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A comprehensive classification system for lipids

Fahy, Eoin, Subramaniam, Shankar, Brown, H. Alex, Glass, Christopher K., Merrill, Alfred H., Murphy, Robert C., Raetz, Christian R.H., Russell, David W., Seyama, Yousuke, Shaw, Walter, Shimizu, Takao, Spener, Friedrich, van Meer, Gerrit, VanNieuwenhze, Michael S., White, Stephen H., Witztum, Joseph L., Dennis, Edward A.·2005·Journal of Lipid Research
DOI 10.1194/jlr.e400004-jlr200
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Figures

Fig. 1 Representative structures for each lipid category.
Fig. 1 Representative structures for each lipid category.CC-BY · From the PDF
Image 2
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Image 3
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Image 4
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Image 5
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Image 9
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Image 11
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Fig. 2 Representative structures for fatty acyls.
Fig. 2 Representative structures for fatty acyls.CC-BY · From the PDF
Image 13
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Image 14
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Image 15
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(t) Epoxyeicosatrienoic acids: 14R,15S-epoxy-5Z,8Z,11Z-eicosatrienoic acid
(t) Epoxyeicosatrienoic acids: 14R,15S-epoxy-5Z,8Z,11Z-eicosatrienoic acidCC-BY · From the PDF
(v) Levuglandins: LGE2; 10,11-seco-9,11-dioxo-15S-hydroxy-5Z,13E-prostadienoic acid
(v) Levuglandins: LGE2; 10,11-seco-9,11-dioxo-15S-hydroxy-5Z,13E-prostadienoic acidCC-BY · From the PDF
Image 18
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Image 19
CC-BY · From the PDF
(u) Hepoxilins: Hepoxilin A3; 8R-hydroxy-11R,12S-epoxy-5Z,9E,14Z-eicosatrienoic acid
(u) Hepoxilins: Hepoxilin A3; 8R-hydroxy-11R,12S-epoxy-5Z,9E,14Z-eicosatrienoic acidCC-BY · From the PDF
(w) Isoprostanes: 9S,11S,15S-trihydroxy-5Z,13E-prostadienoic acid-cyclo{8S,12R]
(w) Isoprostanes: 9S,11S,15S-trihydroxy-5Z,13E-prostadienoic acid-cyclo{8S,12R]CC-BY · From the PDF
Fig. 2 Continued.
Fig. 2 Continued.CC-BY · From the PDF
Image 23
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Image 24
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Fig. 4 Representative structures for glycerophospholipids.
Fig. 4 Representative structures for glycerophospholipids.CC-BY · From the PDF
Fig. 4 Continued.
Fig. 4 Continued.CC-BY · From the PDF
Fig. 5 Representative structures for sphingolipids.
Fig. 5 Representative structures for sphingolipids.CC-BY · From the PDF
Image 28
CC-BY · From the PDF
Fig. 6 Representative structures for sterol lipids.
Fig. 6 Representative structures for sterol lipids.CC-BY · From the PDF
Image 30
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Image 31
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Image 32
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(i) C26 bile acids, alcohols, and derivatives: 3α,7α,12α-trihydroxy-27-nor-5β-cholestan-24-one (i) C26 bile acids, alcohols, and derivatives: 3α,7α,12α-trihydroxy-27-nor-5β-cholestan-24-one
(i) C26 bile acids, alcohols, and derivatives: 3α,7α,12α-trihydroxy-27-nor-5β-cholestan-24-one (i) C26 bile acids, alcohols, and derivatives: 3α,7α,12α-trihydroxy-27-nor-5β-cholestan-24-oneCC-BY · From the PDF
(k) Steroid conjugates: Glucuronides: 5α-androstane-3α-ol-17-one glucuronide
(k) Steroid conjugates: Glucuronides: 5α-androstane-3α-ol-17-one glucuronideCC-BY · From the PDF
(n) Steroid conjugates: Sulfates: 5α-androstane-3α-ol-17-one sulfate
(n) Steroid conjugates: Sulfates: 5α-androstane-3α-ol-17-one sulfateCC-BY · From the PDF
Image 36
CC-BY · From the PDF
(o) Hopanoids: diploptene; hop-22(29)-ene
(o) Hopanoids: diploptene; hop-22(29)-eneCC-BY · From the PDF
Fig. 7 Representative structures for prenol lipids.
Fig. 7 Representative structures for prenol lipids.CC-BY · From the PDF
Fig. 7 Continued.
Fig. 7 Continued.CC-BY · From the PDF
Image 40
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Image 41
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Image 42
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Image 43
CC-BY · From the PDF
Image 44
CC-BY · From the PDF
Image 45
CC-BY · From the PDF
Image 46
CC-BY · From the PDF

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Citations

Cites

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Metadata

Authors
Fahy, E., Subramaniam, S., Brown, H. A., Glass, C. K., Merrill, A. H., Murphy, R. C., Raetz, C. R. H., Russell, D. W., Seyama, Y., Shaw, W., Shimizu, T., Spener, F., van Meer, G., VanNieuwenhze, M. S., White, S. H., Witztum, J. L., & Dennis, E. A.
Venue
Journal of Lipid Research
Publisher
Elsevier BV
Published
2005-05
Volume
46
Issue
5
Pages
839-861
ISSN
0022-2275
DOI
10.1194/jlr.e400004-jlr200
Cited by
1,699
References
1
Language
en
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