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chengmiaojyгæ (СÓÐÃûÆø)
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[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»
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| 13C NMR (75 MHz, MeOD) ¦Ä 29.19, 35.07,38.41, 66.93, 80.30, 96.33,105.22, 106.01, 115.07, 115.77, 116.41, 119.33,129.16,131.69,134.51, 145.83,145.96, 152.05, 153.51,157.28, 170.74. |
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²éѯ½á¹û£º¹²²éµ½101¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ±í¶ù²èËØ-[8,7-e]-4¦Â-(4-ôÇ»ù±½)-3,4-¶þôÇ»ù-2(3H)-ßÁà«Íª ÏàËÆ¶È:95.4% Natural Product Research and Development 2005 17 131-137 Studies on the Active Constituents of Asparagi Radix XU Cong-li; CHEN Hai-sheng *; TAN Xing-qi; XUAN Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ±í¶ù²èËØ-[8,7-e]-4¦Á-(4-ôÇ»ù±½)-3,4-¶þôÇ»ù-2(3H)-ßÁà«Íª ÏàËÆ¶È:95.4% Natural Product Research and Development 2005 17 131-137 Studies on the Active Constituents of Asparagi Radix XU Cong-li; CHEN Hai-sheng *; TAN Xing-qi; XUAN Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Corbulain Ia C24H21O8 ÏàËÆ¶È:87.5% Phytochemistry 2011 72 495-502 Estrogenic and anti-estrogenic compounds from the Thai medicinal plant, Smilax corbularia (Smilacaceae) Boonsong Wungsintaweekul, Kaoru Umehara, Toshio Miyase, Hiroshi Noguchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Corbulain Ib C24H20O8 ÏàËÆ¶È:87.5% Phytochemistry 2011 72 495-502 Estrogenic and anti-estrogenic compounds from the Thai medicinal plant, Smilax corbularia (Smilacaceae) Boonsong Wungsintaweekul, Kaoru Umehara, Toshio Miyase, Hiroshi Noguchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . apocynin C ÏàËÆ¶È:86.3% Chemical & Pharmaceutical Bulletin 1999 47 1049-1050 Apocynins A-D : New Phenylpropanoid-substituted Flavan-3-ols Isolated from Leaves of Apocynum venetum (Luobuma-Ye) Wenzhe FAN,Yasuhiro TEZUKA,Quanbo XIONG,Masao HATTORI,Tsuneo NAMBA and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Epicatechin-(7,8-bc)-48-(4-hydroxyphenyl)-dihydro-2(3H)-pyranone ÏàËÆ¶È:83.3% Phytochemistry 1994 35 545-546 Phenylpropanoid-catechins from bark of Ocotea porosa Jorge M. David, Massayoshi Yoshida, Otto R. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Epicatechin-(7,8-bc)-4a-(4-hydroxyphenyl)-dihydro-2(3H)-pyrunone ÏàËÆ¶È:83.3% Phytochemistry 1994 35 545-546 Phenylpropanoid-catechins from bark of Ocotea porosa Jorge M. David, Massayoshi Yoshida, Otto R. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ±í¶ù²èËØ-[8,7-e]-4¦Á-(3,4-ôÇ»ù±½)-3,-4-¶þôÇ»ù-2(3H-)-ßÁà«Íª ÏàËÆ¶È:83.3% Natural Product Research and Development 2005 17 131-137 Studies on the Active Constituents of Asparagi Radix XU Cong-li; CHEN Hai-sheng *; TAN Xing-qi; XUAN Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . epicatechin-(7,8-bc)-4¦Á-(3,4-dihydroxyphenyl)-dihydro-2(3H)-pyranone ÏàËÆ¶È:82.6% Phytochemistry 1987 26 2825-2830 Phenylpropanoid derivatives of catechin,epicatechin and phylloflavan from Phyllocladus trichomanoides Lai Yeap Foo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . cinchonain Ib C24H20O9 ÏàËÆ¶È:82.6% Chinese Traditional and Herbal Drugs 2008 39 975-977 ÝÃÝÖ»¯Ñ§³É·Ö¼°Æä¿¹Ñõ»¯»îÐÔµÄÑо¿ ÕÔÖÓÏé;·ëÓýÁÖ;Èî½ðÀ¼;×£³¿Êc;ÑîÊÀÁÖ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 1 C24H20O9 ÏàËÆ¶È:79.1% Natural Medicines 2000 54 97-100 Cytotoxic Constituents from Erythroxylum catuaba Isolation and Cytotoxic Activities of Cinchonain SATOH Mitsuru,SATOH Yoshio,FUJIMOTO Yasuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 2 C24H20O9 ÏàËÆ¶È:79.1% Natural Medicines 2000 54 97-100 Cytotoxic Constituents from Erythroxylum catuaba Isolation and Cytotoxic Activities of Cinchonain SATOH Mitsuru,SATOH Yoshio,FUJIMOTO Yasuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Cinchonain Ia C24H20O9 ÏàËÆ¶È:79.1% Natural Product Research and Development 2012 24 8-11 Chemical Constituents of Gaultheria yunnanensis FU Jiao-long; TAN Chang-heng; TAN Jun-jie; CHEN Jia-jia; QIU Ye-xian; ZHU Da-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . apocynin A ÏàËÆ¶È:77.2% Chemical & Pharmaceutical Bulletin 1999 47 1049-1050 Apocynins A-D : New Phenylpropanoid-substituted Flavan-3-ols Isolated from Leaves of Apocynum venetum (Luobuma-Ye) Wenzhe FAN,Yasuhiro TEZUKA,Quanbo XIONG,Masao HATTORI,Tsuneo NAMBA and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . epicatechn-[5,6-e]-4¦Â-(3,4-dihydroxyphenyl)-dihydro-2(3H)-pyranone ÏàËÆ¶È:77.2% Phytochemistry 1989 28 2477-2481 Flavanocoumarins and flavanophenylpropanoids from Phyllocladus trichomanoides Lai Yeap Foo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . smiglabrone B C25H22O9 ÏàËÆ¶È:76% Molecules 2013 18 5265-5287 Chemical Constituents from the Rhizomes of Smilax glabra and Their Antimicrobial Activity Shuo Xu, Ming-Ying Shang, Guang-Xue Liu, Feng Xu, Xuan Wang, Cheng-Chao Shou and Shao-Qing Cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . cinchonain Ib C24H20O9 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1982 30 4268-4276 Tannins and Related Compounds. VII. Phenylpropanoid-substituted Epicatechins, Cinchonains from Cinchona succirubra. (1) GENICHIRO NONAKA and ITSUO NISHIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 1 C24H20O9 ÏàËÆ¶È:75% Zeitschrift f¨¹r Naturforschung C 2002 57 483-488 Two Epimeric Flavalignans from Trichilia catigua (Meliaceae) with Antimicrobial Activity Key words: Trichilia catigua, Flavalignans, Antimicrobial Activity Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . epicatechin-(7,8-bc)-4¦Â-(3,4-dihydroxyphenyl)-dihydro-2(3H)-pyranone ÏàËÆ¶È:73.9% Phytochemistry 1987 26 2825-2830 Phenylpropanoid derivatives of catechin,epicatechin and phylloflavan from Phyllocladus trichomanoides Lai Yeap Foo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . apocynin B ÏàËÆ¶È:72.7% Chemical & Pharmaceutical Bulletin 1999 47 1049-1050 Apocynins A-D : New Phenylpropanoid-substituted Flavan-3-ols Isolated from Leaves of Apocynum venetum (Luobuma-Ye) Wenzhe FAN,Yasuhiro TEZUKA,Quanbo XIONG,Masao HATTORI,Tsuneo NAMBA and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . smiglabrone A C26H24O10 ÏàËÆ¶È:72% Molecules 2013 18 5265-5287 Chemical Constituents from the Rhizomes of Smilax glabra and Their Antimicrobial Activity Shuo Xu, Ming-Ying Shang, Guang-Xue Liu, Feng Xu, Xuan Wang, Cheng-Chao Shou and Shao-Qing Cai Structure 13C NMR ̼Æ×Ä£Äâͼ |
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