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weiwei891203: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-09 11:38:35
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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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½11¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . maesapsin-6-O-glucopyranoside ÏàËÆ¶È:94.1% Phytochemistry 1997 46 97-102 Antimicrobial compounds from Ceanothus americanus against oral pathogens Xing-Cong Li, Linin Cai, Christine D.Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . maesopsin-6-O-glucopyranoside ÏàËÆ¶È:88.2% Chinese Pharmaceutical Journal 2009 44 334-336 Study on Chemical Constituents of Delphinium giraldii HE Yang-qing, MA Zhan-ying, YANG Qian, GAO Li-ming, TIAN Ping, DU Bao-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . hovetrichoside C ÏàËÆ¶È:86.8% Korean Journal of Pharmacognosy 2012 43 127-136 Flavonoids from the Seeds of Zizyphus jujuba var. spinosa Lee, So-Young; Lee, Joo-Young; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . hovetricoside C C21H22O11 ÏàËÆ¶È:81.5% Journal of Natural Products 1998 61 786-790 Hovetrichosides C-G, Five New Glycosides of Two Auronols, Two Neolignans, and a Phenylpropanoid from the Bark of Hovenia trichocarea Kazuko Yoshikawa, Kimura Eiko, Noriko Mimura, Yuko Kondo, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Vatalbinoside D C34H32O12 ÏàËÆ¶È:52.9% Journal of Natural Products 2010 73 1499-1506 Resveratrol Oligomers from Vatica albiramis Naohito Abe, Tetsuro Ito, Kenji Ohguchi, Minori Nasu, Yuichi Masuda, Masayoshi Oyama, Yoshinori Nozawa, Masafumi Ito, and Munekazu Iinuma Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . aprosmosides H C34H42O21S ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2002 50(8) 1035-1040 Iridoids and Anthraquinones from the Malaysian Medicinal Plant,Saprosma scortechinii (Rubiaceae) Sui-Kiong LING,Akiko KOMORITA, Takashi TANAKA,Toshihiro FUJIOKA, Kunihide MIHASHI,and Isao KOUNO Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . quercetin 5,7,4'-tri-O-¦Â-D-glucopyranoside C33H40O22 ÏàËÆ¶È:50% Phytochemistry 2002 59 275-278 Flavonoid 5-glucosides from the cocoon shell of the silkworm, Bombyx mori Yasumori Tamura, Ken-ichi Nakajima, Ken-ichi Nagayasu, Chiyuki Takabayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . kaempferol-3-O-[(6'"-O-trans-sinnapoyl)-¦Â-D-glucopyranosyl (1 ¡ú6)]-¦Â-D-glucopyranoside C38H40O20 ÏàËÆ¶È:50% Chinese Chemical Letters 2009 20 320-321 A new flavonoid glucoside from Cassia angustifolia Qiu Ping Wu, Zhu Ju Wang, Li Ying Tang, Mei Hong Fu, Yan He Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . quercetin-3-O-[¦Á-L-rhamnose-(1 ¡ú 2)-¦Â-D-glucopyranosyl]-5-O-¦Â-D-glucopyranoside C33H40O21 ÏàËÆ¶È:50% Journal of Asian Natural products Research 2010 12 1033-1037 Two new flavone glycosides from the seeds of Impatiens balsamina L. Jing Lei; Shi-Hui Qian; Jian-Qin Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . polygonflavanol A C35H34O15 ÏàËÆ¶È:50% Phytochemistry Letters 2012 5 756-760 Polygonflavanol A, a novel flavonostilbene glycoside from the roots of Polygonum multiflorum Li-Li Chen, Xiao-Jun Huang, Man-Mei Li, Guo-Min Ou, Bing-Xin Zhao, Min-Feng Chen, Qing-Wen Zhang, Ying Wang, Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Saprosmoside H C34H42O21S ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2007 55 159-222 Naturally Occurring Iridoids. A Review, Part 1 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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