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a89812

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198.08, 171.33, 109.10, 80.78, 73.11, 70.97, 32.74, 31.71, 29.67, 29.21, 28.94, 27.11, 25.32, 22.65, 22.57, 17.62
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177.33, 175.66, 73.00, 67.96, 62.57, 49.15, 41.02, 36.41, 33.93, 31.84, 29.58, 29.50, 29.34, 29.28, 29.10, 25.40, 24.77, 22.60, 14.01
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a89812(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-04-29 09:21:26
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1 .     Dihydropyran
C16H26O4     ÏàËÆ¶È:93.7%
Journal of Natural Products          1991          Vol 54          396
New Antibiotics from Strains of Trichoderma harzianum
Faramak Almassi, Emilio L. Ghisalberti, Melissa J. Narbey, Krishnapillai Sivasithamparam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 6
C16H26O4     ÏàËÆ¶È:93.7%
Journal of Natural Products          1993          Vol 56          1799
Antifungal Metabolites from Trichoderma harzianum
Emilio L. Ghisalberti, Catherine Y. Rowland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     koninginin B
    ÏàËÆ¶È:87.5%
Bioscience, Biotechnology, and Biochemistry          1995          59          1747-1749
Koninginin E : Isolation of a Biologically Active Natural Product from Trichoderma koningii
Stephen R. Parker, Horace G. Cutler, Peter R. Schreiner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Koninginin B
    ÏàËÆ¶È:87.5%
Journal of Agricultural and Food Chemistry          1991          39          977-980
Koninginin B: a biologically active congener of koninginin A from Trichoderma koningii
Horace G. Cutler, David S. Himmelsbach, Boris Yagen, Richard F. Arrendale, John M. Jacyno, Patsy D. Cole, Richard H. Cox
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 7
C16H26O4     ÏàËÆ¶È:68.7%
Journal of Natural Products          1993          Vol 56          1799
Antifungal Metabolites from Trichoderma harzianum
Emilio L. Ghisalberti, Catherine Y. Rowland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     koninginin E
    ÏàËÆ¶È:68.7%
Bioscience, Biotechnology, and Biochemistry          1995          59          1747-1749
Koninginin E : Isolation of a Biologically Active Natural Product from Trichoderma koningii
Stephen R. Parker, Horace G. Cutler, Peter R. Schreiner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3,6-dihydroxy-2-[1-oxo-10(E)-tetradecenyl]cyclohex-2-en-1-one
C20H32O4     ÏàËÆ¶È:62.5%
Journal of Natural Products          1987          Vol 50          1126
Isolation and Identification of the Major Component of Setal Exudate from Corythucha ciliata Isolation and Identification of the Major Component of Setal Exudate from Corythucha ciliata
William R. Lusby, James E. Oliver, John W. Neal Jr., Robert R. Heath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 8
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1993          Vol 56          1799
Antifungal Metabolites from Trichoderma harzianum
Emilio L. Ghisalberti, Catherine Y. Rowland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (S)-1-((4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl)prop-2-yn-1-ol
C15H26O3     ÏàËÆ¶È:62.5%
The Journal of Organic Chemistry          2011          76          2029-2039
Enantioselective Synthesis of Possible Diastereomers of Heptadeca-1-ene-4,6-diyne-3,8,9,10-tetrol; Putative Structure of a Conjugated Diyne Natural Product Isolated from Hydrocotyle leucocephala
Kavirayani R. Prasad and Bandita Swain
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (S)-methyl 2-((4R,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl)-2-hydroxyacetate
C15H28O5     ÏàËÆ¶È:62.5%
The Journal of Organic Chemistry          2011          76          2029-2039
Enantioselective Synthesis of Possible Diastereomers of Heptadeca-1-ene-4,6-diyne-3,8,9,10-tetrol; Putative Structure of a Conjugated Diyne Natural Product Isolated from Hydrocotyle leucocephala
Kavirayani R. Prasad and Bandita Swain
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 8a
    ÏàËÆ¶È:62.5%
Tetrahedron Letters          2000          41          5341-5345
Synthesis of chiral, densely functionalized medium-sized rings from carbohydrate precursors via regioselective exo/endo-primary alkyl radical cyclizations
Jos¨¦ Marco-Contelles, Elsa de Opazo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     7,7-dimethyl-8-(2-methyl-1-propenylidenyl)-5-dodecyne
C18H30     ÏàËÆ¶È:62.5%
Tetrahedron Letters          2002          43          1289-1293
A new coupling reaction of propargyl carbonates mediated by Ti(OiPr)2Cl2/Mg
Fanglong Yang, Gang Zhao, Yu Ding, Zongbao Zhao, Yueqing Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 5b
    ÏàËÆ¶È:62.5%
Tetrahedron Letters          2005          46          4753-4756
The synthesis and catalytic application of spacer-modified diol-functionalised Merrifield resins
Philip W. Dyer, Sandeep Handa, Toby B. Reeve, Samuel Suhard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-(13-methylhexadecyloxy)-1,2-(S)-propanediol + homolog 3-(15-methyloctadecyl-oxy)-1,2-(s)-propanediol
    ÏàËÆ¶È:62.5%
Tetrahedron letters          1983          24          5699-5702
Branched chain mono-glycerol ethers from a taiwanese marine sponge of the genus Aaptos
Muu N. Do, Karen L. Erickson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Tridecan-5-olide
C13H24O2     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1994                   2537-2543
Biological Baeyer¨CVilliger oxidation of some monocyclic and bicyclic ketones using monooxygenases from Acinetobacter calcoaceticus NCIMB 9871 and Pseudomonas putida NCIMB 10007
Rene Gagnon, Gideon Grogan, Melissa S. Levitt, Stanley M. Roberts, Peter W. H. Wan and Andrew J. Willetts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     17Z-tetracosenyl glycerol-l-yl
C27H54O3     ÏàËÆ¶È:62.5%
Lipids          1983          18          107-110
17Z-Tetracosenyl 1-glycerol ether from the spongesCinachyra alloclada andUlosa ruetzleri
John H. Cardellina, Clinton J. Graden, Bradley J. Greer and John R. Kern
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (E)-3-decylidenepyrrolidine-2,5-dione
    ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2013          21          660-667
Synthesis and evaluation of thiazolidinedione and dioxazaborocane analogues as inhibitors of AI-2 quorum sensing in Vibrio harveyi
Gilles Brackman, Abed Al Aziz Al Quntar, Claes D. Enk, Izet Karalic, Hans J. Nelis, Serge Van Calenbergh, Morris Srebnik, Tom Coenye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-pentacosox-1,2-propanediol
C28H58O3     ÏàËÆ¶È:62.5%
Chinese Journal of Organic Chemistry          2002          22          138-140
Studies on the Chemical Constituents of the Algae Sargassum polycystcum
XU, Shi-Hai DING, Li-Sheng WANG, Ming-Kui PENG, Shu-Lin LIAO, Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     tert-Butyl Acetate
C16H28O3     ÏàËÆ¶È:62.5%
Journal of Agricultural and Food Chemistry          2002          50          3522-3526
Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals
Mitsuo Miyazawa and Yuya Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Bis(octanoyl (¦Á-D-gluco-oct-pyranosyluronoylhydrazine)ether
C32H58N4O13     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2004          12          6397-6413
Synthesis of trehalose-based compounds and their inhibitory activities against Mycobacterium smegmatis
Jinhua Wang, Bryan Elchert, Yu Hui, Jon Y. Takemoto, Mekki Bensaci, John Wennergren, Huiwen Chang, Ravi Rai, Cheng-Wei Tom Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     R-3-hydroxyundecanoic acid methylester-3-O-¦Á-L-rhamnopyranoside
C18H34O7     ÏàËÆ¶È:61.1%
Marine Drugs          2012          10          598-603
A Fatty Acid Glycoside from a Marine-Derived Fungus Isolated from Mangrove Plant Scyphiphora hydrophyllacea
Yan-Bo Zeng,Hui Wang,Wen-Jian Zuo,Bo Zheng,Tao Yang,Hao-Fu Dai and Wen-Li Mei
Structure      13C NMR   


»¯ºÏÎï2£º

1 .     N-octadecanoyl-phytosphingosine
C36H73NO4     ÏàËÆ¶È:73.6%
Chinese Journal of Marine Drugs          2005          24(5)          22-23
A new natural ceramide N-octadecanoyl-phytosphingosine from soft coral Sinul a ria sp.
YANG Ruo-lin, WANG Hong-zhong, ZHENG Gui-lan, ZHANG Rong-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     N-(2-Hydroxyhexadecanoyl)-4-sphingenine
    ÏàËÆ¶È:68.4%
Helvetica Chimica Acta          2004          Vol. 87          1912
Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis
Fei Wang, Jian-Wen Tan, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     methyl 11S-jalapinolate
    ÏàËÆ¶È:68.4%
Chemical & Pharmaceutical Bulletin          2011          59(9)          1163-1168
Identification and Characterization of Component Organic and Glycosidic Acids of Crude Resin Glycoside Fraction from Calystegia soldanella
Ayako TAKIGAWA, Hiroaki SETOGUCHI, Masafumi OKAWA, Junei KINJO, Hiroyuki MIYASHITA, Kazumi YOKOMIZO, Hitoshi YOSHIMITSU, Toshihiro NOHARA, and Masateru ONO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Compound 6
    ÏàËÆ¶È:68.4%
Bioorganic & Medicinal Chemistry Letters          2001          11          1063-1064
Novel, lipophilic derivatives of 2,5-dideoxy-2,5-imino-D-mannitol (DMDP) are powerful ¦Â-glucosidase inhibitors
Tanja M. Wrodnigg, Stephen G. Withers, Arnold E. St¨¹tz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     2-Deoxy-3-O-tetradecanoyl-D-galactono-1,4-lactone
C20H36O6     ÏàËÆ¶È:68.4%
Bioorganic & Medicinal Chemistry Letters          1993          3          1993-1998
Conformationally constrained analogues of diacylglycerol. 5. 2,5-Dideoxy-3-O-tetradecanoyl-D-galactono-1,4-lactone: A superior homologue of 3-O-tetradecanoyl-2-deoxy-L-ribonolactone with PK-C binding affinity.
Rajiv Sharma, Victor E. Marquez, George W. A. Milne, Nancy E. Lewin, Peter M. Blumberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     2-(13-methyl)-tridecanecaproate
    ÏàËÆ¶È:68.4%
Chinese Traditional and Herbal Drugs          2010          41          1421-1423
Chemical constituents of Toosendan Fructus(¢ñ)
ZHOU Ying; WANG Hui-juan; GUO Dong-gui; WANG Zheng-lin; ZHU Xun; HU Fang; LI Zhou-yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (2S,3R,2'R,4E)-2'-hydroxy-C16-ceramide
C34H67NO4     ÏàËÆ¶È:68.4%
Bioorganic & Medicinal Chemistry          2010          18          7565-7579
Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells
Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 9
    ÏàËÆ¶È:68.4%
Australian Journal of Chemistry          1991          44          843-854
Epoxy Lipids From the Australian Epiphytic Brown Alga Notheia anomala. II.
LM Murray, RA Barrow and RJ Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     4-(hydroxymethyl)-4-[(tetradecanoyloxy)methyl]-4-vi-nyltetrahydro-2-furanone
C20H36O5     ÏàËÆ¶È:68.4%
Journal of Medicinal Chemistry          1996          39          19-28
Conformationally Constrained Analogues of Diacylglycerol. 10. Ultrapotent Protein Kinase C Ligands Based on a Racemic 5-Disubstituted Tetrahydro-2-furanone Template1
Rajiv Sharma, Jeewoo Lee, Shaomeng Wang, George W. A. Milne, Nancy E. Lewin, Peter M. Blumberg, and Victor E. Marquez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     [3S-(3¦Á,3a¦Á,5a¦Â,7¦Â,9a¦Á,9b¦Â)]-3-(1,1-dimethylethoxy)-dodecahydro-3a-methyl-1H-benz[e]indene-7-ethanol
C20H36O2     ÏàËÆ¶È:68.4%
Journal of Medicinal Chemistry          1995          38          4548-4556
Neurosteroid Analogs. 3. The Synthesis and Electrophysiological Evaluation of Benz[e]indene Congeners of Neuroactive Steroids Having the 5.beta.-Configuration
Mingcheng Han, Yuefei Hu, Charles F. Zorumski, Douglas F. Covey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl (11S)-hydroxyhexadecanoate
    ÏàËÆ¶È:68.4%
Phytochemistry          2011          72          773-780
Batatins III¨CVI, glycolipid ester-type dimers from Ipomoea batatas
Daniel Rosas-Ram¨ªrez, Edgar Escalante-S¨¢nchez, Rogelio Pereda-Miranda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     methyl 11-hydroxyheptadecanoate
    ÏàËÆ¶È:68.4%
Phytochemistry          2012          81          165-174
Resin glycosides from the aerial parts of Operculina turpethum
Wenbing Ding, Zi-Hua Jiang, Ping Wu, Liangxiong Xu, Xiaoyi Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Compound KPB-196
C25H43NO2     ÏàËÆ¶È:68.4%
Bioorganic & Medicinal Chemistry          2012          20          6162-6170
Novel amide- and sulfonamide-based aromatic ethanolamines: Effects of various substituents on the inhibition of acid and neutral ceramidases
Krishna P. Bhabak, Christoph Arenz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (2S)-2-(2-Hydroxyhexadecanamido)-4-methylpentanoic acid
C22H43NO4     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2011          19          735-743
Inhibition of secreted phospholipases A2 by 2-oxoamides based on a-amino acids: Synthesis, in vitro evaluation and molecular docking calculations
Varnavas D. Mouchlis, Victoria Magrioti, Efrosini Barbayianni, Nathan Cermak, Rob C. Oslund,Thomas M. Mavromoustakos, Michael H. Gelb, George Kokotos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2R)-2-(2-Hydroxyhexadecanamido)-4-methylpentanoic acid
C22H43NO4     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2011          19          735-743
Inhibition of secreted phospholipases A2 by 2-oxoamides based on a-amino acids: Synthesis, in vitro evaluation and molecular docking calculations
Varnavas D. Mouchlis, Victoria Magrioti, Efrosini Barbayianni, Nathan Cermak, Rob C. Oslund,Thomas M. Mavromoustakos, Michael H. Gelb, George Kokotos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 1a/1b
C38H78NO5     ÏàËÆ¶È:65%
Journal of Natural Products          2001          64          1210-1215
Sex Pheromones of the Hair Crab Erimacrus isenbeckii. II. Synthesis of Ceramides
Naoki Asai, Nobuhiro Fusetani, and Shigeki Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (2S,3S,4R)-2-[(R)-2-acetoxytetracosanoylamino]-1,3,4-hexadecanetriol
    ÏàËÆ¶È:65%
Bulletin of the Chemical Society of Japan          1998          71          259-272
Total Synthesis of Acanthacerebroside A and Astrocerebroside A via a Chiral Epoxide Intermediate Derived from L-Quebrachitol
Noritaka Chida, Noboru Sakata, Katsuyuki Murai, Takahiko Tobe, Toshihiko Nagase, Seiichiro Ogawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (2S,3S,4R)-2-tetracosanoylamino-1,3,4-octadecanetriol
    ÏàËÆ¶È:65%
Natural Product Research and Development          2006          18          411-414
Phytochemical Study on Zehneria maysorensis
LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     4-[(tetradecanoyloxy)methyl]-4-vinyltetrahydro-2-furanone
C21H36O4     ÏàËÆ¶È:65%
Journal of Medicinal Chemistry          1996          39          19-28
Conformationally Constrained Analogues of Diacylglycerol. 10. Ultrapotent Protein Kinase C Ligands Based on a Racemic 5-Disubstituted Tetrahydro-2-furanone Template1
Rajiv Sharma, Jeewoo Lee, Shaomeng Wang, George W. A. Milne, Nancy E. Lewin, Peter M. Blumberg, and Victor E. Marquez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (2S,3R,6S)-(3-Benzyloxy-6-dodecylpiperidin-2-yl)methanol
C25H43NO2     ÏàËÆ¶È:65%
Heterocycles          2004          64          249-259
A Short Synthesis of (-)-Deoxoprosophylline
Ang¨¦lique Jourdant and Jieping Zhu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     gracilamide B
C43H85NO5     ÏàËÆ¶È:63.1%
Journal of Natural Products          2006          69          1488-1491
Gracilarioside and Gracilamides from the Red Alga Gracilaria asiatica
Yi Sun, Youjun Xu, Kai Liu, Huiming Hua, He Zhu, and Yuehu Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (e)-8-oxo-9-oactadecenoic acid
C18H32O3     ÏàËÆ¶È:63.1%
Journal of Natural Products          2002          65          1712-1714
Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes
Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥2013-04-29 08:48:03
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a89812

½ð³æ (ÕýʽдÊÖ)

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2Â¥: Originally posted by wm0629 at 2013-04-29 08:48:03
»¯ºÏÎï1£º

1 .     Dihydropyran
C16H26O4     ÏàËÆ¶È:93.7%
Journal of Natural Products          1991          Vol 54          396
New Antibiotics from Strains of Trichoderma harzianum
Faramak  ...

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4Â¥2013-04-30 18:35:31
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×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
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