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Slotus5389

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[ÇóÖú] 1 C ÒÑÓÐ1È˲ÎÓë

13C NMR (101 MHz, MeOD) ¦Ä 176.49, 141.25, 132.70, 128.18, 126.25, 103.83, 102.92, 100.55, 88.16, 85.78, 76.56, 73.79, 73.64, 72.35, 70.67, 69.70, 68.85, 60.92, 55.09, 54.21, 43.17, 41.77, 41.72, 39.08, 38.00, 36.15, 31.94, 26.85, 25.40, 21.94, 18.01, 17.43, 16.60, 15.55, 15.32.
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Slotus5389: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-12 19:55:26
1 .     Kudinoside
C35H52O8     ÏàËÆ¶È:68.5%
Phytochemistry          1996          41          871-877
Triterpenes and triterpenoid glycosides from the leaves of Ilex kudincha
Ming-An Ouyang, Chong-Ren Yang, Zi-Li Chen, Han-Qing Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     1-deoxy-1-{[(3¦Â,18¦Á,20¦Â)-3-hydroxy-11,29-dioxo-olean-12-en-29-yl]amino}-D-glucitol
    ÏàËÆ¶È:62.8%
Bioorganic & Medicinal Chemistry          2010          18          433-454
Synthesis of glycyrrhetinic acid derivatives for the treatment of metabolic diseases
Igor Beseda, Laszlo Czollner, Priti S. Shah, Rupesh Khunt, Rawindra Gaware, Paul Kosma, Christian Stanetty, Maria Carmen del Ruiz-Ruiz, Hassan Amer, Kurt Mereiter, Thierry Da Cunha, Alex Odermatt, Dirk Claßen-Houben, Ulrich Jordis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 13
    ÏàËÆ¶È:60%
Phytochemistry          1991          30          2699-2702
Acyclic sesquiterpene oligoglycosides from pericarps of Sapindus delavayi
Wong Wu-Hsiung, Ryoji Kasai, Wakako Choshi, Yukie Nakagawa, Kenji Mizutani, Kazuhiro Ohtani, Osamu Tanaka
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Ursolazuroside 2
C36H56O11     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2010          93          457-465
Four New Triterpenes from Anchusa azurea var. azurea
Ayşe Kuru¨¹z¨¹m-Uz, Zuhal G¨¹venalp, Cavit Kazaz, Bekir Salih and L. Öm¨¹r Demirezer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     compound 19
    ÏàËÆ¶È:60%
Phytochemistry          1986          25          871-876
Acyclic sesquiterpene oligoglycosides from pericarps of Sapindus mukurossi
Ryoji Kasai, Hiroko Fujino, Tatsuro Kuzuki, Wu-Hsiung Wong, Chie Goto, Noboru Yata, Osamu Tanaka, Fujiko Yasuhara, Shozo Yamaguchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ilekudinchoside C
C40H60O12     ÏàËÆ¶È:60%
Planta Medica          2011          77          1835-1840
Triterpenes and Triterpenoid Saponins from the Leaves of Ilex kudincha
Zuo, Wen-Jian; Dai, Hao-Fu; Chen, Jing; Chen, Hui-Qin; Zhao, You-Xing; Mei, Wen-Li; Li, Xian; Wang, Jin-Hui:
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3-O-¦Á-L-Rhamnopyranoside of methyl betulinate
C37H60O7     ÏàËÆ¶È:59.4%
Bioorganic & Medicinal Chemistry          2006          14          6713-6725
Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents
Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     20(R)-ginsenoside-Rh2
C36H62O8     ÏàËÆ¶È:58.3%
China Journal of Chinese Materia Medica          1991          16          678-679
Isolation and Identification of 20£¨R)-ginsenoside-Rh2
Zhao Yuqing , Yuan Changlu and Lu Haoran
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Capsugenin-30-O-¦Â-glucopyranoside
    ÏàËÆ¶È:58.3%
Journal of Natural Products          1987          Vol 50          479
Capsugenin-30-O-¦Â-glucopyranoside: A New Glycoside from the Leaves of Corchorus capsularis
Mohammad A. Quader, Mufizud-din Ahmed, Choudhury M. Hasan, Peter G. Waterman
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     rosamultin
C36H60O10     ÏàËÆ¶È:58.3%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxy-urs-12-en-28-oic acid-3-O-¦Â-D-glucopyranosyl ester
C36H60O11     ÏàËÆ¶È:58.3%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     2¦Á,3¦Â,23-trihydroxylurs-12,20(30)-dien-28-oic acid ¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:58.3%
Chinese Chemical Letters          2012          23          827-830
Two new triterpenoids from Psidium guajava
Ji Cheng Shu, Jian Qun Liu, Gui Xin Chou, Zheng Tao Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     ¨¢cido 3-O-¦Â-D-glucopiranos¨ªdeo-quin¨®vico
    ÏàËÆ¶È:58.3%
Qu¨ªmica Nova          2005          28          601-604
Triterpenoid saponins from Tocoyena brasiliensis Mart. (Rubiaceae)
Hamerski, Lidilhone; Carbonezi, Carlos Alberto; Cavalheiro, Alberto Jos¨¦; Bolzani, Vanderlan da Silva; Young, Maria Cl¨¢udia Marx
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     3¦Â,16¦Á,23,28,30-pentahydroxyoleana-11,13(18)-diene 3-O-¦Â-D-fucopyranoside
C36H58O9     ÏàËÆ¶È:58.3%
Natural Product Communications          2008          3          155-157
Saikosaponins from Bupleurum chinense and Inhibition ofHBV DNA Replication Activity
Feng Yin, Ruixiang Pan, Rongmin Chen and Lihong Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     3-O-¦Á-L-Rhamnopyranoside of betulinic acid
C36H58O7     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2006          14          6713-6725
Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents
Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     3-O-¦Â-D-glucopyranosyl-olean-12-ene-3¦Â,27,28,29-tetraol.
C36H60O9     ÏàËÆ¶È:58.3%
Phytochemistry          2013          93          176-181
Triterpene saponins of Genista ulicina Spach
Naima Boutaghane, Laurence Voutquenne-Nazabadioko, Dominique Harakat, Alain Simon, Zahia Kabouche
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     pomolic acid-28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:58.3%
Chinese Traditional and Herbal Drugs          2014          45          2742-2747
Chemical constituents from roots of Potentilla anserine
LIU Yi, CHENG Liang, HE Quan-quan, YEON Jae-ho, KONG De-yun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     rosamultin
    ÏàËÆ¶È:58.3%
Chinese Traditional and Herbal Drugs          2014          45          2742-2747
Chemical constituents from roots of Potentilla anserine
LIU Yi, CHENG Liang, HE Quan-quan, YEON Jae-ho, KONG De-yun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     Grandoside
C36H58O7     ÏàËÆ¶È:58.3%
Phytochemistry Letters          2014          10          86-90
One new flavonoid xyloside and one new natural triterpene rhamnoside from the leaves of Syzygium grande
Mamdouh N. Samy, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Mohamed S. Kamel
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     phrygioside A
C38H65O15SO3Na     ÏàËÆ¶È:57.8%
Russian Chemical Bulletin          2004          53          2634-2638
A new steroidal glycoside phrygioside A and its aglycone from the starfish Hippasteria phrygiana
E. V. Levina, A. I. Kalinovskii, P. V. Andriyashchenko, P. S. Dmitrenok and E. V. Evtushenko, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-02-10 18:35:12
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