Prostaglandin H2

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Prostaglandin H2
Prostaglandin H2 skeletal.svg
Identifiers
42935-17-1 N
ChEBI CHEBI:15554 YesY
ChemSpider 392800 YesY
4483
Jmol 3D model Interactive image
MeSH Prostaglandin+H2
PubChem 445049
  • InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18-14-19(17)25-24-18)10-7-4-5-8-11-20(22)23/h4,7,12-13,15-19,21H,2-3,5-6,8-11,14H2,1H3,(H,22,23)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1 YesY
    Key: YIBNHAJFJUQSRA-YNNPMVKQSA-N YesY
  • InChI=1/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18-14-19(17)25-24-18)10-7-4-5-8-11-20(22)23/h4,7,12-13,15-19,21H,2-3,5-6,8-11,14H2,1H3,(H,22,23)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1
    Key: YIBNHAJFJUQSRA-YNNPMVKQBN
  • O=C(O)CCC/C=C\C[C@H]2[C@H]1OO[C@H](C1)[C@@H]2/C=C/[C@@H](O)CCCCC
Properties
C20H32O5
Molar mass 352.465 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Prostaglandin H2 is a type of prostaglandin and a precursor for many other biologically significant molecules. It is synthesized from arachidonic acid in a reaction catalyzed by a cyclooxygenase enzyme.[1]

Eicosanoid synthesis - prostaglandin H2 near center

It is acted upon by:

It rearranges non-enzymatically to:

Figure 1: Synthetic pathways from PGH2 (the parent compound) to prostaglandins, prostacyclin and thromboxanes

References

  1. Lua error in package.lua at line 80: module 'strict' not found.


<templatestyles src="Asbox/styles.css"></templatestyles>