class name | count |
---|---|
rosids | 19 |
asterids | 17 |
class name | count |
---|---|
Rutaceae | 19 |
Apiaceae | 12 |
Asteraceae | 5 |
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 |
---|---|---|---|---|---|---|
C00019788
![]() |
Anisocoumarin H
|
CHEMBL408980
|
10 / 6 / 3 |
![]() |
||
C00019831
![]() |
6,7-Di-(3,3-dimethylallyloxy)-5-hydroxycoumarin
|
![]() |
||||
C00019832
![]() |
6,7-Di-(3,3-dimethylallyloxy)-5-methoxycoumarin
|
![]() |
||||
C00019891
![]() |
(E)-7-(6-Hydroperoxy-3,7-dimethylocta-2,7-dienyloxy)coumarin
|
![]() |
||||
C00019896
![]() |
7-(6R-Hydroxy-3,7-dimethylocta-2,5-dienyl)-7-hydroxycoumarin
|
CHEMBL2346911
|
![]() |
|||
C00020021
![]() |
Schinilenol
|
![]() |
||||
C00020022
![]() |
Schininallylol
|
![]() |
||||
C00029763
![]() |
Auraptene
|
CHEMBL307341
|
C105832
|
28 / 25 / 26 | 3 / 0 |
![]() |
C00030547
![]() |
Isoschinilenol
|
![]() |
||||
C00033590
![]() |
6-Methoxyaurapten
/ 7-O-Geranylscopoletin / 6-Methoxy-7-geranyloxycoumarin |
CHEMBL2346913
|
![]() |
|||
C00033786
![]() |
Diversin
/ Diversine |
![]() |
||||
C00036626
![]() |
6-Methoxy-7-geranyloxy coumarin
|
CHEMBL2346913
|
![]() |
|||
C00036786
![]() |
Auraptenol
|
![]() |
||||
C00037062
![]() |
Diversinin
|
![]() |
||||
C00037141
![]() |
Ferulagol A
|
![]() |
||||
C00037142
![]() |
Ferulagol B
|
![]() |
||||
C00039185
![]() |
Excavatin A
/ (+)-Excavatin A |
![]() |
||||
C00045665
![]() |
Artekeiskeanol A
|
CHEMBL465504
CHEMBL454286 |
![]() |
|||
C00045666
![]() |
Artekeiskeanol B
|
CHEMBL465504
CHEMBL454286 |
![]() |
|||
C00045667
![]() |
Artekeiskeanol C
|
CHEMBL465505
CHEMBL465492 |
![]() |
|||
C00045668
![]() |
Artekeiskeanol D
|
CHEMBL465505
CHEMBL465492 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00019788 C00029763 | 1 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00019788 C00029763 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00019788 C00029763 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00019788 C00029763 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00019788 C00029763 | 2 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00019788 C00029763 | 2 / 2 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00029763 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00029763 | 0 / 0 |
P41145 | Kappa-type opioid receptor | Opioid receptor | C00019788 | 0 / 0 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00029763 | 1 / 4 |
Q9Y253 | DNA polymerase eta | Enzyme | C00029763 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00029763 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00029763 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00029763 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00029763 | 1 / 1 |
Q96RI1 | Bile acid receptor | NR1H4 | C00029763 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00019788 | 0 / 0 |
P56817 | Beta-secretase 1 | A1A | C00029763 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00029763 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00029763 | 2 / 2 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00029763 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00029763 | 0 / 1 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00029763 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00029763 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00019788 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00029763 | 6 / 4 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00029763 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00029763 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00019788 | 1 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00029763 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00029763 | 1 / 4 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00029763 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00029763
|
5743 | PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 | prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) |
C00029763
|
7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A |
C00029763
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#114500 | Colorectal cancer; crc |
P84022
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|