Cratoxylum formosum
Species
KNApSAcK Entry
| Organism name | Cratoxylum formosum |
|---|---|
| Genus | Cratoxylum |
| Family | Hypericaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Cratoxylum formosum |
|---|---|
| Linked NCBI taxonomy ID | 198761 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Hypericaceae |
|---|---|
| ID | 629714 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | rosids |
|---|---|
| ID | 71275 |
Metabolite list (7)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00002961
|
Macluraxanthone
/ 3-Hydroxyblancoxanthone |
CHEMBL478960
|
5 / 11 / 11 | No. 18 | No. 15 |
|
||
|
C00032517
|
Xanthone V1
|
No. 18 | No. 15 |
|
||||
|
C00034842
|
Formoxanthone A
|
CHEMBL1254112
|
No. 18 | No. 15 |
|
|||
|
C00034843
|
Formoxanthone B
|
No. 44 |
|
|||||
|
C00034844
|
Formoxanthone C
|
No. 47 | No. 15 |
|
||||
|
C00032493
|
Vismiaquinone
/ Vismiaquinone A |
CHEMBL455104
|
No. 1967 | No. 62 |
|
|||
|
C00034872
|
Madagascin
|
CHEMBL1800811
|
No. 1967 | No. 62 |
|
Human Protein / Gene in interactions
5 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q16637 | Survival motor neuron protein | Unclassified protein | C00002961 | 4 / 1 |
| 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 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (11)
| OMIM | preferred title | UniProt |
|---|---|---|
| #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 DISEASE (11)
| 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)
|
| 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)
|