| class name | count |
|---|---|
| rosids | 45 |
| asterids | 3 |
| Liliopsida | 1 |
| class name | count |
|---|---|
| Fabaceae | 23 |
| Moraceae | 20 |
| Cannabaceae | 2 |
| Asteraceae | 2 |
| Apiaceae | 1 |
| Zingiberaceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Chalcones | 1 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Chalcones | C08573 | C00002371 |
| 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 |
|---|---|---|---|---|---|---|
|
C00002371
|
Abyssinone VI
|
CHEMBL508727
|
1 / 0 / 0 |
|
||
|
C00007007
|
Glyinflanin A
|
|
||||
|
C00007010
|
Glyinflanin E
|
|
||||
|
C00007054
|
Spinochalcone A
|
|
||||
|
C00007072
|
Kanzonol C
/ 2',4',4-Trihydroxy-3'-prenylchalcone |
CHEMBL1644933
|
|
|||
|
C00007073
|
4,2',4'-Trihydroxy-3',5'-diprenylchalcone
|
CHEMBL403930
|
|
|||
|
C00007113
|
Antiarone E
|
|
||||
|
C00007115
|
Antiarone D
|
|
||||
|
C00007116
|
Antiarone C
|
|
||||
|
C00007122
|
Flemiwallichin E
|
|
||||
|
C00007124
|
Xanthoangelol
|
CHEMBL494083
CHEMBL457210 |
C068244
|
20 / 30 / 25 | 1 / 0 |
|
|
C00007128
|
3'-Geranyl-2',4',6'-trihydroxychalcone
|
|
||||
|
C00007137
|
Kuwanol D
|
|
||||
|
C00007138
|
Ammothamnidin
|
|
||||
|
C00007139
|
Kushenol D
|
|
||||
|
C00007142
|
5-Deoxyhomoflemingin
|
|
||||
|
C00007148
|
Kuraridin
|
CHEMBL243362
|
3 / 2 / 2 |
|
||
|
C00007149
|
Kuraridinol
|
|
||||
|
C00007151
|
Flemiwallichin C
|
|
||||
|
C00007155
|
Homoflemingin
|
|
||||
|
C00011136
|
Bartericin D
|
|
||||
|
C00011138
|
Angusticornin B
/ 3,5'-di-(2-Hydroxy-3-methylbut-3-enyl)-4,2',4'-trihydroxychalcone |
|
||||
|
C00011140
|
Stipulin
|
CHEMBL1169874
|
|
|||
|
C00011141
|
Bartericin A
|
CHEMBL1169613
|
|
|||
|
C00014441
|
3'-Neryl-2',4',6'-trihydroxychalcone
|
|
||||
|
C00014454
|
Paratocarpin D
/ 3'-Prenyl-3-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone |
|
||||
|
C00014455
|
Paratocarpin E
/ 3-Prenyl-3'-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone |
|
||||
|
C00014457
|
Anthyllin
/ 5-Prenyl-3-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone |
|
||||
|
C00014471
|
3'-Geranylchalconaringenin
/ 3'-Geranyl-4,2',4',6'-tetrahydroxychalcone |
CHEMBL480722
|
|
|||
|
C00014473
|
5'-Prenylxanthohumol
/ 3',5'-Diprenyl-4,2',4'-trihydroxy-6-methoxychalcone |
CHEMBL471777
|
|
|||
|
C00014484
|
3'-Geranyl-3,4,2',4'-tetrahydroxychalcone
|
CHEMBL258707
|
|
|||
|
C00038202
|
2',4'-Dihydroxy-3'-(1''-geranyl)-6'-methoxychalcone
|
CHEMBL255070
|
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00002371 | 0 / 0 |
| P13866 | Sodium/glucose cotransporter 1 | Glucose | C00007148 | 1 / 1 |
| P31639 | Sodium/glucose cotransporter 2 | Glucose | C00007148 | 1 / 1 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00007124 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00007124 | 1 / 1 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00007124 | 1 / 1 |
| P02545 | Prelamin-A/C | Unclassified protein | C00007124 | 11 / 10 |
| P37840 | Alpha-synuclein | Unclassified protein | C00007124 | 4 / 2 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00007124 | 1 / 0 |
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00007148 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00007124 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00007124 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00007124 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00007124 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00007124 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00007124 | 1 / 1 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00007124 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00007124 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00007124 | 4 / 3 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00007124 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00007124 | 1 / 0 |
| O00255 | Menin | Unclassified protein | C00007124 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00007124 | 1 / 2 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00007124 | 1 / 1 |
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00007124
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #127750 | Dementia, lewy body; dlb |
P37840
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #301500 | Fabry disease |
P06280
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #606824 | Glucose/galactose malabsorption; ggm |
P13866
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
| #605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
| #168600 | Parkinson disease, late-onset; pd |
P37840
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #233100 | Renal glucosuria; glys1 |
P31639
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| 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)
|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H01261 | Congenital glucose-galactose malabsorption (GGM) |
P13866
(related)
|
| H01126 | Familial renal glucosuria (FRG) |
P31639
(related)
|
| H00057 | Parkinson's disease (PD) |
P37840
(related)
|
| H00066 | Lewy body dementia (LBD) |
P37840
(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)
|