class name | count |
---|---|
asterids | 28 |
rosids | 3 |
eudicotyledons | 1 |
class name | count |
---|---|
Apiaceae | 28 |
Rutaceae | 2 |
Crassulaceae | 1 |
Moraceae | 1 |
br08003 Category | # of metabolite |
---|---|
Furanocoumarins | 2 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Furanocoumarins | C09279 | C00002486 |
Furanocoumarins | C09309 | C00002496 |
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 |
---|---|---|---|---|---|---|
C00002486
![]() |
Nodakenin
|
CHEMBL459825
|
C471579
|
11 / 8 / 6 |
![]() |
|
C00002496
![]() |
Rutarin
|
![]() |
||||
C00019822
![]() |
Columbianetin-beta-D-glucopyranoside
|
C062747
|
![]() |
|||
C00019919
![]() |
(2R)-2'-Hydroxymarmesin 2'-O-beta-D-glucopyranoside
|
![]() |
||||
C00020008
![]() |
Praeroside II
/ (-)-Praeroside II |
![]() |
||||
C00020009
![]() |
Praeroside III
|
![]() |
||||
C00020010
![]() |
Praeroside IV
|
CHEMBL1159445
|
2 / 0 / 0 |
![]() |
||
C00020028
![]() |
Tortuoside
|
![]() |
||||
C00020036
![]() |
Praeroside V
|
![]() |
||||
C00029680
![]() |
Ammajin
/ Marmesinin / (-)-Marmesinin |
CHEMBL459825
|
11 / 8 / 6 |
![]() |
||
C00031440
![]() |
Yunngnoside A
/ (+)-Yunngnoside A |
![]() |
||||
C00031441
![]() |
Yunngnoside B
/ (+)-Yunngnoside B |
CHEMBL1335374
|
4 / 9 / 5 |
![]() |
||
C00031472
![]() |
(R)-Peucedanol 7-O-beta-D-glucopyranoside
|
CHEMBL1159420
|
2 / 0 / 0 |
![]() |
||
C00031604
![]() |
Apterin
|
CHEMBL1335374
|
4 / 9 / 5 |
![]() |
||
C00035164
![]() |
Turbinatocoumarin
|
![]() |
||||
C00037263
![]() |
Heraclenol 3'-O-beta-D-glucopyranoside
/ (+)-Heraclenol 3'-O-beta-D-glucopyranoside |
![]() |
||||
C00037589
![]() |
Oxypeucedanin hydrate 3'-O-beta-glucopyranoside
|
![]() |
||||
C00042467
![]() |
Devenyoside A
/ (-)-Devenyoside A |
![]() |
||||
C00042468
![]() |
Devenyoside B
/ (-)-Devenyoside B |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002486 C00029680 C00031441 C00031604 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00002486 C00020010 C00029680 C00031472 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002486 C00029680 C00031441 C00031604 | 2 / 2 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002486 C00029680 C00031472 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00002486 C00029680 | 1 / 1 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00031441 C00031604 | 7 / 3 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002486 C00029680 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002486 C00029680 | 2 / 2 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002486 C00029680 | 1 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00031441 C00031604 | 0 / 0 |
P22303 | Acetylcholinesterase | Hydrolase | C00002486 C00029680 | 1 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002486 C00029680 | 1 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002486 C00029680 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00020010 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#301500 | Fabry disease |
P06280
|
#232300 | Glycogen storage disease ii |
P10253
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#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
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H00125 | Fabry disease |
P06280
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(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)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|