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1 .     officinoside B
C19H32O8     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2001          49(8)          974-978
Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis
Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Compound 2a
C21H37O13N     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry Letters          1996          6          1123-1126
Synthesis of lactosamine derivatives using ¦Â--galactosidase from Bacillus circulans
Shuichi Takayama, Makoto Shimazaki, Lei Qiao, Chi-Huey Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     citronellol-1-O-¦Á-L-arabinofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C21H38O10     ÏàËÆ¶È:57.1%
Molecules          2012          17          7629-7636
Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities
Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (1S,2S,4R)-1,8-epoxy-p-methan-2-O-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:54.5%
Pharmazie          2002          57          279-281
New isopimarane diterpene and new cineole type glucoside from Nepeta prattii
Zhen-Fu Hou - Yong-Qiang Tu - Yu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (1R,2R,4S)-1,8-epoxy-p-methan-2-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:54.5%
Pharmazie          2002          57          279-281
New isopimarane diterpene and new cineole type glucoside from Nepeta prattii
Zhen-Fu Hou - Yong-Qiang Tu - Yu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     officinoside A
C19H32O8     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2001          49(8)          974-978
Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis
Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Ovatolactone 7-O-(6'-O-p-Hydroxybenzoyl)-¦Â-D-glucopyranoside
C22H28O10     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2001          49(6)          732-736
Studies on the Constituents of Catalpa Species. VI.Monoterpene Glycosides from the Fallen Leaves of Catalpa ovata G. DON
Koichi MACHIDA, Megumi ANDO, Yasunori YAOITA, Rie KAKUDA, and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     melia-ionoside A
C19H36O8     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          1991          39          2529-2533
Phytochemical Studies on Meliaceous Plants. VII. The Structures of Two New Ionone Glucosides from Melia toosendan SIEB. et ZUCC. and a Novel Type of Selective Biooxidation by a Kind of Protease
Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     melia-ionoside A
C19H36O8     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          1990          38          830-832
THE STRUCTURES OF TWO NEW IONONE GLUCOSIDES FROM MELIA TOOSENDAN AND A NOVEL TYPE OF SELECTIVE BIO-OXIDATION
Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     L-prolinium 4-(methylsulfinyl)butyl glucosinolate
C17H32N2O12S3     ÏàËÆ¶È:52.3%
Fitoterapia          2002          73          177-178
Glucosinolates from Cardaria draba
Antoine F¨¦echard, Nicolas Fabre ,S¨¦bastien Hannedouche, Isabelle Fourast¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     15¦Â-hydroxyisolineolon
C21H32O6     ÏàËÆ¶È:52.3%
Phytochemistry          2000          53          485-498
Steroidal glycosides from the aerial part of Asclepias incarnata
Tsutomu Warashina, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Crassarine D
C20H34O4     ÏàËÆ¶È:52.3%
Marine drugs          2011          9          1955-1968
Bioactive Cembranoids from the Soft Coral Sinularia crassa
Chih-Hua Chao,Kuei-Ju Chou,Chiung-Yao Huang,Zhi-Hong Wen,Chi-Hsin Hsu,Yang-Chang Wu,Chang-Feng Dai and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     sarcaglaboside G
C21H30O9     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2009          57          418-420
Three Novel Sesquiterpene Glycosides of Sarcandra glabra
Xiao-ru Hu, Jun-shan Yang and Xu-dong Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Neolinustatinamide
C17H31NO12     ÏàËÆ¶È:52.3%
Phytochemical Analysis          2010          21          575-581
Synthesis and Characterisation of -Glycosyloxyamides Derived from Cyanogenic Glycosides
Jandirk Sendker and Adolf Nahrstedt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2¦Á,5¦Á,7¦Â,9¦Á,13¦Á-pentahydroxy-10¦Â-acetoxytaxa-4(20),11-diene
C22H34O7     ÏàËÆ¶È:52.3%
Magnetic Resonance in Chemistry          2007          45          527-530
Structural determination of a new 2(3 ¡ú 20)abeotaxane with an unusual 13¦Â-substitution pattern and a new 6/8/6-ring taxane from Taxus cuspidata (pages 527¨C530)
Changhong Huo, Xiaohui Su, Xing Li, Xiping Zhang, Cunfang Li, Yufang Wang, Qingwen Shi and Hiromasa Kiyota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3¦Â,19-Diacetoxy jesromotetrol
C24H32O6     ÏàËÆ¶È:52.3%
Phytochemistry          1985          24          3056-3058
Diterpenes from Palafoxia texana
Antonio G. Gonz¨¢lez, Jos¨¦ J. Mendoza, Javier G. Luis, Angel G. Ravelo, Xorge A. Dom¨ªnguez, G. Cano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 5
C20H36O4     ÏàËÆ¶È:52.3%
Tetrahedron Letters          2002          43          4605-4608
Covilanone: a new rearranged labdane type diterpene
J.M.L. Rodilla, M.I. Ismael, L.A. Silva, J.P. Ces¨¢rio Serrano, J.G. Urones, F. Sanz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (1S,2E,4S,6E,8S,11R,12R)-2,6-cembradiene-4,8,11,12-tetrol
    ÏàËÆ¶È:52.3%
Acta Chemica Scandinavica          1986          40          123-134
Tobacco Chemistry. 69. Five New Labdanic Compounds from Tobacco.
Wahlberg, Inger; Eklund, Ann-Marie; Nordfors, Kerstin; Vogt, Carmen; Enzell, Curt R.; Berg, Jan-Eric
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Ovatolactone-7-O-(6'-O-p-hydroxybenzoyl)-¦Â-D-glucopyranoside
C22H28O10     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2007          55          159-222
Naturally Occurring Iridoids. A Review, Part 1
Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 17
C18H32O13     ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          1999          7          1549-1558
Bacteria targeted by human natural antibodies using ¦Á-gal conjugated receptor-specific glycopolymers
Jun Li, Sima Zacharek, Xi Chen, Jianqiang Wang, Wei Zhang, Adam Janczuk, Peng George Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     17¦ÂH-periplogenin
C23H34O5     ÏàËÆ¶È:52.1%
Phytochemistry          1988          27          2129-2133
Biotransformation of digitoxigenin by cell suspension cultures of Strophanthus gratus
Tsutomu Furuya,Kiichiro Kawaguchi,Masao Hirotani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ent-2-oxo-15,16-dihydroxypima¦Á-8(14)-en-16-O-¦Â-glucopyranoside
C26H42O8     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          1517-1521
Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis
Ying Xiang, Hua Zhang, Cheng-Qi Fan, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     borapetosideA
C26H34O12     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1985          33          4438-4444
Studies on the Constituents of the Stems of Tinospora tuberculata BEUMEE. II. New Diterpenoids, Borapetoside A and Borapetol A
NAOMICHI FUKUDA,MICHIKO YONEMITSU,TAKEATSU KIMURA,SHIZUKO HACHIYAMA,KAZUMOTO MIYAHARA and TOSHIO KAWASAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     N-oxy-tuberostemonine
C22H33NO5     ÏàËÆ¶È:50%
Journal of Chinese Pharmaceutical Sciences          1999          8          1-7
Three New Alkaloids from the Roots of Stemona tuberosa Lour
Lin Wenhan and Fu Hongzheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     13-Ethyl-11-methylene-18,19-dinor-17¦Á-pregn-4-en-20-yn-16¦Â,17-diol
    ÏàËÆ¶È:50%
Steroids          2002          67          111-117
Base promoted air oxidation of 13¦Â-ethyl-11-methylenegon-4-en-17-one
Federica Compostella, Diego Colombo, Emilia Modica, Antonio Scala, Lucio Toma, Bruna Bovio, Fiamma Ronchetti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     borapetoside A
    ÏàËÆ¶È:50%
Phytochemistry          1989          28          2419-2422
A furanoid diterpene glucoside from Tinospora cordifolia
R.K. Bhatt,B.K. Sabata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     15-Hydroxytorreyol 10-O-(6-O-¦Â-D-apiofuranosyl)-¦Â-D-glucopyranoside
C26H44O11     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2010          93          1407-1412
Glycosidic Constituents of Celastrus orbiculatus
Yang Zhang, Chang-Heng Tan, Jun-Jie Tan, Pei-Ming Yang, Shan-Hao Jiang, Xiang Ni and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     compound 2
C29H58NO13P     ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          5305-5308
Synthesis of ¦Â-d-Galp-(1¡ú4)-¦Á-d-Manp methanephosphonate, a substrate analogue for the elongating ¦Á-d-mannosyl phosphate transferase in the Leishmania
Vladimir S Borodkin, Michael A.J Ferguson, Andrei V Nikolaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     daucosterol-6'-O-stearate
    ÏàËÆ¶È:50%
Natural Product Research and Development          1996          8(1)          5-9
THE CONSTITUENTS FROM THE RHIZOMA OF ALTSMA ORIENTALIS (SAM) JUZEP.
Cai Lining; Wang Hongshu; Cao Hongxing; Zhang Ruyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     1-tert-butyl2'-methyl5-iodo-2-oxo-1',5',6',7',8',8a'-hexahydro-2'H-spiro[indole-3,3'-indolizine]-1,2'(2H)-dicarboxylate
C22H27IN2O5     ÏàËÆ¶È:50%
Tetrahedron          2012          68          3103-3111
Skeletal diversity via Pd(0) catalysed three-component cascades of allene and halides or triflates with protected hydroxylamines and formamide
Elghareeb E. Elboray, Chuanjun Gao, Ronald Grigg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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