KCF-S cluster No. 983 (9 metabolites)

Corresponding Phytochemical cluster No. 35



Metabolite list (9)

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
C00010848 External link 512 Oleuropeic acid
CHEMBL1077602
C417926
C00010930 External link 512 p-Menth-1(7)-en-8-ol
C00010931 External link 512 (R)-(+)-alpha-Terpineol
/ (R)-(+)-p-Menth-1-en-8-ol
CHEMBL447597
CHEMBL449810
3 / 16 / 11
C00010932 External link 512 (S)-(-)-alpha-Terpineol
/ (S)-(-)-p-Menth-1-en-8-ol
CHEMBL447597
CHEMBL449810
3 / 16 / 11
C00010971 External link 512 alpha-Sylveterpineol
/ (+)-m-Menth-6-en-8-ol
C00010972 External link 512 m-Menth-1-en-8-ol
C00022008 External link 512 (-)-p-Menth-1-ene-7,8-diol
CHEMBL448219
C00022009 External link 512 Sobrerol
CHEMBL400537
CHEMBL459048
CHEMBL1997575
C003316
C00029674 External link 512 alpha-Terpineol
CHEMBL447597
CHEMBL449810
C016775
3 / 16 / 11

Human Protein / Gene in interactions

3 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00010931 C00010932 C00029674 3 / 0
P02545 Prelamin-A/C Unclassified protein C00010931 C00010932 C00029674 11 / 10
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00010931 C00010932 C00029674 5 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

OMIM preferred title UniProt
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#143500 Gilbert syndrome P22309
P22310
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (11)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00208 Hyperbilirubinemia P22309 (related)