29295
3-环己基-D-丙氨酸 水合物
≥99.0% (calc. based on dry substance, NT), ~1 mol/mol water
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关于此项目
经验公式（希尔记法）:
C9H17NO2 · xH2O
化学文摘社编号:
分子量:
171.24 (anhydrous basis)
Beilstein:
3197315
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
≥99.0% (calc. based on dry substance, NT)
表单
solid
旋光性
[α]20/D −12±1°, c = 1% in 1 M HCl (dry matter)
杂质
~1 mol/mol water
应用
peptide synthesis
SMILES字符串
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
InChI key
HDJQIWAIDCEDEF-DDWIOCJRSA-N
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
K M Armstrong et al.
Journal of molecular biology, 230(1), 284-291 (1993-03-05)
Two models have been considered for the helix-stabilizing Phe-His+ interaction in C-peptide: (1) the H-bond model in which His+ acts as an H-bond donor and the aromatic ring of Phe acts as an acceptor, and (2) a helix dipole model
Development of inhibitors against lipase and alpha-glucosidase from derivatives of monascus pigment.
Jong Hoon Kim et al.
FEMS microbiology letters, 276(1), 93-98 (2007-10-17)
New derivatives of monascus pigment were produced during Monascus fermentation by the addition of unnatural amino acids, and the inhibitory activities of the derivatives against diet-related lipase and alpha-glucosidase were tested. Derivatives with penicillamine (H-Pen), cyclohexylalanine (H-Cha), butylglycine (L-t-Bg), and
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
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