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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½37¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6-Bromo-8-hydroxy-3-benzoylcoumarin C16H9BrO4 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2011 21 4224-4227 MAO inhibitory activity modulation: 3-Phenylcoumarins versus 3-benzoylcoumarins Maria João Matos, Saleta Vazquez-Rodriguez, Eugenio Uriarte, Lourdes Santana, Dolores Viña Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4,4'-di (2amino 4-N,N'dimethylphenyl) pyrimidyl) dibenzo 18-crown-6 C44H50O6N8 ÏàËÆ¶È:55.5% Indian Journal of Chemistry Section B 2008 47B 1915-1917 Synthesis of dibenzo-18-crown-6 ether containing pyrimidine derivatives Deshmukh,M B; Alasundkar,K N; Salunkhe,S M; Salunkhe,D K; Sankpal,S A; Patil,D R; Anbhule,P V Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-Anwulignan ÏàËÆ¶È:55% Chinese Journal of Organic Chemistry 2009 29 1564-1568 A New Triterpenoid Saponin from the Root of Ardisia crispa Huang, Wei Xu, Kangping Li, Fushuang Yuan, Shouhong Li, Zhongkui Xu, Pingsheng Tan, Guishan* Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . kingianic acid C C22H20O4 ÏàËÆ¶È:54.5% Molecules 2014 19 1732-1747 Kingianic Acids A¨CG, Endiandric Acid Analogues from Endiandra kingiana Mohamad Nurul Azmi, Charlotte G¨¦ny, Aur¨¦lie Leverrier, Marc Litaudon, Vincent Dumontet, Nicolas Birlirakis, Françoise Gu¨¦ritte, Kok Hoong Leong, Siti Nadiah Abd. Halim, Khalit Mohamad and Khalijah Awang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . flazine ÏàËÆ¶È:50% Planta Medica 2002 68 730-733 Bioactive Constituents of the Seeds of Brucea javanica Bao-Ning Su,Leng Chee Chang,Eun Jung Park,Muriel Cuendet,Bernard D.Santarsiero, Andrew D.Mesecar, Rajendra G.Mehta,Harry H.S.Fong,John M.Pezzuto,A.Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 4c ÏàËÆ¶È:50% Chinese Chemical Letters 2008 19 37-39 1-[2-(2-Methoxyphenylthio) benzyl]-4-arylpiperazines derivatives:Synthes isa nde valuationf ord ual5 -HT1a/SSRI activities Xin W ang£¬Dong Zhi Liu£¬Ai Jun Li Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . caulidine A C18H23N ÏàËÆ¶È:50% 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 8 . 2-(4-Bromoacetophenon-x-yl)-3-(4-bromophenyl)-5-cyano-6-cyanomethylpyran C22H14Br2N2O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2707-2713 Anti-tumor and anti-leishmanial evaluations of 1,3,4-oxadiazine,pyran derivatives derived from cross-coupling reactions of b-bromo-6H-1,3,4-oxadiazine derivatives Rafat M. Mohareb ,J¨¹rgen Schatz Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-(2-bromophenyl)-2-(1H-indol-1-yl)-4-nitrobutanenitrile C18H14N3O2Br ÏàËÆ¶È:50% Organic Letters 2008 Vol.10,No.1 125-128 First Total Synthesis of Trimeric Indole Alkaloid, Psychotrimine Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-cyano-3-(dimethylamino)-1-(1H-Indol-3-yl)propen-1-one ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 141-145 Synthetic applications of 3-(cyanoacetyl)indoles and related compounds Johnny Sltt,Tomasz Janosik,Niklas Wahlström and Jan Bergman Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6,7-dimethoxy-4-(4'-N,N-dimethylaminophenyl)-8-(2''-pyridyl)quinazoline C23H22N4O2 ÏàËÆ¶È:50% Heterocycles 2007 71 1723-1741 Molecular Design and Synthesis of 4, 8-Di(hetero)arylquinazolines with Potential Applications in Quadratic Nonlinear Optics. Diazines Part 48 Alexandrine Busch, Alain Turck, Kamila Nowicka, Alberto Barsella, Chantal Andraud, and Nelly Pl¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-Methylindole-3-carboxaldehyde(3-fluorophenyl)hydrazone C16H14N3F ÏàËÆ¶È:50% Molecules 2010 15 2187-2202 Novel Indole-Based Analogs of Melatonin: Synthesis and in Vitro Antioxidant Activity Studies Hanif Shirinzadeh, Burcu Eren, Hande Gurer-Orhan, Sibel Suzen and Seçkin Özden Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . flazine ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2007 38 337-339 Chemical constituents of fruiting bodies from basidiomycete Suillus granulatus and their anti-HIV-1 activity DONG Ze-jun; WANG Fei; WANG Rui-rui; YANG Liu-meng; ZHENG Yong-tang; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-(1-(4-methoxyphenyl)-2-nitro ethyl)-1H-indole C17H16N2O3 ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 3859-3862 Samarium triiodide-catalyzed conjugate addition of indoles with electron-deficient olefins Zhuang-Ping Zhan, Rui-Feng Yang, Kai Lang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 6-(Z)-(2-methoxybenzylidene)-2,3-dihydroimidazo-[2,1-b]-thiazol-5(6H)-one C13H12N2O2S ÏàËÆ¶È:50% Archiv der Pharmazie 1997 330 85-90 Fused 2-Thiohydantoin Derivatives: Evaluation as Potential Antioxidants Katarzyna Kiec-Kononowicz, Janina Karolak-Wojciechowska and Jadwiga Robak Structure 13C NMR ̼Æ×Ä£Äâͼ |

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