Page last updated: 2024-11-04

delta(1)-piperidine-2-carboxylic acid

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

Description

delta(1)-piperidine-2-carboxylic acid: proposed intermediate in pathway of lysine metabolism [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-piperideine-2-carboxylic acid zwitterion : A zwitterion resulting from the transfer of a proton from the carboxy group to the nitrogen of 1-piperideine-2-carboxylic acid [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]

Cross-References

ID SourceID
PubMed CID1194
CHEMBL ID308149
CHEBI ID30912
CHEBI ID77631
SCHEMBL ID4674692
MeSH IDM0111168

Synonyms (27)

Synonym
CHEMBL308149
kw6n8nmv9u ,
delta 1-piperideine-2-carboxylate
unii-kw6n8nmv9u
1-p-2-ca
2-pyridinecarboxylic acid, 3,4,5,6-tetrahydro-
CHEBI:30912 ,
2756-89-0
1-piperideine-2-carboxylic acid
3,4,5,6-tetrahydropyridine-2-carboxylic acid
delta(1)-piperidine-2-carboxylic acid
delta1-piperideine-2-carboxylate ,
C04092 ,
1,2-didehydropiperidine-2-carboxylate
delta1-piperidine-2-carboxylate
AKOS006378980
d-1-piperideine-2-carboxylic acid
2,3,4,5-tetrahydropyridine-6-carboxylic acid
SCHEMBL4674692
delta(1)-piperideine-2-carboxylate
3,4,5,6-tetrahydropyridinium-2-carboxylate
1-piperideine-2-carboxylic acid zwitterion
CHEBI:77631
DTXSID80181962
Q27104170
3,4,5,6-tetrahydro-2-pyridinecarboxylic acid
3,4,5,6-tetrahydropyridine-2-carboxylicacid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
piperidinemonocarboxylic acidAny member of the class of piperidines in which one of the carbons of the piperidine ring is substituted by a carboxy group.
zwitterionA neutral compound having formal unit electrical charges of opposite sign on non-adjacent atoms. Sometimes referred to as inner salts, dipolar ions (a misnomer).
[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]

Pathways (1)

PathwayProteinsCompounds
Biochemical pathways: part I0466

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (28.57)18.7374
1990's3 (42.86)18.2507
2000's2 (28.57)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: 12.31

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 Index12.31 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.39 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.31)

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]