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250350663

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13C NMR (100 MHz, CDCl3) ¦Ä12.2, 13.8, 18.8, 20.5, 20.6, 20.8, 24.6, 27.1, 27.4, 29.1, 29.7, 29.8, 40.2, 41.3, 42.0,42.4, 44.7, 51.2, 62.6, 63.1, 68.3, 70.1, 70.3, 71.3, 71.9, 72.7, 73.0, 73.4, 74.0,74.1, 74.2, 74.4, 74.6, 95.2, 96.0, 96.5, 96.8, 98.2, 104.8, 105.1, 112.0, 113.8, 119.3, 120.5,120.9, 131.2, 131.4, 145.3, 149.3, 149.4, 152.4, 166.5, 167.6, 169.3, 170.6, 170.7, 171.6
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lifeliuyan

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250350663: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-25 15:29:00
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1 .     undecaacetate
    ÏàËÆ¶È:54.3%
Planta Medica          1987          53          427-431
New Secoiridoid Glucosides from Ligustrum japonicum
Yoshiyasu Fukuyama,Kazuyo Koshino, Takashi Hasegawat, Toshihide Yamadat, and Kazuyuki Nakagawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     3-O-[¦Á-l-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl]3¦Â,23-dihydroxy olean-18-en-28-oic acid 28-O-[¦Á-L- rhamnopyranosyl-(1¡ú4)-¦Â-D-O-acetyl glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl] ester
C61H98O27     ÏàËÆ¶È:54.0%
Phytochemistry          2002          60          185-195
Triterpenoid saponins from Oreopanax guatemalensis
F.R. Melek, Toshio Miyase, S.M. Abdel-Khalik, M.H. Hetta, I.I. Mahmoud
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     perennisoside VII
C58H92O26     ÏàËÆ¶È:53.4%
Journal of Natural Products          2008          71(5)          828-835
Perennisosides I#VII, Acylated Triterpene Saponins with Antihyperlipidemic Activities from the Flowers of Bellis perennis
Toshio Morikawa, Xuezheng Li, Eriko Nishida, Yuki Ito, Hisashi Matsuda, Seikou Nakamura, Osamu Muraoka, and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Perennisoside IX
C58H92O25     ÏàËÆ¶È:53.4%
Chemical & Pharmaceutical Bulletin          2011          59          889-895
Medicinal Flowers. XXXII. Structures of Oleanane-Type Triterpene Saponins, Perennisosides VIII, IX, X, XI, and XII, from the Flowers of Bellis perennis
Toshio Morikawa, Xuezheng Li, Eriko Nishida, Seikou Nakamura, Kiyofumi Ninomiya, Hisashi Matsuda, Makoto Hamao, Osamu Muraoka, Takao Hayakawa and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     perennisaponin A
C57H90O24     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          2008          56(4)          559-568
Medicinal Flowers. XXI.1) Structures of Perennisaponins A, B, C, D, E,and F, Acylated Oleanane-Type Triterpene Oligoglycosides, from the Flowers of Bellis perennis
Masayuki YOSHIKAWA,Xuezheng LI,Eriko NISHIDA,Seikou NAKAMURA,Hisashi MATSUDA,Osamu MURAOKA,and Toshio MORIKAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     perennisoside I
C52H82O21     ÏàËÆ¶È:52.6%
Journal of Natural Products          2008          71(5)          828-835
Perennisosides I#VII, Acylated Triterpene Saponins with Antihyperlipidemic Activities from the Flowers of Bellis perennis
Toshio Morikawa, Xuezheng Li, Eriko Nishida, Yuki Ito, Hisashi Matsuda, Seikou Nakamura, Osamu Muraoka, and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     perennisoside II
C52H82O21     ÏàËÆ¶È:52.6%
Journal of Natural Products          2008          71(5)          828-835
Perennisosides I#VII, Acylated Triterpene Saponins with Antihyperlipidemic Activities from the Flowers of Bellis perennis
Toshio Morikawa, Xuezheng Li, Eriko Nishida, Yuki Ito, Hisashi Matsuda, Seikou Nakamura, Osamu Muraoka, and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     namonin B
C57H84O26     ÏàËÆ¶È:52.6%
Journal of Natural Products          2001          64          1127-1132
New Spirostanol Steroids and Steroidal Saponins from Roots and Rhizomes of Dracaena angustifolia and Their Antiproliferative Activity
Quan Le Tran, Yasuhiro Tezuka, Arjun Hari Banskota,Qui Kim Tran, Ikuo Saiki, and Shigetoshi Kadota
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3-O-¦Â-D-glucopyranosyl(1¡ú2)[¦Á-L-rhamnopyranosyl(¡ú3)] ¦Â-D-glucuronopyranosyl 28-O-angeloyl-A1-barrigenol
C53H84O21     ÏàËÆ¶È:52.6%
Phytochemistry          1998          49          2081-2085
Saponins from Harpullia cupanioides
Laurence Voutquenne, Catherine Lavaud, Georges Massiot, Cl¨¦ment Delaude
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     3-O-¦Â-D-galactopyranosyl(1¡ú2)[¦Á-L-rhamnopyranosyl(1¡ú3)] ¦Â-D-glucuronopyranosyl 28-O-angeloyl-A1-barrigenol
C53H84O21     ÏàËÆ¶È:52.6%
Phytochemistry          1998          49          2081-2085
Saponins from Harpullia cupanioides
Laurence Voutquenne, Catherine Lavaud, Georges Massiot, Cl¨¦ment Delaude
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     depresteroside deca-acetate
    ÏàËÆ¶È:52.6%
Phytochemistry          1994          36          377-382
Depresteroside, a mixed iridoid-secoiridoid structure from Gentiana depressa
Albert J. Chulia, Joseph Vercauteren, Mourad Kaouadji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     heinsiagenin ¦Á-3¦Â-O-(¦Á-1-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside)
C72H103O26N     ÏàËÆ¶È:52.6%
Phytochemistry          1994          36          1489-1492
Two triterpenoid saponins from Heinsia crinata
Babady-Bila, Chantal Wynants, Suzanne Toppet, Amuri Kilonda, Georges Hoornaert
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     oleoechinacoside
    ÏàËÆ¶È:52.6%
Natural Product Research          2010          24          737-742
Structural revision of oleoacteoside and oleoechinacoside
Koichi Machida; Erika Matsuoka; Masao Kikuchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     Rogchaponin R1
C52H80O21     ÏàËÆ¶È:52.6%
Planta Medica          2011          77          2029-2036
Tea Triterpenoidal Saponins from the Roots of Camellia sinensis Have Inhibitory Effects against Alcohol Dehydrogenase
Varughese, Titto; Manir, Md. Maniruzzaman; Rahaman, Mozahidur; Kim, Jeong Kee; Lee, Byeong-Gon; Moon, Surk-Sik:
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Pavioside D
    ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          2012          20          3280-3286
Paviosides A¨CH, eight new oleane type saponins from Aesculus pavia with cytotoxic activity
Virginia Lanzotti, Pasquale Termolino, Marcello Dolci, Paolo Curir
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     4''-O-[3-({2-[(1-cyclopropyl-1,4-dihydro-3-{[(2-hydroxyethyl)amino]carbonyl}-4-oxo-6-quinolyl)amino]ethyl}amino)-propanoyl]-9-deoxo-9a-methyl-9a-aza-9a-homoerythromycinA
C58H96N6O16     ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          2011          19          7270-7280
Synthesis and activity of new macrolones: Conjugates between 6(7)-(2¡ä-aminoethyl)-amino-1-cyclopropyl-3-carboxylic acid (2¡ä-hydroxyethyl) amides and 4¡å-propenoyl-azithromycin
Samra Kapić, Andrea Fajdetić, Sanja Koštrun, Ana Čikoš, Hana Čipčić Paljetak, Roberto Antolović, David J. Holmes, Sulejman Alihodžić
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     aesculioside C8
C55H88O21     ÏàËÆ¶È:52.6%
Phytochemistry          2013          90          95-105
Cytotoxic triterpenoid saponins from husks of Aesculus californica (Spach) Nutt.
Wei Yuan, Ping Wang, Zushang Su, Victoria S. Wang, Shiyou Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3¦Â,20S,24S-trihydroxydammar-25-ene-21,28-dioic acid 3-O-{-[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Á-L-rhamnopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl(1¡ú3)]-¦Á-L-arabinopyranosyl}-21-O-¦Â-D-glucopyranoside
C59H96O29     ÏàËÆ¶È:52.5%
Journal of Natural Products          2006          69          1394-1398
Triterpene Saponins from Gynostemma cardiospermum
Feng Yin, Yinan Zhang, Zhengyi Yang, Qiuqun Cheng, and Lihong Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     5-benzyloxycarbonylamino-1-pentyl [2-deoxy-4,6-O-di-tert-butylsilylene-2-(2,2,2-trichloroethoxycarbamoyl)-3-O-(2,2,2-trichloroethoxycarbonyl)-¦Á-D-galactopyranosyl]-(1¡ú3)-[2,3,4-tri-O-acetyl-¦Á-L-fucopyranosyl-(1¡ú2)]-(4,6-di-O-acetyl-¦Â-D-galactopyranosyl)-(
C73H95Cl6N3O33Si     ÏàËÆ¶È:52.5%
Molecules          2014          19          414-437
A New Chemical Approach to Human ABO Histo-Blood Group Type 2 Antigens
Atsushi Hara, Akihiro Imamura, Hiromune Ando, Hideharu Ishida and Makoto Kiso
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ciwujianoside A4
C61H98O28     ÏàËÆ¶È:52.4%
Chemical & Pharmaceutical Bulletin          1989          37          42-45
Saponins from Leaves of Acanthopanax senticosus HARMS., Ciwujia. II. : Structures of Ciwujianosides A1, A2, A3, A4 and D7
Chun-Jie SHAO,Ryoji KASAI,Jing-Da XU and Osamu TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     compound 7
C43H64O18     ÏàËÆ¶È:52.4%
Journal of Agricultural and Food Chemistry          1996          44          2020-2025
Studies on the Constituents of Cyclanthera pedata (Caigua) Seeds:  Isolation and Characterization of Six New Cucurbitacin Glycosides
Nunziatina De Tommasi, Francesco De Simone, Giovanna Speranza, and Cosimo Pizza
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     Perennisoside VIII
C58H92O25     ÏàËÆ¶È:51.7%
Chemical & Pharmaceutical Bulletin          2011          59          889-895
Medicinal Flowers. XXXII. Structures of Oleanane-Type Triterpene Saponins, Perennisosides VIII, IX, X, XI, and XII, from the Flowers of Bellis perennis
Toshio Morikawa, Xuezheng Li, Eriko Nishida, Seikou Nakamura, Kiyofumi Ninomiya, Hisashi Matsuda, Makoto Hamao, Osamu Muraoka, Takao Hayakawa and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     3¦Â-[(4-O-¦Á-L-rhamnopyranosyl-6-O-¦Â-D-glucopyranosyl)-¦Â-D-glucopyranosyl) oxy]-16¦Á,20,22,25-tetrahydroxycucurbita-5-en-11-one
C48H80O20     ÏàËÆ¶È:51.7%
Journal of Agricultural and Food Chemistry          1999          47          4512-4519
Studies on the Constituents of Cyclanthera pedata Fruits:  Isolation and Structure Elucidation of New Triterpenoid Saponins
Nunziatina De Tommasi, Francesco De Simone, Giovanna Speranza, and Cosimo Pizza
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl]-28-O-[¦Â-D-glucopyranosyl-(1¡ú2)-{¦Â-D-glucopyranosyl-(1¡ú6)}-¦Â-D-glucopyranosyl]-29-hydroxyhederagenin
    ÏàËÆ¶È:51.7%
Phytochemistry          2001          57          469-478
Triterpenoid saponins from the stem bark of Elattostachys apetala
Catherine Lavaud, Marie-Laure Crublet, Isabelle Pouny, Marc Litaudon, Thierry S¨¦venet
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     petersaponin III
C62H92O26     ÏàËÆ¶È:51.6%
Journal of Natural Products          2000          63          716-719
Petersaponins III and IV, Triterpenoid Saponins from Petersianthus macrocarpus
Tiwalade A. Olugbade,Abiodun Ogundaini, Nicolas Birlirakis, Mary Païs,and Marie-Th¨¦r¨¨se Martin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     solidagosaponin X
C60H94O28     ÏàËÆ¶È:51.6%
Chemical & Pharmaceutical Bulletin          1992          40          946-953
Studies on the Constituents of Solidago virga-aurea L. II. Structures of Solidagosaponins X-XX
Yoshinori INOSE,Toshio MIYASE and Akira UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     solidagosaponin XI
C60H94O28     ÏàËÆ¶È:51.6%
Chemical & Pharmaceutical Bulletin          1992          40          946-953
Studies on the Constituents of Solidago virga-aurea L. II. Structures of Solidagosaponins X-XX
Yoshinori INOSE,Toshio MIYASE and Akira UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
28 .     Floraassamsaponin IV
C60H94O27     ÏàËÆ¶È:51.6%
Tetrahedron          2015          71          846−851
Acylated oleanane-type triterpene oligoglycosides from the flower buds of Camellia sinensis var. assamica
Tomoe Ohta, Seikou Nakamura, Souichi Nakashima, Takahiro Matsumoto, Keiko Ogawa, Katsuyoshi Fujimoto, Masashi Fukaya, Masayuki Yoshikawa, Hisashi Matsuda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-25 13:35:34
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

250350663

ľ³æ (ÕýʽдÊÖ)

ÒýÓûØÌû:
2Â¥: Originally posted by lifeliuyan at 2015-03-25 13:35:34
²éѯ½á¹û£º¹²²éµ½67¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     undecaacetate
    ÏàËÆ¶È:54.3%
Planta Medica          1987          53          427-431
New Secoiridoid Glucosides from Ligustrum japonicum ...

3Â¥2015-03-25 15:28:56
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