595-40-4
Chemical Structure
L-Isovaline
- CAS No.: 595-40-4
- Formula:C5H11NO2
- Molecular Weight:117.15
IUPAC Name: (S)-2-amino-2-methylbutanoic acid
InChIKey: GCHPUFAZSONQIV-YFKPBYRVSA-N
SMILES: OC([C@@](C)(N)CC)=O
Biological Activity: L-Isovaline is a valine derivative[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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L-Isovaline | 99.90% | L-Isovaline is a valine derivative. | ||||||||||||||||||||
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α-Methyl-DL-methionine | α-Methyl-DL-methionine is a Methionine (HY-13694) derivative. | |||||||||||||||||||||
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H-alpha-Prg-D-Ala-OH | H-alpha-Prg-D-Ala-OH is a click chemistry reagent containing an azide group. | |||||||||||||||||||||
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(S)-2-amino-3-hydroxy-2-methylpropanoic acid | 98.0% | (S)-2-amino-3-hydroxy-2-methylpropanoic acid is a serine derivative. | ||||||||||||||||||||
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D-Isovaline | 97.0% | D-Isovaline is a valine derivative. | ||||||||||||||||||||
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(R)-2-amino-2,3-dimethylbutanoic acid | 98.0% | (R)-2-amino-2,3-dimethylbutanoic acid is a valine derivative. | ||||||||||||||||||||
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(S)-2-Amino-2,3-dimethylbutanoic acid | 99.90% | (S)-2-Amino-2,3-dimethylbutanoic acid is a valine derivative. | ||||||||||||||||||||
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2-Amino-3-hydroxy-2-methylpropanoic acid | 2-Amino-3-hydroxy-2-methylpropanoic acid is a serine derivative. | |||||||||||||||||||||
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Dimebutic acid | 99.85% | Dimebutic acid is an orally active short-chain fatty acid. Dimebutic acid stimulates fetal globin production and alters the balance of Bcl family proteins. Dimebutic acid prolongs red blood cell survival. Dimebutic acid exhibits toxicity in rats. Dimebutic acid can be used in the study of β-thalassemia and sickle cell disease. | ||||||||||||||||||||
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α-Methyl-DL-aspartic acid | 99.93% | α-Methyl-DL-aspartic acid is a specific inhibitor of argininosuccinate synthase (ASS), and also is the rate-limiting enzyme for the recycling of 1-citrulline to 1-arginine. | ||||||||||||||||||||
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NSC 16590 (Standard) | 99.91% | NSC 16590 (Standard) is the analytical standard of NSC 16590. This product is intended for research and analytical applications. NSC 16590 inhibits the production of endogenous ethylene in the cotyledonary segments of cocklebur. | ||||||||||||||||||||
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