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H0377

Sigma-Aldrich

DL-5-Hydroxy-lysin -hydrochlorid

≥98% (TLC)

Synonym(e):

2,6-Diamino-5-hydroxy-capronsäure -hydrochlorid, 2,6-Diamino-5-hydroxyhexansäure -hydrochlorid

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About This Item

Lineare Formel:
NH2CH2CH(OH)CH2CH2CH(NH2)COOH · HCl
CAS-Nummer:
13204-98-3
Molekulargewicht:
198.65
Beilstein:
3914368
EG-Nummer:
236-168-9
MDL-Nummer:
MFCD00012878
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24895397
NACRES:
NA.26

product name

DL-5-Hydroxy-lysin -hydrochlorid,

Assay

≥98% (TLC)

Form

powder

Farbe

white

mp (Schmelzpunkt)

225 °C (dec.) (lit.)

Anwendung(en)

detection
peptide synthesis

SMILES String

Cl.NCC(O)CCC(N)C(O)=O

InChI

1S/C6H14N2O3.ClH/c7-3-4(9)1-2-5(8)6(10)11;/h4-5,9H,1-3,7-8H2,(H,10,11);1H

InChIKey

MJXVOTKVFFAZQJ-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung


  • Characterization of acetyl-CoA: L-lysine N6-acetyltransferase, which catalyses the first step of carbon catabolism from lysine in Saccharomyces cerevisiae.: This research investigates the enzyme acetyl-CoA: L-lysine N6-acetyltransferase, which initiates the catabolism of lysine in Saccharomyces cerevisiae. Utilizing DL-5-Hydroxylysine hydrochloride, the study provides insights into the metabolic pathways and regulatory mechanisms of lysine degradation, contributing to the broader understanding of amino acid metabolism in yeast (Bode et al., 1993).

Biochem./physiol. Wirkung

DL-5-Hydroxylysine is a racemic mixture of D- and L- enantiomers of 5-hydroxylysine which may be used as potential target markers for radical-induced protein oxidation.

Sonstige Hinweise

Mixed DL and DL-allo

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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R Bode et al.
Archives of microbiology, 160(5), 397-400 (1993-01-01)
The carbon catabolism of L-lysine starts in Saccharomyces cerevisiae with acetylation by an acetyl-CoA:L-lysine N6-acetyltransferase. The enzyme is strongly induced in cells grown on L-lysine as sole carbon source and has been purified about 530-fold. Its activity was specific for
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Chemical research in toxicology, 11(11), 1265-1273 (1998-11-17)
gamma-Irradiation of several amino acids (Val, Leu, Ile, Lys, Pro, and Glu) in the presence of O2 generates hydroperoxides. We have previously isolated and characterized valine and leucine hydroperoxides, and hydroxides, and have detected these products in both isolated systems
M Droux et al.
Archives of biochemistry and biophysics, 316(1), 585-595 (1995-01-10)
Cystathionine beta-lyase, the second enzyme of the transsulfuration pathway leading to homocysteine synthesis was purified over 16,000-fold from spinach (Spinacia oleracea L.) leaf chloroplasts (soluble fraction). Enzyme activity was followed along the purification scheme by either a colorimetric method for
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International journal of plant sciences, 160(3), 511-519 (2001-09-07)
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[reaction: see text] L-alpha-(1-Cyclobutenyl)glycine (1-Cbg) was targeted as a potentially translatable analogue of isoleucine and valine and as a useful building block for peptides. An enantioselective synthesis was executed in which the key step was diastereoselective addition of 1-cyclobutenylmagnesium bromide
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