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Merck
CN

218693

Sigma-Aldrich

1-氨基环己烷羧酸

98%

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别名:
1-氨基环己甲酸
线性分子式:
H2NC6H10CO2H
CAS号:
分子量:
143.18
Beilstein:
2355692
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

检测方案

98%

形式

solid

反应适用性

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

应用

peptide synthesis

SMILES字符串

NC1(CCCCC1)C(O)=O

InChI

1S/C7H13NO2/c8-7(6(9)10)4-2-1-3-5-7/h1-5,8H2,(H,9,10)

InChI key

WOXWUZCRWJWTRT-UHFFFAOYSA-N

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WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Nicolas Fabresse et al.
Journal of pharmaceutical and biomedical analysis, 141, 149-156 (2017-04-27)
Tranexamic acid is a widely used antifibrinolytic drug but its pharmacology and pharmacokinetics remains poorly understood. Owing to the recent knowledge on phospholipid-induced matrix effects during human plasma analysis, our aim was to develop a liquid chromatography-mass spectrometry method for
Francisco Rodríguez-Ropero et al.
Journal of chemical information and modeling, 48(2), 333-343 (2008-01-19)
Conformationally restricted amino acids are promising candidates to serve as basic pieces in redesigned protein motifs which constitute the basic modules in synthetic nanoconstructs. Here we study the ability of constrained cyclic amino acid 1-aminocyclohexane-1-carboxylic acid (Ac6c) to stabilize highly
B Jastrzebska et al.
The journal of peptide research : official journal of the American Peptide Society, 62(2), 70-77 (2003-06-26)
In this study we describe the synthesis and some pharmacological properties of seven new analogues of arginine vasopressin (AVP) substituted in position 2 or 3 with 1-aminocyclohexane-1-carboxylic acid (Acc). All peptides were tested for the pressor, antidiuretic and uterotonic in
Olga Labudda et al.
Journal of peptide science : an official publication of the European Peptide Society, 12(12), 775-779 (2006-11-30)
A sterically constrained non-coded amino acid, 1-aminocyclopentane-1-carboxylic acid (Apc), was introduced in position 7 or 8 of the bradykinin (BK) B(2) receptor antagonist, [D-Arg(0), Hyp(3), Thi(5, 8), D-Phe(7)]BK, previously synthesized by Stewart's group. This modification is believed to reduce the
A Romanelli et al.
Journal of peptide science : an official publication of the European Peptide Society, 7(1), 15-26 (2001-03-14)
Secondary structure formation and stability are essential features in the knowledge of complex folding topology of biomolecules. To better understand the relationships between preferred conformations and functional properties of beta-homo-amino acids, the synthesis and conformational characterization by X-ray diffraction analysis

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