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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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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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