| ²é¿´: 326 | »Ø¸´: 3 | ||||
ÃÔ;±±¼«½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
άÆÕÇóÖú
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| 13C NMR (600 MHz, DMSO) ¦Ä 56.43, 56.83, 61.07, 63.54, 70.04, 70.10, 73.58, 73.61, 76.92, 76.95, 77.71, 77.83, 95.48, 95.78, 99.96, 100.45, 100.61, 103.91, 104.26, 104.94, 105.81,105.81, 110.75, 116.23, 120.65, 120.96, 121.80, 140.50, 148.52, 148.67, 151.39, 157.38, 157.38,161.56, 163.44, 163.44, 164.61, 164.61,182.53 |
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kerry
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
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- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ

2Â¥2013-07-20 11:08:25
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3Â¥2013-07-20 13:24:17
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
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karl2100: ½ð±Ò+1, лл»Ø¸´£¡ 2013-07-20 15:15:39
karl2100: ½ð±Ò+1, лл»Ø¸´£¡ 2013-07-20 15:15:39
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°´´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£º¹²²éµ½109¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ozturkoside A C39H40O20 ÏàËÆ¶È:69.2% Phytochemistry 2004 65 2095-2099 Three acylated flavone glycosides from Sideritis ozturkii Aytac & Aksoy F. PInar Şahin, Nurten Ezer,İhsan Çalş Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ozturkoside B C37H38O19 ÏàËÆ¶È:66.6% Phytochemistry 2004 65 2095-2099 Three acylated flavone glycosides from Sideritis ozturkii Aytac & Aksoy F. PInar Şahin, Nurten Ezer,İhsan Çalş Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . chrysoeriol-7-O-[2''-O-(5'''-O-feruloyl)-¦Â-D-apiofuranosyl]-¦Â-D-glucopyranoside C37H38O18 ÏàËÆ¶È:61.5% Journal of Natural Products 2009 72 1563-1567 Triterpenoids and Flavonoids from Celery (Apium graWeolens) Kailan Zhou, Feng Zhao, Zhihui Liu, Yulei Zhuang, Lixia Chen,and Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ozturkoside C C39H40O19 ÏàËÆ¶È:61.5% Phytochemistry 2004 65 2095-2099 Three acylated flavone glycosides from Sideritis ozturkii Aytac & Aksoy F. PInar Şahin, Nurten Ezer,İhsan Çalş Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . isorhamnetin-3-O-¦Â-D-glucopyranosyl-7-O-¦Â-gentiobioside ÏàËÆ¶È:61.5% Acta Pharmaceutica Sinica 2004 Vol 39 46-51 Isolation and structure identification of chemical constituents from the seeds of Descurainia sophia (L.) Webb ex Prantl WANG Ai qin; WANG Xiu kun; LI Jun lin; CUI Xiang yu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Kaempferol3-O-[6"-O-sinapoyl-¦Â-D-glucopyranosyl](1¡ú2)-¦Â-D-galactopyranoside C38H40O20 ÏàËÆ¶È:58.9% Phytochemistry 1995 40 577-581 Flavonol sinapoyl glycosides from leaves of Thevetia peruviana Fumiko Abe, Yukiko Iwase, Tatsuo Yamauchi, Shoji Yahara, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ochnaflavone 7-O-¦Â-D-glucopyranoside C36H28O15 ÏàËÆ¶È:58.9% Journal of Shenyang Pharmaceutical University 2009 26 868-870 Chemical constituents from the leaves of Lonicera japonica Thunb. MA Jun-li, LI Ning, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6''-O-(2-O-trans-sinapoyl-¦Â-D-glucopyranosyl)-7-O-trans-sinapoylisovitexin C49H51O23 ÏàËÆ¶È:58.9% Tetrahedron 2005 61 7037-7044 Five novel flavonoids from Wasabia japonica Takahiro Hosoya, Young Sook Yun, Akira Kunugi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . apigenin-7-O-¦Â-D-glucopyranoside-(3'-O-7'')-quercetin-3''-methyl ether C37H30O17 ÏàËÆ¶È:58.9% Journal of the Chinese Chemical Society 2004 51 629-636 Chemical Components of Seriphidium santolium Poljak Yan-Ru Deng, Ai-Xin Song and Han-Qing Wang* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Kaempferol3-O-¦Â-D-glucopyranosyl(1¡ú4)[6"-O-sinapoyl-¦Â-D-glucopyranosyl](1¡ú2)-¦Â-D-galactopyranoside C44H50O25 ÏàËÆ¶È:58.1% Phytochemistry 1995 40 577-581 Flavonol sinapoyl glycosides from leaves of Thevetia peruviana Fumiko Abe, Yukiko Iwase, Tatsuo Yamauchi, Shoji Yahara, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6''-O-(2-O-trans-sinapoyl-¦Â-D-glucopyranosyl)-7-O-trans-sinapoylisovitexin 4'-O-¦Â-D-glucopyranoside C55H61O28 ÏàËÆ¶È:56.8% Tetrahedron 2005 61 7037-7044 Five novel flavonoids from Wasabia japonica Takahiro Hosoya, Young Sook Yun, Akira Kunugi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ginkgetin 7''-O-¦Â-D-glucopyranoside C38H32O15 ÏàËÆ¶È:56.4% Chemical & Pharmaceutical Bulletin 2005 53(9) 1200-1201 Biflavone Glucosides from Ginkgo biloba Yellow Leaves Sook Kyung HYUN,Sam Sik KANG,Kun Ho SON,Hae Young CHUNG,and Jae Sue CHOI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Quercetin3-O-[6"-O-sinapoyl-¦Â-D-glucopyranosyl](1¡ú2)-¦Â-D-galactopyranoside C38H40O21 ÏàËÆ¶È:56.4% Phytochemistry 1995 40 577-581 Flavonol sinapoyl glycosides from leaves of Thevetia peruviana Fumiko Abe, Yukiko Iwase, Tatsuo Yamauchi, Shoji Yahara, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . chrysoeriol-7-O-(2,6-dirhamnosyl)-glucoside ÏàËÆ¶È:56.4% Pharmazie 2001 56 348-349 New methoxyflavone glycosides from Verbena bipinnatifida Nutt H.N. Michael - J.Y. Salib - M.S. Ishak Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . luteolin-7-O-neohesperidoside-4'-O-sophoroside ÏàËÆ¶È:56.4% Acta Chemica Scandinavica 1979 33 675-683 Two New Acyclic Diterpenoids from Nicotiana sylvestris. Wallin, Ingrid; Narbonne, Claudine; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . quercetin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:56.4% Natural Product Research and Development 2013 25 197-200 Chemical Constituents from Root Wood of Cudrania cochinchinensis LIU Zhi-ping, ZHOU Min, LIU Sheng, GAN Chun-fang, WEI Wan-xing Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Pedunculosumoside A C39H50O22 ÏàËÆ¶È:56.4% Journal of Natural Products 2011 74 683-689 Homoflavonoid Glucosides from Ophioglossum pedunculosum and Their Anti-HBV Activity Chuan-Xing Wan, Ping-Hu Zhang, Jian-Guang Luo, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Pedunculosumoside E C34H42O22 ÏàËÆ¶È:56.4% Journal of Natural Products 2011 74 683-689 Homoflavonoid Glucosides from Ophioglossum pedunculosum and Their Anti-HBV Activity Chuan-Xing Wan, Ping-Hu Zhang, Jian-Guang Luo, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Luteolin 7-O-[(6'''-caffeoyl)-¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside C36H36O19 ÏàËÆ¶È:56.4% Chemistry of Natural Compounds 2012 47 888-890 Identification of a new flavone glycoside from Codonopsis nervosa Xian-li Zhou, Qiang Fan, Shuai Huang, Cui-juan Wang and You-song Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . luteolin-7-O-¦Â-D-glucopyranosyl-(1¡ú6)-[6'''-O-caffeoyl]-¦Â-D-glucopyranoside C36H36O19 ÏàËÆ¶È:56.4% Chinese Journal of Natural Medicines 2012 10 366-369 Chemical constituents from the aerial parts of Codonopsis nervosa Er-Bu AGA, Hui-Jun LI, Jun CHEN, Ping LI Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . platanoside M C43H48O24 ÏàËÆ¶È:55.8% Fitoterapia 2012 83 281-285 Acylated flavonol glycoside from Platanus orientalis Mudasir A. Tantry, Seema Akbar, Javid A. Dar, Syed Irtiza, Ahmed Galal, Mohammad A. Khuroo, Khalid Ghazanfar Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . quercetin 3-O-[(6-O-trans-feruloyl-¦Â-glucopyranosyl)-(1¡ú2)-¦Â-arabinopyranoside]-7-O-¦Â-glucopyranoside C42H46O24 ÏàËÆ¶È:54.7% Journal of Natural Products 2000 63 845-847 A New Acylated Flavonol Triglycoside from Carrichtera annua Khaled A. Abdel-Shafeek, Moustafa M. El-Messiry, Abdelaaty A. Shahat, Sandra Apers, Luc Pieters, and Medhat M. Seif-El Nasr Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-07-20 14:02:43














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