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Z-PHE-HIS-LEU-OH is a tetrapeptide consisting of the amino acids phenylalanine, histidine, leucine, and a carboxy-terminal hydroxyl group. It is derived from the N-terminal region of the β-endorphin molecule, an endogenous opioid peptide that functions as a neurotransmitter in the central nervous system. This peptide has potential applications in modulating the body's response to pain and stress, as well as in drug development for pain management.

28458-19-7

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28458-19-7 Usage

Uses

Used in Pharmaceutical Industry:
Z-PHE-HIS-LEU-OH is used as a potential therapeutic agent for pain management due to its ability to modulate the body's response to pain and stress. It is being studied for its potential interactions with opioid receptors and its role in neuronal signaling pathways, which could lead to the development of new drugs for treating pain.
Used in Neurobiological Research:
Z-PHE-HIS-LEU-OH is used as a research tool in the field of neurobiology to investigate the mechanisms of pain perception and stress response. Its interactions with opioid receptors and involvement in neuronal signaling pathways provide valuable insights into the development of novel therapeutic strategies for managing pain and stress-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 28458-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28458-19:
(7*2)+(6*8)+(5*4)+(4*5)+(3*8)+(2*1)+(1*9)=137
137 % 10 = 7
So 28458-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C29H35N5O6/c1-19(2)13-25(28(37)38)33-27(36)24(15-22-16-30-18-31-22)32-26(35)23(14-20-9-5-3-6-10-20)34-29(39)40-17-21-11-7-4-8-12-21/h3-12,16,18-19,23-25H,13-15,17H2,1-2H3,(H,30,31)(H,32,35)(H,33,36)(H,34,39)(H,37,38)

28458-19-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-L-Phe-L-His-L-Leu-OH

1.2 Other means of identification

Product number -
Other names Z-Phe-His-Leu-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28458-19-7 SDS

28458-19-7Downstream Products

28458-19-7Relevant academic research and scientific papers

Mechanism of enantioselective ester cleavage by histidine-containing peptides at a micellar interface. 2. Effect of changing peptide chain length

Cleij, Marco C.,Drenth, Wiendelt,Nolte, Roeland J. M.

, p. 459 - 468 (2007/10/02)

Chiral p-nitrophenyl esters derived from the amino acid phenylalanine are cleaved by various histidine-containing tripeptides and higher oligopeptides as catalysts at a micellar interface.It is assumed that the oligopeptides adopt an internally hydrogen-b

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