29295
3-Cyclohexyl-D-alanine hydrate
≥99.0% (calc. based on dry substance, NT), ~1 mol/mol water
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About This Item
Fórmula empírica (Notação de Hill):
C9H17NO2 · xH2O
Número CAS:
Peso molecular:
171.24 (anhydrous basis)
Beilstein:
3197315
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
≥99.0% (calc. based on dry substance, NT)
Formulário
solid
atividade óptica
[α]20/D −12±1°, c = 1% in 1 M HCl (dry matter)
Impurezas
~1 mol/mol water
aplicação(ões)
peptide synthesis
cadeia de caracteres SMILES
O.N[C@H](CC1CCCCC1)C(O)=O
InChI
1S/C9H17NO2.H2O/c10-8(9(11)12)6-7-4-2-1-3-5-7;/h7-8H,1-6,10H2,(H,11,12);1H2/t8-;/m1./s1
chave InChI
HDJQIWAIDCEDEF-DDWIOCJRSA-N
Código de classe de armazenamento
13 - Non Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Chad D Tatko et al.
Journal of the American Chemical Society, 126(7), 2028-2034 (2004-02-20)
We have examined the impact of C-H...pi and hydrophobic interactions in the diagonal position of a beta-hairpin peptide through comparison of the interaction of Phe, Trp, or Cha (cyclohexylalanine) with Lys or Nle (norleucine). NMR studies, including NOESY and chemical
Nathan A Schnarr et al.
Journal of the American Chemical Society, 124(33), 9779-9783 (2002-08-15)
Specific coiled-coil heterotrimers result from steric matching of hydrophobic core side chains. A 2:1 heterotrimer is formed by peptides containing alanine or cyclohexylalanine, respectively, at a central core residue. Detailed thermodynamic analysis reveals that the designed complex is considerably more
Tuning wasp toxin structure for nicotinic receptor antagonism: cyclohexylalanine-containing analogues as potent and voltage-dependent blockers.
Christian A Olsen et al.
ChemMedChem, 1(3), 303-305 (2006-08-08)
Christopher J Pace et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(19), 5832-5836 (2012-04-05)
CH-π stacks up! Using the protein α(2) D as a model system, we estimate that a CH-π contact between cyclohexylalanine (Cha) and phenylalanine (F) contributes approximately -0.7 kcal mol(-1) to the protein stability. The stacking F-Cha pairs are sequestered in the
Takao Nomura et al.
Biopolymers, 95(6), 410-419 (2011-02-01)
Stabilization of protein structures and protein-protein interactions are critical in the engineering of industrially useful enzymes and in the design of pharmaceutically valuable ligands. Hydrophobic interactions involving phenylalanine residues play crucial roles in protein stability and protein-protein/peptide interactions. To establish
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