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)
|