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CDCL3, C-NMR 56.0, 56.4, 84.6, 109.1, 114.2, 116.2, 120.3, 132.9, 139.0, 145.3, 146.8 |
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wei537113: ½ð±Ò+30 2015-04-27 19:05:28
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wei537113: ½ð±Ò+30 2015-04-27 19:05:28
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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 56.0, 56.4, 84.6, 109.1, 114.2, 116.2, 120.3, 132.9, 139.0, 145.3, 146.8 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O CD3COOD C4D8O2 D2O CF3COOD CD3OD CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½39¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 1-O-methyl-guaiacylglycerol C11H16O5 ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2009 34 1672-1675 Chemical constituents from roots of Incarvillea mairei HUANG Zhengsheng, ZHANG Weidong, LIN Sheng, LIU Chunmei, HUANG Dasen, SONG Taifa, LU Longhai, PEI Yuehu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . nigrolineabiphenyl B C15H16O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2005 68 1218-1221 Benzopyran, Biphenyl, and Tetraoxygenated Xanthone Derivatives from the Twigs of Garcinia nigrolineata Vatcharin Rukachaisirikul, Kwanruthai Tadpetch, Anyarat Watthanaphanit, Neangnoi Saengsanae, and Souwalak Phongpaichit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . rel-(3R,3'S,4R,4'S)-3,3',4,4'-Tetrahydro-6,6'-dimethoxy[3,3'-bi-2H-benzopyran]-4,4'-diol C20H22O6 ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2000 Vol. 83 3344 Chemical Constituents of Tripterygium wilfordii Guangzhong Yang, Xueqiang Yin, and Yuanchao Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 1-(4-hydroxy-3-methoxyphenyl)propan-1,2-diol ÏàËÆ¶È:63.6% Phytochemistry 2004 65 1137-1143 Diarylheptanoids from the rhizomes of Zingiber officinale Jianping Ma, Xiaoling Jin, Li Yang, Zhong-Li Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1-(4-hydroxy-3-methoxyphenyl)-1-methoxypropan-2-ol C11H16O4 ÏàËÆ¶È:63.6% Planta Medica 2008 74 760-763 Constituents from Hoya parasitica and their Cell Growth Inhibitory Activity Samir Kumar Sadhu, Amina Khatun, Takashi Ohtsuki, Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . iso-nectandrin B C20H24O5 ÏàËÆ¶È:63.6% Acta Botanica Yunnanica 1997 19(2) 211-212 CHEMICAL CONSTITUENTSOF PIPER POLYSYPHORUM Zhang Ke, ¡¡Chen Changxiang, ¡¡Chen Defang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Crenulatin(part) C30H40O17 ÏàËÆ¶È:63.6% Chinese Chemical Letters 1992 3 111-112 A NOVEL GALLOTANNIN FROM RHODIOLA CRENULATA WE SHENG YU,XIN MIN CHEN,HONG LI,LEI YANG,YU FEI LI,LI SHENG DING Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . pinoresinol C20H22O6 ÏàËÆ¶È:63.6% Natural Product Research 2002 16 359-363 Pinoresinol from Ipomoea Cairica Cell Cultures Csilla P¨¢ska; Gabbriella Innocenti; Mariagrazia Ferlin; M¨®nika Kunv¨¢ri; Mikl¨®s L¨¢szl¨® Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . pinoresinol C20H22O6 ÏàËÆ¶È:63.6% Fitoterapia 2001 72 80-82 Lignans from Strophanthus gratus S. Cowan, M. Stewart, D.K. Abbiw, Z. Latif ,S.D. Sarker,U, R.J. Nash Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . clemaphenol A C20H22O6 ÏàËÆ¶È:63.6% Acta Pharmaceutica Sinica 2001 Vol 36 278-280 STUDIES ON THE CHEMICAL COMPONENTS OF CLEMATIS CHINENSIS HE Ming; ZHANG Jing-hua; HU Chang-qi Structure 13C NMR ̼Æ×Ä£Äâͼ |

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