| ²é¿´: 202 | »Ø¸´: 1 | ||
ÄûÃÊË®½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú--63
|
|
ÈܼÁ£ºDMSO CÆ×Êý¾Ý£º 54.4,56.2,56.3,63.8,106.0,106.8,127.3,127.8,134.9,141.0,147.6,148.2,197.1 лл£¡ |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¡£¡£¡£
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú(±½»·ÑÜÉúÎïÀà)
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡£¡£¡¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
jasminelw
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 269 (´óѧÉú)
- ½ð±Ò: 8813.7
- É¢½ð: 80
- ºì»¨: 6
- Ìû×Ó: 972
- ÔÚÏß: 604.2Сʱ
- ³æºÅ: 1858727
- ×¢²á: 2012-06-13
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄûÃÊË®(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-09-21 11:19:22
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄûÃÊË®(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-09-21 11:19:22
|
²éѯ½á¹û£º¹²²éµ½948¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (3-Hydroxy-2,4-dimethoxyphenyl)(4-hydroxy-3,5-dimethoxyphenyl)methanone C17H18O7 ÏàËÆ¶È:71.4% Bioorganic & Medicinal Chemistry 2011 19 6042-6054 Synthesis and biological evaluation of phenstatin metabolites Alina Ghinet, Benoît Rigo, Jean-Pierre H¨¦nichart, Delphine Le Broc-Ryckewaert, Jean Pommery, Nicole Pommery, Xavier Thuru, Bruno Quesnel, Philippe Gautret Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4,4'-dihydroxy-3,5,3',5'-tetramethoxychalcone C19H20O7 ÏàËÆ¶È:69.2% Natural Product Research 2002 16 187-193 Synthesis, Dimerization, and Biological Activity of Hexaoxygenated Chalcones Related to Calythropsin and Combretastatins Elisabeth Seguin; Abdelhakim Elomri; Prokopios Magiatis; Alexios-Leandros Skaltsounis; Lin Rui Chao; François Tillequin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . danielone C10H12O5 ÏàËÆ¶È:69.2% Phytochemistry 1997 44 255-256 Danielone, a phytoalexin from papaya fruit Fernando Echeverri, Fernando Torres, Winston Quiñones, Gloria Cardona, Rosendo Archbold, Javier Roldan, Ivan Brito, Javier G. Luis, El-Hassane Lahlou Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone C11H14O5 ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 8 1028-1031 Study on chemical constituents from leaves of Tripterygium wilfordii CAO Xu, LI Chuang jun, YANG Jing zhi, WEI Baixing, LUO Yongming, ZHANG Dongming Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . sinapine ÏàËÆ¶È:69.2% Phytochemistry 1983 22 219-222 Sinapine-O-¦Â-D-glucopyranoside in seeds of Alliaria officinalis Lone Melchior Larsen, Ole Olsen, Annette Plöger, Hilmer Sørensen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5,6-dimethoxy-3-(pyridine-4-yl)spiro[indene-2,2'-oxiran]-1(3H)-one ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2010 58 1157-1160 A New Commercially Viable Synthetic Route for Donepezil Hydrochloride: Anti-Alzheimer's Drug Shailendra Kumar Dubey, Manita Kharbanda, Sushil Kumar Dubey and Chandra Shekhar Mathela Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ethyl 1-formyl-6,7-dimethoxyisoquinoline-3-carboxylate C15H15NO5 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 2120-2127 Efficient Access to C1- and C3-Functionalized Isoquinolines: Towards Potential Lanthanide Ligands Fabien Caill¨¦, Fr¨¦d¨¦ric Buron, ¨¦va T¨®th and Franck Suzenet Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3-Hydroxy-2,4-dimethoxyphenyl)-(3,4,5-trimethoxyphenyl)methanone C18H20O7 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 6042-6054 Synthesis and biological evaluation of phenstatin metabolites Alina Ghinet, Benoît Rigo, Jean-Pierre H¨¦nichart, Delphine Le Broc-Ryckewaert, Jean Pommery, Nicole Pommery, Xavier Thuru, Bruno Quesnel, Philippe Gautret Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-[[N-(2-Methoxyethyl)-N-(2-propenyl)amino]methyl]-2-methyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide hydrochloride C14H21N3O5S3 ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry 2000 8 957-975 2H-Thieno[3,2-e]- and [2,3-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides as ocular hypotensive agents: synthesis, carbonic anhydrase inhibition and evaluation in the rabbit Hwang-Hsing Chen, Sharon Gross, John Liao, Marsha McLaughlin, Tom Dean, William S. Sly, Jesse A. May Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-demethoxymichigazone C14H11NO4 ÏàËÆ¶È:64.2% The Journal of Antibiotics 1996 49 312-313 A Neuronal Cell Protecting Substance, 4-Demethoxymichigazone, Produced by Streptomyces halstedii TOSHIHIRO KUNIGAMI, KAZUO SHIN-YA, KAZUO FURIHATA, KEIKO FURIHATA, YOICHI HAYAKAWA, HARUO SETO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . sodium hydroxyphenstatin diphosphate ÏàËÆ¶È:64.2% Journal of Medicinal Chemistry 2000 43 2731-2737 Antineoplastic Agents. 443. Synthesis of the Cancer Cell Growth Inhibitor Hydroxyphenstatin and Its Sodium Diphosphate Prodrug George R. Pettit, Matthew P. Grealish, Delbert L. Herald, Michael R. Boyd, Ernest Hamel, and Robin K. Pettit Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5,6-dimethoxy-1-oxo-indan-2-carboxylic acid ethyl ester ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry 2013 21 676-683 Design, synthesis and evaluation of novel heterodimers of donepezil and huperzine fragments as acetylcholinesterase inhibitors Yueqing Hu, Jun Zhang, Oormila Chandrashankra, Fanny C.F. Ip, Nancy Y. Ip Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 46 ÏàËÆ¶È:64.2% The Journal of Organic Chemistry 1993 58 4871-4880 Protein tyrosine kinase inhibitory properties of planar polycyclics obtained from the marine sponge Xestospongia cf. carbonaria and from total synthesis Khisal A. Alvi, Jaime Rodriguez, Maria Cristina Diaz, Robert Moretti, Robert S. Wilhelm, Rita H. Lee, Doris L. Slate, Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 5a ÏàËÆ¶È:62.5% Heterocycles 2001 55 635-640 Synthesis of 4-Aryltetrahydroiso-quinolines: Application to the Synthesis of Cherylline Somsak Ruchirawat,* Sopchok Tontoolarug, and Poolsak Sahakitpichan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ciwujiatone C22H26O9 ÏàËÆ¶È:62.5% Journal of Anhui Agricultural Sciences 2012 40 7089-7090 Study on Chemical Constituents of the Ancient Ephedra Species Found in Yanghai,Xinjiang MA Qing-yun et al Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . aryl-8-oxa-bicyclo[3,2,1]-oct-3-en-2-one C16H18O6 ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 2004 52(12) 1483-1486 Two New Lactones and One New Aryl-8-oxa-bicyclo[3,2,1]oct-3-en-2-one from Descurainia sophia Kai SUN,Xian LI,Wen LI,Jinhui WANG,Jianming LIU,and Yi SHA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone C11H14O6 ÏàËÆ¶È:61.5% Journal of Natural Products 2002 65 1497-1500 Five New Phenolics from the Roots of Ficus beecheyana Tzong-Huei Lee,Yuh-Chi Kuo,Guei-Jane Wang,Yueh-Hsiung Kuo,Chi-I Chang, Chung-Kung Lu, and Ching-Kuo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 8 ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1984 32 2622-2627 O-Methylation Effect on the Carbon-13 Nuclear Magnetic Resonance Signals of ortho-Disubstituted Phenols and Its Application to Structure Determination of New Phthalides from Aspergillus silvaticus MASAO FUJITA,MIKIKO YAMADA,SHOICHI NAKAJIMA,KENICHI KAWAI and MASAHIRO NAGAI Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (R)-Calycotomine C12H17NO3 ÏàËÆ¶È:61.5% Molecules 2004 9 650-657 Isolation and X-ray Crystal Structure of Tetrahydroisoquinoline Alkaloids from Calycotome Villosa Subsp. Intermedias Ali El Antri, Ibtissam Messouri, Mohamed Bouktaib, Rachid El Alami, Michael Bolte, Brahim El Bali and Mohammed Lachkar Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2'-hydroxyaucuparin ÏàËÆ¶È:61.5% Phytochemistry 1999 50 231-235 Elicited cell suspension cultures of apple (Malus¡Ádomestica) cv.Liberty produce biphenyl phytoalexins W. Borejsza-Wysocki, C. Lester, A.B. Attygalle, G. Hrazdina Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5-acetyl-7-methoxybenzofuran C11H10O3 ÏàËÆ¶È:61.5% Journal of Natural Products 1994 Vol 57 146 Four New Furans from the Roots of Ligularia przewalskii Zhongjian Jia, Yu Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . syringaldehyde C9H10O4 ÏàËÆ¶È:61.5% Acta Pharmaceutica Sinica 1999 Vol 34 203-206 CHEMICAL CONSTITUENTS FROM MICHELIA SPHAERANTHA C.Y.WU Lin Jia (Lin J); Hao Xiaojiang (Hao XJ) and Liang Guangyi (Liang GY) Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Sinapine C16H23NO5 ÏàËÆ¶È:61.5% Phytochemistry 1995 40 483-485 Sinapinyl but-3-enylglucosinolate from Boreava orientalis Akiyo Sakushima, Maksut Cokun, Takashi Maoka Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 1-(4,7-Dimethoxybenzothiophen-2-yl)-2-propen-1-one C13H12O3S ÏàËÆ¶È:61.5% Molecules 2012 17 1388-1407 Synthesis, Docking Studies and Biological Evaluation of Benzothiophen-2-yl-3-(4-arylpiperazin-1-yl)-propan-1-one Derivatives on 5-HT1A Serotonin Receptors Hern¨¢n Pessoa-Mahana,Gonzalo Recabarren-Gajardo, Jenny Fiedler Temer ,Gerald Zapata-Torres , C. David Pessoa-Mahana, Claudio Saitz Barr¨ªa and Ramiro Araya-Maturana Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 6,7-dimethoxy-thiocoumarin ÏàËÆ¶È:61.5% Organic letters 1999 1 697-700 Microwave-Accelerated Solvent-Free Synthesis of Thioketones, Thiolactones, Thioamides, Thionoesters, and Thioflavonoids Rajender S. Varma and Dalip Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-17 17:57:39














»Ø¸´´ËÂ¥