CAS 147612-86-0

EPQ-PY-EEIPIYL*

Description:

EPQ-PY-EEIPIYL, identified by the CAS number 147612-86-0, is a chemical compound that belongs to a class of materials often utilized in advanced applications such as organic electronics and photonics. While specific details about its physical and chemical properties may not be widely documented, compounds of this nature typically exhibit characteristics such as good thermal stability, solubility in organic solvents, and the ability to form thin films. They may also possess interesting optical properties, making them suitable for use in light-emitting devices or solar cells. The molecular structure often includes functional groups that enhance electron mobility or facilitate charge transport, which are critical for their performance in electronic applications. Additionally, the compound may be synthesized through various organic reactions, allowing for modifications to tailor its properties for specific uses. As with many specialized chemicals, safety data sheets and handling guidelines should be consulted to ensure safe usage and compliance with regulatory standards.

Formula: C₆₆H₉₇N₁₂O₂₄P

Synonyms:

• YEEI PEPTIDE
• H-GLU-PRO-GLN-TYR(H2PO3)-GLU-GLU-ILE-PRO-ILE-TYR-LEU-OH
• GLU-PRO-GLN-PTYR-GLU-GLU-ILE-PRO-ILE-TYR-LEU
• YEEI Peptide, Phosphorylated trifluoroacetate salt
• H-GLU-PRO-GLN-TYR(PO3H2)-GLU-GLU-ILE-PRO-ILE-TYR-LEU-OH
• L-Leucine, L-α-glutamyl-L-prolyl-L-glutaminyl-O-phosphono-L-tyrosyl-L-α-glutamyl-L-α-glutamyl-L-isoleucyl-L-prolyl-L-isoleucyl-L-tyrosyl-
• SH2 DOMAIN LIGAND (2)
• (pY)EEI
• GLU-PRO-GLN-TYR(PO3H2)-GLU-GLU-ILE-PRO-ILE-TYR-LEU
• H-GLU-PRO-GLN-PTYR-GLU-GLU-ILE-PRO-ILE-TYR-LEU-OH
• EPQ-PY-EEIPIYL*

H-Glu-Pro-Gln-Tyr(PO3H2)-Glu-Glu-Ile-Pro-Ile-Tyr-Leu-OH

CAS: 147612-86-0

The target of H-Glu-Pro-Gln-Tyr(PO3H2)-Glu-Glu-Ile-Pro-Ile-Tyr-Leu is the phosphotyrosine residue in tyrosine kinase. This compound has been shown to inhibit the proliferation of cells that express this type of receptor and induce apoptosis. The x-ray structures of ligand binding to the receptor show a hydrogen bond network with the hydroxyl group at position 2, which is believed to be important for binding activity. The molecular modeling studies confirm that this interaction is energetically favorable, with a ΔΔG = -6.5 kcal/mol. H-Glu-Pro-Gln-Tyr(PO3H2)-Glu-Glu-Ile-(OH) has also been found to have antiosteoporotic properties when administered orally in rats.

Formula: C₆₆H₉₇N₁₂O₂₄P

Purity: Min. 95%

Molecular weight: 1,473.52 g/mol

Ref: 3D-FG110365