Metabolite

KNApSAcK Entry

id C00007568
Name 3-Hydroxyanthranilic acid
CAS RN 548-93-6
Standard InChI InChI=1S/C7H7NO3/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3,9H,8H2,(H,10,11)
Standard InChI (Main Layer) InChI=1S/C7H7NO3/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3,9H,8H2,(H,10,11)

Cluster

Phytochemical cluster
KCF-S cluster No. 2138

Link

ChEMBL

By standard InChI CHEMBL445304
By standard InChI Main Layer CHEMBL445304

KEGG

By LinkDB C00632

CTD

By CAS RN D015095

Species

Summary

Plant class

class name count

Family

family name count
Micrococcaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Arthrobacter protophormiae 37930 Micrococcaceae Bacteria

Human Protein / Gene in interaction

9 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P11413 Glucose-6-phosphate 1-dehydrogenase Enzyme CHEMBL445304 CHEMBL1737961 (1)
1 / 2
Q15118 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial Pdhk CHEMBL445304 CHEMBL994900 (1) CHEMBL994901 (1)
CHEMBL994902 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL445304 CHEMBL1794483 (1)
0 / 0
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL445304 CHEMBL1737991 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL445304 CHEMBL1738184 (1)
0 / 0
Q9UBT6 DNA polymerase kappa Enzyme CHEMBL445304 CHEMBL1794536 (1)
0 / 0
P10747 T-cell-specific surface glycoprotein CD28 Unclassified protein CHEMBL445304 CHEMBL994898 (1)
0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme CHEMBL445304 CHEMBL1964002 (1)
1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme CHEMBL445304 CHEMBL2114738 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (2)

OMIM preferred title UniProt
#300908 Anemia, nonspherocytic hemolytic, due to g6pd deficiency P11413
#137800 Glioma susceptibility 1; glm1 O75874

KEGG DISEASE (2)

KEGG disease name UniProt
H00101 Other phagocyte defects P11413 (related)
H00668 Anemia due to disorders of glutathione metabolism P11413 (related)

Diseases related to CTD interactions

2 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D010024 D015095 Osteoporosis marker/mechanism
17042918
D012509 D015095 Sarcoma marker/mechanism
6248561