Metabolite

KNApSAcK Entry

id C00029479
Name Veratric acid / 3,4-dimethoxybenzoic acid
CAS RN 93-07-2
Standard InChI InChI=1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)
Standard InChI (Main Layer) InChI=1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)

Cluster

Phytochemical cluster
KCF-S cluster No. 1073

Link

ChEMBL

By standard InChI CHEMBL118903
By standard InChI Main Layer CHEMBL118903

KEGG

By LinkDB

CTD

By CAS RN C009333

Human Protein / Gene in interaction

10 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P43166 Carbonic anhydrase 7 Lyase CHEMBL118903 CHEMBL2340802 (1)
0 / 0
P00918 Carbonic anhydrase 2 Lyase CHEMBL118903 CHEMBL1670882 (1)
1 / 2
P23280 Carbonic anhydrase 6 Lyase CHEMBL118903 CHEMBL2045824 (1)
0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase CHEMBL118903 CHEMBL2340799 (1)
0 / 0
O43570 Carbonic anhydrase 12 Lyase CHEMBL118903 CHEMBL1670884 (1)
1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL118903 CHEMBL1794584 (1)
2 / 0
P00915 Carbonic anhydrase 1 Lyase CHEMBL118903 CHEMBL1670881 (1)
0 / 0
Q16790 Carbonic anhydrase 9 Lyase CHEMBL118903 CHEMBL1670883 (1)
0 / 1
P51580 Thiopurine S-methyltransferase Enzyme CHEMBL118903 CHEMBL814140 (1)
1 / 1
P22748 Carbonic anhydrase 4 Lyase CHEMBL118903 CHEMBL2045823 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#143860 Hyperchlorhidrosis, isolated O43570
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#600852 Retinitis pigmentosa 17; rp17 P22748
#610460 Thiopurine s-methyltransferase deficiency P51580

KEGG DISEASE (6)

KEGG disease name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)