ÄϿƴóÉúÎïѧ297·Ö£¬Çóµ÷¼ÁÍÆ¼ö
ÒѾÓÐ8È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ27È˻ظ´
³õÊÔ301£¬´úÂë085701»·¾³¹¤³Ì£¬±¾Ë¶Ò»Ö£¬ËÄÁù¼¶Òѹý£¬ÓжþÇøÒ»×÷£¬¹²·¢±í5ƪÂÛÎÄ
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸»ª¶«Àí¹¤085601²ÄÁϹ¤³Ì303·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
372·Ö²ÄÁÏÓ뻯¹¤£¨085600£©Ó¢¶þÊý¶þÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
ÉúÎïÓëÒ½Ò©273Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóάÆÕÊý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú¶«Ñô¹âµÄǰ±²ÃÇ£¬ÖƼÁѧ±ÏÒµµÄ˶ʿ½ø¶«Ñô¹âÄĸö²¿ÃűȽϺã¿Ð»Ð»»Ø´ð¡£¡£
ÒѾÓÐ10È˻ظ´
985ÎÄ¿ÆÀàÕÜѧרҵС˶Ï빫Åɳö¹ú¶Á²©£¬Ï£Íûǰ±²ÃÇÄܸøÐ©½¨Ò飬ллÀ²
ÒѾÓÐ17È˻ظ´
¸ÊËàÑ¡µ÷ÉúÔõôÑù£¿Éϰ¶µÄǰ±²¸øµã¿´·¨°¡ лл
ÒѾÓÐ8È˻ظ´
¹ØÓÚдÈËÎĵØÀíѧÂÛÎÄ£¬µØÀíϵµÄǰ±²ÃǽøÀ´Ò»Ï£¬Ð»Ð»
ÒѾÓÐ8È˻ظ´
ÒºÏàµÄÁ÷¶¯ÏàÖУ¬¸÷ÖÖÑÎÏ࣬Æðʲô×÷Óã¬ÈçºÎÈ·¶¨£¿ÓлúÏàÆøÊ²Ã´×÷ÓÃ?ллǰ±²£¡
ÒѾÓÐ10È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
Çó¸÷λǰ±²°ï棡matlab½â¸´Êý·½³Ì£¬³öÏÖͼÖеľ¯¸æ£¬ÔõÀ´ÐÞ¸ÄÄØ£¿Ð»Ð»Á˰¡
ÒѾÓÐ5È˻ظ´
ÈôÖ»ÄÜÓÃ×ÏÍâ·Ö¹â¹â¶È²â·ÏË®¼°ÎÛÄàÖÐÖØ½ðÊô Çó²â¶¨·½·¨²½Öè~~лл¸÷λǰ±²
ÒѾÓÐ7È˻ظ´
ÎÛÄàÖÐÖØ½ðÊô²â¶¨ Ñ¡ÔñÄÄÖֲⶨ·½·¨±È½ÏºÃ лл¸÷λǰ±²~~
ÒѾÓÐ17È˻ظ´
Çë½Ì¸÷λǰ±²£¬ÎÒÕâÑùµÄÌõ¼þ¿ÉÒÔÉêÇëÍÆÃâÂð£¿ÓÐûÓÐÀÏʦ»áÒª°¡£¿Ð»Ð»~~~
ÒѾÓÐ11È˻ظ´
ʦÐÖ¡¢½ã¡£¡£ÄãÃÇÆ½Ê±Ö÷Òª²éѯʲôÊý¾Ý¿âÄØ£¿
ÒѾÓÐ6È˻ظ´
ÇóÖú--Ͷ¹ýscience of the total environment µÄǰ±²°ï濴һϣ¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
¡¾ÌÖÂÛ¡¿Ò©ÎïµÄ¼±¶¾ºÍ³¤¶¾×ÊÁÏÓ¦¸ÃÈ¥ÄÄÀïÕÒ£¿
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿£¨BOC£©2O±£»¤°±»ùËáµÄ°±»ù·´Ó¦ºó´¦ÀíÔõô×ö°¡
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÇóÂÖÌ¥Éú²ú·½ÃæµÄ×ÊÁÏ Åä·½¹¤ÒÕ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿¸÷λǰ±²£¬ÓиöÎÊÌâ×Éѯ´ó¼Ò£¬¹ØÓÚÒÒ´¼µÄ
ÒѾÓÐ35È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿¼ÑÐÅ®º¢GO: ½ð±Ò+6, ¡ï¡ï¡ïºÜÓаïÖú 2014-03-20 12:29:39
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿¼ÑÐÅ®º¢GO: ½ð±Ò+6, ¡ï¡ï¡ïºÜÓаïÖú 2014-03-20 12:29:39
|
²éѯ½á¹û£º¹²²éµ½55¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (6S,9R)-6-hydroxy-3-one-¦Á-inonol-9-O-¦Â-D-glucopyranoside ÏàËÆ¶È:57.8% Acta Pharmaceutica Sinica 2002 Vol 37 121-123 STUDIES ON WATER-SOLUBLE CONSTITUENTS OF ECHINACEA PRUPUREA LI Ji ren; WANG Bin; QIAO Liang; AI Tie min; ZHAO Yu ying Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . all-trans-crocetin di(¦Â-D-gentiobiosyl) ester C44H64O24 ÏàËÆ¶È:57.1% Archives of Pharmacal Research 2013 36 933-940 Anti-inflammatory activities of crocetin derivatives from processed Gardenia jasminoides Yun-Jung Hong, Ki-Sook Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . carthamoside A2 C16H24O6 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 2006 54(10) 1455-1456 New Acetylenic Glucosides from Carthamus tinctorius Yu-Zhi ZHOU, Hong-Yu MA, Huan CHEN, Li QIAO, Yao YAO, Jia-Qing CAO, and Yue-Hu PEI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . robinioside F ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1997 45 362-366 Oleanene-Type Triterpene Glycosides from Puerariae Radix. IV. Six New Saponins from Pueraria lobata Tomonori ARAO,Junnei KINJO,Toshihiro NOHARA and Ryuichi ISOBE Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . synargentolide E C18H24O10 ÏàËÆ¶È:55.5% Phytochemistry 1998 48 651-656 5,6-Dihydro-¦Á-pyrones from Syncolostemon argenteus Lynne A. Collett, Michael T. Davies-Coleman, Douglas E. A. Rivett Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Dihydrophaseic acid sodium salt 4'-O-¦Â-D-glucopyranoside C21H31O10Na ÏàËÆ¶È:55.5% Chinese Journal of Applied & Environmental Biology 2011 17 350-352 Chemical Constituents from Fructus Xanthii CHENG Zhi; WANG Lun; CHEN Bin; LI Fu & WANG Mingkui Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Crocin C44H64O24 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2007 55(11) 1643-1646 Neocrocin A: a Novel Crocetin Glycoside with a Unique System for Binding Sugars Isolated from Gardenia Yellow Yoshinori UEKUSA,Naoki SUGIMOTO,Kyoko SATO,Young Sook YUN,Akira KUNUGI,Takeshi YAMAZAKI,and Ken-ichi TANAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Micranthin C19H26O7 ÏàËÆ¶È:52.6% Phytochemistry 1992 31 2160-2162 Sesquiterpene lactones from Achillea micrantha Natiq A.R. Hatam, Nahia J. Yousif, Andrea Porzel, Karlheinz Seifert Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . beibersteneolide-a C19H26O7 ÏàËÆ¶È:52.6% Indian Journal of Chemistry Section B 2005 44B 2538-2544 Beibersteneolide-a and -b: Two new sesquiterpene lactones from Achillea beiberstenii Howiriny,Tawfeq A Al; Mossa,Jaber S; Ahmed,Bahar Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 5-(2,4-difluorophenyl)-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-chroman-6-yl acetate ÏàËÆ¶È:52.6% European Journal of Organic Chemistry 2011 2450-2457 Synthesis of 5-(Fluorophenyl)tocopherols as Novel Dioxin Receptor Antagonists Elisabeth Kloser, Stefan Böhmdorfer, Lothar Brecker, Hanspeter Kählig, Thomas Netscher, Kurt Mereiter and Thomas Rosenau Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ixerin W ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 1986 34 4170-4176 Sesquiterpene Lactones from Ixeris dentata NAKAI MAMORU SETO,TOSHIO MIYASE and SEIGO FUKUSHIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . notoserolide A ÏàËÆ¶È:52.3% Acta Pharmaceutica Sinica 2002 Vol 37 37-40 CHEMICAL CONSTITUENTS OF NOTOSERIS RHOMBIFORMIS LIAO Zhi xin; WANG Ming kui; PENG Shu lin; CHEN Yao zu; DING Li sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (3E,6S*, 7R*, 9S*, 10S*, 12R*)-9-chloro-13-bromo-6:12-epoxy-7, 10-diacetoxypentadec-3-en-1-yne C19H26O5BrCl ÏàËÆ¶È:50% Phytochemistry 2002 59 111-116 C15 Acetogenins from the red alga Laurencia obtusa Dimitra Iliopoulou, Constantinos Vagias, Catherine Harvala, Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9¦Â-(tigloyloxy)-atripliciolide ÏàËÆ¶È:50% Planta Medica 2002 68 843-845 Anti-Inflammatory Sesquiterpene Lactones from Lourteigia ballotaefolia Alfredo Rosas-Romero,Carlos Martinez Manchado,Oscar Crescente,Mercedes Acosta, Massimo Curini,Francesco Epifano, Maria Carla Marcotullio, Ornelio Rosati,Aurelia Tubaro,Silvio Sosa Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 7-¦Â-hydroxy-8-epiiridodial glucoside C16H26O8 ÏàËÆ¶È:50% Planta Medica 1982 46 38-41 8-Epiloganic Acid and 7-3-Hydroxy-8-EpiiridodiaI Glucoside Two New Iridoid Glucosides from Linaria cymbalaria Armandodoriano Bianco, Pietro Passacantilli and Giovanna Polidori Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 7,8-dihydroaucubin C15H24O9 ÏàËÆ¶È:50% Planta Medica 1982 44 204-206 Two New Iridoid Glucosides of Plantago asiatica H. Oshio and H. lnouye Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . catapol C15H22O10 ÏàËÆ¶È:50% Acta Botanica Yunnanica 1993 15(1) 83-88 CHEMICAL CONSTITUENTS FROM PICRORHIZA SCROPHULARIIFLORA WANG Da-Qi,HE Zheng-Dan,FENG Bao-Shu,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (2R. 3S)-and (2S,3R)-2-Chloro-2-methyl-2-desoxy-D,L-tetrofuranose C5H9ClO3 ÏàËÆ¶È:50% Helvetica Chimica Acta 1981 64 775-786 Stereoselektive Hydrid-Reduktion von Tetronsäurederivaten. Synthese verzweigtkettiger Tetrofuranosen Heinz Wyss, Ulrich Vögeli, Rolf Scheffold Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Brachysiphonoside C22H26O11 ÏàËÆ¶È:50% Biochemical Systematics and Ecology 2007 35 614-620 Chemical markers in Veronica sect. Hebe Maria Johansen, Tania Surrow Larsen, Maria Ahlm Mattebjerg, Charlotte Held Gotfredsen, Søren Rosendal Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 7 C20H24O10 ÏàËÆ¶È:50% Biochemical Systematics and Ecology 2009 37 230-233 Coumarins, caffeoyl derivatives and a monoterpenoid glycoside from Ferulago asparagifolia R. Alkhatib, T. Hennebelle, V. Roumy, S. Sahpaz, S. S¨¹zgeç, E. Akalın, A.H. Meriçli, F. Bailleul Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5-deoxypulchelloside C17H26O11 ÏàËÆ¶È:50% Natural Product Research 2001 15 345-351 Iridoid and Phenylethanoid Glycosides from Phlomis longifolia var. longifolia Tayfun Ersöz; Wolfgang Sch¨¹hly; Simeon Popov; Nedjalka Handjieva; Otto Sticher; Ihsan Çaliş Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . unedoside ÏàËÆ¶È:50% Phytochemistry 1998 47 1007-1011 Unedoside derivatives in Nuxia and their biosynthesis Søren Rosendal Jensen, Lene Ravnkilde, Jan Schripsema Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . angeloside C15H24O9 ÏàËÆ¶È:50% Phytochemistry 1997 46 371-373 Iridoid glucosides from Angelonia integerrima Gilsane Lino von Poser, Søren Damtoft, Jan Schripsema, Am¨¦lia T. Henriques, Søren Rosendal Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . alatoside ÏàËÆ¶È:50% Phytochemistry 1996 42 1223-1225 Iridoid glycosides from Thunbergia grandiflora Lotfy D. Ismail, Mohamed M. El-Azizi, Taha I. Khalifa, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . lsounedoside C14H20O9 ÏàËÆ¶È:50% Phytochemistry 1996 42 1223-1225 Iridoid glycosides from Thunbergia grandiflora Lotfy D. Ismail, Mohamed M. El-Azizi, Taha I. Khalifa, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . verbenalin C17H24O10 ÏàËÆ¶È:50% Journal of Natural Products 1980 Vol 43 649-707 Iridoids. A Review Leticia J. El-Naggar, Jack L. Beal Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . lamiide ÏàËÆ¶È:50% Journal of Natural Products 1982 Vol 45 462-465 Pondraneoside, A New Iridoid Glucoside From Pondranea ricasoliana Marcella Guiso Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . lamiidol ÏàËÆ¶È:50% Journal of Natural Products 1982 Vol 45 462-465 Pondraneoside, A New Iridoid Glucoside From Pondranea ricasoliana Marcella Guiso Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . catalpol ÏàËÆ¶È:50% Journal of Natural Products 1986 Vol 49 519 Radiatoside, a New Bisiridoid from Argylia radiata Armandodoriano Bianco, Pietro Passacantilli, Claudio Rispoli, Marcello Nicoletti, Irene Messana, Juan A. Garbarino, Vincente Gambaro Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 7 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 583 Structure and Stereochemistry of Pectinolides A-C, Novel Antimicrobial and Cytotoxic 5,6-Dihydro-¦Á-pyrones from Hyptis pectinata Rogelio Pereda-Miranda, Lourdes Hern¨¢ndez, Manuela Judith Villavicencio, Miriam Novelo, Patricia Ibarra, Heebyung Chai, John M. Pezzuto Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 7-O-butylsecologanic acid ÏàËÆ¶È:50% Journal of Natural Products 1995 Vol 58 1756-1758 Isolation of Secoiridoid Artifacts from Lonicera japonica Lamberto Tomassini, M. Francesca Cometa, Mauro Serafini, Marcello Nicoletti Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-31 10:07:11














»Ø¸´´ËÂ¥