| class name | count |
|---|---|
| rosids | 49 |
| Magnoliophyta | 1 |
| class name | count |
|---|---|
| Rutaceae | 48 |
| Notodontidae | 1 |
| Cucurbitaceae | 1 |
| Piperaceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Acridone alkaloids | 4 |
| Quinoline alkaloids | 1 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Acridone alkaloids | C10643 | C00002137 |
| Acridone alkaloids | C10681 | C00002163 |
| Quinoline alkaloids | C10699 | C00002176 |
| Acridone alkaloids | C10722 | C00002186 |
| Acridone alkaloids | C10724 | C00002187 |
| Acridone alkaloids | C10681 | C00024253 |
| 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 |
|---|---|---|---|---|---|---|
|
C00002137
|
Arborinine
|
CHEMBL349609
|
C022784
|
1 / 0 / 0 |
|
|
|
C00002163
|
Furofoline I
|
|
||||
|
C00002176
|
Japonine
|
|
||||
|
C00002186
|
Melicopicine
|
CHEMBL455628
|
|
|||
|
C00002187
|
Melicopine
|
CHEMBL1876999
|
7 / 8 / 4 |
|
||
|
C00024230
|
1-Hydroxy-3-methoxy-N-methylacridone
|
CHEMBL1094824
|
|
|||
|
C00024231
|
1-Hydroxy-N-methylacridone
|
CHEMBL1288799
|
3 / 5 / 4 |
|
||
|
C00024232
|
5-Hydroxyarborinine
|
CHEMBL1928574
|
|
|||
|
C00024243
|
Buxifoliadine-F
|
|
||||
|
C00024245
|
Buxifoliadine-H
|
CHEMBL465629
|
|
|||
|
C00024248
|
Citrusamine
|
|
||||
|
C00024249
|
Citrusinine I
|
CHEMBL451705
|
C062044
|
1 / 0 / 0 |
|
|
|
C00024250
|
Citrusinine II
|
CHEMBL465847
|
1 / 0 / 0 |
|
||
|
C00024251
|
Evoxanthine
|
|
||||
|
C00024253
|
Furacridone
|
|
||||
|
C00024254
|
Furoparadine
|
|
||||
|
C00024264
|
Marshdine
|
|
||||
|
C00024270
|
Normelicopicine
|
CHEMBL453816
|
|
|||
|
C00024271
|
Normelicopidine
|
|
||||
|
C00024272
|
Normelicopine
|
|
||||
|
C00034360
|
1,3-Dimethoxy-N-methylacridone
|
|
||||
|
C00034720
|
Tegerrardin A
|
CHEMBL1095073
|
|
|||
|
C00035416
|
Toddaliopsin B
|
|
||||
|
C00035417
|
Toddaliopsin C
|
|
||||
|
C00035418
|
Toddaliopsin D
|
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| O60911 | Cathepsin L2 | C1A | C00024249 C00024250 | 0 / 0 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002187 | 7 / 3 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002187 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00002187 | 0 / 0 |
| P42858 | Huntingtin | Unclassified protein | C00024231 | 1 / 1 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002187 | 0 / 0 |
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00002137 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002187 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00002187 | 1 / 1 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00024231 | 4 / 3 |
| P11940 | Polyadenylate-binding protein 1 | Unclassified protein | C00002187 | 0 / 0 |
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00024231 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #143100 | Huntington disease; hd |
P42858
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #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
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| KEGG | name | UniProt |
|---|---|---|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|