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T90808

L-Tyrosine methyl ester

Name: <SC>L</SC>-Tyrosine methyl ester
Brand: ALDRICH

98%

Synonym(s):

(S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester, S-Tyrosine methyl ester

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About This Item

Linear Formula:

4-(HO)C₆H₄CH₂CH(NH₂)COOCH₃

CAS Number:

1080-06-4

Molecular Weight:

195.22

NACRES:

NA.22

PubChem Substance ID:

24900583

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

214-095-3

MDL number:

MFCD00002392

Beilstein/REAXYS Number:

2372626

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Properties

Quality Level

200

assay

98%

form

powder with small lumps

optical activity

[α]20/D +26°, c = 2.4 in methanol

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

134-136 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

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

InChI key

MWZPENIJLUWBSY-VIFPVBQESA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Efficient functionalization of alginate biomaterials.

Marianne Ø Dalheim et al.

Biomaterials, 80, 146-156 (2015-12-29)

Peptide coupled alginates obtained by chemical functionalization of alginates are commonly used as scaffold materials for cells in regenerative medicine and tissue engineering. We here present an alternative to the commonly used carbodiimide chemistry, using partial periodate oxidation followed by

Evaluation of the analgesic effects of ammoxetine, a novel potent serotonin and norepinephrine reuptake inhibitor.

Ting-Ting Zhang et al.

Acta pharmacologica Sinica, 37(9), 1154-1165 (2016-07-19)

The selective serotonin (5-HT) and norepinephrine (NE) reuptake inhibitors (SNRIs) are commonly used for the treatment of neuropathic pain and fibromyalgia. Ammoxetine ((±)-3-(benzo[d] [1,3]dioxol-4-yloxy)-N-methyl-3-(thiophen-2-yl)propan-1-amine) has been identified as a novel potent SNRI. In this study, we evaluated the acute analgesic

Inhibition of 3,5,3'-triiodothyronine binding to its receptor in rat liver by protease inhibitors and substrates.

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.

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Global Trade Item Number

SKU	GTIN
T90808-25G	04061832649535
T90808-5G	04061837380495