T2007
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:
Molecular Weight:
507.54
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
assay
≥98% (TLC)
Quality Level
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
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Storage Class
11 - Combustible Solids
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Articles
DISCOVER Bioactive Small Molecules for Neuroscience
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.
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
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