Metabolite list (10)

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
C00002637 External link 512 Antiarol
/ 3,4,5-Trimethoxyphenol
CHEMBL1319047
4 / 6 / 7
C00002646 External link 512 2,6-Dimethoxyphenol
CHEMBL109652
C010120
3 / 5 / 2
C00007558 External link 512 Syringaldehyde
/ 4-Hydroxy-3,5-dimethoxybenzaldehyde
CHEMBL225303
C069665
C00032269 External link 512 Syringol
CHEMBL109652
C010120
3 / 5 / 2
C00035473 External link 512 2,4,6-Trimethoxyphenol
CHEMBL225314
C00035489 External link 512 3,4-Dimethoxyphenol
C00035789 External link 512 2,6-Dimethoxyhydroquinone
C00036456 External link 512 2,4,5-Trimethoxybenzaldehyde
/ 3,4,6-Trimethoxybenzaldehyde
CHEMBL1164301
C034031
9 / 14 / 7
C00042023 External link 512 1,2,3-Trimethoxybenzene
C091694
C00042138 External link 512 4-Hydroxy-2,3-dimethoxybenzaldehyde
CHEMBL454267

Human Protein / Gene in interactions

16 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14867 Gamma-aminobutyric acid receptor subunit alpha-1 GABA-A alpha C00002646 C00032269 1 / 1
P47870 Gamma-aminobutyric acid receptor subunit beta-2 GABA-A beta C00002646 C00032269 0 / 0
P18507 Gamma-aminobutyric acid receptor subunit gamma-2 GABA-A gamma C00002646 C00032269 4 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002637 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00036456 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00036456 7 / 3
P11021 78 kDa glucose-regulated protein Unclassified protein C00002637 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00036456 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002637 2 / 3
Q9UNA4 DNA polymerase iota Enzyme C00036456 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002637 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00036456 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00036456 1 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00036456 3 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00036456 3 / 2
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00036456 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#607208 Dravet syndrome P18507
#607681 Epilepsy, childhood absence, susceptibility to, 2; eca2 P18507
#611136 Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 P14867
#600274 Frontotemporal dementia; ftd P10636
#604233 Generalized epilepsy with febrile seizures plus, type 1; gefsp1 P18507
#611277 Generalized epilepsy with febrile seizures plus, type 3; gefsp3 P18507
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (16)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00808 Idiopathic generalized epilepsies (IGEs) P14867 (related)
P18507 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00783 Febrile seizures P18507 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)