| Organism name | Cudrania cochinchinensis (LOUR.) KUDO & MASAMUNE var.gerontogea (S.& Z.) KUDO & MASAMUNE |
|---|---|
| Genus | Cudrania |
| Family | Moraceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Maclura |
|---|---|
| Linked NCBI taxonomy ID | 3495 |
| Linked level | genus |
| Family in NCBI taxonomy | Moraceae |
|---|---|
| ID | 3487 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00024199
|
Gerontoxanthone H
|
CHEMBL514057
|
9 / 9 / 4 | No. 14 | No. 15 |
|
||
|
C00024194
|
Gerontoxanthone B
|
CHEMBL478938
|
No. 18 | No. 15 |
|
|||
|
C00024193
|
Gerontoxanthone A
|
CHEMBL517514
|
7 / 10 / 6 | No. 18 | No. 15 |
|
||
|
C00024197
|
Gerontoxanthone E
|
No. 47 | No. 15 |
|
||||
|
C00024200
|
Gerontoxanthone I
|
CHEMBL478791
|
11 / 12 / 5 | No. 47 | No. 15 |
|
||
|
C00024198
|
Gerontoxanthone G
|
CHEMBL479107
|
No. 47 | No. 15 |
|
|||
|
C00024195
|
Gerontoxanthone C
|
No. 47 | No. 15 |
|
||||
|
C00024196
|
Gerontoxanthone D
|
No. 1835 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q99700 | Ataxin-2 | Unclassified protein | C00024193 C00024199 C00024200 | 1 / 1 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00024193 C00024199 C00024200 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00024193 C00024199 C00024200 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00024193 C00024199 C00024200 | 0 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00024199 C00024200 | 1 / 1 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00024199 C00024200 | 1 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00024199 C00024200 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00024199 C00024200 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00024193 | 1 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00024200 | 7 / 3 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00024200 | 0 / 0 |
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00024193 | 4 / 2 |
| P07900 | Heat shock protein HSP 90-alpha | Other cytosolic protein | C00024200 | 0 / 0 |
| P37840 | Alpha-synuclein | Unclassified protein | C00024199 | 4 / 2 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00024193 | 2 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #114480 | Breast cancer |
P38398
|
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #127750 | Dementia, lewy body; dlb |
P37840
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #167000 | Ovarian cancer |
P38398
|
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
| #168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
| #605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
| #168600 | Parkinson disease, late-onset; pd |
P37840
|
| #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
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
| KEGG | name | UniProt |
|---|---|---|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H00057 | Parkinson's disease (PD) |
P37840
(related)
|
| H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
| H00027 | Ovarian cancer |
P38398
(related)
|
| H00031 | Breast cancer |
P38398
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|