Metabolite list (64)

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
figure
C00040746 External link 512 Ciliatoside B
/ (-)-Ciliatoside B
CHEMBL445172
CHEMBL499379
No. 174
C00000632 External link 512 (+)-Pinoresinol-beta-D-glucoside
/ Pinoresinol O-beta-D-glucopyranoside
CHEMBL573336
CHEMBL1083218
CHEMBL1302893
9 / 6 / 4 No. 174
C00047704 External link 512 beta-Peltatin-O-beta-D-glucopyranoside
CHEMBL401601
No. 174
C00000648 External link 512 (+)-Phillyrin
CHEMBL462767
C075528
1 / 0 / 0 No. 174
C00037463 External link 512 Patavine
/ (-)-Patavine
No. 174
C00002601 External link 512 Eucommin A
CHEMBL573786
CHEMBL1076999
No. 174
C00047703 External link 512 Styraxlignolide B
/ (-)-Styraxlignolide B
CHEMBL519719
No. 174
C00045470 External link 512 Podorhizol beta-D-glucoside
No. 174
C00002628 External link 512 Alangilignoside D
No. 174
C00002632 External link 512 Tanegoside
No. 174
C00029302 External link 512 Lactucaside
/ (-)-Lactucaside
CHEMBL499481
No. 174
C00030288 External link 512 Staunoside C
No. 174
C00030699 External link 512 Fraxiresinol 4'-O-beta-D-glucopyranoside
/ (-)-Fraxiresinol 4'-O-beta-D-glucopyranoside
CHEMBL501875
No. 174
C00030720 External link 512 1-Hydroxypinoresinol 1-glucoside
/ 1-Hydroxypinoresinol 1-O-beta-D-glucoside
CHEMBL517863
No. 174
C00030867 External link 512 (-)-Massoniresinol 4'-O-beta-D-glucopyranoside
No. 174
C00036439 External link 512 4''-O-Acetylmananthoside B
CHEMBL452903
No. 174
C00036313 External link 512 Diphyllin
/ Cleistanthin C
No. 174
C00031031 External link 512 Tortoside B
/ Manglieside E
/ (-)-Manglieside E
CHEMBL1085531
No. 174
C00031316 External link 512 Foliachinenoside C
/ (-)-Foliachinenoside C
No. 174
C00031451 External link 512 Magnolenin C
No. 174
C00031457 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
No. 174
C00031615 External link 512 (+)-Isolarisiresinol 2a-O-beta-D-glucopyranoside
No. 174
C00036284 External link 512 Arabelline
No. 174
C00034754 External link 512 Majidine
CHEMBL508105
No. 174
C00044851 External link 512 Styraxjaponoside A
/ (+)-Styraxjaponoside A
No. 174
C00032561 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 No. 174
C00043848 External link 512 Styraxlignolide C
/ (-)-Styraxlignolide C
CHEMBL486465
No. 174
C00043511 External link 512 Styraxlignolide E
/ (-)-Styraxlignolide E
CHEMBL459834
CHEMBL520065
No. 174
C00032284 External link 512 Vitecannaside A
No. 174
C00032565 External link 512 Phyllanthusmin C
/ (-)-Phyllanthusmin C
CHEMBL460047
CHEMBL1929098
1 / 0 / 0 No. 174
C00032498 External link 512 Lyoniside
/ (+)-Lyoniside
CHEMBL466738
CHEMBL583884
No. 174
C00032499 External link 512 Nudiposide
CHEMBL466738
CHEMBL583884
No. 174
C00032514 External link 512 (-)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside
CHEMBL464198
CHEMBL1159486
CHEMBL1159487
CHEMBL1813178
CHEMBL1813179
CHEMBL1813180
CHEMBL1813181
CHEMBL2332109
6 / 11 / 5 No. 174
C00032199 External link 512 (+)-Isolariciresinol 2a-O-alpha-L-arabinopyranoside
No. 174
C00042832 External link 512 Styraxlignolide D
/ (-)-Styraxlignolide D
CHEMBL519055
No. 509
C00032712 External link 512 Acutissimalignan A
/ (+)-Acutissimalignan A
No. 509
C00033152 External link 512 Phyllanthusmin B
No. 509
C00033292 External link 512 Patentiflorin A
/ (-)-Patentiflorin A
CHEMBL458904
CHEMBL458905
CHEMBL1929103
1 / 0 / 0 No. 509
C00033456 External link 512 4-O-(3-O-methyl-beta-D-glucopyranosyl)-diphyllin
/ 4-O-(3''-O-methyl-beta-D-glucopyranosyl)-diphyllin
No. 509
C00033721 External link 512 Tuberculatin
No. 509
C00033722 External link 512 Cleistanthin A
C010088
No. 509
C00034173 External link 512 (2E,6R)-2,6-Dimethyl-8-hydroxy-2-octenoic acid 8-O-[6'-O-(E)-p-coumaroyl]-beta-D-glucopyranoside
No. 509
C00031683 External link 512 (-)-Isolariciresinol 3-alpha-O-beta-D-glucopyranoside
CHEMBL459617
No. 509
C00035950 External link 512 Procumbenoside A
/ (-)-Procumbenoside A
CHEMBL508105
No. 509
C00031682 External link 512 (+)-Isolarisiresinol 3a-O-beta-D-glucopyranoside
CHEMBL459617
No. 509
C00031018 External link 512 Alangilignoside C
/ (+)-Alangilignoside C
No. 509
C00031017 External link 512 Prinsepiol 4-O-beta-D-glucopyranoside
CHEMBL479729
No. 509
C00002590 External link 512 (+)-Pinoresinol monomethyl ether O-beta-D-glucopyranoside
No. 509
C00042144 External link 512 Matairesinoside
/ (-)-Matairesinoside
CHEMBL459834
CHEMBL520065
No. 509
C00038357 External link 512 Ciliatoside A
/ (-)-Ciliatoside A
CHEMBL497767
CHEMBL502183
No. 509
C00000629 External link 512 (+)-Cycloolivil 4'-O-beta-D-glucopyranoside
No. 653
C00032370 External link 512 Vitecannaside B
No. 653
C00032217 External link 512 Aviculin
/ (+)-Aviculin
No. 653
C00032216 External link 512 Schizandriside
/ (+)-Schizandriside
CHEMBL2346750
No. 653
C00043931 External link 512 Styraxjaponoside B
/ (-)-Styraxjaponoside B
CHEMBL488098
No. 653
C00043932 External link 512 Styraxlignolide F
/ (-)-Styraxlignolide F
CHEMBL488098
No. 653
C00043933 External link 512 (-)-Arctiin
CHEMBL388452
CHEMBL1526371
C077992
4 / 15 / 11 0 / 2 No. 653
C00000646 External link 512 (-)-Pinoresinol O-beta-D-glucopyranoside
/ (-)-Pinoresinol 4-O-beta-D-glucopyranoside
CHEMBL573336
CHEMBL1083218
CHEMBL1302893
9 / 6 / 4 No. 653
C00043935 External link 512 Tracheloside
/ (-)-Tracheloside
C079169
No. 653
C00032004 External link 512 Woorenoside XI
/ (-)-Woorenoside XI
No. 653
C00002621 External link 512 Lariciresinol-9-O-beta-D-glucoside
No. 653
C00048330 External link 512 Phyllanthostatin A
CHEMBL454500
C058885
No. 653
C00043934 External link 512 (-)-Nortracheloside
CHEMBL574493
No. 653
C00002618 External link 512 Simplexoside
No. 8092

Human Protein / Gene in interactions

21 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
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00031031 C00031451 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
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00036284 C00036313 0 / 0
P37840 Alpha-synuclein Unclassified protein C00031031 C00031451 4 / 2
P11388 DNA topoisomerase 2-alpha Isomerase C00031018 C00042832 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00031031 C00031451 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00031031 C00031451 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00031031 C00031451 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00031031 C00031451 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00031031 C00031451 0 / 0
Q9P0U3 Sentrin-specific protease 1 Enzyme C00036284 C00036313 0 / 0
P00734 Prothrombin S1A C00036284 C00036313 4 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00036284 C00036313 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00000646 0 / 0
O75496 Geminin Unclassified protein C00000646 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000648 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000646 11 / 10
Q16637 Survival motor neuron protein Unclassified protein C00000646 4 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (32)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#127750 Dementia, lewy body; dlb P37840
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#232300 Glycogen storage disease ii P10253
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#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
#275210 Restrictive dermopathy, lethal P02545
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (20)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
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)
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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D005921 Glomerulonephritis C00000646
D011230 Precancerous Conditions C00000646