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²éѯ½á¹û£º¹²²éµ½173¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5-hydroxymethyl-2-furancarboxaldehyde C6H6O3 ÏàËÆ¶È:83.3% Planta Medica 1990 56 472-474 New Furans from Cirsium chiorolepis Yue-mao Shen and Quan-zhang Mu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 5-hydroxymethyl-2-furancarboxaldehyde C6H6O3 ÏàËÆ¶È:83.3% Planta Medica 1990 56 472-474 New Furans from Cirsium chiorolepis Yue-mao Shen and Quan-zhang Mu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-(hydroxymethyl)-2-furfuraldehyde ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1993 41 1469-1471 Studies on Aldose Reductase Inhibitors from Natural Products. V. Active Components of Hachimi-jio-gan (Kampo Medicine) Mineo SHIMIZU,Yutaka ZENKO,Ryoichi TANAKA,Tomoko MATSUZAWA and Naokata MORITA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-Hydroxymethyl-furfural ÏàËÆ¶È:83.3% Journal of Chinese Pharmaceutical Sciences 2006 15 127-129 Chemical Constituents of Roots of Ranunculus ternatus Thunb. HU Xiao-yan; DOU De-qiang; PEI Yu-ping; and FU Wen-wei Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-hydroxymethyl furfural ÏàËÆ¶È:83.3% Natural Product Research 2003 17 337-339 Insecticidal Compounds against Drosophila Melanogaster from Cornus Officinalis Sieb. Et Zucc. Mitsuo Miyazawa; Jun Anzai; Jun Fujioka; Yukio Isikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-hydroxymethyl-furaldehyde ÏàËÆ¶È:83.3% Natural Product Research 2009 23 1013-1020 Fructose-derived carbohydrates from Alisma orientalis Zhen Zhang; Dong Wang; Yun Zhao; Hong Gao; Ying-He Hu; Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5-hydroxymethol-2-furfural ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2009 34 410-413 Chemical constituents from involatile moiety of Pogostemon cablin HUANG Liejun, MU Shuzhen, ZHANG Jianxin, DENG Bin, SONG Zhiqin, HAO Xiaojiang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-hydroxymethyl-2-furancarboxaldehyde ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2009 34 2200-2202 Chemical constituents of Lobelia chinensis HAN Jinglan, Zhang Fengling, LI Zhihong, DU Guanhua, QIN Hailin Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-(hydroxymethyl)furfural ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2008 33 1272-1274 Studies on chemical constituents of Dioscorea opposita BAI Bing, LI Mingjing, WANG Yong, LIU Xiuhua Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-hydroxymethyl-2-furadehyde ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2006 31 656-658 Studies on chemical constituents in root of Phlomis medicinalis I YU Zhenxi, WANG Gangli, BIANBA Ciren, LIN Ruichao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5-hydroxymethyl furfural ÏàËÆ¶È:83.3% Acta Pharmaceutica Sinica 1999 Vol 34 448-450 LIPOSOLUBLE CONSTITUENTS FROM THE ROOTSOF SCROPHULARIA NINGPOENSIS Li Yiming(Li YM); Jiang Shanhao(Jiang SH); Gao Wenyun(Gao WY) and Zhu Dayuan(Zhu DY) Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4-hydroxymethyl-2-furaldehyde C6H6O3 ÏàËÆ¶È:83.3% Acta Pharmaceutica Sinica 1999 Vol 34 297-300 CHEMICAL CONSTITUENTS FROM THE RHIZOMES OF PHLOMIS UMBROSA TURCZ Fu Hongzheng (Fu HZ); Liu Shiwang (Liu SW) and Lin Wenhan (Lin WH) Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5-hydroxymethylfurfural C6H6O3 ÏàËÆ¶È:83.3% Natural Product Sciences 2002 8 30-33 Monoamine Oxidase Inhibitors from Aquilaria agallocha Huong, Dang Thi Lan; Dat, Nguyen Tien; Minh, Chau Van; Kang, Jong-Seong; Kim, Young-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-(hydroxymethyl)-2-furfural ÏàËÆ¶È:83.3% Korean Journal of Pharmacognosy 1999 30(2) 173-176 A Nitric Oxide Synthesis Inhibitor from the Roots of Gentiana scabra in RAW 264.7 Cells Kim, Na-Young; Kang, Tai-Hyun; Kim, Do-Hoon; Kim, Youn-Chul Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 5-ôǼ׻ù¿·È©(5-hydroxym ethyl-2-furalclehyde) C6H6O3 ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 7 881-885 Studies on anti-tumormetastatic constituents from Ardisia Crenata WANG Xue, TANG Shen gan, ZHAI Huiyuan, DUAN Hongquan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 5-ôǼ׻ù-2-߻ૼ×È© ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-hydroxy-methyl furaldehyde C6H6O3 ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 365-367 ¸Ü°å¹éµÄ»¯Ñ§³É·ÖÑо¿(¢ò) ÕÔ³¬;³Â»ª¹ú;¹¨Ð¡¼û;²Ü¹ðºì;ÖÜìøæÂ;ÖÜÐÀ Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-hydroxymethyl-2furaldehyde ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 517-520 Chemical constituents of Baihe Zhimu Decoction(¢ñ) FANG Qian-bo; QIN Kun-ming; PAN Yang; LI Wei-dong; CHEN Zhi-peng; CAI Bao-chang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 5-hydroxymethylfurfural ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 877-881 ¸ÊË컯ѧ³É·ÖµÄÑо¿ ÎâÏþÀÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 5-hydroxymethyl-furaldehyde ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2009 40 98-100 ¶ÀÐв˻¯Ñ§³É·ÖÑо¿ Óà¶«»Ô;Áº¾´îÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Á-ôǼ׻ù¿·È© C6H6O3 ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2009 40 106-108 Ò°Î÷¹Ï»¯Ñ§³É·ÖµÄÑо¿(¢ñ) ·ëС·;ÐÁº£Á¿;ÕÅÀÚ;·½ð²Å;ÍõÓñÁÁ Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 5-hydroxymethyl-2-furaldehyde C6H6O3 ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2008 39 972-975 Chemical constituents from roots of Millettia speciosa WANG Chun-hua; WANG Ying; WANG Guo-cai; YA Ji; ZHANG Xiao-qi; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 2-formyl-5-hydroxymethylfuran C6H6O3 ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2003 34 300-302 Studies on chemical constituents of Isodon eriocalyx var. laxiflora ţѩ÷; Àèʤºì; ÄÉÖÇ; ÷˫ϲ; ÕÔÇÚʵ; Ëﺺ¶ Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 1998 29 730-731 ʯÝÅÆÑË®¼åÒº»¯Ñ§³É·ÖµÄÑо¿ ÑîÏþÑà Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 5-ôǼ׻ù-2-߻ૼ×È© ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 1782-1785 ¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿ ÕÅΰ;ËÎÆôʾ Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 5-methoxyfurfural ÏàËÆ¶È:83.3% Chinese Journal of Natural Medicines 2004 2 149-151 Studies on the Constituents of Citrus medica L.var. Sarcodactylis(Noot.)Swingle YIN Feng; CHENG Liang; LOU Feng-Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 5-hydroxymethyl-furaldehyde ÏàËÆ¶È:83.3% Chinese Journal of Natural Medicines 2006 4 181-184 Chemical Constituents of Asparagus officinalis HUANG Xue-Feng; LUO Jun; ZHANG Yong; KONG Ling-Yi Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 6-Hydroxy-2H-pyran-3-carbaldehyde C6H6O3 ÏàËÆ¶È:83.3% Pharmazie 2008 63 405-407 A new tyrosinase inhibitor from Crinum yemense as potential treatment for hyperpigmentation O. B. Abdel-Halim, A. M. Marzouk, R. Mothana and N. Awadh Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 5-hydroxymethylfurfural ÏàËÆ¶È:83.3% Archives of Pharmacal Research 2002 25 280-284 Phytochemical constituents from the fruits ofAcanthopanax sessiliflorus Sanghyun Lee, Bak-Kwang Kim, Seon Haeng Cho and Kuk Hyun Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 5-(Hydroxymethyl)furfural C6H6O3 ÏàËÆ¶È:83.3% Archives of Pharmacal Research 2003 26 15-20 Chemical constituents from the Hydrangea chinensis Ashraf Taha Khalil, Fang-Rong Chang, Yue-Han Lee, Chung-Yi Chen and Chih-Chuang Liaw, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 5-Hydroxymethyl-2-furancarboxaldehyde ÏàËÆ¶È:83.3% Archives of Pharmacal Research 2004 27 381-385 Phenolic and furan type compounds isolated fromGastrodia elata and their anti-platelet effects Mi Kyung Pyo, Jing Ling Jin, Yean Kyoung Koo and Hye Sook Yun-Choi Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (Hydroxymethyl)-2-furaldehyde ÏàËÆ¶È:83.3% Archives of Pharmacal Research 2007 30 665-669 Two new ¦Á-pyrones and other components from the cladodes of Opuntia dillenii Ying Kun Qiu, Yan Yan Zhao, De Qiang Dou, Bi Xia Xu and Ke Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2000 35 372-374 Studies on the chemical consitituents of Mycena dendrobii GUO Shun xing, CHEN Xiao mei, YANG Jun shan, CAO Wen qin, XIAO Sheng yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 5-hydroxymethyl furaldehyde ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2005 40 1373-1375 Studies on chemical constituents of Ranunculus ternatus (II) CHEN Yun, TIAN Jing-kui, CHENG Yi-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2008 43 971-973 Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . cirsiumaldehyde ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2008 43 1066-1069 Studies on Chemical Constituents in Fruit of Melia toosendan XIE Fan, ZHANG mian, ZHANG Chao-feng, WANG Zheng-tao, YU Bo-yang Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 5-hydroxylmethylfuraldehyde ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2009 44 1372-1374 Chemical Constituents of the Roots of Uritca fissa E.Pritz. JI Bao-quan, FENG Bao-min, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 5-hydroxymethyl furfural ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2009 44 1375-1377 Studies on Chemical Constituents of the Euonymus alatus(Thunb.) Sieb.¢ò ZHOU Xin, LIU Yun, GONG Xiao-jian, ZHAO Chao, CHEN Hua-guo Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Modern Chinese Medicine 2009 11(11) 21-22 Study on the Constituents of Ophiopogonis tuber Wang Qinghui, Li Xian, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Chinese Journal of Medicinal Chemistry 1999 9 48-49 Studies on the Chemical Constituents of Lonicera bournei Hemsl . II Xiang Ting, Wu Lijun, Lin Ruihong, Sun Junwei, Dai Xiaobin Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 5-hydroxymethylfurfural ÏàËÆ¶È:83.3% Chinese Journal of Medicinal Chemistry 2010 20 47-49 Chemical constituents of Lasiosphaera fenzlii Reich. GAO Yun-jia, ZHAO Qing-chun, MIN Peng, SHI Guo-bing, YAN M ing Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 5-hydroxymethylfuraldehyde ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2011 28 21-24 Isolation and identification of chemical constituents of root of Girardinia suborbiculata C. J. Chen subsp. Triloba FENG Bao-min, LIU Jing-yan, WANG Hui-guo, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 5-hydroxym ethyl furaldehyde ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2010 27 354-356 Isolation and identification of chemical constituents from aerial part of Euphorbia chrysocoma L¨¦v.i et Vant. (II) JIANG Chun-yong, MU Shu-zhen, DENG Bin, GE Yong-hui, ZHANG Jian-x in, HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 5-ôǼ׻ù¿·È© ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2008 25 796-799 Chemical constituents of the aerial parts of Polygonum capitatum YU Ming, LI Zhan-lin, LI Ning, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 5-(hydroxymethyl)-2-furfural ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2006 23 84-87 Chemistry study of Stellaria dichatoma L. var. lanceolata Bge. SUN Bo-hang, Yashikawa, CHEN Ying-jie, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . 5-hydroxymethyl furfural ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2005 22 12-14 Study on chemical constituents of Descurainia sophia (L.)Webb ex Prantl SUN Kai, LI Xian, KANG Xing-dong, LIU Li Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 5-hydroxymethyl furaldehyde ÏàËÆ¶È:83.3% Journal of Shenyang Pharmaceutical University 2002 19 27-29 Study on the chemical constituents of Achyranthes bidentata Bl. MENG Da-li, LI Xian, XIONG Yin-hua, WANG Jin-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 5-(hydroxymethyl)-2-furfuraldehyde ÏàËÆ¶È:83.3% Natural Product Research and Development 2010 22 54-57 Study on the Chemical Constituents of Pyrola calliantha H. Andres REN Feng-xia; ZHANG Ai-jun; ZHAO Yi-min Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 5-hydroxymethyl.-2-furancarboxaldehyde ÏàËÆ¶È:83.3% Natural Product Research and Development 2009 21 424-427 Chemical Constituents from the Endophytic Fungus Rhizoctonia sp. J5 of Antiaris toxicaria QUE Dong-mei; DAI Hao-fu; HUANG Gui-xiu; DAI Wen-jun; MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 5-hydroxymethyl-furfural ÏàËÆ¶È:83.3% Natural Product Research and Development 2009 21 239-241 Chemical Constituents from Radix Polygoni multiflori Thunb.after Preparing LIU Zhen-li; LI Lin-fu; CHAO Zhi-mao; SONG Zhi-qian; WANG Chun; ZHANG Ling Structure 13C NMR ̼Æ×Ä£Äâͼ |
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