Cephalotaxus wilsoniana
Species
KNApSAcK Entry
| Organism name | Cephalotaxus wilsoniana |
|---|---|
| Genus | Cephalotaxus |
| Family | Cephalotaxaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Cephalotaxus wilsoniana |
|---|---|
| Linked NCBI taxonomy ID | 50179 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Cephalotaxaceae |
|---|---|
| ID | 50175 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | Spermatophyta |
|---|---|
| ID | 58024 |
Metabolite list (4)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00002324
|
Cephalotaxine
|
CHEMBL276462
CHEMBL1476895 |
C001597
|
4 / 7 / 7 | No. 1451 | No. 4 |
|
|
|
C00027112
|
Epiwilsonine
/ epi-Wilsonine / 3-epi-wilsonine |
No. 2621 |
|
|||||
|
C00044604
|
C-3-epi-wilsonione
/ (+)-C-3-epi-wilsonione |
CHEMBL456524
|
No. 2621 |
|
||||
|
C00014754
|
Taiwanhomoflavone C
|
No. 3412 |
|
Human Protein / Gene in interactions
4 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002324 | 3 / 3 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002324 | 0 / 1 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00002324 | 4 / 3 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002324 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (7)
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG DISEASE (7)
| KEGG | name | UniProt |
|---|---|---|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|