LBF20406CV11: Difference between revisions
(New page: {{Lipid/Header}} {{Hierarchy|{{PAGENAME}}}} {{Metabolite |LipidBank=XPR8007 |LipidMaps=LMFA03120007 |SysName=Methyl-4R- (5-trans,7-cis) -4-acetoxy-7- [ 2S-acetoxy-2- [cis-7-acetoxy-2-oct...) |
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|LipidBank=XPR8007 | |LipidBank=XPR8007 | ||
|LipidMaps=LMFA03120007 | |LipidMaps=LMFA03120007 | ||
|SysName=Methyl-4R- (5- | |SysName=Methyl-4R- (trans-5,cis-7) -4-acetoxy-7- [ 2S-acetoxy-2- (cis-7-acetoxy-2-octenyl) -5-oxo-3-cyclopentenylidene ] -5-heptenoic acid | ||
|Common Name=&&20-Acetoxyclavulone III&&Methyl-4R- (5E,7Z) -4-acetoxy-7- [ 2S-acetoxy-2- | |Common Name=&&20-Acetoxyclavulone III&&Methyl-4R- (5E,7Z) -4-acetoxy-7- [ 2S-acetoxy-2- (7Z-acetoxy-2-octenyl) -5-oxo-3-cyclopentenylidene ] -5-heptenoic acid&& | ||
|Optical=[ alpha ]_D +26.4°(C 0.86, CHCl_3 )[[Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433|{{RelationTable/GetFirstAuthor|Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433}}]] | |Optical=[ alpha ]_D +26.4°(C 0.86, CHCl_3 )[[Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433|{{RelationTable/GetFirstAuthor|Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433}}]] | ||
|Solubility=20-Acetoxyclavulones are soluble in MeOH, EtOH, CHCl_3 , or hexane. | |Solubility=20-Acetoxyclavulones are soluble in MeOH, EtOH, CHCl_3 , or hexane. | ||
Latest revision as of 06:02, 21 October 2010
| LipidBank Top (トップ) |
Fatty acid (脂肪酸) |
Glycerolipid (グリセロ脂質) |
Sphingolipid (スフィンゴ脂質) |
Journals (雑誌一覧) |
How to edit (ページの書き方) |
| IDs and Links | |
|---|---|
| LipidBank | XPR8007 |
| LipidMaps | LMFA03120007 |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20406CV11 |
| 20-Acetoxyclavulone III | |
|---|---|
| |
| Structural Information | |
| Methyl-4R- (trans-5,cis-7) -4-acetoxy-7- [ 2S-acetoxy-2- (cis-7-acetoxy-2-octenyl) -5-oxo-3-cyclopentenylidene ] -5-heptenoic acid | |
| |
| Formula | C27H36O9 |
| Exact Mass | 504.23593274999996 |
| Average Mass | 504.56934 |
| SMILES | C(C[C@](OC(C)=O)(C=1)C(=CC=C[C@@H](CCC(=O)OC)OC(C)=O)C(=O)C1)=CCCCCCOC(C)=O |
| Physicochemical Information | |
| [ α ]D +26.4°(C 0.86, CHCl3) IguchiKet al. | |
| 20-Acetoxyclavulones are soluble in MeOH, EtOH, CHCl3, or hexane. | |
| 20-Acetoxyclavulones were isolated from Japanese soft coral, Stolonifer Clavularia viridis Quoy and Gaimard. Iguchi_K et al. | |
| 20-Acetoxyclavulones showed a significant anti-inflammatory effect at 30 mu g/ml by the fertile egg test. Kikuchi_H et al. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | λ max(EtOH) 230 nm( ε 12400),295 nm( ε 12100) IguchiKet al. |
| IR Spectra | ν max(film)1730,1695,1640,and 1235cm-1 IguchiKet al. |
| NMR Spectra | 1H-NMR(270MHz,CDCl3) δ ppm2.02(3H,s),2.05(3H,s),2.10(3H,s),2.39(2H,t,J=7.6Hz),2.62(1H,dd,J=7.6,14.2Hz),2.87(1H,dd,J=7.3,14.2Hz),3.68(3H,s),4.04(2H,t,J=6.9Hz),5.21(1H,m),5.44(1H,q,J=5.9Hz),5.51(1H,m),6.03(1H,dd,J=5.9,15.5Hz),6.36(1H,d,J=6.3Hz),6.52(1H,d,J=11.2Hz),7.50(1H,d,J=6.3Hz),7.47(1H,dd,J=11.2,15.5Hz). IguchiKet al.13C-NMR(67.8MHz,CDCl3) δ ppm21.0(q,2C),21.7(q),25.6(t),27.3(t),28.5(t),29.0(t),29.2(t),29.8(t),35.6(t),51.7(q),64.4(t),72.5(d),85.2(s),121.8(d),126.4(d),133.5(d),134.2(d),135.6(s),136.9(d),141.1(d),156.0(d),169.9(s),170.1(s),171.2(s),173.1(s),194.0(s). IguchiKet al. |
| Other Spectra | CD λ ext(EtOH)( Δ ε )nm 243(+2.5),291(-0.6). KikuchiHet al. IguchiKet al. |
| Chromatograms | |
| Reported Metabolites, References | |||||||||||||||
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