class name | count |
---|---|
asterids | 36 |
rosids | 7 |
class name | count |
---|---|
Apiaceae | 34 |
Moraceae | 5 |
Rutaceae | 2 |
Asteraceae | 2 |
br08003 Category | # of metabolite |
---|---|
Furanocoumarins | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Furanocoumarins | C09141 | C00002453 |
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 |
---|---|---|---|---|---|---|
C00002453
![]() |
Byakangelicin
/ (+)-Byakangelicin |
CHEMBL508648
|
C434685
|
5 / 2 / 0 |
![]() |
|
C00019845
![]() |
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-5-methoxycoumarin
|
CHEMBL1574904
|
8 / 9 / 7 |
![]() |
||
C00019846
![]() |
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-6-methoxycoumarin
|
![]() |
||||
C00029597
![]() |
8-(3-Chloro-2-hydroxy-3-methylbutoxy)psoralen
/ (+)-8-(3-Chloro-2-hydroxy-3-methylbutoxy)psoralen |
![]() |
||||
C00030905
![]() |
Oxypeucedanin hydrate
/ (+)-Oxypeucedanin hydrate |
CHEMBL454060
CHEMBL1438253 |
13 / 5 / 8 |
![]() |
||
C00032665
![]() |
5-O-(3-Chloro-2-hydroxy-3-methylbutyl)-8-methoxypsoralen
|
![]() |
||||
C00033364
![]() |
Saxalin
|
![]() |
||||
C00035023
![]() |
5-Methoxy-3-(3-methyl-2,3-dihydroxybutyl)psoralen
/ (-)-5-Methoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen |
![]() |
||||
C00035717
![]() |
(+)-Oxypeucedanin
/ Oxypeucedanin hydrate |
CHEMBL454060
CHEMBL1438253 |
13 / 5 / 8 |
![]() |
||
C00036590
![]() |
5,8-Dimethoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen
/ (-)-5,8-Dimethoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen |
![]() |
||||
C00036599
![]() |
5-Methoxy-8-(1,1-dimethyl-2,3-dihydroxypropyl)-psoralen
/ (+)-5-Methoxy-8-(1,1-dimethyl-2,3-dihydroxypropyl)-psoralen |
![]() |
||||
C00036625
![]() |
6-Methoxy-5-(3-methyl-2,3-dihydroxybutyl)-angelicin
|
![]() |
||||
C00037262
![]() |
Heraclenol
|
CHEMBL1173444
|
C087805
|
3 / 0 / 0 |
![]() |
|
C00037677
![]() |
Pranferol
/ (-)-Pranferol |
C042677
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P56817 | Beta-secretase 1 | A1A | C00002453 C00030905 C00035717 C00037262 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002453 C00019845 C00030905 C00035717 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00019845 C00030905 C00035717 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00019845 C00030905 C00035717 | 2 / 2 |
O75496 | Geminin | Unclassified protein | C00030905 C00035717 C00037262 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00019845 C00030905 C00035717 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00019845 C00030905 C00035717 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00019845 C00030905 C00035717 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00030905 C00035717 | 1 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00030905 C00035717 | 1 / 4 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00030905 C00035717 | 0 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00030905 C00035717 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00030905 C00035717 | 1 / 1 |
P04062 | Glucosylceramidase | Enzyme | C00019845 | 6 / 4 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00037262 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002453 | 1 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002453 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002453 | 1 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00019845 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#301500 | Fabry disease |
P06280
|
#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
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#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)
|
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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|