Page last updated: 2024-11-07

glycyl-histidyl-glycine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Glycyl-histidyl-glycine (GH3) is a tripeptide composed of the amino acids glycine and histidine. It has been studied for its potential therapeutic effects in various conditions, including its role in wound healing, its antioxidant activity, and its potential to improve cognitive function. GH3 is a naturally occurring peptide found in various tissues and organs and is known to be involved in cell signaling and communication. Its synthesis can be achieved through various methods, including enzymatic synthesis and chemical synthesis. Research on GH3 aims to understand its mechanisms of action and explore its potential therapeutic applications. The study of GH3 is driven by its unique properties and its potential to offer novel therapeutic strategies.'

Cross-References

ID SourceID
PubMed CID97396
CHEMBL ID1221712
CHEBI ID163724
SCHEMBL ID259179
MeSH IDM0257869

Synonyms (16)

Synonym
CHEMBL1221712
7758-33-0
gly-his-gly
2-[[(2s)-2-[(2-aminoacetyl)amino]-3-(1h-imidazol-5-yl)propanoyl]amino]acetic acid
CHEBI:163724
glycyl-l-histidylglycine
glycyl-histidyl-glycine
nsc 120776
glycine, n-(n-glycyl-l-histidyl)-
n-(n-glycyl-l-histidyl)glycine
glycine,glycyl-l-histidyl-
SCHEMBL259179
h-gly-his-gly-oh
glycyl-l-histidyl-glycine
mfcd00022369
(s)-2-(2-(2-aminoacetamido)-3-(1h-imidazol-4-yl)propanamido)acetic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
oligopeptideA peptide containing a relatively small number of amino acids.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID500816Inhibition of nitrogen-starved wild type sigma1278b yeast Gap1-mediated amino acid uptake at 5 mM after 60 secs relative to L-citrulline2009Nature chemical biology, Jan, Volume: 5, Issue:1
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's2 (40.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.66

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.66 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.73 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.66)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (16.67%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]