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27655-56-7

27655-56-7 | 1,3-Cyclohexadiene-1-carboxylic acid, 3,4,5-trihydroxy-, (R)- (9CI)

CAS No: 27655-56-7 Catalog No: AG002UC9 MDL No:

Product Description

Catalog Number:
AG002UC9
Chemical Name:
1,3-Cyclohexadiene-1-carboxylic acid, 3,4,5-trihydroxy-, (R)- (9CI)
CAS Number:
27655-56-7
Molecular Formula:
C7H8O5
Molecular Weight:
172.1354
IUPAC Name:
(5R)-3,4,5-trihydroxycyclohexa-1,3-diene-1-carboxylic acid
InChI:
InChI=1S/C7H8O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1,5,8-10H,2H2,(H,11,12)/t5-/m1/s1
InChI Key:
HFMGXSXAGHUXTI-RXMQYKEDSA-N
SMILES:
OC(=O)C1=CC(=C([C@@H](C1)O)O)O

Properties

Complexity:
276  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
172.037g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
172.136g/mol
Monoisotopic Mass:
172.037g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
98A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1  

Literature

Title Journal
Mechanism of gallic acid biosynthesis in bacteria (Escherichia coli) and walnut (Juglans regia). Plant molecular biology 20110401
Insights into the mechanism of type I dehydroquinate dehydratases from structures of reaction intermediates. The Journal of biological chemistry 20110204
Conversion of quinate to 3-dehydroshikimate by Ca-alginate-immobilized membrane of Gluconobacter oxydans IFO 3244 and subsequent asymmetric reduction of 3-dehydroshikimate to shikimate by immobilized cytoplasmic NADP-shikimate dehydrogenase. Bioscience, biotechnology, and biochemistry 20100101
Structural studies of shikimate dehydrogenase from Bacillus anthracis complexed with cofactor NADP. Journal of molecular modeling 20090201
The missing link in petrobactin biosynthesis: asbF encodes a (-)-3-dehydroshikimate dehydratase. Biochemistry 20081125
A novel 3-dehydroquinate dehydratase catalyzing extracellular formation of 3-dehydroshikimate by oxidative fermentation of Gluconobacter oxydans IFO 3244. Bioscience, biotechnology, and biochemistry 20080601
Directed evolution of 2-keto-3-deoxy-6-phosphogalactonate aldolase to replace 3-deoxy-D-arabino-heptulosonic acid 7-phosphate synthase. Journal of the American Chemical Society 20070516
Enzymatic preparation of metabolic intermediates, 3-dehydroquinate and 3-dehydroshikimate, in the shikimate pathway. Bioscience, biotechnology, and biochemistry 20061201
Benzene-free synthesis of catechol: interfacing microbial and chemical catalysis. Journal of the American Chemical Society 20050309
A thermostable shikimate 5-dehydrogenase from the archaeon Archaeoglobus fulgidus. FEMS microbiology letters 20040901
Conversion of (-)-3-dehydroshikimic acid into derivatives of the (+)-enantiomer. The Journal of organic chemistry 20030822
The 2.3-A crystal structure of the shikimate 5-dehydrogenase orthologue YdiB from Escherichia coli suggests a novel catalytic environment for an NAD-dependent dehydrogenase. The Journal of biological chemistry 20030523
Antioxidant activity of 3-dehydroshikimic acid in liposomes, emulsions, and bulk oil. Journal of agricultural and food chemistry 20030423
Altered glucose transport and shikimate pathway product yields in E. coli. Biotechnology progress 20030101
Pulse experiments as a prerequisite for the quantification of in vivo enzyme kinetics in aromatic amino acid pathway of Escherichia coli. Biotechnology progress 20020101
Modulation of phosphoenolpyruvate synthase expression increases shikimate pathway product yields in E. coli. Biotechnology progress 20020101
Hydroaromatic equilibration during biosynthesis of shikimic acid. Journal of the American Chemical Society 20011024

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