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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£º¹²²éµ½110¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Irisflorentine ÏàËÆ¶È:65% Archives of Pharmacal Research 2002 25 306-312 Isoflavonoids from the rhizomes of Belamcanda chinensis and their effects on aldose reductase and sorbitol accumulation in streptozotocin induced diabetic rat tissues Sang Hoon Jung, Yeon Sil Lee, Sanghyun Lee, Soon Sung Lim and Yeong Shik Kim, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-hydroxy-2',3',4'-trimethyl isoflavan ÏàËÆ¶È:63.1% Journal of Natural Products 1991 Vol 54 810 Constituents of Astragalus membranaceus Zheng-Quan He, John A. Findlay Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-7-hydroxy-2',3',4'-trimethoxyisoflavan ÏàËÆ¶È:63.1% Phytochemistry 1994 36 1387-1389 Antimicrobial isoflavans from Astragalus species Nadia A. El-Sebakhy, Aya M. Asaad, Rokia M. Abdallah, Soad M. Toaima, Maged S. Abdel-Kader, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . isomucronulatol ÏàËÆ¶È:63.1% Chinese Traditional and Herbal Drugs 2007 38 985-987 Ïã¸ÛÔ¶Ö¾»¯Ñ§³É·ÖµÄ·ÖÀëÓë¼ø¶¨ Îâ½£·å;³ÂËı£;³ÂÊ¿ÁÖ;ÍÀÅô·É;ÎâÁ¢¾ü;ÑîÀöÄÈ Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-isomucronulatol ÏàËÆ¶È:63.1% Journal of Shenyang Pharmaceutical University 2003 20 104-106 Chemical constituents of the pericarp of Sphaerophysa salsula DC. LI Guo-yu, WANG Jin-hui, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3R)-7,2'-dihydroxy-3',4'-dimethoxyisoflavan ÏàËÆ¶È:57.8% Chemistry & Biodiversity 2007 Vol. 4 2172 Phenolic Derivatives with Free-Radical-Scavenging Activities from Ixeridium gracile (DC.) Shih Xue-Mei Ma, Yong Liu, and Yan-Ping Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . R(-)-3-(4-Hydroxybenzyl)-5-hydroxy-6, 7,8-trimethoxychroman-4-one C19H20O7 ÏàËÆ¶È:57.8% Planta Medica 1996 62 534-539 Constituents of Veitheimia viridifolia;I. Homoisoflavanones of the Bulbs Gudrun Amschler, August W. Frahm, Armin Hatzelmann, Ulrich Kilian, Dieter M¨¹Iler-Doblies,and Ulrike M¨¹ller-Doblies Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-hydroxy-3,4',6,7-tetramethoxyflavone C19H18O7 ÏàËÆ¶È:57.8% Acta Botanica Yunnanica 1994 16(4) 434-436 THE FLAVONOLS FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3',7-dihydroxy-2',4'-dimethoxy isoflavan C17H18O5 ÏàËÆ¶È:57.8% China Journal of Chinese Materia Medica 2007 32 318-322 Studies on flavonoids of Oxytropis falcata LU Fang, XU Xiaojie Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (3R)-(-)-7,2'-dihydroxy-3,4-dimethoxy isoflavan ÏàËÆ¶È:57.8% Journal of Natural Products 1991 Vol 54 810 Constituents of Astragalus membranaceus Zheng-Quan He, John A. Findlay Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Irisjaponin B C19H18O8 ÏàËÆ¶È:57.8% Phytochemistry 1996 41 1219-1221 Highly oxygenated isoflavones from Iris japonica Hiroyuki Minami, Aya Okubo, Mitsuaki Kodama |

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²éѯ½á¹û£º¹²²éµ½64¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 10 C38H42O10 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2010 5056-5062 Synthesis of A Bis-Macrotricyclic Host and Its Complexation with Secondary Ammonium Salts: An Acid¨CBase Switchable Molecular Handcuff Jia-Bin Guo, Jun-Feng Xiang and Chuan-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1-[4-(2-Ethoxyethoxymethyl)-2-methoxyphenyl]piperazine ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2012 20 455-466 Bivalent molecular probes for dopamine D2-like receptors Daniela Huber, Stefan Löber, Harald H¨¹bner, Peter Gmeiner Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 13,22,39,40,-tetraaza-6,16,19,29-trioxa-3,9,11,21,24,26,32-hexathiotetracyclo-[32,3,1,110.13,122.25]-heptatriaconta-1(38),10(39),25(40),34(35),36(37)-pentaene-12,23-dione C26H36N4O6S6 ÏàËÆ¶È:57.1% Heterocycles 2008 75 1457-1466 Metalloreceptors Composed of Organopalladium Complexes Containing 5-Mercapto-3H-1, 3, 4-thiadiazolin-2-ones Nam Sook Cho, Sang Beom Kim, Min Hye Kim, Seong Gyun Park, Sung Kown Kang, Se Jin Lee, and Yeong-Joon Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-4-methoxyaniline C17H30N2O4 ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 2011 6240-6253 Copper-Catalyzed Arylation of Oxadiamines and Polyamines Maxim V. Anokhin, Alexei D. Averin and Irina P. Beletskaya Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 9 C38H46O12S2 ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 2010 5056-5062 Synthesis of A Bis-Macrotricyclic Host and Its Complexation with Secondary Ammonium Salts: An Acid¨CBase Switchable Molecular Handcuff Jia-Bin Guo, Jun-Feng Xiang and Chuan-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-{[(2,6-dichlorophenyl)methyl]sulfanyl}-1-ferrocenylethanol C19H18Cl2FeOS ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2012 9 2236-2253 Sulfur-Containing Ferrocenyl Alcohols and Oximes: New Promising Antistaphylococcal Agents Danijela Ilić, Ivan Damljanović, Dragana Stevanović, Mirjana Vukićević, Polina Blagojević, Niko Radulović and Rastko D. Vukićević Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Tweezer-Shaped Host C60H68O16 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2012 95 2604-2620 2,3,10,11-Tetrahydroxytetraphenylene and Its Application in Molecular Recognition Jian-Fang Cui, Chao Chen, Xiang Gao, Zong-Wei Cai, Jian-Wei Han and Henry N. C. Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 3 C22H28O8 ÏàËÆ¶È:56.2% Tetrahedron Letters 2005 46 1575-1577 Intramolecular Cannizzaro desymmetrization of tetraethylene glycol assisted by a cation binding template Yolanda Vida, Ezequiel Perez-Inestrosa, Rafael Suau Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . lincomycin HCl ÏàËÆ¶È:53.3% The Journal of Antibiotics 1981 34 596-599 STRUCTURE OF ANTIBIOTIC Bu-2545, A NEW MEMBER OF THE CELESTICETIN-LINCOMYCIN CLASS SOICHIRO TODA, SUSUMU NAKAGAWA, TAKAYUKI NAITO, HIROSHI KAWAGUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . celesticetin HCl ÏàËÆ¶È:53.3% |

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