Home Other Building Blocks 2,3-dihydroxyphenylpropionic acid

2,3-dihydroxyphenylpropionic acid

CAS No.:
3714-73-6
Catalog Number:
AG00C971
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00C971
Chemical Name:
2,3-dihydroxyphenylpropionic acid
CAS Number:
3714-73-6
MDL Number:
MFCD12923244
IUPAC Name:
3-(2,3-dihydroxyphenyl)propanoic acid
InChI:
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)
InChI Key:
QZDSXQJWBGMRLU-UHFFFAOYSA-N
UNII:
PUH669YNEK
Properties
Complexity:
181  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
182.058g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
182.175g/mol
Monoisotopic Mass:
182.058g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1  
Literature
Title Journal
Biomimetic formation of 2-tropolones by dioxygenase-catalysed ring expansion of substituted 2,4-cyclohexadienones. Chembiochem : a European journal of chemical biology 20100125
The complete multipartite genome sequence of Cupriavidus necator JMP134, a versatile pollutant degrader. PloS one 20100101
Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function. PloS one 20100101
Degradation of chloroaromatics by Pseudomonas putida GJ31: assembled route for chlorobenzene degradation encoded by clusters on plasmid pKW1 and the chromosome. Microbiology (Reading, England) 20091201
3-Hydroxyphenylpropionate and phenylpropionate are synergistic activators of the MhpR transcriptional regulator from Escherichia coli. The Journal of biological chemistry 20090807
Metabolic reconstruction of aromatic compounds degradation from the genome of the amazing pollutant-degrading bacterium Cupriavidus necator JMP134. FEMS microbiology reviews 20080801
Exploiting the pathway structure of metabolism to reveal high-order epistasis. BMC systems biology 20080101
Directed evolution of a non-heme-iron-dependent extradiol catechol dioxygenase: identification of mutants with intradiol oxidative cleavage activity. Chembiochem : a European journal of chemical biology 20061201
Xenobiotic reductase A in the degradation of quinoline by Pseudomonas putida 86: physiological function, structure and mechanism of 8-hydroxycoumarin reduction. Journal of molecular biology 20060804
3-phenylpropionate catabolism and the Escherichia coli oxidative stress response. Research in microbiology 20050401
Lactone synthesis activity in a site-directed mutant of an extradiol catechol dioxygenase enzyme. Chemical communications (Cambridge, England) 20050207
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). Biochemistry 20041026
Extradiol oxidative cleavage of catechols by ferrous and ferric complexes of 1,4,7-triazacyclononane: insight into the mechanism of the extradiol catechol dioxygenases. Journal of the American Chemical Society 20010530
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