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²éѯ½á¹û£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 13 C18H19ClO7 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2009 17 4622-4635 Synthesis and structure¨Cactivity relationships of radicicol derivatives and WNT-5A expression inhibitory activity Hideki Shinonaga, Toshiya Noguchi, Akiko Ikeda, Mari Aoki, Natsuko Fujimoto, Akira Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . epirhododendrin ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1983 31 1917-1922 Studies on the Constituents of Aceraceae Plants. IV. Carbon-13 Nuclear Magnetic Resonance Spectra of Acerogenin A, Rhododendrol and Related Compounds, and Structure of Aceroside IV from Acer nikoense MASAYOSHI KUBO,MASAHIRO NAGAI and TAKAO INOUE Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1'S-dihydrophayomphenol A2 C17H16O6 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2012 20 832-840 Antidiabetogenic oligostilbenoids and 3-ethyl-4-phenyl-3,4-dihydroisocoumarins from the bark of Shorea roxburghii Toshio Morikawa,Saowanee Chaipech, Hisashi Matsuda,Makoto Hamao,Yohei Umeda,Hiroki Sato, Haruka Tamura, Haruka Kon'I, Kiyofumi Ninomiya,Masayuki Yoshikawa,Yutana Pongpiriyadacha, Takao Hayakawa,Osamu Muraoka Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Orcinoside A C27H36O14 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2010 93 504-510 Three New Dimeric Orcinol Glucosides from Curculigo orchioides Ai-Xue Zuo, Yong Shen, Zhi-Yong Jiang, Xue-Mei Zhang, Jun Zhou, Jun L¨¹ and Ji-Jun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . isosalicin C13H18O7 ÏàËÆ¶È:53.3% Journal of Chemistry 2008 46 292-297 Study on chemical constituents of Paeonia veitchii Lynch. var Beresowskii Shiff. Phạm Hải Yến, Phan Văn Kiệm, L¨º Ngọc Thanh Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 9-[4-O-(¦Â-D-Galactopyranosyl)-(2Z)-(2-butenyl)]-2,6-diamino-(9H)purine C15H22O6N6 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2012 20 3111-3118 An enzymatic glycosylation of nucleoside analogues using ¦Â-galactosidase from Escherichia coli Jiř¨ª Blažek, Petr Jansa, Ondřej Baszczy¨¾ski, Martin Maxmilian Kaiser, Miroslav Otmar, Marcela Krečmerov¨¢, Martin Dranč¨ªnský, Anton¨ªn Holý, Blanka Kr¨¢lov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-(1,5-anhydro-2-deoxy-D-galactitol-2-yl)-4-(4-trifluoromethylsulfonamidophenoxy) methyl-1,2,3-triazole C16H19F3N4O7S ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2009 17 7254-7264 Design, synthesis and evaluation of monovalent ligands for the asialoglycoprotein receptor (ASGP-R) Daniela Stokmaier, Oleg Khorev, Brian Cutting, Rita Born, Daniel Ricklin, Thomas O.G. Ernst, Fabienne Böni, Kathrin Schwingruber, Martin Gentner, Matthias Wittwer, Morena Spreafico, Angelo Vedani, Said Rabbani, Oliver Schwardt, Beat Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . stachyline C C13H18O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2011 74 21-25 Stachylines A−D from the Sponge-Derived Fungus Stachylidium sp. Celso Almeida, Natalja Part, Sarah Bouhired, Stefan Kehraus, and Gabriele M. König Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound Mi 2 ÏàËÆ¶È:52.9% Molecules 2009 14 1098-1110 Polyphenols with Antiulcerogenic Action from Aqueous Decoction of Mango Leaves (Mangifera indica L.) Juliana Aparecida Severi, Zeila Pinheiro Lima, H¨¦lio Kushima, Alba Regina Monteiro Souza Brito, Lourdes Campaner dos Santos, Wagner Vilegas and Cl¨¦lia Akiko Hiruma-Lima Structure 13C NMR ̼Æ×Ä£Äâͼ |
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