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103425-21-4

H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2 is a sequence of amino acids that form the backbone of a specific protein in the human body. The sequence begins with a hydrogen atom (H) and ends with an amide group (NH2), with the amino acids Alanine (ALA), Lysine (LYS), Phenylalanine (PHE), Aspartic Acid (ASP), Tyrosine (TYR), Glycine (GLY), Leucine (LEU), and Methionine (MET) in between. The precise order of these amino acids is crucial, as it determines the protein's function and behavior, enabling a wide range of biological processes such as digestion, immune response, oxygen transport, and neural communication.

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  • 103425-21-4 Structure

  • Basic information

    1. Product Name: H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2
    2. Synonyms: SHARK SUBSTANCE P RELATED PEPTIDE;SCY 1;SCYLIORHININ I;SCYLIORHININ I AMIDE (DOGFISH);ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2;AKFDKFYGLM;H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2;H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-OH
    3. CAS NO:103425-21-4
    4. Molecular Formula: C59H87N13O13S
    5. Molecular Weight: 1218.47
    6. EINECS: N/A
    7. Product Categories: peptide
    8. Mol File: 103425-21-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1590.2 °C at 760 mmHg
    3. Flash Point: 915.5 °C
    4. Appearance: /
    5. Density: 1.264 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.585
    8. Storage Temp.: -15°C
    9. Solubility: N/A
    10. CAS DataBase Reference: H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2(CAS DataBase Reference)
    11. NIST Chemistry Reference: H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2(103425-21-4)
    12. EPA Substance Registry System: H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2(103425-21-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103425-21-4(Hazardous Substances Data)

103425-21-4 Usage

Uses

Used in Pharmaceutical Industry:
H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2 is used as a therapeutic agent for targeting specific diseases and conditions. The unique sequence of amino acids allows for the development of protein-based drugs that can modulate biological pathways, treat genetic disorders, or enhance the body's natural healing processes.
Used in Nutritional Supplements:
H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2 is used as a dietary supplement to support overall health and well-being. The specific amino acid composition can provide essential nutrients that may be lacking in some individuals' diets, promoting muscle growth, immune function, and cognitive health.
Used in Cosmetics Industry:
H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2 is used as an active ingredient in skincare products for its potential anti-aging and skin-repairing properties. The amino acid sequence may contribute to collagen production, skin elasticity, and the reduction of wrinkles and fine lines.
Used in Research and Development:
H-ALA-LYS-PHE-ASP-LYS-PHE-TYR-GLY-LEU-MET-NH2 is used as a research tool for studying protein structure, function, and interactions with other molecules. Understanding the properties of this specific amino acid sequence can provide insights into the development of new drugs, therapies, and diagnostic tools for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 103425-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,2 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103425-21:
(8*1)+(7*0)+(6*3)+(5*4)+(4*2)+(3*5)+(2*2)+(1*1)=74
74 % 10 = 4
So 103425-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C59H87N13O13S/c1-35(2)29-44(56(82)66-41(51(63)77)25-28-86-4)65-49(74)34-64-53(79)45(32-39-21-23-40(73)24-22-39)69-57(83)46(30-37-15-7-5-8-16-37)71-55(81)43(20-12-14-27-61)68-59(85)48(33-50(75)76)72-58(84)47(31-38-17-9-6-10-18-38)70-54(80)42(19-11-13-26-60)67-52(78)36(3)62/h5-10,15-18,21-24,35-36,41-48,73H,11-14,19-20,25-34,60-62H2,1-4H3,(H2,63,77)(H,64,79)(H,65,74)(H,66,82)(H,67,78)(H,68,85)(H,69,83)(H,70,80)(H,71,81)(H,72,84)(H,75,76)/t36-,41-,42-,43-,44-,45-,46-,47-,48-/m0/s1

103425-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Scyliorhinin I, Scy I: Shark Substance P Related Peptide,AKFDKFYGLM

1.2 Other means of identification

Product number -
Other names AKFDKFYGLM

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:103425-21-4 SDS

103425-21-4Upstream product

103425-21-4Downstream Products

103425-21-4Relevant articles and documents

A New Class of Amino Protecting Group Removable by Reductive Acidolysis: the 4-Methylsulphinylbenzyloxycarbonyl (Msz) Group

Kiso, Yoshiaki,Kimura, Tooru,Yoshida, Makoto,Shimokura, Masanori,Akaji, Kenichi,Mimoto, Tsutomu

, p. 1511 - 1513 (2007/10/02)

A safety-catch type of amino protecting group, the 4-methylsulphinylbenzyloxycarbonyl (Msz) group is stable under both acidic and basic conditions, but can be smoothly removed by a one-pot reaction involving reductive acidolysis using tetrachlorosilane-tr

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