Isocoproporphyrin

Isocoproporphyrin
Identifiers
3D model (JSmol)
ChemSpider
MeSH C005524
  • InChI=1S/C36H38N4O8/c1-5-20-17(2)25-13-26-18(3)21(6-9-33(41)42)29(38-26)15-31-23(8-11-35(45)46)24(12-36(47)48)32(40-31)16-30-22(7-10-34(43)44)19(4)27(39-30)14-28(20)37-25/h13-16,37,40H,5-12H2,1-4H3,(H,41,42)(H,43,44)(H,45,46)(H,47,48)/b25-13-,26-13-,27-14-,28-14-,29-15-,30-16-,31-15-,32-16- X markN
    Key: UHKZSWAPQUEURH-TXUIXYGZSA-N X markN
  • CCC1=C(C2=CC3=NC(=CC4=C(C(=C(N4)C=C5C(=C(C(=N5)C=C1N2)C)CCC(=O)O)CC(=O)O)CCC(=O)O)C(=C3C)CCC(=O)O)C
Properties
C36H38N4O8
Molar mass 654.70892
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)
Infobox references

Isocoproporphyrin is a tetrapyrrole and prophyrin compound. It has been identified among porphyrins excreted by patients with porphyria cutanea tarda.[1][2]

See also

References

  1. ↑ Stoll, M. S.; Elder, G. H.; Games, D. E.; O'Hanlon, P.; Millington, D. S.; Jackson, A. H. (1 February 1973). "Isocoproporphyrin: nuclear-magnetic-resonance-and mass-spectral methods for the determination of porphyrin structure". The Biochemical Journal. 131 (2): 429–432. doi:10.1042/bj1310429. ISSN 0264-6021. PMC 1177486. PMID 4737320.
  2. ↑ Jackson, Anthony H.; Lash, Timothy D.; Ryder, David J. (1987). "Synthetic and biosynthetic studies of porphyrins. Part 9. Synthesis of isocoproporphyrin, dehydroisocoproporphyrin, and de-ethylisocoproporphyrin". Journal of the Chemical Society, Perkin Transactions 1: 287. doi:10.1039/p19870000287. ISSN 0300-922X.
This page is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.