Record Information Version
1.0 Update Date
1/22/2018 11:54:54 AM
Metabolite ID PAMDB110426
Identification Name:
ferroheme b Description: Not Available
Structure
Synonyms:
protoheme IX
ferroprotoporphyrin IX
Chemical Formula:
C34 H30 N4 O4 Fe
Average Molecular Weight:
614.48 Monoisotopic Molecular
Weight:
616.1772976364 InChI Key:
KABFMIBPWCXCRK-RGGAHWMASA-J InChI:
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-4/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-; CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: C=CC1(C(C)=C7(C=C8(C(C)=C(CCC(=O)[O-])C6(=[N+]([Fe--]24(N(C=1C=C3(C(C)=C(C=C)C(=[N+]23)C=C5(C(C)=C(CCC(=O)[O-])C(N45)=C6)))7))8))))
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as metallotetrapyrroles. These are polycyclic compounds containing a tetrapyrrole skeleton combined with a metal atom.
Kingdom
Organic compounds Super Class Organoheterocyclic compounds
Class
Tetrapyrroles and derivatives Sub Class Metallotetrapyrroles
Direct Parent
Metallotetrapyrroles Alternative Parents
Substituents
Metallotetrapyrrole skeleton Dicarboxylic acid or derivatives Substituted pyrrole Pyrrole Heteroaromatic compound Carboxylic acid salt Carboxylic acid derivative Carboxylic acid Metalloheterocycle Organic transition metal salt Organic metal salt Azacycle Hydrocarbon derivative Organooxygen compound Organonitrogen compound Organic nitrogen compound Organic oxygen compound Carbonyl group Organic salt Organic oxide Organopnictogen compound Organic anion Aromatic heteropolycyclic compound Molecular Framework
Aromatic heteropolycyclic compounds External Descriptors
Not Available
Physical Properties State:
Not Available Charge: Not Available
Melting point:
Not Available Experimental Properties:
Not Available Predicted Properties
Biological Properties Cellular Locations:
Not Available Reactions:
Pathways:
heme biosynthesis II (anaerobic)HEMESYN2-PWY superpathway of heme biosynthesis from glycinePWY-5920 superpathay of heme biosynthesis from glutamatePWY-5918 superpathway of heme biosynthesis from uroporphyrinogen-IIIPWY0-1415 heme biosynthesis from uroporphyrinogen-III I (aerobic)HEME-BIOSYNTHESIS-II
Spectra Spectra:
Not Available
References References:
Not Available Synthesis Reference:
Not Available Material Safety Data Sheet (MSDS)
Not Available
Links External Links:
This project is supported by
the University of Maryland ,
School of Pharmacy ,
Mass Spectrometry Center , a Waters Center of Excellence. The center is an NIH-investigator funded research and core facility that supports a wide range of cutting-edge metabolomic studies. The Center is supported through a center grant from the University of Maryland and NIH grants to its members. The PAMDB project is affiliated with
The Metabolomics Innovation Centre (TMIC) a leading metabolomics research and service center funded through Genome Alberta, Genome British Columbia and Genome Canada.
