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626-51-7 | 3-Methylpentanedioic acid
CAS No: 626-51-7 Catalog No: AG003JRC MDL No:MFCD00002727
Product Description
Catalog Number:
AG003JRC
Chemical Name:
3-Methylpentanedioic acid
CAS Number:
626-51-7
Molecular Formula:
C6H10O4
Molecular Weight:
146.1412
MDL Number:
MFCD00002727
IUPAC Name:
3-methylpentanedioic acid
InChI:
InChI=1S/C6H10O4/c1-4(2-5(7)8)3-6(9)10/h4H,2-3H2,1H3,(H,7,8)(H,9,10)
InChI Key:
XJMMNTGIMDZPMU-UHFFFAOYSA-N
SMILES:
CC(CC(=O)O)CC(=O)O
EC Number:
210-951-5
UNII:
3Q0P190C7B
NSC Number:
14870
Properties
Complexity:
125
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.058g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
146.142g/mol
Monoisotopic Mass:
146.058g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
74.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1
Literature
| Title | Journal |
|---|---|
| Anaerobic degradation of 4-methylbenzoate via a specific 4-methylbenzoyl-CoA pathway. | Environmental microbiology 20120501 |
| The 3-methylglutaconic acidurias: what's new? | Journal of inherited metabolic disease 20120101 |
| Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies. | Progress in retinal and eye research 20110301 |
| Neurochemical evidence that 3-methylglutaric acid inhibits synaptic Na+,K+-ATPase activity probably through oxidative damage in brain cortex of young rats. | International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 20110201 |
| Carboxylated hyperbranched poly(glycidol)s for preparation of pH-sensitive liposomes. | Journal of controlled release : official journal of the Controlled Release Society 20110105 |
| Computational analysis of a novel mutation in ETFDH gene highlights its long-range effects on the FAD-binding motif. | BMC structural biology 20110101 |
| OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria. | Molecular genetics and metabolism 20100601 |
| Striatum is more vulnerable to oxidative damage induced by the metabolites accumulating in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency as compared to liver. | International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 20090601 |
| Inherited mitochondrial optic neuropathies. | Journal of medical genetics 20090301 |
| Costeff optic atrophy syndrome: new clinical case and novel molecular findings. | Journal of inherited metabolic disease 20081201 |
| Induction of oxidative stress by the metabolites accumulating in 3-methylglutaconic aciduria in cerebral cortex of young rats. | Life sciences 20080312 |
| 3-methylglutaconic aciduria type 4 manifesting as Leigh syndrome in 2 siblings. | Journal of child neurology 20070201 |
| 3-Methylglutaric acid as a 13C solid-state NMR standard. | Solid state nuclear magnetic resonance 20061001 |
| NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism. | NMR in biomedicine 20060401 |
| A new sensitive isotropic-anisotropic separation experiment-SPEED MAS. | Journal of magnetic resonance (San Diego, Calif. : 1997) 20040601 |
| Vitamin E analogues as inducers of apoptosis: structure-function relation. | British journal of cancer 20030616 |
| 3-methyglutaconic aciduria in a Chinese patient with glycogen storage disease Ib. | Journal of inherited metabolic disease 20030101 |
| 3-Methylglutaconic aciduria type III in a non-Iraqi-Jewish kindred: clinical and molecular findings. | Molecular genetics and metabolism 20020701 |
| Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews. | American journal of human genetics 20011201 |
| 3-Hydroxy-3-methylglutaric aciduria in an Italian patient is caused by a new nonsense mutation in the HMGCL gene. | Molecular genetics and metabolism 20010701 |
| Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria. | Journal of child neurology 20010201 |
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