| ²é¿´: 320 | »Ø¸´: 1 | ||
magicalgangÌú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
14.01,22.53,30.83,31.49,32.11,36.02,55.22,76.69,77.01,77.33,98.68,106.73,107.91,145.74,156.57,160.79 ÈܼÁ ÂÈ·Â |
» ²ÂÄãϲ»¶
333Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
321Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
348Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0703»¯Ñ§
ÒѾÓÐ8È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ11È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ10È˻ظ´
0703Çóµ÷¼Á383·Ö
ÒѾÓÐ7È˻ظ´
0703»¯Ñ§µ÷¼Á325·Ö
ÒѾÓÐ4È˻ظ´
329Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
magicalgang: ½ð±Ò+15, ¡ïÓаïÖú 2014-10-26 00:01:12
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
magicalgang: ½ð±Ò+15, ¡ïÓаïÖú 2014-10-26 00:01:12
|
²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5-Pentyl-3-methoxy-N-butylaniline ÏàËÆ¶È:75% Phytochemistry 2009 70 1233-1238 Anti-mosquito and antimicrobial nor-halimanoids, isocoumarins and an anilinoid from Tessmannia densiflora Charles Kihampa, Mayunga H.H. Nkunya, Cosam C. Joseph, Stephen M. Magesa, Ahmed Hassanali, Matthias Heydenreich , Erich Kleinpeter Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . monomethyl olivetol C12H18O2 ÏàËÆ¶È:75% Journal of Natural Products 1985 Vol 48 660-663 Microbial Transformation of Olivetol by Fusarium roseum Robert H. McClanahan, Larry W. Robertson Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-methoxy-5-pentane-1-phenol ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2006 37 818-821 Phenolic constituents in Embelia ribes LIN Peng-cheng; LI Shuai; WANG Su-juan; YANG Yong-chun; SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . eleocharinol A ÏàËÆ¶È:75% Natural Product Research and Development 2013 25 1615-1620 Phenolic Constituents and Antioxidant Activity of Eleocharis tuberosa Peels LI Xing-ren, LUO Yang-he*, HE Juan, PENG Li-yan, WU Xing-de, DU Ru-nan, ZHAO Qin-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-heptadecyl-5-methoxy-phenol C24H42O2 ÏàËÆ¶È:70.5% Journal of Ethnopharmacology 2003 88 241-247 Bioactive alkyl phenols and embelin from Oxalis erythrorhiza Gabriela Egly Feresin, Alejandro Tapia, Maximiliano Sortino, Susana Zacchino, Antonieta Rojas de Arias, Alba Inchausti, Gloria Yaluff, Jaime Rodriguez, Cristina Theoduloz, Guillermo Schmeda-Hirschmann Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,3-dimethoxy-5-pentadecylbenzene ÏàËÆ¶È:68.7% Journal of Asian Natural Products Research 2011 13 290-296 Synthesis and biological evaluation of bilobol and adipostatin A Ayano Tanaka; Yasuhiro Arai; Su-Nam Kim; Jungyeob Ham; Toyonobu Usuki Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-Heptadecyl-5-methoxyphenol C24H42O2 ÏàËÆ¶È:62.5% Phytochemistry Letters 2012 5 206-210 Allelopathic potential of alkylphenols from Dactylis glomerata subsp. Hispanica (Roth) Nyman Monica Scognamiglio,Vittorio Fiumano,Brigida D'Abrosca,Severina Pacifico,Anna Messere,Assunta Esposito,Antonio Fiorentino Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-Nonadecyl-5-methoxyphenol C26H46O2 ÏàËÆ¶È:62.5% Phytochemistry Letters 2012 5 206-210 Allelopathic potential of alkylphenols from Dactylis glomerata subsp. Hispanica (Roth) Nyman Monica Scognamiglio,Vittorio Fiumano,Brigida D'Abrosca,Severina Pacifico,Anna Messere,Assunta Esposito,Antonio Fiorentino Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Henicosyl-5-methoxyphenol C28H50O2 ÏàËÆ¶È:62.5% Phytochemistry Letters 2012 5 206-210 Allelopathic potential of alkylphenols from Dactylis glomerata subsp. Hispanica (Roth) Nyman Monica Scognamiglio,Vittorio Fiumano,Brigida D'Abrosca,Severina Pacifico,Anna Messere,Assunta Esposito,Antonio Fiorentino Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . stilbostemin N C16H18O3 ÏàËÆ¶È:56.2% Phytochemistry 2008 69 457-463 Antibacterial stilbenoids from the roots of Stemona tuberosa Li-Gen Lin, Xin-Zhou Yang, Chun-Ping Tang, Chang-Qiang Ke, Ji-Bao Zhang, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cyperusol D C15H24O3 ÏàËÆ¶È:56.2% Journal of Natural Products 2004 67 569-576 Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Stilbostemin O C16H18O3 ÏàËÆ¶È:56.2% Journal of Asian Natural Products Research 2007 9 509-515 Antibacterial constituents from Stemona sessilifolia TONG ZHANG, YA-ZHONG ZHANG and JIAN-SHENG TAO Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Stilbostemin J C16H18O4 ÏàËÆ¶È:56.2% Journal of Asian Natural Products Research 2006 8 47-53 Stilbenoids from Stemona japonica XIN-ZHOU YANG, CHUN-PING TANG and YANG YE Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-(8-pentadecenyl)-1,3-benzenediol ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2006 37 818-821 Phenolic constituents in Embelia ribes LIN Peng-cheng; LI Shuai; WANG Su-juan; YANG Yong-chun; SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . l-(3,5-Dimethoxyphenyl)heptane C15H24O2 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 1998 6 2383-2396 Synthesis and pharmacology of the isomeric methylheptyl-¦¤8-tetrahydrocannabinols John W. Huffman, John Liddle, Sammy G. Duncan Jr., Shu Yu, Billy R. Martin, Jenny L. Wiley Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1,3-dimethoxy-5-octylbenzene ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 2010 333-337 Solid-Phase Reactive Chromatography (SPRC): A New Methodology for Wittig and Horner¨CEmmons Reactions on a Column under Microwave Irradiation Saada C. Dakdouki, Didier Villemin and Nathalie Bar Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 2a ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 1987 35 3016-3020 Antitumor Principles from Ginkgo biloba L. HIDER ITOKAWA,NOBUO TOTSUKA,KEISUKE NAKAHARA,KOICHI TAKEYA,JEAN-PIERRE LEPOITTEVIN and YOSHINORI ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (R)-8-(3-hydroxy-5-pentylphenoxy)-N-(1-hydroxypropan-2-yl)octanamide C22H37NO4 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2014 22 4770-4783 Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (R)-11-(3-hydroxy-5-pentylphenoxy)-N-(1-hydroxypro-pan-2-yl)undecanamide C25H43NO4 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2014 22 4770-4783 Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . N-allyl-11-(3-hydroxy-5-pentylphenoxy)undecana-mide C25H41NO3 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2014 22 4770-4783 Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . N-(2,2,2-trifluoroethyl)-11-(3-hydroxy-5-pentylphen-oxy)undecanamide C24H38F3NO3 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2014 22 4770-4783 Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . gigantol ÏàËÆ¶È:50% Planta Medica 2006 72 1181-1187 Gigantol Isolated from the Whole Plants of Cymbidium goeringii Inhibits the LPS-Induced iNOS and COX-2 Expression via NF- kB Inactivation in RAW 264.7 Macrophages Cells Jong-Heon Won,Ji-Yeon Kim,Kyung-Jin Yun,Jin-Hee Lee,Nam-In Back,Hae-Gon Chung,Sun A. Chung,Tae-Sook Jeong, Myung-Sook Choi,Kyung-Tae Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (10'R)-5-(10-hydroxytridecyl)-1-O-methylresorcinol C20H34O3 ÏàËÆ¶È:50% Phytochemistry 1994 36 189-194 Resorcinol derivatives and other components from Ononis viscosa subsp. breviflora Alejandro.F. Barrero, Eduardo Cabrera, Ignacio Rodr¨ªguez, Eva M. Fern¨¢ndez-Gallego Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Lactapiperanol A ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2005 60b 1065-1067 A New Marasmane Sesquiterpene from the Basidiomycete Russula foetens Xing-Na Wang, Fei Wang, Jian-Chang Du, Hui-Ming Ge, Ren-Xiang Tan, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . [2-(4,5-bis-hexylsulfanyl[1,3]dithiol-2-ylidene)-tetrahydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]-methanol C21H32OS8 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2002 39 1071-1075 Synthesis of zincic phthalocyanine derivative functionalized with four peripheral tetrathiafulvalene units Yingyu Hu and Yongjia Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (R)-1-(3,5-Dimethoxyphenyl)-3-methylheptane C16H26O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 2383-2396 Synthesis and pharmacology of the isomeric methylheptyl-¦¤8-tetrahydrocannabinols John W. Huffman, John Liddle, Sammy G. Duncan Jr., Shu Yu, Billy R. Martin, Jenny L. Wiley Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-10-25 23:17:53














»Ø¸´´ËÂ¥