KCF-S cluster No. 174 (34 metabolites)

Corresponding Phytochemical cluster No. 22



Metabolite list (34)

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
C00000632 External link 512 Lariciresinol-9-O-beta-D-glucoside
C00000648 External link 512 (+)-Phillyrin
CHEMBL462767
C075528
1 / 0 / 0
C00002601 External link 512 Eucommin A
CHEMBL573786
CHEMBL1076999
C00002628 External link 512 Simplexoside
C00002632 External link 512 Acanthoside B
/ Eleutheroside E1
/ (+)-Syringaresinol O-beta-D-glucoside
/ (+)-Syringaresinol 4'-O-beta-glucopyranoside
/ (+)-Syringaresinol-4-O-beta-D-glucopyranoside
CHEMBL573710
CHEMBL1077080
C087806
C00029302 External link 512 (+)-Isolariciresinol 2a-O-alpha-L-arabinopyranoside
C00030288 External link 512 Foliachinenoside C
/ (-)-Foliachinenoside C
C00030699 External link 512 Lyoniside
/ (+)-Lyoniside
CHEMBL466738
CHEMBL583884
C00030720 External link 512 Tortoside B
/ Manglieside E
/ (-)-Manglieside E
CHEMBL1085531
C00030867 External link 512 Nudiposide
CHEMBL466738
CHEMBL583884
C00031031 External link 512 (+)-Pinoresinol-beta-D-glucoside
/ Pinoresinol O-beta-D-glucopyranoside
CHEMBL573336
CHEMBL1083218
CHEMBL1302893
9 / 6 / 4
C00031316 External link 512 Schizandriside
/ (+)-Schizandriside
CHEMBL2346750
C00031451 External link 512 (-)-Pinoresinol O-beta-D-glucopyranoside
/ (-)-Pinoresinol 4-O-beta-D-glucopyranoside
CHEMBL573336
CHEMBL1083218
CHEMBL1302893
9 / 6 / 4
C00031457 External link 512 (+)-Pinoresinol monomethyl ether O-beta-D-glucopyranoside
C00031615 External link 512 Aviculin
/ (+)-Aviculin
C00032199 External link 512 Staunoside C
C00032284 External link 512 Tanegoside
C00032498 External link 512 Vitecannaside A
C00032499 External link 512 Vitecannaside B
C00032514 External link 512 Woorenoside XI
/ (-)-Woorenoside XI
C00032561 External link 512 (-)-Massoniresinol 4'-O-beta-D-glucopyranoside
C00032565 External link 512 (+)-Isolarisiresinol 2a-O-beta-D-glucopyranoside
C00034754 External link 512 (+)-Cycloolivil 4'-O-beta-D-glucopyranoside
C00036284 External link 512 (-)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside
CHEMBL464198
CHEMBL1159486
CHEMBL1159487
CHEMBL1813178
CHEMBL1813179
CHEMBL1813180
CHEMBL1813181
CHEMBL2332109
6 / 11 / 5
C00036313 External link 512 (+)-Lyoniresinol 3alpha-O-beta-glucopyranoside
/ (+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside
CHEMBL464198
CHEMBL1159486
CHEMBL1159487
CHEMBL1813178
CHEMBL1813179
CHEMBL1813180
CHEMBL1813181
CHEMBL2332109
6 / 11 / 5
C00036439 External link 512 1-Hydroxypinoresinol 1-glucoside
/ 1-Hydroxypinoresinol 1-O-beta-D-glucoside
CHEMBL517863
C00037463 External link 512 Magnolenin C
C00040746 External link 512 (+)-Isolarisiresinol 3a-O-beta-D-glucopyranoside
CHEMBL459617
C00043511 External link 512 Fraxiresinol 4'-O-beta-D-glucopyranoside
/ (-)-Fraxiresinol 4'-O-beta-D-glucopyranoside
CHEMBL501875
C00043848 External link 512 Prinsepiol 4-O-beta-D-glucopyranoside
CHEMBL479729
C00044851 External link 512 Lactucaside
/ (-)-Lactucaside
CHEMBL499481
C00045470 External link 512 (-)-Isolariciresinol 3-alpha-O-beta-D-glucopyranoside
CHEMBL459617
C00047703 External link 512 Alangilignoside C
/ (+)-Alangilignoside C
C00047704 External link 512 Alangilignoside D

Human Protein / Gene in interactions

16 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00036284 C00036313 0 / 0
P06746 DNA polymerase beta Enzyme C00031031 C00031451 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00031031 C00031451 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00036284 C00036313 0 / 0
P37840 Alpha-synuclein Unclassified protein C00031031 C00031451 4 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00031031 C00031451 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00036284 C00036313 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00031031 C00031451 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00036284 C00036313 0 / 0
P00734 Prothrombin S1A C00036284 C00036313 4 / 2
Q9UNA4 DNA polymerase iota Enzyme C00031031 C00031451 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00031031 C00031451 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00031031 C00031451 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00031031 C00031451 0 / 0
Q9P0U3 Sentrin-specific protease 1 Enzyme C00036284 C00036313 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000648 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#127750 Dementia, lewy body; dlb P37840
#232300 Glycogen storage disease ii P10253
#174800 Mccune-albright syndrome; mas P63092
#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
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (9)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)