Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:33:15 UTC |
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Update date | 2017-01-19 02:36:40 UTC |
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FoodComEx ID | PC000893 |
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FoodDB Record | FDB022986 |
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Chemical Information |
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Name | Mesoporphyrin IX |
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Description | Mesoporphyrins are porphyrins with four methyl, two ethyl, and two propionic acid side chains attached to the pyrrole rings. There are fifteen isomers of mesoporphyrin.
Mesoporphyrin has anti-inflammatory action. Mesoporphyrin inhibits interferon-gamma and interleukin-6 production, which is closely related to the suppression of prostaglandin E2 generation by interfering cyclooxygenase 1 and 2 enzyme activities suggesting that the inhibition of cytokine production is one of the anti-inflammatory mechanisms of mesoporphyrin. (PMID: 10446754) [HMDB] |
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CAS Number | 493-90-3 |
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Structure | |
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Synonyms | Synonym | Source |
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7,12-diethyl-3,8,13,17-tetramethyl-2,18-Porphinedipropionic acid | hmdb | 7,12-diethyl-3,8,13,17-tetramethyl-21H,23H-Porphine-2,18-dipropanoate | hmdb | 7,12-diethyl-3,8,13,17-tetramethyl-21H,23H-Porphine-2,18-dipropanoic acid | hmdb | Mesoporphyrin | hmdb | Mesoporphyrin IX | hmdb | MPIX | hmdb |
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Chemical Formula | C34H38N4O4 |
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IUPAC name | 3-[20-(2-carboxyethyl)-10,15-diethyl-5,9,14,19-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1,3(24),4,6,8,10,12,14,16,18(21),19-undecaen-4-yl]propanoic acid |
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InChI Identifier | InChI=1S/C34H38N4O4/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/h13-16,35-36H,7-12H2,1-6H3,(H,39,40)(H,41,42)/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16- |
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InChI Key | NCAJWYASAWUEBY-UJJXFSCMSA-N |
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Isomeric SMILES | CCC1=C(C)/C2=C/C3=C(CC)C(C)=C(N3)\C=C3/N=C(/C=C4\N=C(\C=C\1/N\2)C(C)=C4CCC(O)=O)C(CCC(O)=O)=C3C |
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Average Molecular Weight | 566.6899 |
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Monoisotopic Molecular Weight | 566.289305724 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as porphyrins. Porphyrins are compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure. |
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Kingdom | Organic compounds |
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Super Class | Organoheterocyclic compounds |
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Class | Tetrapyrroles and derivatives |
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Sub Class | Porphyrins |
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Direct Parent | Porphyrins |
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Alternative Parents | Not Available |
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Substituents | Not Available |
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Molecular Framework | Not Available |
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External Descriptors | Not Available |
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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | Not Available | |
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Experimental Water Solubility | Not Available | |
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Melting Point | Not Available | |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 5 mg |
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Delivery Time | Not Available |
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Storage Form | solid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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Not Available |