| ²é¿´: 211 | »Ø¸´: 2 | ||
ÏòÎÄ·ÇÖÁ×ðľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
¼±ÇóÁ½×é΢Æ×Êý¾Ý лл
|
|
50.6, 114.0, 115.3, 121.6, 126.4, 145.1, 145.5, 148.1, 167.5 48.4, 111.5, 120.6, 122.0, 126.1, 131.6, 136.4, 165.8 §Ý§Ý |
» ²ÂÄãϲ»¶
081700£¬311£¬Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ17È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ21È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703µ÷¼Á
ÒѾÓÐ18È˻ظ´
0702ÎïÀíѧѧ˶299Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ19È˻ظ´
085600²ÄÁÏÓ뻯¹¤×¨Ë¶329 Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
ÉúÎïÓëÒ½Ò©273Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¼±Çó£ºÎ¢Æ×Êý¾ÝÇóÖú,лл
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú»¯ºÏÎï΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖúһ΢Æ×Êý¾Ý 15 лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
Çó²é΢Æ×Êý¾Ý¿â£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÔÚexcelÀï´¦ÀíÒ»ÏÂÊý¾ÝÇó΢·Ö£¬Çë¸ßÊÖÖ¸½ÌÒ»ÏÂ~ллÀ²~
ÒѾÓÐ15È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½418¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Methyl caffeate ÏàËÆ¶È:100% Archives of Pharmacal Research 2002 25 325-328 Anti-platelet effect of the constituents isolated from the barks and fruits of Magnolia obovata Mi Kyung Pyo, YongYook Lee and Hye Sook Yun-Choi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . trans-Caffeic acid methylate ÏàËÆ¶È:90% Journal of Chinese Pharmaceutical Sciences 2007 16 20-23 Chemical constituents of the unripe fruits of Evodia rutaecarpa Xiu-Wei Yang and Jie Teng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 1-methyl caffeic acid ÏàËÆ¶È:90% Natural Product Sciences 2005 11 75-78 A New Acetophenone of Aerial Parts from Rumex aquatica Yoon, Hwan-Min; Park, Ji-Yeun; Oh, Mi-Hyun; Kim, Kyung-Hee; Han, Jung-Hoon; Whang, Wan-Kyunn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . methylcaffeate ÏàËÆ¶È:90% China Journal of Chinese Materia Medica 2010 35 1142-1144 Flavonoids and phenolic acid derivatives from Flos Farfarae WU Di; ZHANG Mian; ZHANG Chaofeng; WANG Zhengtao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . caffeic acid methyl ester ÏàËÆ¶È:90% Chinese Pharmaceutical Journal 2011 46 338-340 Study on Chemical Constituents of Lonicerae Japonicae Flos FENG Wei-shenga, CHEN Xinga, ZHENG Xiao-keb, ZHANG Chun-lei, LI Dan-dana Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . caffeic acid methyl ester ÏàËÆ¶È:90% Food Chemistry 2010 118 228-238 Unusual sesquiterpene lactones with a new carbon skeleton and new acetylenes from Ajania przewalskii Ying Zhu, Li-Xia Zhang, Yan Zhao, Guo-Du Huang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . methyl caffeate C10H10O4 ÏàËÆ¶È:90% 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 -------------------------------------------------------------------------------- 8 . ¿§·ÈËá¼×õ¥ C10H10O4 ÏàËÆ¶È:90% Chinese Traditional and Herbal Drugs 2011 42 1481-1484 Chemical constituents from rhizome of Matteuccia orientalis SHAO, Peng, ZHANG, Xue, LI, Chang, SONG, Ying, WANG, Nai-li, YAO, Xin-sheng, Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . trans-caffeic acid C9H8O4 ÏàËÆ¶È:88.8% Journal of Natural Products 1998 61 993-996 Metabolism of Rosmarinic Acid in Rats Takahiro Nakazawa and Keisuke Ohsawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . caffeic acid ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2009 34 1002-1004 Chemical constituents from Neo -Taraxacum siphonathum SHI Shuyun, ZHOU Honghao, ZHANG Yup ing, HUANG Kel ong, LIU Suqin Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-25 07:50:15
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
ÏòÎÄ·Ç: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-09-25 17:20:58
ÏòÎÄ·Ç: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-09-25 17:20:58
|
²éѯ½á¹û£º¹²²éµ½388¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 1H-indole-3-carboxylicacid ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2009 34 994-998 Chemical constituents of A lisma orientalis and their immunosuppressive function ZHANG Chaofeng, ZHOU Aichun, ZHANG mian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . indolyl-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2010 41 870-873 Áõ¼ÄÅ«µÄ»¯Ñ§³É·ÖÑо¿ Î¾§;Ê·º£Ã÷;êÃçæ;ÁõÑÞ·¼;ÖÜÓêºç;³ÂÓñƽ;ÍÀÅô·É Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Antibiotics 2001 54 628-634 TMC-205 a New Transcriptional Up-Regulator of SV40 Promoter Produced by an Unidentified Fungus. Fermentation, Isolation, Physico-chemical Properties, Structure Determination and Biological Activities MASAAKI SAKURAI,JUN KOHNO,MAKI NISHIO,KOZO YAMAMOTO,TORU OKUDA,KIMIO KAWANO and NORIYUKI NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Organic Chemistry 1996 61 6591-6593 Arthrichitin. A New Cell Wall Active Metabolite from Arthrinium phaeospermum E. K. S. Vijayakumar, Kirity Roy, Sugata Chatterjee, S. K. Deshmukh, and B. N. Ganguli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Natural Product Research 2013 27 1366-1371 A new 20-membered macrolide produced by a marine-derived Micromonospora strain Peng Fei, Wang Chuan-xi, Xie Yang, Jiang Hong-lei, Chen Lu-jie, Paulina Uribe, Alan T. Bull, Michael Goodfellow, Jiang Hong & Lian Yun-yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ßÅßá-3-¼×Ëá ÏàËÆ¶È:77.7% Chinese Journal of Medicinal Chemistry 2012 22 38-43 Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:75% Modern Chinese Medicine 2008 10(12) 29-31 Studies on the Metabolites of Salvianolic Acid B Yuan Zheng, Li Guoyu, , Zeng Yimei, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 4-hydroxy isophthalic acid ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 2006 54 790-795 Novel Antioxidant Compounds from the Aqueous Extract of the Roots of Decalepis hamiltonii (Wight and Arn.) and Their Inhibitory Effect on Low-Density Lipoprotein Oxidation Anup Srivastava, R. Harish, and T. Shivanandappa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2011 28 938-946 Isolation and identification of the secondary metabolites from marine actinomycete KSC2-1 CAO, Guo-xiu, CHEN, Gang, XU, Wen-feng, WU, Hong-hua, PEI, Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ßÅßá-3-¼×Ëá¼×õ¥ C10H9O2N ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2009 26 964-967 Chemical constituents of aerial parts of Asarum heterotropides Fr. Schmidt var. mandshuricum (Maxim.)Kitaga. (2) XU Lei, WU Di, WU Zhao-hua, LV Shuai, GAO Hui-yuan, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . W2(S*,S*,S*)-(bino)3 ÏàËÆ¶È:66.6% Angewandte Chemie International Edition 1992 31 66-68 Unprecedented Stereospecific Ligand Exchange at a WGW Template Steven D. Dietz,Nancy W Eilerts,and Joseph A. Heppert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . bis(3-indolyl) ketone C17H12N2O ÏàËÆ¶È:66.6% Heterocycles 2004 63 2371-2377 Effect of Sodium Naphthalenide, a Key Set Reagent, on 3-Substituted Indoles Avijit Banerji*, Debasish Bandyopadhyay, and Bidyut Basak Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . indole-3-carboxylic acid ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung C 2011 66 485-490 Effects of Indole Amides on Lettuce and Onion Germination and Growth T. F. Borgati and M. A. D. Boaventura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:66.6% Plant Diversity and Resources 2012 34 101-106 New Withanolides from Nicandra physaloides (Solanaceae) YI Qian-Kun, LI Bo, LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . quindoline ÏàËÆ¶È:62.5% Planta Medica 1996 62 22-27 In Vitro Biological Activities of Alkaloids from Cryptolepis sanguinolenta Kanyanga Cimanga, TessDeBruyne. AleidisLasure, Bart Van Poel, Luc Pieters, Magda Claeys. Dirk VandenBerghe. Kabangu Kambu, Lutete Tona, andArnoldi Vlietinck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 16-epiaffinine ÏàËÆ¶È:62.5% Journal of Natural Products 1985 Vol 48 571-580 Chemistry of the Annonaceae, Part 18. Benzylated Indoles and Dihydrochalcones in Uvaria angolensis from Tanzania Ilias Muhammad, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . indole ÏàËÆ¶È:62.5% Journal of Natural Products 1986 Vol 49 534 3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia A. O. Adeoye, B. O. Oguntimein, A. M. Clark, C. D. Hufford Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 4 ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 2010 88 548-555 The dehydrogenation of combined organic and inorganic hydrogen-storage carriers Dominik Wechsler, Boyd Davis, and Philip G. Jessop Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 1c C10H8ClN ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2000 37 15-24 Synthesis and nuclear magnetic resonance spectroscopic studies of 1-arylpyrroles Chang Kiu Lee, Jung Ho Jun and Ji Sook Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 1H-dibenzo[2,3:6,7]oxepino[4,5-d]imidazole C15H11N2O ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2010 47 640-656 Novel tetracyclic imidazole derivatives: Synthesis, dynamic NMR study, and anti-inflammatory evaluation Renata Rupčić, Marina Modrić, Antun Hutinec, Ana Čikoš, Barbara Stanić, Milan Mesić, Dijana Pešić and Mladen Merćep Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-09-25 07:53:17














»Ø¸´´ËÂ¥