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250350663ľ³æ (ÕýʽдÊÖ)
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[ÇóÖú]
191 ÒÑÓÐ1È˲ÎÓë
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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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250350663: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-25 15:29:00
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250350663: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-25 15:29:00
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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 Yoshiyasu Fukuyama,Kazuyo Koshino, Takashi Hasegawat, Toshihide Yamadat, and Kazuyuki Nakagawa Structure 13C NMR Structure & 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
2Â¥2015-03-25 13:35:34
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3Â¥2015-03-25 15:28:56













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