Weight | 89.094 g/mol |
---|---|
Formula | C3H7NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
D-alanine (338-69-2)
Score:
#777 in Biochemistry
,
#916 in Physics
,
#2118 in Biology
,
#2600 in Chemistry
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- D-alanine added to antipsychotics for the treatment of schizophrenia (Biological Psychiatry, 1998)
- Mechanism of action of penicillins: a proposal based on their structural similarity to acyl-D-alanyl-D-alanine (Proceedings of the National Academy of Sciences of the United States of America, 1965)
- Tissue fractionation studies. 17. Intracellular distribution of monoamine oxidase, aspartate aminotransferase, alanine aminotransferase, d-amino acid oxidase and catalase in rat-liver tissue (Biochemical Journal, 1964)
- Structure of vancomycin and its complex with acetyl-D-alanyl-D-alanine (Nature, 1978)
- Enzymes in the D-alanine branch of bacterial cell wall peptidoglycan assembly. (Journal of Biological Chemistry, 1989)
- Modifications of the acyl-d-alanyl-d-alanine terminus affecting complex-formation with vancomycin (Biochemical Journal, 1971)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C(=O)O)N
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InChIKeyQNAYBMKLOCPYGJ-UHFFFAOYSA-N
- Pubchem - D-alanine
- Wikipedia - D-alanine
Alanine (abbreviated as Ala or A) is an -amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated form, NH3+, under biological conditions), an -carboxylic acid group (which is in the deprotonated form, COO, under biological conditions), and a side chain methyl group, making it a nonpolar, aliphatic amino acid. It is non-essential in humans: because the body can synthesize it, it does not need to be present in the diet.
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