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T2007

Sigma-Aldrich

Tyr-Tyr-Tyr

Synonym(s):

L-tyrosyl-L-tyrosyl- L-tyrosine

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About This Item

Empirical Formula (Hill Notation):
C27H29N3O7
CAS Number:
7390-78-5
Molecular Weight:
507.54
MDL number:
MFCD00055745
UNSPSC Code:
12352202
PubChem Substance ID:
24900005
NACRES:
NA.26

assay

≥98% (TLC)

form

powder

technique(s)

HPLC: suitable

color

white

storage temp.

−20°C

SMILES string

NC(Cc1ccc(O)cc1)C(=O)NC(Cc2ccc(O)cc2)C(=O)NC(Cc3ccc(O)cc3)C(O)=O

InChI

1S/C27H29N3O7/c28-22(13-16-1-7-19(31)8-2-16)25(34)29-23(14-17-3-9-20(32)10-4-17)26(35)30-24(27(36)37)15-18-5-11-21(33)12-6-18/h1-12,22-24,31-33H,13-15,28H2,(H,29,34)(H,30,35)(H,36,37)

InChI key

RMRFSFXLFWWAJZ-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Asako Narai-Kanayama et al.
Journal of biotechnology, 150(3), 343-347 (2010-09-28)
Papain-catalyzed polymerization of L-tyrosine ethyl ester in aqueous media was efficient for synthesis of oligo-tyrosine peptides having angiotensin I-converting enzyme inhibitory activity. Di-, tri-, and tetra-tyrosine accumulated in the soluble fraction of reaction mixture. On the other hand, the peptide
Anne Beilvert et al.
Chemical communications (Cambridge, England), 47(19), 5506-5508 (2011-04-02)
This communication reports the synthesis, characterization and in vivo evaluation in mice of a new tri-tyrosine conjugated MR contrast agent, which may help to identify vulnerable plaques in atherosclerosis by targeting the lipid core.
Javiera Cortés-Ríos et al.
Analytical biochemistry, 608, 113904-113904 (2020-08-18)
Amongst the available methodologies for protein determination, the bicinchoninic acid (BCA) assay highlights for its simplicity, sensitivity, repeatability and reproducibility. Nevertheless, in spite that the general principle behind this methodology is known, there are still unanswered questions regarding the chemistry
Shun Hirota et al.
Biochemical and biophysical research communications, 314(2), 452-458 (2004-01-22)
Effect of a hydrophobic peptide on folding of oxidized cytochrome c (cyt c) is studied with trityrosine. Folding of cyt c was initiated by pH jump from 2.3 (acid-unfolded) to 4.2 (folded). The Soret band of the 2-ms transient absorption

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