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²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (1S,2S,2'Z)-2-(5'-Hydroxy-pent-2'-enyl)-3-oxo-cyclopentaneacetic acid C12H18O4 ÏàËÆ¶È:83.3% Bioscience, Biotechnology, and Biochemistry 2008 72 2867-2876 Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 4 ÏàËÆ¶È:83.3% Bioscience, Biotechnology, and Biochemistry 1996 60 732-735 Two Jasmonoid Glucosides and a Phenylvaleric Acid Glucoside from Perilla frutescens Tomoyuki FUJITA, Kenji TERATO, Mitsuru NAKAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 8b C15H20N4O ÏàËÆ¶È:53.8% Tetrahedron Letters 2001 42 6015-6018 Preparation of ¡®carba¡¯ dipeptides bearing a basic side-chain at the C-terminus: synthesis of enantiopure Boc-d-Phe-¦·[CH2CH2]-l-Arg(NO2)-OH and Boc-d-Phe-¦·[CH2CH2]-d-Arg(NO2)-OH Andrew S. Kende, Han-Qing Dong, Adam W. Mazur, Frank H. Ebetino Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate C13H18O4 ÏàËÆ¶È:53.8% Bioscience, Biotechnology, and Biochemistry 2008 72 2867-2876 Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate C13H18O4 ÏàËÆ¶È:53.8% Bioscience, Biotechnology, and Biochemistry 2008 72 2867-2876 Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . pichiacin B C12H16O3 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(5) 869-872 Furan Metabolites from the Sponge-Derived Yeast Pichia membranifaciens Mohamed Elbandy, Pramod B. Shinde, Hung The Dang, Jongki Hong, Kyung Sook Bae, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . desmethylenylnocardamine C26H46N6O9 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 623-625 Cyclic Peptides of the Nocardamine Class from a Marine-Derived Bacterium of the Genus Streptomyces Hyi-Seung Lee, Hee Jae Shin, Kyoung Hwa Jang, Tae Sik Kim, Ki-Bong Oh, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . caiophoraenin C11H18O5 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 1628-1631 A Novel Antibacterial Iridoid and Triterpene from Caiophora coronata Smriti Khera,Girma M. Woldemichael, Maya P. Singh,Enrique Suarez, and Barbara N. Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . aglaiduline C20H24N2O2 ÏàËÆ¶È:50% Phytochemistry 1999 52 1085-1088 Bisamides from Aglaia edulis Ekarin Saifah, Rutt Suttisri, Srisuda Shamsub, Thitima Pengsuparp, Vimolmas Lipipun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Lonicerin C12H20O6 ÏàËÆ¶È:50% Natural Product Sciences 2009 15 121-124 Alqasoumi, Saleh I.; Al-Rehaily, Adnan J.; Abdel-Kader, Maged S. Alqasoumi, Saleh I.; Al-Rehaily, Adnan J.; Abdel-Kader, Maged S. Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . intetrazole ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2002 12 2553-2556 Glutathione-like tripeptides as inhibitors of glutathionylspermidine synthetase. Part 1: Substitution of the glycine carboxylic acid group Katie Amssoms, Sandra L. Oza, Esteban Ravaschino, Abdellah Yamani, Anne-Marie Lambeir, Padinchare Rajan, Gunther Bal, Juan Bautista Rodriguez, Alan H. Fairlamb, Koen Augustyns, Achiel Haemers Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 1c C9H15O5NS ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 115-118 Synthesis of all isomers of pulcherrimine, a bitter principle in the sea urchin ovary Noriko U Sata, Ryuji Kuwahara, Yuko Murata Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 1d C9H15O5NS ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 115-118 Synthesis of all isomers of pulcherrimine, a bitter principle in the sea urchin ovary Noriko U Sata, Ryuji Kuwahara, Yuko Murata Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S)-2-amino-6-{[(E)-3-(1H-imidazol-4-yl)-2-propenoyl]-amino}hexanoic acid C12H16N4O3 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 2004 47 2243-2255 Novel Amino Acid Derived Natural Products from the Ascidian Atriolum robustum: Identification and Pharmacological Characterization of a Unique Adenosine Derivative Stefan Kehraus, Simone Gorzalka, Christian Hallmen, Jamshed Iqbal, Christa E. M¨¹ller, Anthony D. Wright, Michael Wiese, and Gabriele M. König Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . N-benzoyl-¦Â-alanine n-butylamide C14H20N2O2 ÏàËÆ¶È:50% Chemical Research in Toxicology 2004 17 110-118 Model Studies on the Metal-Catalyzed Protein Oxidation: Structure of a Possible His-Lys Cross-Link Yahua Liu, Gang Sun, Adrian David, and Lawrence M. Sayre Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Sodium 2-(6-aminohexylcarbamoyl)-3-methyl-1H-indole-5-carboxylate C17H23N3O3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4346-4354 Synthesis and evaluation of bidentate ligands designed to interact with PDZ domains Benjamin Boucherle, Alexandre Vogrig, Hemantkumar Deokar, Naoual Bouzidi, Isabelle Ripoche, Isabelle Thomas, Philippe Marin, Sylvie Ducki Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-(S)-Methyl 2-amino-3-(4-benzyloxy-3,5-dibromophenyl)-propanoate C17H18BrBrNO3 ÏàËÆ¶È:50% Organic & Biomolecular Chemistry 2012 10 1246-1254 Syntheses of pseudoceramines A¨CD and a new synthesis of spermatinamine, bromotyrosine natural products from marine sponges J. Mikael Hillgren, Christopher T. Öberg and Mikael Elofsson Structure 13C NMR ̼Æ×Ä£Äâͼ |

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