KCF-S cluster No. 1312 (7 metabolites)

Corresponding Phytochemical cluster No. 63


Plant Species


Cumulative plant class count

class name count
Magnoliophyta 8
Liliopsida 5
asterids 2

Cumulative family count

class name count
Piperaceae 6
Zingiberaceae 5
Lauraceae 2
Gesneriaceae 2

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
alpha-Pyrones 2

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
alpha-Pyrones C09925 C00002987
alpha-Pyrones C09980 C00003024
alpha-Pyrones C09925 C00029550

Metabolite list (7)

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
C00002987 External link 512 5,6-Dehydrokawain
CHEMBL254218
C052297
12 / 16 / 44
C00003024 External link 512 Yangonin
CHEMBL1098658
C110481
16 / 25 / 49
C00029373 External link 512 10-Methoxyyagonin
C00029550 External link 512 5,6-Dehydrokawain
/ Desmethoxyyangonin
CHEMBL254218
12 / 16 / 44
C00029551 External link 512 5,6-Dehydromethysticin
CHEMBL1946690
C00043208 External link 512 5,6-Dehydro-7,8-dihydromethysticin
CHEMBL1376695
3 / 0 / 0
C00045571 External link 512 p-Hydroxy-5,6-dehydrokawain
/ 4'-Hydroxy-5,6-dehydrokawain
CHEMBL464111

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00002987 C00003024 C00029550 7 / 37
Q16637 Survival motor neuron protein Unclassified protein C00002987 C00003024 C00029550 4 / 1
P35869 Aryl hydrocarbon receptor Transcription Factor C00002987 C00003024 C00029550 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00002987 C00003024 C00029550 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002987 C00003024 C00029550 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002987 C00003024 C00029550 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00002987 C00003024 C00029550 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002987 C00003024 C00029550 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002987 C00003024 C00029550 2 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002987 C00029550 0 / 1
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002987 C00029550 0 / 0
P10275 Androgen receptor NR3C4 C00002987 C00029550 3 / 4
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00003024 3 / 3
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00003024 5 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00043208 0 / 0
P55210 Caspase-7 C14 C00003024 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003024 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00003024 4 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00043208 0 / 0
P10145 Interleukin-8 Secreted protein C00003024 0 / 0
P29466 Caspase-1 C14 C00003024 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00043208 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (28)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (53)

KEGG name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
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)
H00026 Endometrial Cancer P04637 (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)
P37231 (related)
H00033 Adrenal carcinoma 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)
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)
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)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)