所有图片(1)
About This Item
线性分子式:
H2NC6H10CO2H
CAS号:
分子量:
143.18
Beilstein:
2802522
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案
95%
表单
powder
mp
299-301 °C (lit.)
SMILES字符串
N[C@H]1CC[C@H](CC1)C(O)=O
InChI
1S/C7H13NO2/c8-6-3-1-5(2-4-6)7(9)10/h5-6H,1-4,8H2,(H,9,10)/t5-,6+
InChI key
DRNGLYHKYPNTEA-OLQVQODUSA-N
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一般描述
cis-4-aminocyclohexanecarboxylic acid (C4-ACHC, cis-ACCA) exists in zwitterionic form. Cyclohexane ring in the molecule of cis-4-aminocyclohexanecarboxylic acid is present in chair conformation. The carboxylate and ammonium groups in the molecule occupy axial and equatorial positions, respectively. It co-crystallizes with water molecules in a 2:1 (amino acid:water ratio). H-Cys-Leu-Gly-Gly-Leu-Leu-Thr-Met-Val-OH (CLG) peptide analogue containing cis-ACCA has been prepared and its activity has been studied.
应用
cis-4-Aminocyclohexanecarboxylic acid may be used in the synthesis of new analogs of arginine vasopressin (AVP). It may be used in the synthesis of cis-4-[[[(2-chloroethyl)nitrosoamino]carbonyl]methylamino]cyclohexanecarboxylic acid.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Hydrogen-bonding patterns in cis-4-ammoniocyclohexanecarboxylate hemihydrate.
Edward E Avila et al.
Acta crystallographica. Section C, Crystal structure communications, 60(Pt 10), o759-o761 (2004-10-07)
T P Johnston et al.
Journal of medicinal chemistry, 27(1), 97-99 (1984-01-01)
cis-4-[[[(2-Chloroethyl)nitrosoamino]carbonyl]methylamino] cyclohexanecarboxylic acid (N-Me-cis-CCCNU) was synthesized in five steps from cis-4-aminocyclohexanecarboxylic acid via an N-tosylated intermediate. N-Me-cis-CCCNU, which is incapable of the facile decomposition that characterizes the clinically useful nitrosoureas, effected a significant cure rate of both early and established
Katherine E S Locock et al.
Neurochemical research, 34(10), 1698-1703 (2009-06-03)
The incorporation of extra binding groups onto known ligands is a powerful tool for the development of more potent and selective agents at target sites such as the GABA receptors. In the present work we have attempted to build on
Mauro Marastoni et al.
Bioorganic & medicinal chemistry, 10(9), 3061-3066 (2002-07-12)
In order to improve the immunotherapeutical potential of H-Cys-Leu-Gly-Gly-Leu-Leu-Thr-Met-Val-OH (CLG) peptide, an Epstein-Barr virus (EBV) subdominant epitope derived from the membrane protein LMP2, we have synthesized and tested CLG analogues containing cis- and/or trans-4-aminocyclohexanecarboxylic acid (ACCA) replacing Gly-Gly and/or Thr-Met
S K Lo et al.
Journal of applied physiology (Bethesda, Md. : 1985), 58(5), 1421-1427 (1985-05-01)
We examined the effect of fibrinolysis depression on thrombin-induced pulmonary microembolism in awake sheep prepared with chronic lung lymph fistulas. Fibrinolysis was depressed by an intravenous infusion (100 mg) of tranexamic acid [trans-4-(Aminomethyl)cyclohexanecarboxylic acid]. Pulmonary microembolism was induced by an
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