Organism name | Cratoxylum cochinchinense (Lour.) Blume |
---|---|
Genus | Cratoxylum |
Family | Hypericaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Cratoxylum cochinchinense |
---|---|
Linked NCBI taxonomy ID | 271749 |
Linked level | species |
Family in NCBI taxonomy | Hypericaceae |
---|---|
ID | 629714 |
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 |
---|---|---|---|---|---|---|---|---|
C00034819
![]() |
Cochinchinone B
|
CHEMBL1173563
|
No. 14 | No. 15 |
![]() |
|||
C00030356
![]() |
Garcinone B
|
CHEMBL560332
|
No. 18 | No. 15 |
![]() |
|||
C00002961
![]() |
Macluraxanthone
/ 3-Hydroxyblancoxanthone |
CHEMBL478960
|
5 / 11 / 11 | No. 18 | No. 15 |
![]() |
||
C00030358
![]() |
Garcinone D
|
CHEMBL462879
|
3 / 2 / 2 | No. 47 | No. 15 |
![]() |
||
C00034820
![]() |
Cochinchinone D
|
No. 2057 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00002961 | 4 / 1 |
Q04206 | Transcription factor p65 | Transcription Factor | C00030358 | 0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00030358 | 2 / 2 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00030358 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002961 | 4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002961 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002961 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002961 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#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
|
#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
|
#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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
H00794 | Aromatase excess syndrome |
P11511
(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)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|