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H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 is a peptide composed of 20 amino acids, including alanine, arginine, leucine, aspartic acid, valine, serine, glutamic acid, phenylalanine, lysine, tryptophan, asparagine, and a C-terminal amide group. This sequence of amino acids may have potential therapeutic applications or be utilized in laboratory experiments related to protein function and structure.

150238-87-2

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150238-87-2 Usage

Uses

Used in Pharmaceutical Applications:
H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 is used as a research tool for understanding the structure and function of proteins, as well as for the development of new therapeutic agents.
Used in Laboratory Experiments:
In the field of molecular biology and biochemistry, H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 serves as a model peptide for studying protein interactions, folding, and stability.
Used in Drug Discovery:
H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 is used as a lead compound in drug discovery, potentially targeting specific biological pathways or receptors for the treatment of various diseases.
Used in Peptide Synthesis:
In the chemical synthesis of peptides, H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 can be employed as a template or building block for the creation of novel peptide-based drugs or diagnostic agents.
Used in Cosmetics Industry:
H-ALA-ARG-LEU-ASP-VAL-ALA-SER-GLU-PHE-ARG-LYS-LYS-TRP-ASN-LYS-TRP-ALA-LEU-SER-ARG-NH2 may be utilized in the development of cosmetic products, where peptides are known to have potential benefits for skin health and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 150238-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,2,3 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150238-87:
(8*1)+(7*5)+(6*0)+(5*2)+(4*3)+(3*8)+(2*8)+(1*7)=112
112 % 10 = 2
So 150238-87-2 is a valid CAS Registry Number.

150238-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name PAMP

1.2 Other means of identification

Product number -
Other names Proadrenomedullin Fragment 1-20 human

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:150238-87-2 SDS

150238-87-2Downstream Products

150238-87-2Relevant academic research and scientific papers

Boosting Fmoc Solid-Phase Peptide Synthesis by Ultrasonication

Merlino, Francesco,Tomassi, Stefano,Yousif, Ali M.,Messere, Anna,Marinelli, Luciana,Grieco, Paolo,Novellino, Ettore,Cosconati, Sandro,Di Maro, Salvatore

supporting information, p. 6378 - 6382 (2019/09/06)

We investigated the ultrasonication-mediated effects on the Fmoc-based solid-phase peptide synthesis (SPPS). Our study culminated with the development of an ultrasound-assisted strategy (US-SPPS) that allowed for the synthesis of different biologically active peptides (up to 44-mer), with a remarkable savings of material and reaction time. Noteworthy, ultrasonic irradiation did not exacerbate the main side reactions and improved the synthesis of peptides endowed with "difficult sequences", placing the US-SPPS among the current high-efficient peptide synthetic strategies.

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