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²éѯ½á¹û£º¹²²éµ½31¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,3-dieaproyl-2-oleoyl-glycerol ÏàËÆ¶È:68.9% Bioorganic & Medicinal Chemistry 1996 4 345-348 Two step synthesis of 1,3-aeetylated, -butyroylated and -eaproylated triglycerides from a microorganism oil rich in Docosahexaenoic Acid (DHA) Yves Bayon , and Ran¨¦ Dolmazon Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 11 ÏàËÆ¶È:65.5% Journal of Natural Products 1997 60 1251-1260 New Acylated Sulfoglycolipids and Digalactolipids and Related Known Glycolipids from Cyanobacteria with a Potential To Inhibit the Reverse Transcriptase of HIV-1 Vered Reshef, Erez Mizrachi, Tal Maretzki, Colin Silberstein, Shoshana Loya, Amnon Hizi, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 12 C37H67O4 ÏàËÆ¶È:65.5% Journal of Natural Products 1997 60 1251-1260 New Acylated Sulfoglycolipids and Digalactolipids and Related Known Glycolipids from Cyanobacteria with a Potential To Inhibit the Reverse Transcriptase of HIV-1 Vered Reshef, Erez Mizrachi, Tal Maretzki, Colin Silberstein, Shoshana Loya, Amnon Hizi, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Compound 6 ÏàËÆ¶È:65.5% Bioorganic & Medicinal Chemistry Letters 2000 10 2679-2681 Total synthesis of mololipids: A new series of anti-HIV Moloka'iamine derivatives Ryan C. Schoenfeld, Jean-Philip Lumb, Jacques Fantini, Bruce Ganem Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (11Z,19E)-3-Acetoxy-11,19-octacosadien-1-ol C30H56O3 ÏàËÆ¶È:65.5% Tetrahedron 2012 68 3750-3760 Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers Original Resear Yasumasa Shikichi, Kazuaki Akasaka, Shigeyuki Tamogami, Shruti Shankar, Joanne Y. Yew, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-O-(¦Â-D-galactofuranosyl)-1,2-di-O-myristoyl-sn-glycerol C37H70O10 ÏàËÆ¶È:65.5% Bioorganic & Medicinal Chemistry 2010 18 3696-3702 Synthesis of the lipoteichoic acid of the Streptococcus species DSM 8747 Yan Qiao, Buko Lindner, Ulrich Zähringer, Peter Truog, Richard R. Schmidt Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,3-dibutyroyl-2-oleoylglycerol C29H52O6 ÏàËÆ¶È:65.5% Pharmacy and Pharmacology Communications 1999 5 311-313 First Total Synthesis of 1,3-Diacetyl- and -Dibutyroyl-2-oleoylglycerol, Previously Isolated From Natural Products J. GUILLON, B. LELONG, J.-P. RIOULT and M. ROBBA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . palmitate C36H70O2 ÏàËÆ¶È:65.5% Natural Product Communications 2011 6 767-772 Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1,2-(10',12'-Heptadecadiynoyl)-sn-glycero-3-phophatidylcholine C42H68NO8P ÏàËÆ¶È:65.5% Journal of the Brazilian Chemical Society 2001 12 64-72 Synthesis of the Diacetylenic Phospholipids 1,2-(10',12'-Heptadecadiynoyl)-sn-Glycero-3-Phophatidylcholine and 1,2-(4',6'-Tricosadiynoyl)-sn-Glycero-3-Phophatidylcholine Paulo T. Hennies, Maria H. C. Santana and Carlos R. D. Correia Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . PX7 ÏàËÆ¶È:64.5% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . balansenate I C32H62O2 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2003 Vol. 86 2452 New Long-Chain Esters and Adenine Analogs from the Leaves of Formosan Bridelia balansae Yeh-Hsin Tsai, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N-palmitoyl-D-erythro-(2S,3R)-17-methyl-octadecasphinga-4(E),8(E)-dienine C35H67NO3 ÏàËÆ¶È:63.3% Journal of Natural Products 1995 Vol 58 948-953 Isolation of New Ceramides from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6-O-tert-Butyldiphenylsilyl-3,4-di-O-tetradecanoyl-L-glucal C50H80O6Si ÏàËÆ¶È:63.3% Bioorganic & Medicinal Chemistry 1993 1 119-123 Conformationally constrained analogues of diacylglycerol (DAG)-II. Differential interaction of ¦Ä-lactones and ¦Ã-lactones with protein kinase C (PK-C) Jeewoo Lee, Victor E. Marquez, Peter M. Blumberg, Kristopher W. Krausz, Marcelo G. Kazanietz Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . strongylodiol G C24H42O2 ÏàËÆ¶È:62.0% Journal of Natural Products 2005 68 1001-1005 Acetylenic Strongylodiols from a Petrosia (Strongylophora) Okinawan Marine Sponge Kinzo Watanabe, Yuichiro Tsuda, Maki Hamada, Miki Omori, Go Mori,Kazuo Iguchi, Hideo Naoki, Tsuyoshi Fujita, and Rob W. M. Van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 19 ÏàËÆ¶È:62.0% Journal of Natural Products 1997 60 1251-1260 New Acylated Sulfoglycolipids and Digalactolipids and Related Known Glycolipids from Cyanobacteria with a Potential To Inhibit the Reverse Transcriptase of HIV-1 Vered Reshef, Erez Mizrachi, Tal Maretzki, Colin Silberstein, Shoshana Loya, Amnon Hizi, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . M-2 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 1982 30 3544-3547 Marine Natural Products. X. Pharmacologically Active Glycolipids from the Okinawan Marine Sponge Phyllospongia foliascens (PALLAS) HIROYUKI KIKUCHI,YASUMASA TSUKITANI,TOSHITAKA MANDA,TAKASHI FUJII,HAJIME NAKANISHI,MOTOMASA KOBAYASHI and ISAO KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (E)-(7,7-Dimethoxy-4-oxohept-5-enoyl)-1-palmitoyl-snglycero-3-phosphatidylcholine C33H63NO11P ÏàËÆ¶È:62.0% Bioorganic & Medicinal Chemistry 2011 19 580-587 An efficient synthesis of ¦Ã-hydroxy-¦Á,¦Â-unsaturated aldehydic esters of 2-lysophosphatidylcholine Jaewoo Choi, James M. Laird, Robert G. Salomon Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . hydroxybenzoic acid 2,3-bis-hexadecanoyloxypropyl esters(b) ÏàËÆ¶È:62.0% Canadian Journal of Chemistry 2006 84 1411-1415 Synthesis and characterization of a series of novel phenol- and polyphenol-based glycerolipids1 Rolf Schmidt, Joseph G. Carrigan, and Christine E. DeWolf Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Compound 9 ÏàËÆ¶È:62.0% Bioorganic & Medicinal Chemistry Letters 2000 10 2679-2681 Total synthesis of mololipids: A new series of anti-HIV Moloka'iamine derivatives Ryan C. Schoenfeld, Jean-Philip Lumb, Jacques Fantini, Bruce Ganem Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . PX8 ÏàËÆ¶È:62.0% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . PX23 ÏàËÆ¶È:62.0% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (11E,19E)-3-Acetoxy-11,19-octacosadien-1-ol C30H56O3 ÏàËÆ¶È:62.0% Tetrahedron 2012 68 3750-3760 Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers Original Resear Yasumasa Shikichi, Kazuaki Akasaka, Shigeyuki Tamogami, Shruti Shankar, Joanne Y. Yew, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (11E,19Z)-3-Acetoxy-11,19-octacosadien-1-ol C30H56O3 ÏàËÆ¶È:62.0% Tetrahedron 2012 68 3750-3760 Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers Original Resear Yasumasa Shikichi, Kazuaki Akasaka, Shigeyuki Tamogami, Shruti Shankar, Joanne Y. Yew, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . convolutamide B C26H37NO4Br2 ÏàËÆ¶È:62.0% Tetrahedron 1994 50 10201-10206 Convolutamides A ¡« F, novel ¦Ã-lactam alkaloids from the marine bryozoan Amathia convoluta Hui-ping Zhang, Hideyuki Shigemori, Masami Ishibashi, Toshiyuki Kosaka, George R. Pettit, Yoshiaki Kamano, Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . phytoceramide C36H71NO4 ÏàËÆ¶È:62.0% Molecules 2011 16 9090-9100 Phytoceramide Shows Neuroprotection and Ameliorates Scopolamine-Induced Memory Impairment Jae-Chul Jung, Yeonju Lee, Sohyeon Moon, Jong Hoon Ryu and Seikwan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2-butoxyethyl linoleate ÏàËÆ¶È:62.0% Journal of the Chinese Chemical Society 2000 47 1131-1136 The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 1,2-(10',12'-Tricosadiynoyl)-sn-glycero-3-phophatidylcholine C54H92NO8P ÏàËÆ¶È:62.0% Journal of the Brazilian Chemical Society 2001 12 64-72 Synthesis of the Diacetylenic Phospholipids 1,2-(10',12'-Heptadecadiynoyl)-sn-Glycero-3-Phophatidylcholine and 1,2-(4',6'-Tricosadiynoyl)-sn-Glycero-3-Phophatidylcholine Paulo T. Hennies, Maria H. C. Santana and Carlos R. D. Correia Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . tripalmitolein ÏàËÆ¶È:61.2% Magnetic Resonance in Chemistry 2009 47 771-781 A novel approach to the rapid assignment of 13C NMR spectra of major components of vegetable oils such as avocado, mango kernel and macadamia nut oils (pages 771¨C781) Liezel Retief, Jean M. McKenzie and Klaus R. Koch Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 12-O-palmitoyl-16-hydroxyphorbol-13-acetate C38H60O9 ÏàËÆ¶È:61.2% Agricultural and Biological Chemistry 1979 43 2523-2529 Piscicidal Constituents and Related Diterpene Esters from Aleurites fordii Mitsuru HIROTA, Hajime OHIGASHI, Koichi KOSHIMIZU Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . PX2 ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Glomeraside B C30H54O8 ÏàËÆ¶È:60% Phytochemistry 2012 82 149-157 Cyclic glycolipids from glandular trichome exudates of Cerastium glomeratum Teigo Asai, Yuki Nakamura, Yui Hirayama, Kiyoshi Ohyama, Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ |
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