Metabolite

KNApSAcK Entry

id C00001387
Name L-Pipecolic acid
CAS RN 535-75-1
Standard InChI InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
Standard InChI (Main Layer) InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)

Cluster

Phytochemical cluster No. 1
KCF-S cluster No. 1523

Link

ChEMBL

By standard InChI CHEMBL322883
By standard InChI Main Layer CHEMBL308408 CHEMBL322883 CHEMBL1231898

KEGG

By LinkDB C00408

CTD

By CAS RN C031345

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Fabaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Phaseolus vulgaris 3885 Fabaceae rosids Viridiplantae

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P35354 Prostaglandin G/H synthase 2 Oxidoreductase CHEMBL308408 CHEMBL1014033 (1)
0 / 3
Q9P0Z9 Peroxisomal sarcosine oxidase Enzyme CHEMBL308408 CHEMBL322883 CHEMBL700838 (1) CHEMBL700620 (1)
CHEMBL878698 (1) CHEMBL700621 (1)
0 / 0
Q7Z2H8 Proton-coupled amino acid transporter 1 Unclassified protein CHEMBL322883 CHEMBL1231898 CHEMBL1919336 (4)
0 / 0

CTD interaction (2)

compound gene gene name gene description interaction interaction type form reference
pmid
C031345 51268 PIPOX
LPIPOX
pipecolic acid oxidase (EC:1.5.3.1 1.5.3.7) PIPOX protein results in increased oxidation of and results in increased degradation of pipecolic acid increases degradation
/ increases oxidation
protein 10642506
C031345 51268 PIPOX
LPIPOX
pipecolic acid oxidase (EC:1.5.3.1 1.5.3.7) PIPOX protein results in increased oxidation of pipecolic acid increases oxidation
protein 10772957

Related Disease

Diseases related to proteins in ChEMBL interactions

KEGG DISEASE (3)

KEGG disease name UniProt
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)

Diseases related to CTD interactions

1 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D018901 C031345 Peroxisomal Disorders marker/mechanism
10642506