CAS 51887-89-9
:(1R)-1-carboxy-2-chloroethanaminium chloride
Formula:C3H7Cl2NO2
InChI:InChI=1/C3H6ClNO2.ClH/c4-1-2(5)3(6)7;/h2H,1,5H2,(H,6,7);1H/t2-;/m0./s1
InChI key:IENJPSDBNBGIEL-DKWTVANSSA-N
SMILES:C([C@@H](C(=O)O)N)Cl.Cl
Synonyms:- 3-Chloro-L-alanine hydrochloride (1:1)
- L-alanine, 3-chloro-, hydrochloride (1:1)
- 3-Chloro-L-alanine Hydrochloride
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H-β-Chloro-Ala-OH · HCl
CAS:Non-competitive inhibitor of alanine racemase, Ki 1.71 mM.Formula:C3H6ClNO2·HClPurity:> 99%Color and Shape:White Crystalline PowderMolecular weight:160.03-Chloro-L-alanine Hydrochloride
CAS:3-Chloro-L-alanine HydrochlorideFormula:C3H7Cl2NO2Purity:95%Molecular weight:160.0H-Ala(3-Cl)-OH.HCl
CAS:3-Chloro-L-alanine HydrochlorideFormula:C3H7Cl2NO2Purity:95%Molecular weight:160.0(R)-2-Amino-3-chloropropanoic acid hydrochloride
CAS:Formula:C3H7Cl2NO2Purity:98%Color and Shape:SolidMolecular weight:159.993-Chloro-L-alanine Hydrochloride
CAS:Formula:C3H7Cl2NO2Purity:95%Color and Shape:SolidMolecular weight:159.9992b-Chloro-L-alanine hydrochloride
CAS:b-Chloro-L-alanine hydrochloride (BCA) is a synthetic compound that has been shown to have anticarcinogenic and antioxidant effects. It can be produced by the hydrogen peroxide-dependent oxidation of b-chloroalanine. BCA's effect on cancer cells is attributed to its ability to inhibit the synthesis of sulfoxides, which are needed for the biosynthesis of pyrimidine nucleotides. BCA also inhibits oxidative stress by scavenging free radicals and reactive oxygen species. This product has been shown to be effective in treating Aeropyrum pernix infections, which are caused by a type of anaerobic bacteria with a metabolic pathway that includes sulfide oxidation.
Formula:C3H6NO2Cl·HClPurity:Min. 95%Color and Shape:White PowderMolecular weight:160 g/mol
