| Weight | 131.175 g/mol |
|---|---|
| Formula | C6H13NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
l-isoleucine (73-32-5, 443-79-8)
Isoleucine · Alloisoleucine · Isoleucine, L Isomer
Score:
#222 in Biochemistry
,
#869 in Biology
,
#962 in Chemistry
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- The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. (The Plant Cell, 2004)
- (+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate (Nature Chemical Biology, 2009)
- Site of Action of Chlorsulfuron: Inhibition of Valine and Isoleucine Biosynthesis in Plants (Plant Physiology, 1984)
- Naturally Occurring Human Glutathione Stransferase GSTP11 Isoforms with Isoleucine and Valine in Position 104 Differ in Enzymic Properties (FEBS Journal, 1994)
- Crystal structure of an isoleucine-zipper trimer. (Nature, 1994)
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine Content (Journal of the American Chemical Society, 1958)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Isoleucine
- Alloisoleucine
- Isoleucine, L Isomer
- L-Isomer Isoleucine
-
SMILESCCC(C)C(C(=O)O)N
-
InChIKeyAGPKZVBTJJNPAG-UHFFFAOYSA-N
- Pubchem - l-isoleucine
- Wikipedia - L-Isoleucine
Isoleucine (abbreviated as Ile or I), encoded by the codons ATT, ATC, ATA, is an -amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated NH+ 3 form under biological conditions), an -carboxylic acid group (which is in the deprotonated COO form under biological conditions), and a hydrocarbon side chain, classifying it as a non-polar, uncharged (at physiological pH), aliphatic amino acid. It is essential in humans, meaning the body cannot synthesize it, and must be ingested in our diet.
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l-isoleucine
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