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850489

Sigma-Aldrich

L-Tyrosine methyl ester hydrochloride

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About This Item

Fórmula linear:
HOC6H4CH2CH(NH2)COOCH3 · HCl
Número CAS:
3417-91-2
Peso molecular:
231.68
Beilstein:
3917353
Número CE:
222-313-3
Número MDL:
MFCD00012607
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
24888297
NACRES:
NA.22

Formulário

powder

atividade óptica

[α]25/D +74.0°, c = 3 in pyridine

adequação da reação

reaction type: solution phase peptide synthesis

pf

192 °C (dec.) (lit.)

aplicação(ões)

peptide synthesis

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Cl.COC(=O)[C@@H](N)Cc1ccc(O)cc1

InChI

1S/C10H13NO3.ClH/c1-14-10(13)9(11)6-7-2-4-8(12)5-3-7;/h2-5,9,12H,6,11H2,1H3;1H/t9-;/m0./s1

chave InChI

VXYFARNRGZWHTJ-FVGYRXGTSA-N

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Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BGBC0359V
BGBB8603
1433117V
1433117
12224JH

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Francesca Fontana et al.
Molecules (Basel, Switzerland), 26(2) (2021-01-14)
Configurationally stable 5-aza[6]helicene (1) was envisaged as a promising scaffold for non-conventional ionic liquids (IL)s. It was prepared, purified, and separated into enantiomers by preparative HPLC on a chiral stationary phase. Enantiomerically pure quaternary salts of 1 with appropriate counterions
S Criado et al.
Photochemistry and photobiology, 68(4), 453-458 (1998-10-31)
This paper studies the dye-sensitized photooxidation of tyrosine (tyr) and tyr di- and tripeptides (tyr-tyr and tyr-tyr-tyr) mediated by singlet molecular oxygen (O2[1 delta g]) in alkaline media. Photooxidation quantum efficiencies (phi r) were obtained by determining the overall and
J Brtko et al.
Molecular and cellular endocrinology, 93(1), 81-86 (1993-05-01)
Various protease inhibitors (e.g. phenylmethanesulfonyl fluoride (PMSF), tosyl-phenylalanine chloromethyl ketone (TosPheCH2Cl)) and substrates (e.g., tosyl-arginine methyl ester (TosArgOMe), tryptophan methyl ester (TrpOMe)) inhibit the binding of adrenal and sex steroids to their cognate receptors (Hubbard and Kalimi (1985) Mol. Cell.
János Elek et al.
Journal of pharmaceutical and biomedical analysis, 38(4), 601-608 (2005-06-22)
Different dual selector systems containing a cyclodextrin derivative (methyl-beta-cyclodextrin and dimethyl-beta-cyclodextrin) and a new diaza-crown-ether derivative (N-[2-(1,4,10,13-tetraoxa-7,16-diazacyclooctadecan-7-yl)propanoyl]glycine) were studied in the enantioselective separation of tryptophan-methylester and tyrosine-methylester enantiomers. This paper deals with the systematic study of the effects of changing
H Iishi et al.
International journal of cancer, 73(1), 113-116 (1997-10-23)
The effects of combined administration of a catecholamine precursor, tyrosine methyl ester (TME), and an ornithine decarboxylase (ODC) inhibitor, 1,3-diaminopropane (DAP), on the incidence of gastric cancers induced by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), the norepinephrine (NE) concentration and ODC activity of the
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