KCF-S cluster No. 623 (13 metabolites)

Corresponding Phytochemical cluster No. 2



Metabolite list (13)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00002085 External link 512 Echimidine
C00002088 External link 512 Heliosupine
C00002097 External link 512 Lasiocarpine
CHEMBL498236
CHEMBL1999554
CHEMBL2138247
C005136
2 / 7 / 3
C00002098 External link 512 Latifoline
C00002122 External link 512 Symlandine
C00002123 External link 512 Symphytine
C020639
C00002124 External link 512 Triangularine
C00026158 External link 512 Acetylheliosupine
/ 3'-Acetylheliosupine
/ Acetylcynoglossophine
/ Heliosupine 3'-acetate
/ Cynoglossophine acetate
C00026166 External link 512 7-Angeloyl-9-(2,3-dihydroxybutyryl)heliotridine
C00026167 External link 512 7-Angeloyl-9-(2-methylbutyryl)heliotridine
C00026170 External link 512 7-Angeloylrindrine
/ 7-Angeloylrinderine
/ O-Demethylheliotrine 7-angelate
C00026180 External link 512 Acetyllasiocarpine
/ Lasiocarpine monoacetate
C00026188 External link 512 Echihumiline

Human Protein / Gene in interactions

2 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00002097 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002097 7 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#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 (3)

KEGG name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)