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1 . Ball(1)12-s-neu5ac12 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2009 17 5451-5464 Systematic syntheses of influenza neuraminidase inhibitors: A series of carbosilane dendrimers uniformly functionalized with thioglycoside-type sialic acid moieties Jun-Ichi Sakamoto, Tetsuo Koyama, Daisei Miyamoto, Sangchai Yingsakmongkon, Kazuya I.P.J. Hidari, Wipawee Jampangern, Takashi Suzuki, Yasuo Suzuki, Yasuaki Esumi, Takemichi Nakamura, Ken Hatano, Daiyo Terunuma, Koji Matsuoka Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . fumifungin C22H41NO7 ÏàËÆ¶È:66.6% The Journal of Antibiotics 1987 40 1050-1052 FUMIFUNGIN, A NEW ANTIFUNGAL ANTIBIOTIC FROM ASPERGILLUS FUMIGATUS FRESENIUS 1863 TRIPTIKUMAR MUKHOPADHYAY, KIRITY ROY, Louis COUTINHO, R. H. RUPP, B. N. GANGULI, H. W. FEHLHABER Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (8'Z,10'R)-2,4-dihydroxy-6-(10-acetoxy-8-pentadecenyl)benzoic acid ÏàËÆ¶È:63.6% Journal of Natural Products 1993 Vol 56 1737 Use of Alkenylresorcinols from Ononis speciosa as Synthetic Precursors of Compounds with Potential Biological Activity Alejandro F. Barrero, Juan F. S¨¢nchez, Ignacio Rodr¨ªguez, Mercedes Maqueda Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-{4-[(3-Hexadecanoylamino)propanoylamino]phenylsul-fonyl}methionine methyl ester C31H53N3O6S2 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2000 8 1991-2006 Design, synthesis and early structure¨Cactivity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate Martin Schlitzer, Markus Böhm, Isabel Sattler, Hans-Martin Dahse Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 4 C29H57NO8 ÏàËÆ¶È:61.9% Phytochemistry 2006 67 1378-1384 Rourinoside and rouremin, antimalarial constituents from Rourea minor Zhen-Dan He, Cui-Ying Ma, Ghee Teng Tan, Kongmany Sydara, Pamela Tamez,Bounhoong Southavong, Somsanith Bouamanivong, D. Doel Soejarto,John M. Pezzuto, Harry H.S. Fong, Hong-Jie Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5R,10¦Â,13-triacetoxycyclomyltaylan-9¦Â-ol C21H30O7 ÏàËÆ¶È:61.9% Phytochemistry 2006 67 2616-2622 Chemical constituents of Malagasy liverworts: Cyclomyltaylanoids from Bazzania madagassa Liva Harinantenaina, Ritsu Kurata, Shigeru Takaoka, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . awajanomycin derivative 3 C17H29NO6 ÏàËÆ¶È:61.9% Journal of Natural Products 2006 69 1358-1360 Awajanomycin, a Cytotoxic ¦Ã-Lactone-¦Ä-lactam Metabolite from Marine-Derived Acremonium sp. AWA16-1 Jae-Hyuk Jang, Kaneo Kanoh, Kyoko Adachi, and Yoshikazu Shizuri Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (E)-11-hydroxy-octadeca-12-enoic acid C18H34O3 ÏàËÆ¶È:61.9% Zeitschrift f¨¹r Naturforschung B 2009 64b 1199-1207 Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile Ghada S. E. Abou-ElWafa, Mohamed Shaaban, Khaled A. Shaaban,Mohamed E. E. El-Naggar, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . comppound 2 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2012 20 667-671 Resin-based investigation of acyl carrier protein interaction networks in Escherichia coli Michael Rothmann, Sherry Niessen, Robert W. Haushalter,Benjamin F. Cravatt,Michael D. Burkart Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 16 C23H43N2O2 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 1998 6 1481-1489 Synthesis and evaluation of morpholino- and pyrrolidinosphingolipids as inhibitors of glucosylceramide synthase Tsuyoshi Miura, Tetsuya Kajimoto, Masayuki Jimbo, Kiwamu Yamagishi, Jin-Chi Inokuchi, Chi-Huey Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (2R,3R)-2-Decanoylamino-1-morpholino-4-(E)-octadecen-3-ol C32H62N2O3 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 1998 6 1481-1489 Synthesis and evaluation of morpholino- and pyrrolidinosphingolipids as inhibitors of glucosylceramide synthase Tsuyoshi Miura, Tetsuya Kajimoto, Masayuki Jimbo, Kiwamu Yamagishi, Jin-Chi Inokuchi, Chi-Huey Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (4'aS,7'R,70aR,2S)-Hexadecane acid-2-hydroxy-2-(hexa-hydro-2',4'a-dihydroxy-7'a-propyloxy-5'-oxo-20H-furo-[3,4-b]pyran-7'-yl)-ethyl ester C28H50O9 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2000 8 807-813 Inhibition of protein phosphatases by Michael adducts of ascorbic acid analogues with ¦Á,¦Â-unsaturated carbonyl compounds U.G Witt, J.E Schultz, M Dölker, K Eger Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl (3S,6R,7S,9R,E)-C6,C7-O-isopropilydene-3,6,7,9-tetrahydroxydodec-4-enoate C20H36O6 ÏàËÆ¶È:61.9% Tetrahedron 2009 65 7464-7467 Absolute stereochemistry and conformational analysis of achaetolide isolated from Ophiobolus sp. Wilanfranco Caballero Tayone, Saori Shindo, Takanori Murakami, Masaru Hashimoto, Kazuaki Tanaka, Noboru Takada Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . all(0)4-amide-S-Neu5Ac4 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2009 17 5451-5464 Systematic syntheses of influenza neuraminidase inhibitors: A series of carbosilane dendrimers uniformly functionalized with thioglycoside-type sialic acid moieties Jun-Ichi Sakamoto, Tetsuo Koyama, Daisei Miyamoto, Sangchai Yingsakmongkon, Kazuya I.P.J. Hidari, Wipawee Jampangern, Takashi Suzuki, Yasuo Suzuki, Yasuaki Esumi, Takemichi Nakamura, Ken Hatano, Daiyo Terunuma, Koji Matsuoka Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . octyl3,4,6-tri-O-acetyl-2-deoxy-¦Â-D-arabino-hexopyranoside C20H34O8 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2008 16 4083-4092 Alkyl deoxy-arabino-hexopyranosides: Synthesis, surface properties, and biological activities Filipa V.M. Silva, Margarida Goulart, Jorge Justino, Ana Neves, Fernando Santos, João Caio, Susana Lucas, Ana Newton, Diana Sacoto, Ester Barbosa, Maria-Soledade Santos, Am¨¦lia P. Rauter Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . D-threo-PipDMP ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry Letters 2004 14 1487-1490 New PDMP analogues inhibit process outgrowth in an insect cell line Jacob P. Slavish, Donna K. Friel, Lynne A. Oland, Robin Polt Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 15 ÏàËÆ¶È:59.0% 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 18 . ¦¤4,5(E),¦¤8,9(E)-sphingol-n-hexadecamide ÏàËÆ¶È:59.0% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (24S)-ergost-5-ene-3¦Â,7¦Á-diol ÏàËÆ¶È:59.0% Acta Scientiarum Naturalium Universitatis Sunyatseni 2005 44(5) 113-115 Studies on the Secondary Metabolite of the Soft Coral Lobophytum sp. (¢ò) HE Xi-xin, YAN Su-jun, ZENG Long-mei, SU Jing-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:59.0% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(6) 38-41 Studies on the Secondary Metabolites of the Soft Coral Sinularia grayi Tix.-Dur. MA Xiang-quan, ZHANG Guang-wen, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:59.0% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(2) 114-116 Studies on Chemical Constitutions of the Soft Coral Sinularia cervicornis Tix.-Dur. HE Xi-xin, YANG Ruo-lin, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . melophlins S C21H37NO ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2006 54(6) 852-854 Melophlins P, Q, R, and S: Four New Tetramic Acid Derivatives, from Two Palauan Marine Sponges of the Genus Melophlus Jinzhong XU,Masateru HASEGAWA,Ken-ichi HARADA,Hisayoshi KOBAYASHI, Hiroshi NAGAI,and Michio NAMIKOSHI Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . batzellaside A C18H37NO4 ÏàËÆ¶È:57.1% Journal of Natural Products 2005 68 118-121 A Madagascar Sponge Batzella sp. as a Source of Alkylated Iminosugars Nathaniel L. Segraves, and Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 4¦Â-acetoxytetrahydrobotryslactone C20H30O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2002 65 1724-1726 Four New Lactones from Botrytis cinerea Ana J. Colmenares, Rosa M. Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-03-29 13:07:37














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