3-[18-(2-carboxylatoethyl)-7-ethenyl-12-[(1S,4E,8E)-1-hydroxy-5,9,13-trimethyltetradeca-4,8,12-trienyl]-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl]propanoate;iron(2+) (BioCAD00000729030)

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Metabolite Card

Formula: C49H56FeN4O5-2 (836.36)
SMILES: CC1=C(C2=CC3=NC(=CC4=C(C(=C([N-]4)C=C5C(=C(C(=N5)C=C1[N-]2)C=C)C)[C@H](CC/C=C(\C)/CC/C=C(\C)/CCC=C(C)C)O)C)C(=C3CCC(=O)[O-])C)CCC(=O)[O-].[Fe+2]

Synonyms [en]

heme O; 3-[18-(2-carboxylatoethyl)-7-ethenyl-12-[(1S,4E,8E)-1-hydroxy-5,9,13-trimethyltetradeca-4,8,12-trienyl]-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl]propanoate;iron(2+)

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

3-[18-(2-carboxylatoethyl)-7-ethenyl-12-[(1S,4E,8E)-1-hydroxy-5,9,13-trimethyltetradeca-4,8,12-trienyl]-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl]propanoate;iron(2+). 数据之源，洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000729030). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Heme O is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).

Entity Information

DBLinks

  • CAS Registry Number:
  • PubChem CID: 49792067
  • ChEBI:
  • HMDB:
  • LipidMaps:
  • KEGG:
  • BioCyc:
  • NCBI MeSH: heme O
  • Wikipedia: Heme_O
Other DBLinks
  • PubChem: 49792067
  • NCBI MeSH: heme O
  • Wikipedia: Heme_O

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
PathBank:SMP0000953 Porphyrin Metabolism
PathBank:SMP0120492 Hereditary Coproporphyria (HCP)
PathBank:SMP0120544 Porphyria Variegata (PV)
PathBank:SMP0000024 Porphyrin Metabolism
PathBank:SMP0120689 Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
PathBank:SMP0120447 Acute Intermittent Porphyria
PathBank:SMP0000345 Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
PathBank:SMP0087397 Porphyrin Metabolism
PathBank:SMP0063655 Porphyrin Metabolism
PathBank:SMP0120668 Acute Intermittent Porphyria
PathBank:SMP0120712 Hereditary Coproporphyria (HCP)
PathBank:SMP0120764 Porphyria Variegata (PV)
PathBank:SMP0120469 Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
PathBank:SMP0121321 Porphyrin Metabolism
PathBank:SMP0000344 Acute Intermittent Porphyria
PathBank:SMP0002363 Porphyrin Metabolism
PathBank:SMP0087336 Porphyrin Metabolism
PathBank:SMP0000346 Porphyria Variegata (PV)
PathBank:SMP0000342 Hereditary Coproporphyria (HCP)
PathBank:SMP0087243 Porphyrin Metabolism
View All Pathways