KCF-S cluster No. 1938 (5 metabolites)

Corresponding Phytochemical cluster No. 21


Plant Species


Cumulative plant class count

class name count
rosids 5
Liliopsida 2
eudicotyledons 1

Cumulative family count

class name count
Zygophyllaceae 4
Zingiberaceae 2
Betulaceae 1
Viscaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Lignans 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Lignans C10719 C00000693

Metabolite list (5)

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
C00000693 External link 512 Nordihydroguaiaretic acid
CHEMBL52
CHEMBL313972
CHEMBL185893
70 / 73 / 92
C00002747 External link 512 Gingerenone A
CHEMBL1086746
C00031488 External link 512 1,7-bis(3,4-Dihydroxyphenyl)-5-hydroxy-3-heptanone
CHEMBL455297
1 / 0 / 0
C00035640 External link 512 Hexahydrocurcumin
CHEMBL479650
1 / 2 / 0
C00037272 External link 512 Hirsutanone
CHEMBL464274
1 / 0 / 0

Human Protein / Gene in interactions

72 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P17252 Protein kinase C alpha type Alpha C00031488 C00037272 0 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00000693 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00000693 7 / 37
P61981 14-3-3 protein gamma Unclassified protein C00000693 0 / 0
Q99700 Ataxin-2 Unclassified protein C00000693 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00000693 2 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00000693 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00000693 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000693 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000693 2 / 2
P08069 Insulin-like growth factor 1 receptor TK tyrosine-protein kinase INSR subfamily C00000693 1 / 3
P06746 DNA polymerase beta Enzyme C00000693 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000693 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000693 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00000693 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000693 11 / 10
P37840 Alpha-synuclein Unclassified protein C00000693 4 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000693 0 / 1
P54132 Bloom syndrome protein Enzyme C00000693 1 / 2
P11473 Vitamin D3 receptor NR1I1 C00000693 2 / 3
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000693 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000693 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000693 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000693 0 / 0
P39748 Flap endonuclease 1 Enzyme C00000693 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00000693 0 / 0
P11413 Glucose-6-phosphate 1-dehydrogenase Enzyme C00000693 1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000693 2 / 0
O75496 Geminin Unclassified protein C00000693 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00000693 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000693 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00000693 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00000693 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000693 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000693 2 / 2
Q15722 Leukotriene B4 receptor 1 Leukotriene receptor C00000693 0 / 0
P06280 Alpha-galactosidase A Enzyme C00000693 1 / 1
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00000693 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000693 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000693 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000693 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000693 2 / 2
Q01453 Peripheral myelin protein 22 Unclassified protein C00000693 5 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000693 0 / 0
P03372 Estrogen receptor NR3A1 C00000693 1 / 1
P26358 DNA (cytosine-5)-methyltransferase 1 Transferase C00035640 2 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000693 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00000693 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000693 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000693 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00000693 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00000693 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000693 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000693 4 / 3
P42345 Serine/threonine-protein kinase mTOR Enzyme C00000693 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000693 0 / 0
P10275 Androgen receptor NR3C4 C00000693 3 / 4
Q9UBT6 DNA polymerase kappa Enzyme C00000693 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000693 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000693 0 / 0
P40225 Thrombopoietin Unclassified protein C00000693 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000693 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000693 1 / 1
O00255 Menin Unclassified protein C00000693 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000693 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00000693 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000693 1 / 4
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00000693 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00000693 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000693 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00000693 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000693 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (75)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#300908 Anemia, nonspherocytic hemolytic, due to g6pd deficiency P11413
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#604121 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant; adcadn P26358
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#114500 Colorectal cancer; crc P18054
P84022
Q14191
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#270450 Insulin-like growth factor i, resistance to P08069
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#614116 Neuropathy, hereditary sensory, type ie; hsn1e P26358
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#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
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (92)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (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)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
P08069 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00125 Fabry disease P06280 (related)
H00050 Synovial sarcoma P08069 (related)
H01274 Growth delay due to insulin-like growth factor I resistance P08069 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00101 Other phagocyte defects P11413 (related)
H00668 Anemia due to disorders of glutathione metabolism P11413 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)