PCIDB

KNApSAcK Metabolite C00001198

Metabolite

KNApSAcK Entry

id C00001198
Name Oxalic acid
CAS RN 144-62-7
Standard InChI InChI=1S/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)
Standard InChI (Main Layer) InChI=1S/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)

Cluster

Phytochemical cluster
KCF-S cluster No. 7540

Link

ChEMBL

By standard InChI CHEMBL146755
By standard InChI Main Layer CHEMBL146755

KEGG

By LinkDB C00209

CTD

By CAS RN D019815

Human Protein / Gene in interaction

2 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein CHEMBL146755 CHEMBL2077322 (1)
0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src CHEMBL146755 CHEMBL823240 (1)
0 / 0

CTD interaction (2)

compound gene gene name gene description interaction interaction type form reference
pmid
D019815 26762 HAVCR1
HAVCR
HAVCR-1
KIM-1
KIM1
TIM
TIM-1
TIM1
TIMD-1
TIMD1
hepatitis A virus cellular receptor 1 Oxalic Acid results in increased expression of HAVCR1 mRNA increases expression
mRNA 22984472
D019815 26762 HAVCR1
HAVCR
HAVCR-1
KIM-1
KIM1
TIM
TIM-1
TIM1
TIMD-1
TIMD1
hepatitis A virus cellular receptor 1 Oxalic Acid results in increased expression of HAVCR1 protein increases expression
protein 22984472

Related Disease

Diseases related to CTD interactions

6 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D058186 D019815 Acute Kidney Injury marker/mechanism
4416261
D006959 D019815 Hyperoxaluria marker/mechanism
22984472
D006960 D019815 Hyperoxaluria, Primary marker/mechanism
22984472
D009397 D019815 Nephrocalcinosis marker/mechanism
4416261
D053040 D019815 Nephrolithiasis marker/mechanism
22984472
D051437 D019815 Renal Insufficiency marker/mechanism
5095537