Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10O4 |
| Molecular Weight | 182.1733 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CCC1=CC=CC(O)=C1O
InChI
InChIKey=QZDSXQJWBGMRLU-UHFFFAOYSA-N
InChI=1S/C9H10O4/c10-7-3-1-2-6(9(7)13)4-5-8(11)12/h1-3,10,13H,4-5H2,(H,11,12)
| Molecular Formula | C9H10O4 |
| Molecular Weight | 182.1733 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function. | 2010-09-21 |
|
| The complete multipartite genome sequence of Cupriavidus necator JMP134, a versatile pollutant degrader. | 2010-03-22 |
|
| Biomimetic formation of 2-tropolones by dioxygenase-catalysed ring expansion of substituted 2,4-cyclohexadienones. | 2010-01-25 |
|
| Degradation of chloroaromatics by Pseudomonas putida GJ31: assembled route for chlorobenzene degradation encoded by clusters on plasmid pKW1 and the chromosome. | 2009-12 |
|
| 3-Hydroxyphenylpropionate and phenylpropionate are synergistic activators of the MhpR transcriptional regulator from Escherichia coli. | 2009-08-07 |
|
| Metabolic reconstruction of aromatic compounds degradation from the genome of the amazing pollutant-degrading bacterium Cupriavidus necator JMP134. | 2008-08 |
|
| Exploiting the pathway structure of metabolism to reveal high-order epistasis. | 2008-04-30 |
|
| Directed evolution of a non-heme-iron-dependent extradiol catechol dioxygenase: identification of mutants with intradiol oxidative cleavage activity. | 2006-12 |
|
| Xenobiotic reductase A in the degradation of quinoline by Pseudomonas putida 86: physiological function, structure and mechanism of 8-hydroxycoumarin reduction. | 2006-08-04 |
|
| 3-phenylpropionate catabolism and the Escherichia coli oxidative stress response. | 2005-04 |
|
| Lactone synthesis activity in a site-directed mutant of an extradiol catechol dioxygenase enzyme. | 2005-02-07 |
|
| Acid-base catalysis in the extradiol catechol dioxygenase reaction mechanism: site-directed mutagenesis of His-115 and His-179 in Escherichia coli 2,3-dihydroxyphenylpropionate 1,2-dioxygenase (MhpB). | 2004-10-26 |
|
| Extradiol oxidative cleavage of catechols by ferrous and ferric complexes of 1,4,7-triazacyclononane: insight into the mechanism of the extradiol catechol dioxygenases. | 2001-05-30 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:16:55 GMT 2025
by
admin
on
Mon Mar 31 19:16:55 GMT 2025
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| Record UNII |
PUH669YNEK
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| Record Status |
Validated (UNII)
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| Record Version |
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18136
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DTXSID70958342
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3714-73-6
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