KCF-S cluster No. 282 (24 metabolites)

Corresponding Phytochemical cluster No. 21



Metabolite list (24)

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
C00000604 External link 512 (-)-Secoisolariciresinol
CHEMBL368347
C060283
2 / 1 / 1 1 / 0
C00000605 External link 512 (+)-Secoisolariciresinol
CHEMBL368347
2 / 1 / 1
C00007214 External link 512 Dihydroguaiaretic acid
CHEMBL430464
CHEMBL375927
CHEMBL1976696
C015816
16 / 18 / 12
C00007215 External link 512 Mesodihydroguaiaretic acid
CHEMBL430464
CHEMBL375927
CHEMBL1976696
16 / 18 / 12
C00030517 External link 512 Isoanwulignan
C00030746 External link 512 meso-Dihydroguaiaretic acid
CHEMBL430464
CHEMBL375927
CHEMBL1976696
16 / 18 / 12
C00031082 External link 512 Pregomisin
CHEMBL1081697
C00031533 External link 512 2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)-methyl]-1,4-butanediol
C00031992 External link 512 Macelignan
CHEMBL254071
8 / 10 / 9
C00032046 External link 512 Myristargenol B
/ (+)-Myristargenol B
C00032176 External link 512 Sphenanlignan
C00034637 External link 512 Piperphilippinin VI
C00034968 External link 512 (-)-Dihydroguaiaretic acid
CHEMBL430464
CHEMBL375927
CHEMBL1976696
16 / 18 / 12
C00034969 External link 512 Sauriol A
/ (-)-Sauriol A
C00034970 External link 512 Sauriol B
/ (-)-Sauriol B
C00038929 External link 512 Daphneresinol
/ (-)-Daphneresinol
CHEMBL574120
C00039517 External link 512 Kadangustin H
/ (-)-Kadangustin H
CHEMBL458390
C00039518 External link 512 Kadangustin I
/ (-)-Kadangustin I
C00039519 External link 512 Kadangustin J
/ (+)-Kadangustin J
C00039520 External link 512 Kadangustin K
C00049243 External link 512 Oleiferin B
C00049244 External link 512 Oleiferin F
/ (+)-Oleiferin F
C00049245 External link 512 Oleiferin G
/ (+)-Oleiferin G
C00049246 External link 512 Oleiferin H
/ (-)-Oleiferin H

Human Protein / Gene in interactions

21 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007214 C00007215 C00030746 C00031992 C00034968 1 / 1
Q99700 Ataxin-2 Unclassified protein C00007214 C00007215 C00030746 C00031992 C00034968 1 / 1
O75496 Geminin Unclassified protein C00007214 C00007215 C00030746 C00031992 C00034968 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00007214 C00007215 C00030746 C00031992 C00034968 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007214 C00007215 C00030746 C00031992 C00034968 2 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00007214 C00007215 C00030746 C00034968 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00007214 C00007215 C00030746 C00034968 0 / 0
P37840 Alpha-synuclein Unclassified protein C00007214 C00007215 C00030746 C00034968 4 / 2
P00918 Carbonic anhydrase 2 Lyase C00007214 C00007215 C00030746 C00034968 1 / 2
P17405 Sphingomyelin phosphodiesterase Enzyme C00007214 C00007215 C00030746 C00034968 2 / 2
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00007214 C00007215 C00030746 C00034968 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00007214 C00007215 C00030746 C00034968 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00007214 C00007215 C00030746 C00034968 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00007214 C00007215 C00030746 C00034968 0 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00007214 C00007215 C00030746 C00034968 7 / 3
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00007214 C00007215 C00030746 C00034968 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000604 C00000605 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000604 C00000605 1 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00031992 1 / 1
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00031992 1 / 4
P10636 Microtubule-associated protein tau Unclassified protein C00031992 4 / 3

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00000604

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#208900 Ataxia-telangiectasia; at Q13315
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (20)

KEGG name UniProt
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (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)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)