200,000+ products from a single source!

sales@angenechem.com

Home > Carboxes > 13052-73-8

13052-73-8

13052-73-8 | 1,2,4-Butanetricarboxylic acid, 2-hydroxy-, (2R)-

CAS No: 13052-73-8 Catalog No: AG000UK0 MDL No:

Product Description

Catalog Number:
AG000UK0
Chemical Name:
1,2,4-Butanetricarboxylic acid, 2-hydroxy-, (2R)-
CAS Number:
13052-73-8
Molecular Formula:
C7H10O7
Molecular Weight:
206.1501
IUPAC Name:
(2R)-2-hydroxybutane-1,2,4-tricarboxylic acid
InChI:
InChI=1S/C7H10O7/c8-4(9)1-2-7(14,6(12)13)3-5(10)11/h14H,1-3H2,(H,8,9)(H,10,11)(H,12,13)/t7-/m1/s1
InChI Key:
XKJVEVRQMLKSMO-SSDOTTSWSA-N
SMILES:
OC(=O)CC[C@](C(=O)O)(CC(=O)O)O

Properties

Complexity:
259  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
206.043g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
206.15g/mol
Monoisotopic Mass:
206.043g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
132A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.7  

Literature

Title Journal
Electronic dimensions of FeMo-co, the active site of nitrogenase, and its catalytic intermediates. Inorganic chemistry 20110103
Formation of a homocitrate-free iron-molybdenum cluster on NifEN: implications for the role of homocitrate in nitrogenase assembly. Dalton transactions (Cambridge, England : 2003) 20100328
Mechanism of substrate recognition and insight into feedback inhibition of homocitrate synthase from Thermus thermophilus. The Journal of biological chemistry 20100205
Transcriptional upregulation of four genes of the lysine biosynthetic pathway by homocitrate accumulation in Penicillium chrysogenum: homocitrate as a sensor of lysine-pathway distress. Microbiology (Reading, England) 20091201
Host plant genome overcomes the lack of a bacterial gene for symbiotic nitrogen fixation. Nature 20091126
Formations of mixed-valence oxovanadiumV,IV citrates and homocitrate with N-heterocycle chelated ligand. Inorganic chemistry 20081006
Evidence for nifU and nifS participation in the biosynthesis of the iron-molybdenum cofactor of nitrogenase. The Journal of biological chemistry 20071221
Acid-base chemical mechanism of homocitrate synthase from Saccharomyces cerevisiae. Biochemistry 20061003
Syntheses, spectroscopies and structures of molybdenum(VI) complexes with homocitrate. Inorganic chemistry 20061002
Evidence for a dynamic role for homocitrate during nitrogen fixation: the effect of substitution at the alpha-Lys426 position in MoFe-protein of Azotobacter vinelandii. The Biochemical journal 20060715
Kinetics and product analysis of the reaction catalysed by recombinant homoaconitase from Thermus thermophilus. The Biochemical journal 20060615
Synthesis of trimethyl (2S,3R)- and (2R,3R)-[2-2H1]-homocitrates and dimethyl (2S,3R)- and (2R,3R)-[2-2H1]-homocitrate lactones-an assay for the stereochemical outcome of the reaction catalysed both by homocitrate synthase and by the Nif-V protein. Organic & biomolecular chemistry 20060207
Binding modes for the first coupled electron and proton addition to FeMoco of nitrogenase. Journal of the American Chemical Society 20020501
Mechanistic features and structure of the nitrogenase alpha-Gln195 MoFe protein. Biochemistry 20010213
Requirement of homocitrate for the transfer of a 49V-labeled precursor of the iron-vanadium cofactor from VnfX to nif-apodinitrogenase. The Journal of biological chemistry 20010209

© 2019 Angene International Limited. All rights Reserved.