Metabolite list (9)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00002674 External link 512 Syringic acid
/ 4-Hydroxy-3,5-dimethoxybenzoic acid
CHEMBL1414
C001945
12 / 3 / 5
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0
C00029476 External link 512 Eudesmic acid
/ Trimethylgallic acid
/ 3,4,5-Trimethoxybenzoic acid
CHEMBL377172
C005854
3 / 2 / 2
C00029479 External link 512 Veratric acid
/ 3,4-dimethoxybenzoic acid
CHEMBL118903
C009333
10 / 6 / 6
C00029502 External link 512 3-Hydroxy-4-methoxybenzoic acid
CHEMBL88700
C045317
2 / 1 / 4
C00034769 External link 512 4-Hydroxy-2-methoxybenzoic acid
C00035926 External link 512 3,4-dimethoxybenzoic acid
CHEMBL118903
C009333
10 / 6 / 6
C00035948 External link 512 4-Ethoxy-3-methoxybenzoic acid
CHEMBL1363623
7 / 12 / 8
C00040794 External link 512 2,6-Dimethoxy-benzoic acid
CHEMBL488609
C472445
6 / 2 / 4

Human Protein / Gene in interactions

28 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9ULX7 Carbonic anhydrase 14 Lyase C00002674 C00029479 C00035926 C00040794 0 / 0
P51580 Thiopurine S-methyltransferase Enzyme C00002682 C00029479 C00029502 C00035926 1 / 1
Q16790 Carbonic anhydrase 9 Lyase C00002674 C00029479 C00035926 C00040794 0 / 1
P00915 Carbonic anhydrase 1 Lyase C00002674 C00029479 C00035926 C00040794 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00002674 C00029479 C00035926 C00040794 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00002674 C00029479 C00035926 C00040794 1 / 2
O43570 Carbonic anhydrase 12 Lyase C00002674 C00029479 C00035926 C00040794 1 / 2
P22748 Carbonic anhydrase 4 Lyase C00002674 C00029479 C00035926 1 / 1
P23280 Carbonic anhydrase 6 Lyase C00002674 C00029479 C00035926 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00029479 C00035926 2 / 0
P15121 Aldose reductase Enzyme C00002674 C00002682 0 / 0
P42858 Huntingtin Unclassified protein C00002682 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00035948 0 / 1
O75496 Geminin Unclassified protein C00029476 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00035948 3 / 2
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00002674 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00035948 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00029476 0 / 0
P51843 Nuclear receptor subfamily 0 group B member 1 Nuclear hormone receptor subfamily 0 group B member 1 C00029476 2 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00035948 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00002674 0 / 0
P03372 Estrogen receptor NR3A1 C00002682 1 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00029502 0 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00035948 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00035948 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00002682 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00002674 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00035948 1 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00002682
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00002682

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

OMIM preferred title UniProt
#300018 46,xy sex reversal 2; srxy2 P51843
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300200 Adrenal hypoplasia, congenital; ahc P51843
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#143100 Huntington disease; hd P42858
#143860 Hyperchlorhidrosis, isolated O43570
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#600852 Retinitis pigmentosa 17; rp17 P22748
#610460 Thiopurine s-methyltransferase deficiency P51580

KEGG DISEASE (21)

KEGG 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)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00552 Glycerol kinase deficiency (GKD) P51843 (related)
H00607 46,XY disorders of sex development (Disorders of gonadal development) P51843 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)