KCF-S cluster No. 1811 (6 metabolites)

Corresponding Phytochemical cluster No. 62


KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Anthraquinone type 2

metabolites link (2)

br08003 Category KEGG ID KNApSAcK ID
Anthraquinone type C10394 C00002856
Anthraquinone type C10401 C00002861

Metabolite list (6)

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
C00002856 External link 512 Pseudopurpurin
C00002861 External link 512 Rhein
CHEMBL418068
C020491
60 / 65 / 46 8 / 1
C00016317 External link 512 NSC 624610
/ Emodic acid
/ 9,10-Dihydro-4,5,7-trihydroxy-9,10-dioxo-2-anthroic acid
CHEMBL290914
32 / 18 / 20
C00018257 External link 512 Endocrocin
C023523
C00032095 External link 512 Ophiohayatone C
C00033228 External link 512 Munjistin

Human Protein / Gene in interactions

69 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00002861 C00016317 2 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002861 C00016317 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002861 C00016317 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002861 C00016317 1 / 2
O00255 Menin Unclassified protein C00002861 C00016317 2 / 5
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002861 C00016317 1 / 1
P08246 Neutrophil elastase S1A C00002861 C00016317 2 / 1
P06746 DNA polymerase beta Enzyme C00002861 C00016317 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002861 C00016317 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002861 C00016317 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002861 C00016317 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002861 C00016317 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002861 C00016317 4 / 3
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002861 C00016317 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002861 C00016317 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002861 C00016317 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002861 C00016317 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002861 C00016317 0 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002861 C00016317 2 / 2
Q9Y253 DNA polymerase eta Enzyme C00002861 C00016317 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002861 C00016317 0 / 0
P08311 Cathepsin G S1A C00002861 C00016317 0 / 0
P39748 Flap endonuclease 1 Enzyme C00002861 C00016317 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002861 5 / 3
O75496 Geminin Unclassified protein C00002861 0 / 0
P10145 Interleukin-8 Secreted protein C00002861 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002861 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002861 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00016317 0 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00002861 1 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00002861 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00016317 0 / 0
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00002861 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00002861 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002861 2 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002861 2 / 0
Q96RI1 Bile acid receptor NR1H4 C00002861 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00002861 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00016317 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002861 3 / 3
Q15149 Plectin Unclassified protein C00002861 4 / 3
Q9Y3R4 Sialidase-2 Enzyme C00002861 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00002861 0 / 0
P03372 Estrogen receptor NR3A1 C00002861 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00002861 0 / 0
P55210 Caspase-7 C14 C00002861 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002861 2 / 3
P54132 Bloom syndrome protein Enzyme C00002861 1 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00002861 3 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00002861 3 / 2
P02545 Prelamin-A/C Unclassified protein C00002861 11 / 10
Q13547 Histone deacetylase 1 Hydrolase C00016317 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002861 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002861 0 / 0
P29466 Caspase-1 C14 C00002861 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002861 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00016317 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002861 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00002861 2 / 0
Q99700 Ataxin-2 Unclassified protein C00016317 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00016317 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00016317 1 / 4
Q92731 Estrogen receptor beta NR3A2 C00002861 0 / 1
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00002861 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00002861 0 / 0
P09619 Platelet-derived growth factor receptor beta Pdgfr C00002861 5 / 1
P16234 Platelet-derived growth factor receptor alpha Pdgfr C00002861 2 / 1
Q16637 Survival motor neuron protein Unclassified protein C00002861 4 / 1
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00016317 0 / 0

8 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00002861
1950 EGF, HOMG4, URG epidermal growth factor C00002861
2064 ERBB2, CD340, HER-2, HER-2/neu, HER2, MLN_19, NEU, NGL, TKR1 v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (EC:2.7.10.1) C00002861
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00002861
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002861
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002861
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002861
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00002861

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (67)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#615007 Basal ganglia calcification, idiopathic, 4; ibgc4 P09619
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
P84022
Q14191
#162800 Cyclic neutropenia P08246
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#226670 Epidermolysis bullosa simplex with muscular dystrophy Q15149
#612138 Epidermolysis bullosa simplex with pyloric atresia Q15149
#131950 Epidermolysis bullosa simplex, ogna type Q15149
#133239 Esophageal cancer P18054
#615363 Estrogen resistance; estrr P03372
#612219 Ewing sarcoma; es P11308
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P16234
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#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
#607685 Hypereosinophilic syndrome, idiopathic; hes P16234
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#607785 Juvenile myelomonocytic leukemia; jmml P09619
#601626 Leukemia, acute myeloid; aml P09619
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#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
#613723 Muscular dystrophy, limb-girdle, type 2q; lgmd2q Q15149
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#131440 Myeloproliferative disorder, chronic, with eosinophilia P09619
#228550 Myofibromatosis, infantile, 1; imf1 P09619
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P37231
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (49)

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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
Q15149 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
Q15149 (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)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00100 Neutropenic disorders P08246 (related)
H00036 Osteosarcoma P08684 (marker)
H00042 Glioma P09619 (related)
P16234 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (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)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00585 Epidermolysis bullosa, hemidesmosomal Q15149 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008106 Liver Cirrhosis, Experimental C00002861