Page last updated: 2024-11-08

sq 24798

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

Description

2-mercaptomethyl-5-guanidinopentanoic acid: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID194328
CHEMBL ID236822
SCHEMBL ID5415499
MeSH IDM0091153

Synonyms (18)

Synonym
5-carbamimidamido-2-(sulfanylmethyl)pentanoic acid
2-mercaptomethyl-5-guanidinopentanoic acid
5-guanidino-2-(mercaptomethyl)pentanoic acid
(+/-)-5-guanidino-2-(mercaptomethyl)pentanoic acid
bdbm50201438
69734-02-7
CHEMBL236822 ,
sq-24798
5-(diaminomethylideneamino)-2-(sulfanylmethyl)pentanoic acid
sq-24,798
sq 24798
sq 24,798
SCHEMBL5415499
gtpl8656
70873-80-2
AKOS030556047
DTXSID40989901
Q27088854
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carboxypeptidase BSus scrofa (pig)IC50 (µMol)0.01000.01000.01000.0100AID305879
Carboxypeptidase BSus scrofa (pig)Ki0.00040.00040.00040.0004AID304049
Carboxypeptidase N catalytic chainHomo sapiens (human)IC50 (µMol)0.00200.00202.70105.4000AID305880
Carboxypeptidase N catalytic chainHomo sapiens (human)Ki0.00200.00200.00200.0020AID304052
Carboxypeptidase B2Homo sapiens (human)IC50 (µMol)0.00800.00150.54291.8000AID305878
Carboxypeptidase B2Homo sapiens (human)Ki0.00400.00400.22700.4500AID304051
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (15)

Processvia Protein(s)Taxonomy
bradykinin catabolic processCarboxypeptidase N catalytic chainHomo sapiens (human)
protein catabolic processCarboxypeptidase N catalytic chainHomo sapiens (human)
response to glucocorticoidCarboxypeptidase N catalytic chainHomo sapiens (human)
peptide metabolic processCarboxypeptidase N catalytic chainHomo sapiens (human)
protein processingCarboxypeptidase N catalytic chainHomo sapiens (human)
positive regulation of extracellular matrix constituent secretionCarboxypeptidase B2Homo sapiens (human)
blood coagulationCarboxypeptidase B2Homo sapiens (human)
response to xenobiotic stimulusCarboxypeptidase B2Homo sapiens (human)
negative regulation of plasminogen activationCarboxypeptidase B2Homo sapiens (human)
protein catabolic processCarboxypeptidase B2Homo sapiens (human)
negative regulation of fibrinolysisCarboxypeptidase B2Homo sapiens (human)
cellular response to glucose stimulusCarboxypeptidase B2Homo sapiens (human)
liver regenerationCarboxypeptidase B2Homo sapiens (human)
negative regulation of hepatocyte proliferationCarboxypeptidase B2Homo sapiens (human)
proteolysisCarboxypeptidase B2Homo sapiens (human)
fibrinolysisCarboxypeptidase B2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (3)

Processvia Protein(s)Taxonomy
protein bindingCarboxypeptidase N catalytic chainHomo sapiens (human)
zinc ion bindingCarboxypeptidase N catalytic chainHomo sapiens (human)
metallocarboxypeptidase activityCarboxypeptidase N catalytic chainHomo sapiens (human)
zinc ion bindingCarboxypeptidase B2Homo sapiens (human)
metallocarboxypeptidase activityCarboxypeptidase B2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (3)

Processvia Protein(s)Taxonomy
extracellular regionCarboxypeptidase N catalytic chainHomo sapiens (human)
extracellular spaceCarboxypeptidase N catalytic chainHomo sapiens (human)
extracellular regionCarboxypeptidase B2Homo sapiens (human)
extracellular exosomeCarboxypeptidase B2Homo sapiens (human)
extracellular spaceCarboxypeptidase B2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (9)

Assay IDTitleYearJournalArticle
AID305880Inhibition of human carboxypeptidase N2007Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
3-Mercaptopropionic acids as efficacious inhibitors of activated thrombin activatable fibrinolysis inhibitor (TAFIa).
AID304050Selectivity for porcine pancreatic carboxypeptidase B over bovine pancreatic carboxypeptidase A2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
AID304049Inhibition of porcine pancreatic carboxypeptidase B2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
AID304052Inhibition of human plasma carboxypeptidase N2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
AID305878Inhibition of human activated thrombin activatable fibrinolysis inhibitor2007Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
3-Mercaptopropionic acids as efficacious inhibitors of activated thrombin activatable fibrinolysis inhibitor (TAFIa).
AID305879Inhibition of porcine pancreatic carboxypeptidase B2007Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
3-Mercaptopropionic acids as efficacious inhibitors of activated thrombin activatable fibrinolysis inhibitor (TAFIa).
AID304051Inhibition of human TAFIa2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
AID1345703Human Carboxypeptidase B2 (plasma) (M14: Carboxypeptidase A)2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
AID1345390Human Carboxypeptidase N, polypeptide 1 (M14: Carboxypeptidase A)2007Journal of medicinal chemistry, Nov-29, Volume: 50, Issue:24
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
[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-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)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: 12.34

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 Index12.34 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.14 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.34)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]