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DL-2-Aminocaprylsäure
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Synonym(e):
DL-2-Aminooctansäure
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About This Item
Lineare Formel:
CH3(CH2)5CH(NH2)CO2H
CAS-Nummer:
Molekulargewicht:
159.23
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352106
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
99%
Form
solid
Eignung der Reaktion
reaction type: solution phase peptide synthesis
mp (Schmelzpunkt)
260 °C (dec.) (lit.)
Anwendung(en)
peptide synthesis
SMILES String
CCCCCCC(N)C(O)=O
InChI
1S/C8H17NO2/c1-2-3-4-5-6-7(9)8(10)11/h7H,2-6,9H2,1H3,(H,10,11)
InChIKey
AKVBCGQVQXPRLD-UHFFFAOYSA-N
Verwandte Kategorien
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Seon-Hee Kim et al.
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Fatty acid (FA) binding proteins (FABPs) of helminths are implicated in acquisition and utilization of host-derived hydrophobic substances, as well as in signaling and cellular interactions. We previously demonstrated that secretory hydrophobic ligand binding proteins (HLBPs) of Taenia solium metacestode
Paper chromatography of 56 amino compounds using phenol and butanol-acetic acid as solvents with illustrative chromatograms of normal and abnormal urines.
T E PARRY
Clinica chimica acta; international journal of clinical chemistry, 2(2), 115-125 (1957-04-01)
Milica Markovic et al.
Pharmaceutics, 11(4) (2019-04-19)
In ulcerative colitis (UC), the inflammation is localized in the colon, and one of the successful strategies for colon-targeting drug delivery is the prodrug approach. In this work, we present a novel phospholipid (PL)-based prodrug approach, as a tool for
Arik Dahan et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 108, 78-85 (2017-06-20)
The enzyme phospholipase A
Sarah A Almahboub et al.
Applied microbiology and biotechnology, 102(2), 789-799 (2017-11-28)
Terminal modification of peptides is frequently used to improve their hydrophobicity. While N-terminal modification with fatty acids (lipidation) has been reported previously, C-terminal lipidation is limited as it requires the use of linkers. Here we report the use of a
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