| Weight | 226.232 g/mol |
|---|---|
| Formula | C10H14N2O4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 6 |
porphobilinogen (487-90-1)
Score:
#1465 in Biochemistry
,
#3459 in Biology
,
#4319 in Chemistry
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- THE OCCURRENCE AND DETERMINATION OF -AMINOLEVULINIC ACID AND PORPHOBILINOGEN IN URINE (Journal of Biological Chemistry, 1956)
- Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Two tissue-specific factors bind the erythroid promoter of the human porphobilinogen deaminase gene. (Nucleic Acids Research, 1989)
- Intermittent Acute Porphyria Demonstration of a Genetic Defect in Porphobilinogen Metabolism (The New England Journal of Medicine, 1972)
- Tissue-specific expression of porphobilinogen deaminase: two isoenzymes from a single gene (FEBS Journal, 1987)
- Structure of porphobilinogen deaminase reveals a flexible multidomain polymerase with a single catalytic site. (Nature, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=C(N1)CN)CC(=O)O)CCC(=O)O
-
InChIKeyQSHWIQZFGQKFMA-UHFFFAOYSA-N
- Pubchem - porphobilinogen
- Wikipedia - porphobilinogen
Porphobilinogen (PBG) is a pyrrole-containing intermediate in the biosynthesis of porphyrins (such a hemes). It is generated from aminolevulinate (ALA) by the enzyme ALA dehydratase. PBG is then converted into hydroxymethyl bilane by the enzyme porphobilinogen deaminase, also known as hydroxymethylbilane synthase.
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Synthesis
Reactant
+
3-Chloropropanoic acid
(Friedel-Crafts alkylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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porphobilinogen
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