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T-6: 13C in MeOD 20.68, 22.00, 30.73, 64.59, 71.39, 74.84, 75.78, 77.53, 103.26, 120.94, 123.04, 123.22, 124.98, 125.32, 136.70, 136.80, 149.52, 159.66, 172.66, 183.67 |
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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£º¹²²éµ½38¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . chrysophanol glucuronide C21H18O10 ÏàËÆ¶È:71.4% The Journal of Antibiotics 2008 61 464-473 Genoketides A1 and A2, New Octaketides and Biosynthetic Intermediates of Chrysophanol Produced by Streptomyces sp. AK 671 Hans-Peter Fiedler, Anke Dieter, Tobias A M Gulder, Inga Kajahn, Andreas Hamm, Ros Brown, Amanda L Jones, Michael Goodfellow, Werner E G M¨¹ller and Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-hydroxy-¦Â-ionyl-¦Â-D-glucopyranoside C19H34O7 ÏàËÆ¶È:55% Phytochemistry 1993 32 747-754 Phenolic, iridoid and ionyl glycosides from Homalium ceylanicum Opinya A. Ekabo, Norman R. Farnsworth, Thawatchai Santisuk, Vichai Reutrakul Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-ethyl-2-n-pentyl-4,9-dihydro-3H-3,4-carbazoldione C19H21NO2 ÏàËÆ¶È:55% Journal of Heterocyclic Chemistry 2003 40 411-417 Synthesis and biological evaluation of structural variants of carbazoquinocin C Alparslan Ayg¨¹n and Ulf Pindur Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-[3-(2-Pyridilmethoxy)propylamine]-4-chlorobenzo[g]phthalazine C21H19ON4Cl ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2007 15 2081-2091 1,4-Bis(alkylamino)benzo[g]phthalazines able to form dinuclear complexes of Cu(II) which as free ligands behave as SOD inhibitors and show efficient in vitro activity against Trypanosoma cruzi Marinela Rodr¨ªguez-Ciria, Ana M. Sanz, Mar¨ªa J.R. Yunta, Fernando G¨®mez-Contreras, Pilar Navarro, Manuel S¨¢nchez-Moreno, Samira Boutaleb-Charki, Antonio Osuna, Alfonso Castiñeiras, Mercedes Pardo, Carmen Cano, Lucrecia Campayo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6 C22H21NO5S ÏàËÆ¶È:54.5% Indian Journal of Chemistry Section B 2008 47B 1113-1116 Synthesis of highly functionalised linear pentacyclic compounds from Baylis-Hillman adduct of heteroaldehydes with azomethine ylides via [3+2] cycloaddition Shanmugam,Ponnusamy; Madhavan,Suchithra; Viswambharan,Baby; Vaithiyanathan,Vadivel Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Chrysophanol 1-O-¦Â-D-(6-O-Malonyl)glucoside C24H22O12 ÏàËÆ¶È:54.1% Chemical & Pharmaceutical Bulletin 2012 60(2) 241-246 Three New Phenolic Glucosides from the Roots of Rheum palmatum Zhi-Wei Wang,Jun-Song Wang,Jun Luo,Dan-Dan Wei,and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . quercetin 3-O-(6"-O-acetyl)-(¦Â-o-glucopyranosi ÏàËÆ¶È:52.1% Planta Medica 1987 53 434-437 Flavonoid Glycosides from Arnica montana and Arnica chamissonis lrmgard Merfort und Detlef Wendisch Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . okanin 4'-O-(6''-O-acetyl-¦Â-D-glucopyranoside ) ÏàËÆ¶È:52.1% Chemical & Pharmaceutical Bulletin 1992 40 689-691 New Acylated Glucosides of Chalocone from the Leaves of Bidens frondosa Hiroyuki KARIKOME,Kazunori OGAWA and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . rosiridoside C C18H30O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2008 56(5) 695-700 Reinvestigation of Absolute Stereostructure of (-)-Rosiridol: Structures of Monoterpene Glycosides, Rosiridin, Rosiridosides A, B, and C, from Rhodiola sachalinensis Masayuki YOSHIKAWA,Seikou NAKAMURA, Xuezheng LI, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . dichotomoside E C20H30O9 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2004 52(10) 1194-1199 Bioactive Constituents from Chinese Natural Medicines. XIV.1)New Glycosides of ¦Â-Carboline-Type Alkaloid, Neolignan, and Phenylpropanoid from Stellaria dichotoma L. var. lanceolata and Their Antiallergic Activities Toshio MORIKAWA,Bohang SUN,Hisashi MATSUDA,Li Jun WU,Shoichi HARIMA,and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 7-O-(6'-acetoxy-¦Â-D-glucopyranosyl)-8-hydroxy coumarin C17H18O10 ÏàËÆ¶È:50% Phytochemistry 2002 59 447-450 Coumarin glucosides from Cruciata taurica Salvatore De Rosa, Maya Mitova, Nedjalka Handjieva, İhsan Çalış Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gentiorigenoside A C22H30O12 ÏàËÆ¶È:50% Acta Botanica Yunnanica 2006 28(6) 669-672 A New Secoiridoidal Glucoside from Gentiana rigescens ( Gentianaceae) XU Min,WANGDong,ZHANG Ying-Jun, YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ |

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