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T9505

L-Tyrosine benzyl ester p-toluenesulfonate salt

Name: <SC>L</SC>-Tyrosine benzyl ester <I>p</I>-toluenesulfonate salt
Brand: SIGMA

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About This Item

Empirical Formula (Hill Notation):

C₁₆H₁₇NO₃ · C₇H₈O₃S

CAS Number:

53587-11-4

Molecular Weight:

443.51

Beilstein:

3855339

EC Number:

258-650-8

MDL number:

MFCD00038959

UNSPSC Code:

12352200

PubChem Substance ID:

24900424

Assay

≥97% (TLC)

form

powder

color

white

storage temp.

−20°C

SMILES string

Cc1ccc(cc1)S(O)(=O)=O.N[C@@H](Cc2ccc(O)cc2)C(=O)OCc3ccccc3

InChI

1S/C16H17NO3.C7H8O3S/c17-15(10-12-6-8-14(18)9-7-12)16(19)20-11-13-4-2-1-3-5-13;1-6-2-4-7(5-3-6)11(8,9)10/h1-9,15,18H,10-11,17H2;2-5H,1H3,(H,8,9,10)/t15-;/m0./s1

InChI key

PJGVHBLZZQDFFM-RSAXXLAASA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Purification, characterization and partial amino acid sequencing of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase from tobacco cell-suspension cultures.

J Negrel et al.

European journal of biochemistry, 247(3), 1127-1135 (1997-08-01)

We report the purification of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase (THT) to apparent homogeneity in 12% yield from tobacco (Nicotiana tabacum L. cv. Xanthi) cell-suspension cultures elicited with a commercial preparation of pronase. The purification procedure employs only four chromatography steps and takes

Endosperm-specific expression of tyramine N-hydroxycinnamoyltransferase and tyrosine decarboxylase from a single self-processing polypeptide produces high levels of tyramine derivatives in rice seeds.

Sangkyu Park et al.

Biotechnology letters, 31(6), 911-915 (2009-02-21)

The plant-specific tyramine derivatives, feruloyltyramine (FT) and 4-coumaroyltyramine (CT), represent bioactive compounds found at low levels in many plant species. We generated transgenic rice seeds that produce high levels of CT (14 microg g(-1) seeds) and FT (2.7 microg g(-1)

Effect of protease inhibitors and substrates on 3,5,3'-triiodothyronine binding to rat liver nuclear receptors.

J Brtko et al.

Endocrine regulations, 26(3), 127-131 (1992-09-01)

The effect of protease inhibitors N-tosyl-L-phenylalanine chloromethyl ketone (TPCK) and N-carbobenzoxy-L-phenylalanine chloromethyl ketone (ZPCK) at concentrations ranging from 1.5 x 10(-6) mol/l to 1.5 x 10(-4) mol/l on the specific binding of 3,5,3'-triiodothyronine (T3) to rat liver nuclear receptors was

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