KCF-S cluster No. 285 (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
C00000611 External link 512 Justicidin E
CHEMBL304236
1 / 0 / 0
C00000700 External link 512 Justicidin A
CHEMBL508532
C049719
C00000701 External link 512 Justicidin B
C00000711 External link 512 Retrojusticidin B
CHEMBL292540
1 / 0 / 0
C00000720 External link 512 Neojusticin A
CHEMBL455369
C00000721 External link 512 Taiwanin E
CHEMBL468453
C00000727 External link 512 Prostalidin A
C00000728 External link 512 Prostalidin B
C00000729 External link 512 Prostalidin C
C00002600 External link 512 Diphyllin
CHEMBL221190
C010130
24 / 43 / 38
C00007210 External link 512 Dehydropodophyllotoxin
/ Tetradehydropodophyllotoxin
CHEMBL487214
C00007211 External link 512 Helioxanthin
CHEMBL436474
C00030455 External link 512 Haplomyrtin
C00031016 External link 512 Phyllanthusmin A
C00031681 External link 512 Cleistanone
/ (+)-Cleistanone
C00036091 External link 512 Chaihunaphthone
C00036092 External link 512 Chinensinaphthol
CHEMBL495476
C00037881 External link 512 Taiwanin C
CHEMBL65755
1 / 0 / 0
C00049571 External link 512 Cilinaphthalide A
CHEMBL491523
C00049572 External link 512 Cilinaphthalide B
CHEMBL521623
C00049574 External link 512 Chinensinaphthol methyl ether
CHEMBL510411
C00049575 External link 512 Neojusticin B
CHEMBL455623
C00049576 External link 512 Taiwanin E methyl ether
CHEMBL495475
C00049959 External link 512 5-Methoxyjusticidin A

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00000611 C00000711 C00037881 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002600 0 / 0
Q9Y5X4 Photoreceptor-specific nuclear receptor NR2E3 C00002600 2 / 2
P02545 Prelamin-A/C Unclassified protein C00002600 11 / 10
P11388 DNA topoisomerase 2-alpha Isomerase C00002600 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002600 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002600 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002600 2 / 2
P42858 Huntingtin Unclassified protein C00002600 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002600 2 / 0
O75496 Geminin Unclassified protein C00002600 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002600 4 / 2
Q99700 Ataxin-2 Unclassified protein C00002600 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002600 7 / 3
P51843 Nuclear receptor subfamily 0 group B member 1 Nuclear hormone receptor subfamily 0 group B member 1 C00002600 2 / 2
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002600 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002600 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00002600 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002600 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002600 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002600 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002600 1 / 0
O00255 Menin Unclassified protein C00002600 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002600 1 / 2
P01215 Glycoprotein hormones alpha chain Unclassified protein C00002600 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (43)

OMIM preferred title UniProt
#300018 46,xy sex reversal 2; srxy2 P51843
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300200 Adrenal hypoplasia, congenital; ahc P51843
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#268100 Enhanced s-cone syndrome; escs Q9Y5X4
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#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
#275210 Restrictive dermopathy, lethal P02545
#611131 Retinitis pigmentosa 37; rp37 Q9Y5X4
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (38)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
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)
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)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00552 Glycerol kinase deficiency (GKD) P51843 (related)
H00607 46,XY disorders of sex development (Disorders of gonadal development) P51843 (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) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00527 Retinitis pigmentosa (RP) Q9Y5X4 (related)
H00805 Vitreoretinal degeneration Q9Y5X4 (related)