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CAS

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23067-32-5

H-GLY-TRP-GLY-OH is a peptide composed of the amino acids glycine (GLY) and tryptophan (TRP), which are essential for various biological processes in the body. Glycine is the simplest amino acid and plays a vital role in protein synthesis and the production of important molecules. Tryptophan is crucial for the synthesis of serotonin and melatonin, neurotransmitters that regulate mood and sleep. H-GLY-TRP-GLY-OH may have potential applications in pharmaceuticals, research, and other fields related to biochemistry and medicine.

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  • 23067-32-5 Structure

  • Basic information

    1. Product Name: H-GLY-TRP-GLY-OH
    2. Synonyms: H-GLY-TRP-GLY-OH;GLYCYL-L-TRYPTOPHYL GLYCINE
    3. CAS NO:23067-32-5
    4. Molecular Formula: C15H18N4O4
    5. Molecular Weight: 318.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23067-32-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -15°C
    8. Solubility: N/A
    9. CAS DataBase Reference: H-GLY-TRP-GLY-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: H-GLY-TRP-GLY-OH(23067-32-5)
    11. EPA Substance Registry System: H-GLY-TRP-GLY-OH(23067-32-5)

  • 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: 23067-32-5(Hazardous Substances Data)

23067-32-5 Usage

Uses

Used in Pharmaceutical Industry:
H-GLY-TRP-GLY-OH is used as a pharmaceutical compound for its potential therapeutic effects. The presence of tryptophan, which is a precursor to serotonin and melatonin, may contribute to the regulation of mood and sleep disorders. Additionally, its potential interactions with other biological molecules could lead to the development of new drugs for various conditions.
Used in Research:
H-GLY-TRP-GLY-OH is used as a research tool in biochemistry and medicine. Its unique structure and composition allow scientists to study the interactions between amino acids and their role in various biological processes. H-GLY-TRP-GLY-OH can be used to investigate the mechanisms of protein synthesis, neurotransmitter production, and other cellular functions.
Used in Biochemical Applications:
H-GLY-TRP-GLY-OH is used in biochemical applications to understand the role of amino acids in the body. Its composition of glycine and tryptophan provides insights into the synthesis of proteins and the production of essential neurotransmitters. This knowledge can be applied to develop new therapies and interventions for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 23067-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23067-32:
(7*2)+(6*3)+(5*0)+(4*6)+(3*7)+(2*3)+(1*2)=85
85 % 10 = 5
So 23067-32-5 is a valid CAS Registry Number.

23067-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]acetyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names Trp-gly-gly

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:23067-32-5 SDS

23067-32-5Upstream product

23067-32-5Downstream Products

23067-32-5Relevant articles and documents

Indole derivatives and a method for production of peptides

-

, (2008/06/13)

An indole group in an amino acid or a peptide can be protected with a group shown by the formula: STR1 wherein R1 and R5 each is hydrogen, methyl or methoxy; R2 and R4 each is hydrogen or methyl; and R3 is methyl or methoxy, and said group may easily be removed without affecting the amino acid or the peptide to be derived from the protected amino acid or peptide. Thus, the present invention is useful in the synthesis of a peptide containing an indole group.

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