Leukotriene A4

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Leukotriene A4
Names
IUPAC name
4-{(2S,3S)-3-[(1E,3E,5Z,8Z)-1,3,5,8-Tetradecatetraen-1-yl]-2-oxiranyl}butanoic acid
Systematic IUPAC name
4-{(2S,3S)-3-[(1E,3E,5Z,8Z)-1,3,5,8-Tetradecatetraen-1-yl]-2-oxiranyl}butanoic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
MeSH D017572
  • InChI=1S/C20H30O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-19(23-18)16-14-17-20(21)22/h6-7,9-13,15,18-19H,2-5,8,14,16-17H2,1H3,(H,21,22)/b7-6-,10-9-,12-11+,15-13+/t18-,19-/m0/s1 ☒N
    Key: UFPQIRYSPUYQHK-WAQVJNLQSA-N ☒N
  • InChI=1/C20H30O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-19(23-18)16-14-17-20(21)22/h6-7,9-13,15,18-19H,2-5,8,14,16-17H2,1H3,(H,21,22)/b7-6-,10-9-,12-11+,15-13+/t18-,19-/m0/s1
    Key: UFPQIRYSPUYQHK-WAQVJNLQBZ
  • CCCCC/C=C\C/C=C\C=C\C=C\[C@H]1[C@@H](O1)CCCC(=O)O
Properties
C20H30O3
Molar mass 318.450
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Leukotriene A4 is a leukotriene. Leukotriene A4 hydrolase converts it to leukotriene B4. Leukotriene C4 synthase converts it to leukotriene C4.

Eicosanoid synthesis. (Leukotrienes at right.)

References