CAS 207727-86-4
:(2S)-2-amino-3-[4-[(2-nitrophenyl)methoxy]phenyl]propanoic acid hydrochloride
Description:
(2S)-2-amino-3-[4-[(2-nitrophenyl)methoxy]phenyl]propanoic acid hydrochloride, with CAS number 207727-86-4, is a synthetic amino acid derivative characterized by its specific stereochemistry and functional groups. This compound features an amino group (-NH2), a carboxylic acid group (-COOH), and a side chain that includes a methoxy-substituted phenyl group and a nitrophenyl moiety, contributing to its potential biological activity. The hydrochloride form indicates that it is a salt, which enhances its solubility in water, making it suitable for various applications in biochemical research and pharmaceutical development. The presence of the nitro group suggests potential interactions with biological targets, while the chiral center at the second carbon atom implies that it may exhibit specific stereochemical properties that can influence its biological activity. Overall, this compound is of interest in medicinal chemistry, particularly in the design of drugs targeting specific pathways or receptors.
Formula:C16H17ClN2O5
InChI:InChI=1/C16H16N2O5.ClH/c17-14(16(19)20)9-11-5-7-13(8-6-11)23-10-12-3-1-2-4-15(12)18(21)22;/h1-8,14H,9-10,17H2,(H,19,20);1H/t14-;/m0./s1
SMILES:c1ccc(c(c1)COc1ccc(cc1)C[C@@H](C(=O)O)N)N(=O)=O.Cl
Synonyms:- L-Tyrosine, O-[(2-nitrophenyl)methyl]-, hydrochloride (1:1)
- O-(2-Nitrobenzyl)-L-tyrosine hydrochloride (1:1)
- O-(2-NITROBENZYL)-L-TYROSINE HCL
- O-[(2-Nitrophenyl)Methyl]-L-tyrosine Hydrochloride
- (S)-2-amino-3-(4-(2-nitrobenzyloxy)phenyl)propanoic acid hydrochloride
- O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride USP/EP/BP
- -2-Amino-3-(4-((2-nitrobenzyl)
- ONBY
- NB-caged Tyrosine hydrochloride
- Ortho-(2-Nitrobenzyl)-L-Tyrosine Hydrochloride
- O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride
- o-nitrobenzyl-O-tyrosine.HCl
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 7 products.
L-Tyrosine, O-[(2-nitrophenyl)methyl]-, hydrochloride (1:1)
CAS:Formula:C16H17ClN2O5Purity:96%Color and Shape:SolidMolecular weight:352.7696L-Tyrosine, O-[(2-nitrophenyl)methyl]-, hydrochloride (1:1)
CAS:<p>L-Tyrosine, O-[(2-nitrophenyl)methyl]-, hydrochloride (1:1)</p>Purity:96%Molecular weight:352.77g/molO-(2-Nitrobenzyl)-L-tyrosine hydrochloride
CAS:Formula:C16H16N2O5·HClPurity:≥ 96.0%Color and Shape:Off-white to light-yellow solid or powderMolecular weight:352.77NB-caged Tyrosine hydrochloride
CAS:<p>NB-caged Tyrosine hydrochloride: photosensitive, releases tyrosine under UV light (300-350 nm), used in E.coli protein synthesis.</p>Formula:C16H17ClN2O5Color and Shape:SolidMolecular weight:352.77(S)-2-Amino-3-(4-((2-nitrobenzyl)oxy)phenyl)propanoic acid hydrochloride
CAS:Formula:C16H17ClN2O5Purity:96%Color and Shape:SolidMolecular weight:352.77O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride
CAS:Controlled ProductFormula:C16H16N2O5·ClHColor and Shape:NeatMolecular weight:352.77O-(2-nitrobenzyl)-l-tyrosine hydrochloride
CAS:<p>O-(2-nitrobenzyl)-l-tyrosine hydrochloride is a stable covalent inhibitor of human tyrosinase, which is an enzyme that catalyzes the first two steps in the synthesis of melanin. This drug has been shown to inhibit the growth of cancer cells in culture and has been used to treat bone cancer in animal models. O-(2-nitrobenzyl)-l-tyrosine hydrochloride also inhibits inflammatory responses by inhibiting enzyme activity, thereby preventing the production of proinflammatory cytokines such as TNF-α and IL1β. This drug binds to active enzymes, which may lead to intracellular targets.</p>Formula:C16H17ClN2O5Purity:Min. 95%Molecular weight:352.77 g/mol







