class name | count |
---|---|
asterids | 33 |
rosids | 31 |
Magnoliophyta | 1 |
Spermatophyta | 1 |
Embryophyta | 1 |
class name | count |
---|---|
Asteraceae
![]() |
12 |
Fabaceae
![]() |
11 |
Apiaceae
![]() |
5 |
Oleaceae
![]() |
4 |
Solanaceae
![]() |
3 |
Hippocastanaceae
![]() |
3 |
Moraceae
![]() |
3 |
Rutaceae
![]() |
3 |
Caprifoliaceae
![]() |
2 |
Rosaceae
![]() |
2 |
Brassicaceae
![]() |
2 |
Thymelaeaceae
![]() |
2 |
Cannabaceae
![]() |
1 |
Aceraceae
![]() |
1 |
Euphorbiaceae
![]() |
1 |
Araliaceae
![]() |
1 |
Apocynaceae
![]() |
1 |
Malvaceae
![]() |
1 |
Anacardiaceae
![]() |
1 |
Gentianaceae
![]() |
1 |
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 |
---|---|---|---|---|---|---|
C00002458
![]() |
Cichoriin
|
C410941
|
![]() |
|||
C00002472
![]() |
Esculin
|
CHEMBL359043
CHEMBL482581 CHEMBL1434042 CHEMBL1515174 CHEMBL1536019 CHEMBL1619714 CHEMBL1624854 |
D004929
|
22 / 18 / 24 | 0 / 1 |
![]() |
C00002474
![]() |
Fraxin
|
CHEMBL293864
|
C080614
|
11 / 3 / 5 |
![]() |
|
C00002500
![]() |
Scopolin
|
CHEMBL225024
|
C417572
|
7 / 3 / 4 |
![]() |
|
C00019796
![]() |
Bergaptol-O-beta-D-glucopyranoside
|
C067416
|
![]() |
|||
C00019835
![]() |
(-)-2,3-Dihydro-9-O-beta-glucosyloxy-2-isopropenyl-7H-furo[3,2-g][1]benzopyran-7-one
|
![]() |
||||
C00019844
![]() |
6,7-Dihydroxy-5-methoxycoumarin 6-beta-D-glucopyranoside
|
![]() |
||||
C00019957
![]() |
5-Methoxy-8-O-beta-D-glucosyloxy-psoralen
|
![]() |
||||
C00030984
![]() |
Phellodenol G
|
![]() |
||||
C00030985
![]() |
Phellodenol H
|
![]() |
||||
C00032165
![]() |
Skimmin
/ (-)-Skimmin |
CHEMBL526377
|
![]() |
|||
C00037003
![]() |
Daphnin
|
CHEMBL1879316
|
3 / 2 / 3 |
![]() |
||
C00044063
![]() |
Gerberinside
/ 4-Hydroxy-5-methylcoumarin 4-O-beta-D-glucopyranoside |
C058371
|
![]() |
|||
C00047445
![]() |
Euoniside
/ (+)-Euoniside |
![]() |
||||
C00047500
![]() |
Mandshurin
|
![]() |
||||
C00047677
![]() |
5-Hydroxy-6-methoxy-7-O-beta-D-glucosylcoumarin
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75496 | Geminin | Unclassified protein | C00002472 C00002474 C00037003 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002472 C00002474 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00002474 C00002500 | 0 / 0 |
P43166 | Carbonic anhydrase 7 | Lyase | C00002474 C00002500 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00002474 C00002500 | 0 / 1 |
O43570 | Carbonic anhydrase 12 | Lyase | C00002474 C00002500 | 1 / 2 |
P00918 | Carbonic anhydrase 2 | Lyase | C00002474 C00002500 | 1 / 2 |
Q8N1Q1 | Carbonic anhydrase 13 | Lyase | C00002474 C00002500 | 0 / 0 |
P42226 | Signal transducer and activator of transcription 6 | Unclassified protein | C00002472 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002472 | 0 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | C00037003 | 2 / 3 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002472 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002472 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002472 | 1 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002472 | 1 / 1 |
P04062 | Glucosylceramidase | Enzyme | C00002472 | 6 / 4 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00002472 | 0 / 3 |
P29466 | Caspase-1 | C14 | C00002472 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00037003 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002472 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00002472 | 1 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002472 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00002474 | 1 / 1 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002472 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002472 | 2 / 2 |
P22303 | Acetylcholinesterase | Hydrolase | C00002500 | 1 / 0 |
P55210 | Caspase-7 | C14 | C00002472 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002472 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002472 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002474 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002472 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002472 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002472 | 1 / 2 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002474 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#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
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(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)
|