284637
7-Aminoheptanoic acid
98%
Synonym(s):
7-Aminooenanthic acid
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About This Item
Linear Formula:
H2N(CH2)6CO2H
CAS Number:
Molecular Weight:
145.20
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-197-5
Beilstein/REAXYS Number:
906887
MDL number:
Product Name
7-Aminoheptanoic acid, 98%
InChI key
XDOLZJYETYVRKV-UHFFFAOYSA-N
InChI
1S/C7H15NO2/c8-6-4-2-1-3-5-7(9)10/h1-6,8H2,(H,9,10)
SMILES string
NCCCCCCC(O)=O
assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
192-195 °C (lit.)
application(s)
peptide synthesis
Quality Level
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Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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V S De Serrano et al.
Biochemistry, 31(47), 11698-11706 (1992-12-01)
The properties of the cationic locus within the recombinant (r) kringle 2 domain (residues 180-261) of tissue-type plasminogen activator ([K2tPA]) that are responsible for stabilization of its interaction with the carboxylate moiety of omega-amino acid ligands have been assessed by
Tomoyuki Sasaki et al.
Thrombosis research, 130(4), e222-e228 (2012-07-17)
Thrombin-activatable fibrinolysis inhibitor (TAFI) is a plasma zymogen that is activated by thrombin in plasma. In fibrinolytic processes, carboxy-terminal lysine (Lys) residues in partially degraded fibrin are important sites for plasminogen binding and activation, and an active form of TAFI
Is there any need for a TAFI(a) inhibitor as thrombolytic drug?
Ellen Vercauteren et al.
Thrombosis research, 130(4), 574-575 (2012-07-31)
V S De Serrano et al.
Biochemistry, 32(14), 3540-3548 (1993-04-13)
The involvement of specific aspartic acid (D) and glutamic acid (E) residues of the recombinant (r) kringle 2 (K2) domain of tissue-type plasminogen activator (tPA) in stabilizing its interaction with omega-amino acid ligands has been assessed by examination of these
Surface interactions of a homologous series of alpha,omega-amino acids on colloidal silver and gold.
A A Ooka et al.
Biospectroscopy, 5(1), 9-17 (1999-04-29)
Surface enhanced Raman spectroscopy (SERS) was used to characterize a homologous series of alpha,omega-amino acids on colloidal gold and silver. Raman and SER spectra of the alpha,omega-amino acids, NH2(CH2)nCOOH (n = 3-7), are presented and analyzed, revealing the probable conformations
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