| Organism name | Swartzia madagascariensis |
|---|---|
| Genus | Swartzia |
| Family | Fabaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Swartzia |
|---|---|
| Linked NCBI taxonomy ID | 53925 |
| Linked level | genus |
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00003526
|
Gypsogenin 3-O-rhamnosylglucuronide
|
No. 9 | No. 51 |
|
||||
|
C00009694
|
Anhydrovariabilin
/ 3,9-Dimethoxypterocarpene |
CHEMBL1520512
|
9 / 11 / 12 | No. 27 | No. 15 |
|
||
|
C00009761
|
3,9-Dimethylcoumestan
/ Di-O-methylcoumestrol / Coumestrol dimethyl ether / 3,9-Dimethoxy-6-oxopterocarpene |
No. 54 | No. 17 |
|
||||
|
C00009620
|
4-Methoxymedicarpin
/ 3-Hydroxy-4,9-dimethoxypterocarpan |
CHEMBL404648
|
No. 66 | No. 15 |
|
|||
|
C00009616
|
Pterocarpin
/ 3-Methoxy-8,9-methylenedioxypterocarpan |
CHEMBL21103
CHEMBL242128 CHEMBL1983713 |
7 / 8 / 10 | No. 66 | No. 15 |
|
||
|
C00009613
|
Baphinitone
/ (-)-Homopterocarpin / 3,9-Dimethoxypterocarpan |
CHEMBL277682
CHEMBL396671 CHEMBL2007304 |
No. 66 | No. 15 |
|
|||
|
C00009623
|
4-Methoxymaackiain
|
CHEMBL458847
|
No. 66 | No. 15 |
|
|||
|
C00009625
|
4-Methoxyhomopterocarpin
|
No. 66 | No. 15 |
|
||||
|
C00009630
|
4-Methoxypterocarpin
|
CHEMBL480288
|
No. 66 | No. 15 |
|
|||
|
C00002547
|
(-)-Medicarpin
/ 3-Hydroxy-9-methoxypterocarpan |
CHEMBL238845
CHEMBL413297 |
C047353
|
3 / 1 / 1 | No. 66 | No. 15 |
|
|
|
C00002546
|
Inermin
/ Maackiain / (-)-Maackiain / Demethylpterocarpin / 3-Hydroxy-8,9-methylenedioxypterocarpan |
CHEMBL334918
CHEMBL239047 CHEMBL445279 |
3 / 2 / 3 | No. 66 | No. 15 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P13866 | Sodium/glucose cotransporter 1 | Glucose | C00002546 C00009616 | 1 / 1 |
| P31639 | Sodium/glucose cotransporter 2 | Glucose | C00002546 C00009616 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002546 C00009694 | 0 / 1 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00009616 C00009694 | 4 / 3 |
| O75496 | Geminin | Unclassified protein | C00002547 | 0 / 0 |
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00009694 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00009616 | 0 / 0 |
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00009694 | 0 / 0 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00009694 | 0 / 0 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00009694 | 4 / 1 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002547 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00009694 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00009616 | 1 / 1 |
| O00255 | Menin | Unclassified protein | C00009694 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00009694 | 1 / 2 |
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00009616 | 0 / 1 |
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00009616 | 1 / 4 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002547 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #606824 | Glucose/galactose malabsorption; ggm |
P13866
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
| #233100 | Renal glucosuria; glys1 |
P31639
|
| #253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
| #253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
| #253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
| #271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #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)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| 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)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
| H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
| H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
| H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|