Cudrania cochinchinensis (LOUR.) KUDO & MASAMUNE var.gerontogea (S.& Z.) KUDO & MASAMUNE


Species

KNApSAcK Entry

Organism name Cudrania cochinchinensis (LOUR.) KUDO & MASAMUNE var.gerontogea (S.& Z.) KUDO & MASAMUNE
Genus Cudrania
Family Moraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Maclura
Linked NCBI taxonomy ID 3495
Linked level genus

Family

Family in NCBI taxonomy Moraceae
ID 3487

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (8)

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 External link 512 Gerontoxanthone H
CHEMBL514057
9 / 9 / 4 No. 14 No. 15
C00024194 External link 512 Gerontoxanthone B
CHEMBL478938
No. 18 No. 15
C00024193 External link 512 Gerontoxanthone A
CHEMBL517514
7 / 10 / 6 No. 18 No. 15
C00024197 External link 512 Gerontoxanthone E
No. 47 No. 15
C00024200 External link 512 Gerontoxanthone I
CHEMBL478791
11 / 12 / 5 No. 47 No. 15
C00024198 External link 512 Gerontoxanthone G
CHEMBL479107
No. 47 No. 15
C00024195 External link 512 Gerontoxanthone C
No. 47 No. 15
C00024196 External link 512 Gerontoxanthone D
No. 1835

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (23)

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 DISEASE (12)

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)