CAS 118021-35-5
:O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
Description:
O-(2-Aminoethyl)-L-serine hydrochloride, with the CAS number 118021-35-5, is a derivative of the amino acid L-serine, characterized by the presence of an aminoethyl group attached to the hydroxyl group of the serine molecule. This compound is typically a white to off-white crystalline powder, soluble in water due to the presence of the hydrochloride salt, which enhances its solubility and stability. It is often used in biochemical research and pharmaceutical applications, particularly in studies related to neurotransmitter synthesis and metabolic pathways. The aminoethyl group can participate in various chemical reactions, making it a versatile building block in organic synthesis. Additionally, this compound may exhibit biological activity, influencing cellular processes and potentially serving as a precursor for other bioactive molecules. As with many amino acid derivatives, it is important to handle it with care, following appropriate safety protocols in laboratory settings.
Formula:C5H13ClN2O3
InChI:InChI=1/C5H12N2O3.ClH/c6-1-2-10-3-4(7)5(8)9;/h4H,1-3,6-7H2,(H,8,9);1H/t4-;/m0./s1
SMILES:C(COC[C@@H](C(=O)O)N)N.Cl
Synonyms:- 4-Oxy-L-Lysine Hydrochloride
- H-Ser(Etnh2)-Oh Hcl
- H-Lys[*4(
- H-LYS[*4(<-O)]-OH HCL
- (S)-(+)-2-AMINO-3-(2-AMINOETHOXY)PROPANOIC ACID, MONOHYDROCHLORIDE
- L-4-OXALYSINE HCL
- (S)-(+)-2-AMINO-3-(2-AMINOETHOXY)-PROPAN OIC ACID HYDROCHLORIDE, 98%
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Found 3 products.
L-4-Oxalysine hydrochloride
CAS:<p>L-4-Oxalysine hydrochloride has shown antitumor activities, is a natural product isolated from the culture media of Streptomyces roseovirdofuscus in China.</p>Formula:C5H13ClN2O3Purity:98%Color and Shape:SolidMolecular weight:184.62L-4-Oxalysine hydrochloride
CAS:<p>L-4-Oxalysine hydrochloride is a halogenated, amidino, acid derivative of the amino acid, L-lysine. It is an inhibitor of the enzyme oxide synthase and has been shown to be effective in treating rheumatoid arthritis. L-4-Oxalysine hydrochloride inhibits the production of prostaglandin E2 (PGE2) by inhibiting the enzyme cyclooxygenase and by blocking the conversion of arachidonic acid to PGE2. This drug also has anti-inflammatory properties and can inhibit protein synthesis in cells.</p>Formula:C5H12N2O3•HClPurity:Min. 95%Molecular weight:184.62 g/mol


