| 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)
|