class name | count |
---|---|
rosids | 6 |
class name | count |
---|---|
Simaroubaceae | 6 |
br08003 Category | # of metabolite |
---|---|
Dammarenes | 5 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Dammarenes | C08749 | C00003699 |
Dammarenes | C08750 | C00003700 |
Dammarenes | C08751 | C00003701 |
Dammarenes | C08754 | C00003704 |
Dammarenes | C08782 | C00003730 |
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 |
---|---|---|---|---|---|---|
C00003699
![]() |
Bruceantin
|
CHEMBL509895
CHEMBL1700569 |
C002550
|
12 / 12 / 8 | 0 / 1 |
![]() |
C00003700
![]() |
Bruceantinol
|
CHEMBL450145
|
![]() |
|||
C00003701
![]() |
Bruceine B
|
CHEMBL140809
|
C024965
|
![]() |
||
C00003704
![]() |
Brusatol
|
CHEMBL450464
CHEMBL1702665 |
C020237
|
9 / 15 / 8 | 2 / 0 |
![]() |
C00003730
![]() |
Sergeolide
|
CHEMBL521373
CHEMBL1975433 |
C045844
|
1 / 0 / 0 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P05412 | Transcription factor AP-1 | Transcription Factor | C00003699 C00003704 C00003730 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00003699 C00003704 | 0 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003699 C00003704 | 2 / 0 |
P37840 | Alpha-synuclein | Unclassified protein | C00003699 C00003704 | 4 / 2 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00003699 C00003704 | 1 / 2 |
Q99700 | Ataxin-2 | Unclassified protein | C00003699 C00003704 | 1 / 1 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003699 C00003704 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003699 C00003704 | 0 / 0 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00003699 | 1 / 2 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00003704 | 7 / 3 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003699 | 1 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003699 | 1 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00003699 | 1 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
9817 | KEAP1, INrf2, KLHL19 | kelch-like ECH-associated protein 1 |
C00003704
|
4780 | NFE2L2, NRF2 | nuclear factor, erythroid 2-like 2 |
C00003704
|
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#612219 | Ewing sarcoma; es |
P11308
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#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
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | name | UniProt |
---|---|---|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|