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2624-63-7 | 21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 5,10,15,20,22,24-hexahydro-3,8,13,17-tetramethyl-
CAS No: 2624-63-7 Catalog No: AG002SEZ MDL No:
Product Description
Catalog Number:
AG002SEZ
Chemical Name:
21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 5,10,15,20,22,24-hexahydro-3,8,13,17-tetramethyl-
CAS Number:
2624-63-7
Molecular Formula:
C36H44N4O8
Molecular Weight:
660.7566
IUPAC Name:
3-[8,12,17-tris(2-carboxyethyl)-3,7,13,18-tetramethyl-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid
InChI:
InChI=1S/C36H44N4O8/c1-17-21(5-9-33(41)42)29-14-27-19(3)22(6-10-34(43)44)30(39-27)15-28-20(4)24(8-12-36(47)48)32(40-28)16-31-23(7-11-35(45)46)18(2)26(38-31)13-25(17)37-29/h37-40H,5-16H2,1-4H3,(H,41,42)(H,43,44)(H,45,46)(H,47,48)
InChI Key:
NIUVHXTXUXOFEB-UHFFFAOYSA-N
SMILES:
OC(=O)CCc1c2Cc3[nH]c(c(c3C)CCC(=O)O)Cc3[nH]c(Cc4[nH]c(Cc(c1C)[nH]2)c(CCC(=O)O)c4C)c(c3CCC(=O)O)C
Properties
Complexity:
1170
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
660.316g/mol
Formal Charge:
0
Heavy Atom Count:
48
Hydrogen Bond Acceptor Count:
8
Hydrogen Bond Donor Count:
8
Isotope Atom Count:
0
Molecular Weight:
660.768g/mol
Monoisotopic Mass:
660.316g/mol
Rotatable Bond Count:
12
Topological Polar Surface Area:
212A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6
Literature
| Title | Journal |
|---|---|
| Cerium relieves the inhibition of chlorophyll biosynthesis of maize caused by magnesium deficiency. | Biological trace element research 20111001 |
| Normal and abnormal heme biosynthesis. Part 7. Synthesis and metabolism of coproporphyrinogen-III analogues with acetate or butyrate side chains on rings C and D. Development of a modified model for the active site of coproporphyrinogen oxidase. | Bioorganic & medicinal chemistry 20110215 |
| The oxygen-independent coproporphyrinogen III oxidase HemN utilizes harderoporphyrinogen as a reaction intermediate during conversion of coproporphyrinogen III to protoporphyrinogen IX. | Biological chemistry 20100101 |
| Cloning, expression, and biochemical properties of CPOX4, a genetic variant of coproporphyrinogen oxidase that affects susceptibility to mercury toxicity in humans. | Toxicological sciences : an official journal of the Society of Toxicology 20090601 |
| Identification of tetrapyrrole compounds excreted by Rhodobacter sphaeroides and sources of the methyl hydrogens of bacteriochlorophyll a biosynthesized by R. sphaeroides, based on 13C-NMR spectral analysis of coproporphyrin III tetramethyl ester. | Chemical & pharmaceutical bulletin 20070701 |
| Investigation of the catalytic and structural roles of conserved histidines of human coproporphyrinogen oxidase using site-directed mutagenesis. | Medical science monitor : international medical journal of experimental and clinical research 20070101 |
| Identification of a mammalian mitochondrial porphyrin transporter. | Nature 20061005 |
| Density-functional study of mechanisms for the cofactor-free decarboxylation performed by uroporphyrinogen III decarboxylase. | The journal of physical chemistry. B 20050929 |
| Crystal structure of the oxygen-dependant coproporphyrinogen oxidase (Hem13p) of Saccharomyces cerevisiae. | The Journal of biological chemistry 20040910 |
| Unprecedented overmetabolism of a porphyrinogen substrate by coproporphyrinogen oxidase. | Bioorganic & medicinal chemistry letters 20020408 |
| Metabolism of analogues of coproporphyrinogen-III with modified side chains: implications for binding at the active site of coproporphyrinogen oxidase. | Bioorganic & medicinal chemistry letters 20020211 |
| Kinetic studies of novel di- and tri-propionate substrates for the chicken red blood cell enzyme coproporphyrinogen oxidase. | Journal of biochemistry 20020201 |
| Normal and abnormal heme biosynthesis. 3.(1)Synthesis and metabolism of tripropionate analogues of coproporphyrinogen-III: novel probes for the active site of coproporphyrinogen oxidase. | The Journal of organic chemistry 20010601 |
| The heme synthesis and degradation pathways: role in oxidant sensitivity. Heme oxygenase has both pro- and antioxidant properties. | Free radical biology & medicine 20000115 |
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