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| 13C NMR (126 MHz, cd3od) ¦Ä61.08,70.15,74.61,75.00,77.27,93.10,98.26,99.12,104.44,109.15,114.69,115.63,120.06,121.73,121.93,133.50,138.42,144.53,144.89,148.24,156.80,156.86,161.67,164.27,166.38,177.65 |
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-19 20:50:55
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-19 20:50:55
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²éѯ½á¹û£º¹²²éµ½263¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Quercetin 3-O-¦Â-D-(6''-galloyl)glucopyranoside ÏàËÆ¶È:92.3% Journal of Agricultural and Food Chemistry 2003 51 6689-6695 Chemical Composition and Antioxidant Activity of Phenolic Compounds from Wild and Cultivated Sclerocarya birrea (Anacardiaceae) Leaves Alessandra Braca, Matteo Politi, Rokia Sanogo, Haby Sanou, Ivano Morelli, Cosimo Pizza, and Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Quercetin 3-O-¦Á-D-(6''-galloyl)galactopyranoside ÏàËÆ¶È:84.6% Journal of Agricultural and Food Chemistry 2003 51 6689-6695 Chemical Composition and Antioxidant Activity of Phenolic Compounds from Wild and Cultivated Sclerocarya birrea (Anacardiaceae) Leaves Alessandra Braca, Matteo Politi, Rokia Sanogo, Haby Sanou, Ivano Morelli, Cosimo Pizza, and Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Quercetin 3-O-(2''-O-galloyl)-¦Â-D-galactopyranoside ÏàËÆ¶È:84.6% Archives of Pharmacal Research 2013 36 1533-1540 Flavonoid constituents in the leaves of Myrica rubra sieb. et zucc. with anti-inflammatory activity Han Hyuk Kim, Dong Hee Kim, Manh Heun Kim, Myoeng Hwan Oh, So Ra Kim, Kwang Jun Park, Min Won Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . quercetin 3-O-(6''-O-Galloyl)-¦Â-galactoside C28H24O16 ÏàËÆ¶È:80.7% Chemistry of Natural Compounds 2012 48 477-479 Phenolic compounds from the leaves of Psidium guajava II. Quercetin and its glycosides Byoung-Jae Park, Tomohiko Matsuta, Tsutomu Kanazawa, Cheol-Ho Park and Kwang-Jin Chang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . quercetin-3-O-2''-galloyl-rhamnoside ÏàËÆ¶È:76.9% Chinese Traditional and Herbal Drugs 2013 44 1391-1396 Phenolic constituents from twigs of Acer rubrum and their anti-oxidation and anti-¦Á-glucosidase activities WAN Chun-peng, ZHOU Shou-ran Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . quercetin-3-O-(2''-O-coumaroyl)-¦Â-D-glucoside C30H26O14 ÏàËÆ¶È:76.6% Food Chemistry 2012 135 1929-1937 Antioxidant and ¦Á-glucosidase inhibitory phenolics isolated from highbush blueberry flowers Chunpeng Wan, Tao Yuan, Amanda L. Cirello, Navindra P. Seeram Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Quercetin-3-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:74.0% Archives of Pharmacal Research 2010 33 67-70 Tribuli fructus constituents protect against tacrine-induced cytotoxicity in HepG2 cells Erisa Byun, Gil-Saeng Jeong, Ren-Bo An, Tae Sun Min and Youn-Chul Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Quercetin-3-O-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranoside ÏàËÆ¶È:74.0% Bioorganic & Medicinal Chemistry 2014 22 937-944 Synthesis of quercetin glycosides and their melanogenesis stimulatory activity in B16 melanoma cells Kosei Yamauchi, Tohru Mitsunaga, Irmanida Batubara Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . quercetin 3-O-¦Â-D-glucoside ÏàËÆ¶È:73.0% Natural Product Sciences 2009 15 90-95 Phytochemical Constituents of Nelumbo nucifera Kim, Ki-Hyun; Chang, Sang-Wook; Ryu, Shi-Yong; Choi, Sang-Un; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . quercetin 3-O-¦Â-D-glucoside ÏàËÆ¶È:73.0% Molecules 2010 15 2593-2599 A New Sulfated ¦Á-Ionone Glycoside from Sonchus erzincanicus Matthews Ufuk Ozgen, Handan Sevindik, Cavit Kazaz, Demet Yigit, Ali Kandemir, Hasan Secen and Ihsan Calis Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . isoquercitrin ÏàËÆ¶È:73.0% Chinese Journal of Natural Medicines 2008 6 418-420 Chemical Constituents of Gardenia jasminoides Ellis FU Xiao-Mei; ; CHOU Gui-Xin; WANG Zheng-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . myricetin 3-O-(2''-galloyl)-¦Â-D-galactopyranoide ÏàËÆ¶È:73.0% Molecules 2011 16 8305-8318 Inhibitory Effects of Constituents from Euphorbia lunulata on Differentiation of 3T3-L1 Cells and Nitric Oxide Production in RAW264.7 Cells Zhi-Gang Yang, Liu-Nan Jia, Yan Shen, Atsuko Ohmura and Susumu Kitanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . quercetin 3-O-¦Â-glucopyranoside ÏàËÆ¶È:73.0% Phytotherapy Research 1998 12 562-567 Flavonol monoglycosides isolated from the antiviral fractions of Persea americana (Lauraceae) leaf infusion A. P. de Almeida, M. M. F. S. Miranda, I. C. Simoni, M. D. Wigg, M. H. C. Lagrota and S. S. Costa Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isoquercetrin C21H20O12 ÏàËÆ¶È:73.0% Turkish Journal of Chemistry 2009 33 521-526 Chemical constituents and mushroom tyrosinase inhibition activity of Chloroxylon swietenia leaves G. VENKATATESWARA RAO, K. SAMBASIVA RAO, TIRUGANASAMBANDHAM ANNAMALAI, NARAYANASAMY RADHAKRISHNAN, TRIPTIKUMAR MUKHOPADHYAY Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . quercetin-3-O-¦Â-glucoside ÏàËÆ¶È:73.0% Korean Journal of Pharmacognosy 2012 43 201-205 Flavonoids Constituents of Duchesnea chrysantha Liu, Qing; Ahn, Jong-Hoon; Kim, Seon-Beom; Hwang, Bang-Yeon; Lee, Mi-Kyeong Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . quercetin-3-O-¦Â-D-glucoside C21H20O12 ÏàËÆ¶È:73.0% Food Chemistry 2012 135 1929-1937 Antioxidant and ¦Á-glucosidase inhibitory phenolics isolated from highbush blueberry flowers Chunpeng Wan, Tao Yuan, Amanda L. Cirello, Navindra P. Seeram Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Quercetin-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:73.0% Bioorganic & Medicinal Chemistry 2014 22 937-944 Synthesis of quercetin glycosides and their melanogenesis stimulatory activity in B16 melanoma cells Kosei Yamauchi, Tohru Mitsunaga, Irmanida Batubara Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Quercetin-3-O-¦Â-D-glucopyranoside (Isoquercitrin) ÏàËÆ¶È:73.0% Archives of Pharmacal Research 2011 34 543-550 A dimeric triterpenoid glycoside and flavonoid glycosides with free radical-scavenging activity isolated from Rubus rigidus var. camerunensis T¨¦lesphore Benoît Nguelefack, F¨¦licit¨¦ Hermine Kamga Mbakam, L¨¦on Az¨¦fack Tapondjou, Pierre Watcho and Elvine Pami Nguelefack-Mbuyo, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . quercetin-3-O-¦Â-D-glucoside ÏàËÆ¶È:73.0% China Journal of Chinese Materia Medica 2013 38 3295-3298 A new eremophilane derivative from Senecio dianthus HAN He-dong, HU Hai-qing, LI Yan, WANG Xiao-ling* Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . astragalin-2'',6''-di-O-gallate C35H28O19 ÏàËÆ¶È:70.9% Natural Product Research and Development 1997 9(3) 12-18 NEW GALLOYLATED FLAVONOIDAL GLYCOSIDE AND GALLOTANNINS FROM THE LEAVES OF LOROPETALUM CHINENSE OLIV. Liu Yanze; Wu Yangjie; Yuan Ke; Ji Chunru; Wang Ling Takashi Yoshida; Takuo Okuda Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . rutin ÏàËÆ¶È:70.3% Chinese Journal of Natural Medicines 2008 6 418-420 Chemical Constituents of Gardenia jasminoides Ellis FU Xiao-Mei; ; CHOU Gui-Xin; WANG Zheng-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ |
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