Organism name | Baphia nitida |
---|---|
Genus | Baphia |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Baphia nitida |
---|---|
Linked NCBI taxonomy ID | 162666 |
Linked level | species |
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 |
---|---|---|---|---|---|---|---|---|
C00009459
![]() |
Santal
/ 5,3',4'-Trihydroxy-7-methoxyisoflavone |
No. 3 | No. 15 |
![]() |
||||
C00020669
![]() |
Santarubin C
|
No. 34 | No. 18 |
![]() |
||||
C00009616
![]() |
Pterocarpin
/ 3-Methoxy-8,9-methylenedioxypterocarpan |
CHEMBL21103
CHEMBL242128 CHEMBL1983713 |
7 / 8 / 10 | No. 66 | No. 15 |
![]() |
||
C00002570
![]() |
Sativan
/ (-)-Sativan |
No. 73 | No. 15 |
![]() |
||||
C00009754
![]() |
6,7,3'-Trihydroxy-2',4'-dimethoxyisoflavene
|
No. 400 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P13866 | Sodium/glucose cotransporter 1 | Glucose | C00009616 | 1 / 1 |
P31639 | Sodium/glucose cotransporter 2 | Glucose | C00009616 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00009616 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00009616 | 4 / 3 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00009616 | 1 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00009616 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00009616 | 1 / 4 |
OMIM | preferred title | UniProt |
---|---|---|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#606824 | Glucose/galactose malabsorption; ggm |
P13866
|
#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
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#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)
|
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) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|