| Weight | 129.159 g/mol |
|---|---|
| Formula | C6H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
cycloleucine (52-52-8)
Aminocyclopentanecarboxylic Acid · 1-Aminocyclopentanecarboxylic Acid · 1 Aminocyclopentanecarboxylic Acid
Score:
#1160 in Biochemistry
,
#2950 in Biology
,
#3692 in Chemistry
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- Synthesis and Structural Characterization of Helix-Forming -Peptides: trans-2-Aminocyclopentanecarboxylic Acid Oligomers (Journal of the American Chemical Society, 1999)
- cis2Aminocyclopentanecarboxylic Acid Oligomers Adopt a Sheetlike Structure: Switch from Helix to Nonpolar Strand (Angewandte Chemie, 2002)
- RNA methylation and control of eukaryotic RNA biosynthesis. Effects of cycloleucine, a specific inhibitor of methylation, on ribosomal RNA maturation. (FEBS Journal, 1977)
- Theoretical and Experimental Circular Dichroic Spectra of the Novel Helical Foldamer Poly[(1R,2R)-trans-2-aminocyclopentanecarboxylic acid] (Journal of the American Chemical Society, 1998)
- Stereoselective Synthesis of 3-Substituted 2-Aminocyclopentanecarboxylic Acid Derivatives and Their Incorporation into Short 12-Helical -Peptides That Fold in Water (Journal of the American Chemical Society, 2002)
- Cycloleucine competitively antagonizes the strychnine-insensitive glycine receptor (European Journal of Pharmacology, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aminocyclopentanecarboxylic Acid
- 1-Aminocyclopentanecarboxylic Acid
- 1 Aminocyclopentanecarboxylic Acid
- NSC 1026
-
SMILESC1CCC(C1)(C(=O)O)N
-
InChIKeyNILQLFBWTXNUOE-UHFFFAOYSA-N
- Pubchem - cycloleucine
- Wikipedia - cycloleucine
Cycloleucine is a non-proteinogenic amino acid. It could be classified as a cyclic derivate of norleucine, having two hydrogen atoms less. Leading structure is a cyclopentane-ring.
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