| Organism name | Cedrela sinensis |
|---|---|
| Genus | Cedrela |
| Family | Meliaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Toona sinensis |
|---|---|
| Linked NCBI taxonomy ID | 443222 |
| Linked level | species |
| Family in NCBI taxonomy | Meliaceae |
|---|---|
| ID | 43707 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00031038
|
Piscidinol A
/ (-)-Piscidinol A |
CHEMBL1508930
|
12 / 23 / 20 | No. 119 | No. 51 |
|
||
|
C00041290
|
7-Deacetoxy-7alpha,11alpha-dihydroxygedunin
/ (+)-7-Deacetoxy-7alpha,11alpha-dihydroxygedunin |
CHEMBL463400
CHEMBL513222 |
No. 204 | No. 51 |
|
|||
|
C00041234
|
11beta-Hydroxygedunin
/ (+)-11beta-Hydroxygedunin |
CHEMBL462806
CHEMBL480303 |
No. 204 | No. 51 |
|
|||
|
C00041291
|
7-Deacetoxy-7alpha,11beta-Dihydroxygedunin
|
CHEMBL463400
CHEMBL513222 |
No. 204 | No. 51 |
|
|||
|
C00041233
|
11alpha-Hydroxygedunin
/ (+)-11alpha-Hydroxygedunin |
CHEMBL462806
CHEMBL480303 |
No. 204 | No. 51 |
|
|||
|
C00029846
|
Bourjotinolone A
|
No. 264 | No. 51 |
|
||||
|
C00030484
|
Hispidol B
|
No. 264 | No. 51 |
|
||||
|
C00029764
|
Azadirone
|
CHEMBL338847
CHEMBL1215753 |
No. 453 |
|
||||
|
C00030427
|
Grandifoliolenone
|
CHEMBL1356418
|
1 / 4 / 3 | No. 1247 |
|
|||
|
C00031287
|
Sapelin E acetate
|
No. 1247 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00030427 C00031038 | 4 / 3 |
| O75496 | Geminin | Unclassified protein | C00031038 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00031038 | 0 / 0 |
| Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00031038 | 1 / 4 |
| P42858 | Huntingtin | Unclassified protein | C00031038 | 1 / 1 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00031038 | 2 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00031038 | 1 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00031038 | 7 / 3 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00031038 | 4 / 1 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00031038 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00031038 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00031038 | 1 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #208900 | Ataxia-telangiectasia; at |
Q13315
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #143100 | Huntington disease; hd |
P42858
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
| #103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
| #603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
| #612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
| #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
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #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)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(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)
|
| H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
| H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
| H00094 | DNA repair defects |
Q13315
(related)
|
| H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|