Weight | 117.148 g/mol |
---|---|
Formula | C5H11NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
L-norvaline (6600-40-4)
norvaline · alpha-aminovaleric acid · norvaline, (DL)-isomer
Score:
#2131 in Biochemistry
,
#5533 in Chemistry
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- Kinetic studies of glutamate dehydrogenase with glutamate and norvaline as substrates. Coenzyme activation and negative homotropic interactions in allosteric enzymes (Biochemical Journal, 1969)
- Effect of temperature on partial molar volumes and viscosities of aqueous solutions of -dl-Aminobutyric acid, dl-Norvaline and dl-Norleucine (Physics and Chemistry of Liquids, 2004)
- Ornithine Transcarbamylase from Streptococcus faecalis and Bovine Liver II. MULTIPLE BINDING SITES FOR CARBAMYL-P AND l-NORVALINE, CORRELATION WITH STEADY STATE KINETICS (Journal of Biological Chemistry, 1972)
- Incorporation of Norvaline at Leucine Positions in Recombinant Human Hemoglobin Expressed in Escherichia coli (Journal of Biological Chemistry, 1997)
- 5-Diazo-4-Oxo-L-Norvaline: Reactive Asparagine Analog with Biological Specificity (Science, 1968)
- Conformational analysis of protected norvaline oligopeptides by high resolution proton magnetic resonance. (Journal of the American Chemical Society, 1977)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - norvaline
- alpha-aminovaleric acid
- norvaline, (DL)-isomer
-
SMILESCCCC(C(=O)O)N
-
InChIKeySNDPXSYFESPGGJ-UHFFFAOYSA-N
- Pubchem - L-norvaline
- Wikipedia - norvaline
Norvaline (abbreviated as Nva) is an amino acid with the formula CH3(CH2)2CH(NH2)CO2H. The compound is an isomer of the more common amino acid valine. Like most other -amino acids, norvaline is chiral.
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