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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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