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SUC-PHE-GLU-PRO-ILE-PRO-GLU-GLU-TYR(SO3H)-LEU-D-GLU-OH is a peptide composed of a specific sequence of amino acids, including phenylalanine, glutamic acid, proline, isoleucine, tyrosine with a sulfonate group, leucine, and D-glutamic acid. The presence of the sulfonate group on the tyrosine residue contributes to its unique chemical properties. This peptide is commonly utilized in research and pharmaceuticals for its potential therapeutic effects and for studying the impact of specific peptide sequences on biological systems.

131791-98-5

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131791-98-5 Usage

Uses

Used in Pharmaceutical Research:
SUC-PHE-GLU-PRO-ILE-PRO-GLU-GLU-TYR(SO3H)-LEU-D-GLU-OH is used as a research tool for understanding the interactions between peptides and biological targets. Its unique sequence and the presence of the sulfonate group on tyrosine allow researchers to investigate its binding affinity and specificity, which can be crucial for developing new drugs.
Used in Drug Development:
In the pharmaceutical industry, SUC-PHE-GLU-PRO-ILE-PRO-GLU-GLU-TYR(SO3H)-LEU-D-GLU-OH is used as a potential therapeutic agent. Its specific amino acid composition and the sulfonate group may confer biological activities that could be beneficial in treating certain diseases or conditions. The peptide's effects are being studied for possible applications in medicine.
Used in Biochemical Studies:
SUC-PHE-GLU-PRO-ILE-PRO-GLU-GLU-TYR(SO3H)-LEU-D-GLU-OH serves as a subject in biochemical research to explore the mechanisms of peptide-protein interactions, enzymatic activities, and other cellular processes. The peptide's structure provides insights into how specific sequences can modulate biological functions.
Used in Diagnostics:
This peptide may also be employed in the development of diagnostic tools, where its binding properties can be leveraged to detect or measure the presence of specific biological molecules, offering a method for disease monitoring or therapeutic response evaluation.

Check Digit Verification of cas no

The CAS Registry Mumber 131791-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,9 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131791-98:
(8*1)+(7*3)+(6*1)+(5*7)+(4*9)+(3*1)+(2*9)+(1*8)=135
135 % 10 = 5
So 131791-98-5 is a valid CAS Registry Number.

131791-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Suc-Phe-Glu-Pro-Ile-Pro-Glu-Glu-Tyr(OSO3H)-Leu-D-Glu-OH

1.2 Other means of identification

Product number -
Other names Succinyl-(Pro58,D-Glu65)-Hirudin (56-65) (sulfated)

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:131791-98-5 SDS

131791-98-5Downstream Products

131791-98-5Relevant academic research and scientific papers

Positional Effects of Sulfation in Hirudin and Hirudin PA Related Anticoagulant Peptides

Payne, Marguerite H.,Krstenansky, John L.,Yates, Mark T.,Mao, Simon J. T.

, p. 1184 - 1187 (2007/10/02)

C-Terminal fragment analogues of the leech protein hirudin or the related protein hirudin PA block thrombin's cleavage of fibrinogen.Three series of synthetic peptides were synthesized to study the effects of sulfation in hirudin-derived peptides.Potency

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