Species

KNApSAcK Entry

Organism name Coleus forskohlii WILLD.BRIQ.
Genus Coleus
Family Lamiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Coleus
Linked NCBI taxonomy ID 587658
Linked level genus

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (5)

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
C00022388 External link 512 Coleonol B
/ Isoforskolin
CHEMBL147617
CHEMBL1519619
5 / 12 / 5 No. 531 No. 41
C00030314 External link 512 Forskoditerpenoside C
/ (-)-Forskoditerpenoside C
No. 2270
C00030316 External link 512 Forskoditerpenoside E
/ (-)-Forskoditerpenoside E
No. 2270
C00030315 External link 512 Forskoditerpenoside D
/ (-)-Forskoditerpenoside D
No. 2270
C00030311 External link 512 Forskoditerpene A
No. 7248

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P37840 Alpha-synuclein Unclassified protein C00022388 4 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00022388 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00022388 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00022388 0 / 0
Q9GZV3 High affinity choline transporter 1 Choline Na-symporter C00022388 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#127750 Dementia, lewy body; dlb P37840
#174800 Mccune-albright syndrome; mas P63092
#158580 Neuronopathy, distal hereditary motor, type viia; hmn7a Q9GZV3
#166350 Osseous heteroplasia, progressive; poh P63092
#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

KEGG DISEASE (5)

KEGG name UniProt
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)