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13C NMR (151 MHz, MeOD)
13.01,22.31,24.71,25.36,25.39,28.82,28.97,29.02,29.18,29.33,29.36,29.45,31.65,33.61,37.01,71.03,176.38

»¯ºÏÎï2(0410-5)
13C NMR (151 MHz, MeOD)

13.04,22.32,24.65,24.68,25.17,28.78,28.83,28.88,29.01,29.12,29.19,29.32,29.44,31.64,31.86,33.56,37.04,66.78,72.36,130.85,131.09,132.60,133.07,176.28
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1 .     menthalactone
C23H41NO3     ÏàËÆ¶È:70.8%
Zeitschrift f¨¹r Naturforschung C          2009          64          809-812
Menthalactone, a New Analgesic from Mentha cordifolia Opiz. Leaves
I. M. Villaseñor and A. C. Sanchez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Compound 24b
    ÏàËÆ¶È:64%
Bioorganic & Medicinal Chemistry          2008          16          2212-2225
¦Á- and ¦Â-Substituted phosphonate analogs of LPA as autotaxin inhibitors
Peng Cui, William F. McCalmont, Jose L. Tomsig, Kevin R. Lynch, Timothy L. Macdonald
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     eushearilide
C29H54NO6P     ÏàËÆ¶È:61.5%
The Journal of Antibiotics          2006          59          597-600
A New Antifungal Macrolide, Eushearilide, Isolated from Eupenicillium shearii FREE
Tomoo Hosoe, Kazutaka Fukushima, Kayoko Takizawa, Takeshi Itabashi, Nobuo Kawahara, Valerio Vidotto and Ken-ichi Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Compound 4a
C21H44O6P     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry Letters          2004          14          5323-5328
Alkyl lysophosphatidic acid and fluoromethylene phosphonate analogs as metabolically-stabilized agonists for LPA receptors
Yong Xu, Masayuki Tanaka, Hiroyuki Arai, Junken Aoki, Glenn D. Prestwich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     rac-1-hexadecyl-2-hexadec-9-encyl-3-phosphoglycerol
C38H78O8P     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry Letters          2007          17          113-117
Synthesis and surface activity of diether-linked phosphoglycerols: Potential applications for exogenous lung surfactants
Robert H. Notter, Zhongyi Wang, Zhengdong Wang, Jason A. Davy, Adrian L. Schwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (3aR,5R,6S,7R,7aR)-6,7-Dihydroxy-5-(tetradecanoyloxymethyl)2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]thiazole
    ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2009          17          1831-1836
GlcNAc-Thiazoline conformations
Spencer Knapp, David Fash, Mohannad Abdo, Thomas J. Emge, Paul R. Rablen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (S)-1-(tetradecyloxy)-1-oxopropan-2-aminium methanesulfonate
    ÏàËÆ¶È:58.3%
Molecules          2011          16          8733-8744
Efficient Microwave-Assisted Synthesis of Ionic Esterified Amino Acids
Ricardo Cer¨®n-Camacho, Jorge Aburto, Luisa E. Montiel, Eugenio A. Flores, Frisia Cuellar and Rafael Mart¨ªnez-Palou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     sphingofungin F
C21H39NO6     ÏàËÆ¶È:58.3%
The Journal of Antibiotics          1992          45          1692-1696
SPHINGOFUNGINS E AND F: NOVEL SERINEPALMITOYL TRANS-FERASE INHIBITORS FROM Paecilomyces variotii
WENDY S. HORN, JACK L. SMITH, GERALD F. BILLS, SUSAN L. RAGHOOBAR, GREGORY L. HELMS, MYRA B. KURTZ, JEAN A. MARRINAN, BETH R. FROMMER, ROSEMARY A. THORNTON, SUZANNE M. MANDALA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (¡À)-trans-2-(ethoxycarbonyl)-2-hexadecylcyclopentyl-2-(trimethylammonio) ethyl phosphate
C29H58NO6P     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2013          21          2018-2024
Synthesis, characterization and Akt phosphorylation inhibitory activity of cyclopentanecarboxylate-substituted alkylphosphocholines
Md. Maqusood Alam, Eun-Ha Joh, Hyerim Park, Baek Kim, Dong-Hyun Kim, Yong Sup Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 22
    ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
11 .     (2S)-1,2-di-O-palmitoyl-3-O-(6-sulpho-¦Á-D-quinovopyranosyl) glycerol
C41H78O12S     ÏàËÆ¶È:54.1%
Chemical & Pharmaceutical Bulletin          2004          52(8)          986-988
Glycerol Derivatives and Sterols from Sargassum parvivesiculosum
Shu-Hua QI,Si ZHANG,Jian-She HUANG, Zhi-Hui XIAO,Jun WU,and Li-Juan LONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Malhamensilipin A
C24H40Cl6NaO8S2     ÏàËÆ¶È:54.1%
Journal of Natural Products          2010          73          279-283
Structure Revision and Absolute Configuration of Malhamensilipin A from the Freshwater Chrysophyte Poterioochromonas malhamensis
Alban R. Pereira, Tara Byrum, Grant M. Shibuya, Christopher D. Vanderwal and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Compound 3
C41H87NO6PS     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry Letters          2004          14          5983-5986
Synthesis and interfacial behavior of sulfur-containing analogs of lung surfactant dipalmitoyl phosphatidylcholine
Yusuo Chang, Zhengdong Wang, Robert H. Notter, Zhongyi Wang, Long Qu, Adrian L. Schwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Compound 4
C48H95NO9     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry Letters          2010          20          3475-3478
Synthesis and biological activity of ¦Á-glucosyl C24:0 and C20:2 ceramides
Peter J. Jervis, Natacha Veerapen, Gabriel Bricard, Liam R. Cox, Steven A. Porcelli, Gurdyal S. Besra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     O-oleyl-L-glutamine
C23H42N2O4     ÏàËÆ¶È:54.1%
Tetrahedron          1999          55          11275-11280
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2-(hexadecyloxy)-2-oxoethanaminium methanesulfonate
    ÏàËÆ¶È:54.1%
Molecules          2011          16          8733-8744
Efficient Microwave-Assisted Synthesis of Ionic Esterified Amino Acids
Ricardo Cer¨®n-Camacho, Jorge Aburto, Luisa E. Montiel, Eugenio A. Flores, Frisia Cuellar and Rafael Mart¨ªnez-Palou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2-(octadecyloxy)-2-oxoethanaminium methanesulfonate
    ÏàËÆ¶È:54.1%
Molecules          2011          16          8733-8744
Efficient Microwave-Assisted Synthesis of Ionic Esterified Amino Acids
Ricardo Cer¨®n-Camacho, Jorge Aburto, Luisa E. Montiel, Eugenio A. Flores, Frisia Cuellar and Rafael Mart¨ªnez-Palou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-(dodecanoyloxy)-2-(isobutyryloxy)-4-methylpentanoic acid
C22H40O6     ÏàËÆ¶È:54.1%
Molecules          2012          17          12469-12477
A Novel Antibacterial Compound from Siegesbeckia glabrescens
Young-Soo Kim, Hyungil Kim, Eunsun Jung, Jang-Hyun Kim, Wangtaek Hwang, Eun-Ju Kang, Sanghyun Lee, Byung-Jo Ha, Jongsung Lee and Deokhoon Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     [1S-[1¦Á,2¦Á(Z),3¦Á,4¦Á]]-7-[3-[[[[(1-oxoheptyl)amino]acetyl]amino]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid
C23H38O6N2     ÏàËÆ¶È:54.1%
Journal of Medicinal Chemistry          1990          33          2465-2476
7-Oxabicyclo[2.2.1]heptyl carboxylic acids as thromboxane A2 antagonists: aza .omega.-chain analogs
Masami Nakane, Joyce A. Reid, Wen Ching Han, Jagabandhu Das, Vu Chi Truc, Martin F. Haslanger, Dianne Garber, Don N. Harris, Anders Hedberg,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     [1R-[1¦Á,2¦Á(Z),3¦Á,4¦Á]]-7-[3-[[[[(1-oxoheptyl)amino]acetyl]amino]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid
C23H38N2O5     ÏàËÆ¶È:54.1%
Journal of Medicinal Chemistry          1990          33          2465-2476
7-Oxabicyclo[2.2.1]heptyl carboxylic acids as thromboxane A2 antagonists: aza .omega.-chain analogs
Masami Nakane, Joyce A. Reid, Wen Ching Han, Jagabandhu Das, Vu Chi Truc, Martin F. Haslanger, Dianne Garber, Don N. Harris, Anders Hedberg,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (2S,3R,4E,8 Z,2'R)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydrox yhexadecanoyl)-4,8-sphingadienin
    ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          1988          1988          807-814
Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides
Kenji Mori and Takeshi Kinsho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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xmcwebpasser(¶¹¸ç´ú·¢): ½ð±Ò+50, лл 2013-06-03 08:25:17
1 .     9,10,13-trihydroxy-(E)-11-octadecenoic acid
C18H32O5     ÏàËÆ¶È:72.2%
Natural Product Research and Development          1996          8(4)          28-32
SYNTHESIS OF NATURAL INSECTICIDE p-PHELLANDRENE
Lu Kui; Liu Yanqi; Zhao Yingjie; Lu Chunming; Zhang Xiaolin; Jiang Yongjia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Compound 18
    ÏàËÆ¶È:70.5%
Bioorganic & Medicinal Chemistry Letters          2004          14          4919-4923
Synthesis and biological evaluation of novel cytotoxic phospholipids for prostate cancer
Veeresa Gududuru, Eunju Hurh, Gangadhar G. Durgam, Seoung Soo Hong, Vineet M. Sardar, Huiping Xu, James T. Dalton, Duane D. Miller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 2
C17H34O4     ÏàËÆ¶È:70.5%
The Journal of Organic Chemistry          2009          74          5267-5275
Structural and Synthetic Investigations of Tanikolide Dimer, a SIRT2 Selective Inhibitor, and Tanikolide seco-Acid from the Madagascar Marine Cyanobacterium Lyngbya majuscula
Marcelino Gutierrez, Eric H. Andrianasolo, Won Kyo Shin, Douglas E. Goeger, Alexandre Yokochi, Jorg Schemies, Manfred Jung, Dennis France, Susan Cornell-Kennon, Eun Lee and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Compound 4a
C21H44O6P     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2004          14          5323-5328
Alkyl lysophosphatidic acid and fluoromethylene phosphonate analogs as metabolically-stabilized agonists for LPA receptors
Yong Xu, Masayuki Tanaka, Hiroyuki Arai, Junken Aoki, Glenn D. Prestwich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Compound 2
C41H87NO4PS     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2004          14          5983-5986
Synthesis and interfacial behavior of sulfur-containing analogs of lung surfactant dipalmitoyl phosphatidylcholine
Yusuo Chang, Zhengdong Wang, Robert H. Notter, Zhongyi Wang, Long Qu, Adrian L. Schwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-(dodecanoyloxy)-2-(isobutyryloxy)-4-methylpentanoic acid
C22H40O6     ÏàËÆ¶È:65%
Molecules          2012          17          12469-12477
A Novel Antibacterial Compound from Siegesbeckia glabrescens
Young-Soo Kim, Hyungil Kim, Eunsun Jung, Jang-Hyun Kim, Wangtaek Hwang, Eun-Ju Kang, Sanghyun Lee, Byung-Jo Ha, Jongsung Lee and Deokhoon Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     batzellaside A
C18H37NO4     ÏàËÆ¶È:61.1%
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
8 .     Compound 6
    ÏàËÆ¶È:61.1%
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
9 .     (E)-9-octadecenoic acid
C18H34O2     ÏàËÆ¶È:61.1%
Journal of Agricultural and Food Chemistry          2002          50          6993-6996
Repellent Activity of Constituents Identified in Foeniculum vulgare Fruit against Aedes aegypti (Diptera:  Culicidae)
Do-Hyoung Kim, Soon-Il Kim, Kyu-Sik Chang, and Young-Joon Ahn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     linoleic acid
C18H32O2     ÏàËÆ¶È:61.1%
Chinese Journal of Medicinal Chemistry          2012          22          47-50
Chemical constituents of Lysimachia stenosepala
CAO Xian-ping; LIANG Xin; ZHONG Hui-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Compound 8a
C22H44PF2O5     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2004          14          5323-5328
Alkyl lysophosphatidic acid and fluoromethylene phosphonate analogs as metabolically-stabilized agonists for LPA receptors
Yong Xu, Masayuki Tanaka, Hiroyuki Arai, Junken Aoki, Glenn D. Prestwich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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