class name | count |
---|---|
rosids | 16 |
asterids | 8 |
Liliopsida | 5 |
Magnoliophyta | 3 |
eudicotyledons | 2 |
class name | count |
---|---|
Rutaceae
![]() |
5 |
Celastraceae
![]() |
3 |
Moraceae
![]() |
2 |
Euphorbiaceae
![]() |
2 |
Fabaceae
![]() |
2 |
Zingiberaceae
![]() |
2 |
Orchidaceae
![]() |
2 |
Asteraceae
![]() |
2 |
Magnoliaceae
![]() |
1 |
Myrtaceae
![]() |
1 |
Posidoniaceae
![]() |
1 |
Acanthaceae
![]() |
1 |
Gesneriaceae
![]() |
1 |
Lauraceae
![]() |
1 |
Hydrangeaceae
![]() |
1 |
Piperaceae
![]() |
1 |
Apiaceae
![]() |
1 |
Viscaceae
![]() |
1 |
Brassicaceae
![]() |
1 |
Rubiaceae
![]() |
1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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
![]() |
Antiarol
/ 3,4,5-Trimethoxyphenol |
CHEMBL1319047
|
4 / 6 / 7 |
![]() |
||
C00002646
![]() |
2,6-Dimethoxyphenol
|
CHEMBL109652
|
C010120
|
3 / 5 / 2 |
![]() |
|
C00007558
![]() |
Syringaldehyde
/ 4-Hydroxy-3,5-dimethoxybenzaldehyde |
CHEMBL225303
|
C069665
|
![]() |
||
C00032269
![]() |
Syringol
|
CHEMBL109652
|
C010120
|
3 / 5 / 2 |
![]() |
|
C00035473
![]() |
2,4,6-Trimethoxyphenol
|
CHEMBL225314
|
![]() |
|||
C00035489
![]() |
3,4-Dimethoxyphenol
|
![]() |
||||
C00035789
![]() |
2,6-Dimethoxyhydroquinone
|
![]() |
||||
C00036456
![]() |
2,4,5-Trimethoxybenzaldehyde
/ 3,4,6-Trimethoxybenzaldehyde |
CHEMBL1164301
|
C034031
|
9 / 14 / 7 |
![]() |
|
C00042023
![]() |
1,2,3-Trimethoxybenzene
|
C091694
|
![]() |
|||
C00042138
![]() |
4-Hydroxy-2,3-dimethoxybenzaldehyde
|
CHEMBL454267
|
![]() |
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 |
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 | 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)
|