Record Information
Version 1.0
Update Date 1/22/2018 12:54:54 PM
Metabolite IDPAMDB120520
Identification
Name: 131-oxo-magnesium-protoporphyrin IX 13-monomethyl ester
Description:The conjugate base of magnesium 131-oxoprotoporphyrin 13-monomethyl ester, formed by deprotonation of the carboxyethyl group at C-17. It is the principal species at pH 7.3.
Structure
Thumb
Synonyms:
  • magnesium 131-oxoprotoporphyrinate 13-monomethyl ester
  • Mg-131-oxoprotoporphyrin 13-monomethyl ester
Chemical Formula: C35H31N4O5MG
Average Molecular Weight: 611.959
Monoisotopic Molecular Weight: 612.2223
InChI Key: IOQIILLGNAOXJE-JXBSUKTBSA-K
InChI:InChI=1S/C35H34N4O5.Mg/c1-8-21-17(3)24-12-25-19(5)23(10-11-33(41)42)30(38-25)15-31-35(32(40)16-34(43)44-7)20(6)27(39-31)14-29-22(9-2)18(4)26(37-29)13-28(21)36-24;/h8-9,12-15H,1-2,10-11,16H2,3-7H3,(H3,36,37,38,39,40,41,42);/q;+2/p-3/b24-12-,25-12-,26-13-,27-14-,28-13-,29-14-,30-15-,31-15-;
CAS number: Not Available
IUPAC Name:{3-[18-(3-methoxy-3-oxopropanoyl)-3,7,12,17-tetramethyl-8,13-divinylporphyrin-2-yl-κ4N21,N22,N23,N24]propanoato(3−)}magnesate(1−)
Traditional IUPAC Name: Not Available
SMILES:C=CC2(C(C)=C6(C=C1(C(C)=C(CCC(=O)[O-])C(=N1)C=C4(N5([Mg]N(C=2C=C3(C(C)=C(C=C)C(=N3)C=C(C(C)=C(C(=O)CC(=O)OC)4)5))6)))))
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as metalloporphyrins. These are polycyclic compounds containing a porphyrin moiety and a metal atom.
Kingdom Organic compounds
Super ClassOrganoheterocyclic compounds
Class Tetrapyrroles and derivatives
Sub ClassMetallotetrapyrroles
Direct Parent Metalloporphyrins
Alternative Parents
Substituents
  • Metalloporphyrin
  • Porphyrin
  • Aryl alkyl ketone
  • Aryl ketone
  • Beta-keto acid
  • Fatty acid ester
  • Dicarboxylic acid or derivatives
  • Keto acid
  • Fatty acyl
  • Substituted pyrrole
  • 1,3-dicarbonyl compound
  • Heteroaromatic compound
  • Pyrrole
  • Methyl ester
  • Ketone
  • Carboxylic acid salt
  • Carboxylic acid ester
  • Azacycle
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic nitrogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Organic salt
  • Carbonyl group
  • Organic cation
  • Aromatic heteropolycyclic compound
Molecular Framework Aromatic heteropolycyclic compounds
External Descriptors Not Available
Physical Properties
State: Not Available
Charge:-1
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
3D Conformer of Parent6327075 PubChem
Molecular Weight611.961 g/molPubChem
Hydrogen Bond Donor Count0 PubChem
Hydrogen Bond Acceptor Count9 PubChem
Rotatable Bond Count8 PubChem
Exact Mass611.214 g/molPubChem
Monoisotopic Mass611.214 g/molPubChem
Topological Polar Surface Area110 A^2PubChem
Heavy Atom Count45 PubChem
Formal Charge-1 PubChem
Complexity1670 PubChem
Isotope Atom Count0 PubChem
Defined Atom Stereocenter Count0 PubChem
Undefined Atom Stereocenter Count0 PubChem
Defined Bond Stereocenter Count0 PubChem
Undefined Bond Stereocenter Count0 PubChem
Covalently-Bonded Unit Count2 PubChem
Biological Properties
Cellular Locations: Not Available
Reactions:
Pathways:
  • chlorophyllide a biosynthesis III (aerobic, light independent)PWY-7159
  • chlorophyllide a biosynthesis I (aerobic, light-dependent)CHLOROPHYLL-SYN
  • chlorophyllide a biosynthesis II (anaerobic)PWY-5531
    Spectra
    Spectra: Not Available
    References
    References:
    Synthesis Reference: Not Available
    Material Safety Data Sheet (MSDS) Not Available
    External Links:
    ResourceLink
    CHEBI60490
    PUBCHEM44229101
    LIGAND-CPDC11830