Page last updated: 2024-12-10

cholecystokinin pentapeptide

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

Description

cholecystokinin pentapeptide: RN given refers to all (L)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID3081446
CHEMBL ID353181
MeSH IDM0140912

Synonyms (13)

Synonym
l-phenylalaninamide, glycyl-l-tryptophyl-l-methionyl-l-alpha-aspartyl-
cholecystokinin pentapeptide
(3s)-3-[[(2s)-2-[[(2s)-2-[(2-aminoacetyl)amino]-3-(1h-indol-3-yl)propanoyl]amino]-4-methylsulfanylbutanoyl]amino]-4-[[(2s)-1-amino-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid
CHEMBL353181
cck-5
18917-24-3
gly-trp-met-asp-phe-nh2
glycyl-tryptophyl-methionyl-aspartyl-phenylalaninamide
DTXSID00172312
gly-trp-met-asp-phe-nh(2)
h-gly-trp-met-asp-phe-nh2
gly(29)-trp(30)-met(31)-asp(32)-phe(33)-nh(2)
(s)-4-(((s)-1-amino-1-oxo-3-phenylpropan-2-yl)amino)-3-((s)-2-((s)-2-(2-aminoacetamido)-3-(1h-indol-3-yl)propanamido)-4-(methylthio)butanamido)-4-oxobutanoic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID169972Compound was evaluated for (in vivo) gastrin like activity measured on perfused rat stomach after intravenous administration1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
Synthesis of potent heptapeptide analogues of cholecystokinin.
AID109526Anticonvulsive potency against picrotoxin induced (6 mg/kg sc) convulsions in mice, first tonic seizure1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
Synthesis of potent heptapeptide analogues of cholecystokinin.
AID109525Anticonvulsive activity against picrotoxin-induced (6 mg/kg sc) convulsions in mice, time of death1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
Synthesis of potent heptapeptide analogues of cholecystokinin.
AID167754Compound was evaluated for cholecystokinin activity measured in isolated rabbit gallbladder strips (in vitro)1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
Synthesis of potent heptapeptide analogues of cholecystokinin.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (40.00)18.7374
1990's3 (30.00)18.2507
2000's3 (30.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.82

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 Index11.82 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.31 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.82)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (10.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other9 (90.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]