| ²é¿´: 375 | »Ø¸´: 1 | ||
ÄûÃÊË®½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×Êý¾Ý²éѯ
|
|
ÈܼÁDMSO, CÆ×Êý¾Ý£º19.9, 27.8, 50.8, 103.7, 110.4, 111.9, 119.2, 119.7, 121.0, 125.2, 126.3, 135.4, 144.2, 145.4, 160.2, 166.7 |
» ²ÂÄãϲ»¶
324Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085404£¬285·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
µ÷¼Á
ÒѾÓÐ3È˻ظ´
ÉúÎïÓëÒ½Ò©273Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
0703»¯Ñ§
ÒѾÓÐ26È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Á½¸öÈýÝÆÀ໯ºÏÎï΢Æ×̼Æ×Êý¾Ý²éѯ
ÒѾÓÐ9È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ivyasspring
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 46 (СѧÉú)
- ½ð±Ò: 1023.6
- ºì»¨: 5
- Ìû×Ó: 152
- ÔÚÏß: 39.8Сʱ
- ³æºÅ: 1764251
- ×¢²á: 2012-04-18
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄûÃÊË®(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-05-29 15:25:37
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄûÃÊË®(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-05-29 15:25:37
|
1 . 2-methoxy-5,10-dihydro-indeno[1,2-b]indole C16H13NO ÏàËÆ¶È:68.7% Bioorganic & Medicinal Chemistry 2009 17 6583-6589 Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part Oktay Talaz, İlhami G¨¹lçin, S¨¹leyman Göksu, Nurullah Saracoglu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-methoxy-5,10-dihydroindeno[1,2-b]indol C16H13NO ÏàËÆ¶È:68.7% Bioorganic & Medicinal Chemistry 2009 17 6583-6589 Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part Oktay Talaz, İlhami G¨¹lçin, S¨¹leyman Göksu, Nurullah Saracoglu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . neoechinulin A ÏàËÆ¶È:68.4% Chemical & Pharmaceutical Bulletin 2004 52(3) 375-376 Golmaenone, a New Diketopiperazine Alkaloid from the Marine-Derived Fungus Aspergillus sp. Yong LI,Xifeng LI,Se-Kwon KIM,Jung Sook KANG,Hong Dae CHOI,Jung Rae RHO,and Byeng Wha SON Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . neoechinulin A ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2008 33 1032-1035 Studies on chemical constituents of Saussurea laniceps DAWA Zhuoma, ZHOU Yan, BAI Yang, GESANG Suolang, XIE Ping, DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . neoechinulin A C19H21O2N3 ÏàËÆ¶È:63.1% Natural Product Research and Development 2007 19 48-50 Neoechinulin A:An Indole Alkaloid Isolated from Metabolites of Plant Endophyte WANG Wei; CHEN Chao; YANG Jun; HU Chang-qi* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . aristolochic acid IIIa ÏàËÆ¶È:62.5% Phytochemistry 1994 37 237-239 Eleven aristolochic acid derivatives from Aristolochia cinnabarina Hong Li, Sakagami Youji, Marumo Shingo, Xinmin Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Luteoride B C16H17N3O2 ÏàËÆ¶È:62.5% Tetrahedron Letters 2011 52 7042-7045 Histone deacetylase inhibitor induced the production of three novel prenylated tryptophan analogs in the entomopathogenic fungus,Torrubiella luteorostrata Teigo Asai, Takashi Yamamoto, Yoshiteru Oshima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . variecolorin H C20H23N3O3 ÏàËÆ¶È:60% Journal of Natural Products 2007 70 1558-1564 Isoechinulin-type Alkaloids, Variecolorins A¨CL, from Halotolerant Aspergillus Wariecolor Wen-Liang Wang, Zhen-Yu Lu, Hong-Wen Tao, Tian-Jiao Zhu, Yu-Chun Fang, Qian-Qun Gu, and Wei-Ming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Aristolochic acid Iva ÏàËÆ¶È:58.8% Pharmazie 2005 60 789-791 A new biflavonoid from Aristolochia contorta Li-Li Yu, Rong Huang, Yu-Ping Lv, Yong Zhao and Yegao Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 4-(4-(4-bromophenoxy)quinazolin-2-ylamino)benzonitrile C21H13N4OBr ÏàËÆ¶È:58.8% Bioorganic & Medicinal Chemistry 2010 18 5039-5047 Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy Zhao-Sen Zeng, Qiu-Qin He, Yong-Hong Liang, Xiao-Qing Feng, Fen-Er Chen, Erik De Clercq, Jan Balzarini, Christophe Pannecouque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . rutaecarpine C18H13N3O ÏàËÆ¶È:58.8% Korean Journal of Pharmacognosy 2012 43 122-126 Cholinesterase Inhibitors Isolated from the Fruits Extract of Evodia officinalis Lee, Ji-Young; Cha, Mi-Ran; Choi, Chun-Whan; Kim, Young-Sup; Lee, Bong-Ho; Ryu, Shi-Yong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . cristatumin A C19H21N3O3 ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry Letters 2012 22 4650-4653 Cristatumins A¨CD, new indole alkaloids from the marine-derived endophytic fungus Eurotium cristatum EN-220 Feng-Yu Du, Xiao-Ming Li, Chun-Shun Li, Zhuo Shang, Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Brevianamide Q C21H23N3O3 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2010 93 2075-2080 Four New Alkaloids, Brevianamides O ¨C R, from the Fungus Aspergillus versicolor Guo-You Li, Li-Mei Li, Tao Yang, Xiao-Zhen Chen, Dong-Mei Fang and Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 1,2-dihydroisoquinoline minor C14H15NO5 ÏàËÆ¶È:56.2% Journal of Natural Products 1999 62 780-781 A New 1, 2-Dihydroisoquinoline from the Sponge Petrosia similis P. Ramesh, N. Srinivasa Reddy, and Y. Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 6-(4-oxo-but-2-enyl)-1H-indole C12H11NO ÏàËÆ¶È:56.2% Natural Product Research 2004 18 253-258 Prenylindoles from Tanzanian Monodora and Isolona Species Mayunga H. H. Nkunya; John J. Makangara; Stephan A. Jonker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . phoebegrandine E C16H16N3 ÏàËÆ¶È:56.2% Natural Product Research 2006 20 567-572 New alkaloids from Phoebe grandis (Nees) Merr. Khalijah Awang; Mat Ropi Mukhtar; A. Hamid; A. Hadi; Marc Litaudon; Jalifah Latip; Noor Rain Abdullah Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . clausine-TY C15H13NO4 ÏàËÆ¶È:56.2% Natural Product Research 2007 21 810-813 A new cytotoxic carbazole alkaloid from Clausena excavata Y. H. Taufiq-Yap; T. H. Peh; G. C. L. Ee; M. Rahmani; M. A. Sukari; A. M. Ali; R. Muse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . aristolochic acid C C16H9NO7 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2010 58 1093-1095 Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities Yu Cai and Tian-Ge Cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 7-methoxy-2-(4-nitrophenyl)-4,5-dihydro-2H-benzo[g]indazole C18H15N3O3 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2006 43 389-394 Selective synthesis of some 4,5-dihydro-2H-benzo[g]indazoles and 8,9-dihydro-2H-benzo[e]indazoles via the vilsmeier-haack reaction under thermal and microwave assisted conditions Ganesabaskaran Sivaprasad,Radhakrishnan Sridhar and Paramasivan T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 3-methoxy-5,10-dihydroindeno[1,2-b]indole C16H13N ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2006 43 695-699 One pot synthesis of substituted dihydroindeno[1,2-b]indoles and dihydrobenzo[a]carbazoles by photostimulated reactions of o-iodoaniline with carbanions by the SRN1 mechanism Silvia M. Barolo,Roberto A. Rossi,Cecir¨¦a Rosales and Jorge E. Angel Gu¨ªo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 2-(N,N-diallylamino)-3-(6-chlorobenzotriazol-1-yl)-2H-indazole C19H17ClN6 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2010 47 98-111 n-Butyllithium-mediated reactions of 1-(2-azidoarylmethyl)- 1H-benzotriazoles with alkyl halides Taehoon Kim and Kyongtae Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . compound 8b C15H19N5O ÏàËÆ¶È:56.2% Indian Journal of Chemistry 2009 48B 134-136 Tungstate-catalyzed oxidation of triptans with hydrogen peroxide: A novel method for the synthesis of N,N- dimethyltryptamine N-oxides Ray,Purna Chandra; Mittapelli,Vasantha; Chauhan,Yogendra Kumar; Konudula,Babu Rao; Tyagi,Om Dutt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 2-(2,4-difluorobenzoyl)-1-oxo-1,2,3,4-tetrahydro-¦Â-carboline C18H12F2N2O2 ÏàËÆ¶È:56.2% Heterocycles 2009 79 1073-1080 Design, Synthesis, and Biological Effect of (1-Oxo-1,2,3,4-Tetrahydro- ¦Â-Carbolin-9-yl)-acetic Acids as Inhibitor of Aldose Reductase 2 Naoki Toyooka, Daisuke Takeda, Yuka Minoshima, Atsushi Kato, and Isao Adachi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 1-ethyl-2-formyl-1-methyl-1,2,3,4-tetrahydro-¦Â-carboline C15H18N2O ÏàËÆ¶È:56.2% Heterocycles 2003 59 691-705 A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 2-formyl-1,2,3,4-tetrahydro-¦Â-carboline-1-spirocyclohexane C17H20N2O ÏàËÆ¶È:56.2% Heterocycles 2003 59 691-705 A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 3-[4-(N-acetylamino)-1,3-dimethylpyrazol-5-yl]indole C15H16N4O ÏàËÆ¶È:56.2% Heterocycles 2003 60 1339-1350 Synthesis and Dopamine Receptor Binding of Some Pyrazolo[3',4':6,7]azepino[5,4,3-cd]indoles Peter Gmeiner, Harald H¨¹bner, Kayed A. Abu Safieh, Ismail I. Fasfous, Mustafa M. El-Abadelah,* Salim S. Sabri, and Wolfgang Voelter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 4-[(1H-indol-6-yl)(1H-1,2,4-triazol-1-yl)methyl]benzonitrile C18H13N5 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry Letters 2008 18 4713-4715 Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors Marie-Pierre L¨¦z¨¦, Anja Palusczak, Rolf W. Hartmann, Marc Le Borgne Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . compound 2a ÏàËÆ¶È:56.2% Tetrahedron Letters 2004 45 8419-8422 Palladium-catalyzed functionalization of indoles with 2-acetoxymethyl substituted electron-deficient alkenes Shengming Ma, Shichao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . clausine L C15H13NO3 ÏàËÆ¶È:56.2% Organic & Biomolecular Chemistry 2008 6 2481-2483 First total synthesis of clausine L and pityriazole, a metabolite of the human pathogenic yeast Malassezia furfur Ronny Forke, Anne Jäger and Hans-Joachim Knölker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 1-methoxy-5,10-dihydroindeno[1,2-b]indole C16H13NO ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2009 17 6583-6589 Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part Oktay Talaz, İlhami G¨¹lçin, S¨¹leyman Göksu, Nurullah Saracoglu Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-24 20:07:45














»Ø¸´´ËÂ¥