Glutamate-1-semialdehyde

Source: Wikipedia, the free encyclopedia.
Glutamate-1-semialdehyde
Names
Preferred IUPAC name
(4S)-4-Amino-5-oxopentanoic acid
Identifiers
3D model (
JSmol
)
ChemSpider
MeSH glutamate-1-semialdehyde
UNII
  • InChI=1S/C5H9NO3/c6-4(3-7)1-2-5(8)9/h3-4H,1-2,6H2,(H,8,9)/t4-/m0/s1 ☒N
    Key: MPUUQNGXJSEWTF-BYPYZUCNSA-N ☒N
  • InChI=1/C5H9NO3/c6-4(3-7)1-2-5(8)9/h3-4H,1-2,6H2,(H,8,9)/t4-/m0/s1
    Key: MPUUQNGXJSEWTF-BYPYZUCNBY
  • C(CC(=O)O)[C@@H](C=O)N
Properties
C5H9NO3
Molar mass 131.131 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Glutamate-1-semialdehyde is a molecule formed from by the reduction of

porphyrins, including heme and chlorophyll.[1][2]

See also

References

  1. PMID 16667613
    .
  2. ISBN 0-8247-4268-0
    .


Stub icon

This biochemistry article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Glutamate-1-semialdehyde&oldid=1175939991"