Home Aminos Dl-alpha-aminosuberic acid

Dl-alpha-aminosuberic acid

CAS No.:
3054-07-7
Catalog Number:
AG0030HZ
Molecular Formula:
C8H15NO4
Molecular Weight:
189.2090
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
>95.0%(T)
1 week
United States
$430
- +
Product Description
Catalog Number:
AG0030HZ
Chemical Name:
Dl-alpha-aminosuberic acid
CAS Number:
3054-07-7
Molecular Formula:
C8H15NO4
Molecular Weight:
189.2090
MDL Number:
MFCD21606318
IUPAC Name:
2-aminooctanedioic acid
InChI:
InChI=1S/C8H15NO4/c9-6(8(12)13)4-2-1-3-5-7(10)11/h6H,1-5,9H2,(H,10,11)(H,12,13)
InChI Key:
YOFPFYYTUIARDI-UHFFFAOYSA-N
SMILES:
OC(=O)CCCCCC(C(=O)O)N
Properties
Complexity:
181  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
189.1g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
189.211g/mol
Monoisotopic Mass:
189.1g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
101A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-2.2  
Literature
Title Journal
Comparative gene expression profiling of P. falciparum malaria parasites exposed to three different histone deacetylase inhibitors. PloS one 20120101
Histone deacetylases play a major role in the transcriptional regulation of the Plasmodium falciparum life cycle. PLoS pathogens 20100101
Design, synthesis, potency, and cytoselectivity of anticancer agents derived by parallel synthesis from alpha-aminosuberic acid. Journal of medicinal chemistry 20061228
Aliphatic amino diacid Asu functions as an effective mimic of Tyr(SO3H) in sulfakinins for myotropic and food intake-inhibition activity in insects. Peptides 20050101
The peptides of alpha-aminosuberic acid II. Synthesis of deamino-dicarba-eel-calcitonin sequence 1-9. Amino acids 20010101
A new highly selective metabotropic excitatory amino acid agonist: 2-amino-4-(3-hydroxy-5-methylisoxazol-4-yl)butyric acid. Journal of medicinal chemistry 19960802
Properties