Metabolite list (25)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
figure
C00002797 External link 512 Cassialoin
CHEMBL1721715
2 / 0 / 0 No. 826
C00044223 External link 512 Chrysophanic acid 9-anthrone
CHEMBL122196
C010430
No. 826
C00044143 External link 512 Pseudohypericin
CHEMBL1614664
C056602
1 / 0 No. 826
C00044047 External link 512 Hypericin
CHEMBL286494
C004965
23 / 24 / 24 7 / 2 No. 826
C00036708 External link 512 Mayoside C
/ (-)-Mayoside C
No. 826
C00034664 External link 512 Picramnioside F
/ (-)-Picramnioside F
No. 826
C00034663 External link 512 10-Hydroxycascaroside C
/ (-)-10-Hydroxycascaroside C
No. 826
C00034662 External link 512 Cascaroside A
No. 826
C00034661 External link 512 Cascaroside B
/ (-)-Cascaroside B
No. 826
C00031656 External link 512 Deacetyllittoraloin
/ (-)-Deacetyllittoraloin
No. 826
C00034660 External link 512 Cascaroside D
No. 826
C00044224 External link 512 Sennoside A
CHEMBL54481
CHEMBL448894
CHEMBL445268
CHEMBL1314924
CHEMBL1356785
CHEMBL1362935
CHEMBL1644069
58 / 59 / 53 No. 1163
C00002799 External link 512 10-Hydroxyaloin B
No. 1163
C00031652 External link 512 Aloin
/ Aloin A
/ Barbaloin
CHEMBL123026
CHEMBL497001
CHEMBL1569106
C045601
2 / 2 / 2 No. 1163
C00031651 External link 512 Aloin B
CHEMBL123026
CHEMBL497001
CHEMBL1569106
2 / 2 / 2 No. 1163
C00031490 External link 512 Rumejaposide C
/ (-)-Rumejaposide C
No. 1163
C00037637 External link 512 Protopseudohypericin
C108324
No. 1163
C00037488 External link 512 Protohypericin
CHEMBL1078768
C108325
No. 1163
C00036884 External link 512 Littoraloside
/ (-)-Littoraloside
No. 1163
C00002855 External link 512 Rumejaposide A
/ (+)-Rumejaposide A
No. 2632
C00034650 External link 512 Littoraloin
/ (-)-Littoraloin
No. 2632
C00002829 External link 512 Rumejaposide E
/ (-)-Rumejaposide E
No. 2632
C00034651 External link 512 Cascaroside C
No. 2632
C00002806 External link 512 Rumejaposide D
/ (-)-Rumejaposide D
No. 3961
C00002863 External link 512 Rumejaposide B
/ (-)-Rumejaposide B
No. 7714

Human Protein / Gene in interactions

65 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00002797 C00002863 C00036708 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002829 C00002863 C00031656 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002829 C00002863 4 / 3
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002829 C00002863 1 / 2
O00255 Menin Unclassified protein C00002829 C00002863 2 / 5
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002829 C00002863 1 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002829 C00002863 1 / 4
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002829 C00002863 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002829 C00002863 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002829 C00002863 3 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00002829 C00002863 0 / 1
P54132 Bloom syndrome protein Enzyme C00002829 C00002863 1 / 2
P11473 Vitamin D3 receptor NR1I1 C00002829 C00002863 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002829 C00002863 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002829 C00002863 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002829 C00002863 0 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002829 C00002863 2 / 2
Q92830 Histone acetyltransferase KAT2A Enzyme C00002829 C00002863 0 / 0
Q9H244 P2Y purinoceptor 12 Purine receptor C00002797 C00036708 1 / 1
O75496 Geminin Unclassified protein C00002863 C00031656 0 / 0
Q2TB90 Putative hexokinase HKDC1 Enzyme C00002863 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002863 4 / 2
P35462 D(3) dopamine receptor Dopamine receptor C00002829 1 / 0
Q9Y253 DNA polymerase eta Enzyme C00002863 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002863 0 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00002863 1 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00002863 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002829 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002863 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002863 2 / 0
P06280 Alpha-galactosidase A Enzyme C00002863 1 / 1
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002829 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002863 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002863 3 / 3
P39748 Flap endonuclease 1 Enzyme C00002863 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002863 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002863 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00002863 0 / 0
P55210 Caspase-7 C14 C00002863 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002863 2 / 2
O75164 Lysine-specific demethylase 4A Enzyme C00002863 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002829 0 / 0
P34998 Corticotropin-releasing factor receptor 1 Corticotropin releasing factor receptor C00002829 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002863 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002863 11 / 10
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002863 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002863 0 / 0
O00167 Eyes absent homolog 2 Enzyme C00002863 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002863 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002863 0 / 0
P29466 Caspase-1 C14 C00002863 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002863 0 / 3
P49798 Regulator of G-protein signaling 4 Unclassified protein C00002863 2 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002829 4 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002863 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002863 0 / 1
P03372 Estrogen receptor NR3A1 C00002863 1 / 1
P19429 Troponin I, cardiac muscle Unclassified protein C00002863 4 / 4
P45379 Troponin T, cardiac muscle Unclassified protein C00002863 3 / 5
P63316 Troponin C, slow skeletal and cardiac muscles Other cytosolic protein C00002863 2 / 2
P63165 Small ubiquitin-related modifier 1 Unclassified protein C00002863 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002863 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00002863 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00002863 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002863 1 / 1

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002829 C00002855
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00002829
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002829
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00002829
2938 GSTA1, GST2, GSTA1-1, GTH1 glutathione S-transferase alpha 1 (EC:2.5.1.18) C00002829
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00002829
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00002829

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (66)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#609821 Bleeding disorder, platelet-type, 8; bdplt8 Q9H244
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#601494 Cardiomyopathy, dilated, 1d; cmd1d P45379
#613286 Cardiomyopathy, dilated, 1ff; cmd1ff P19429
#611879 Cardiomyopathy, dilated, 1z; cmd1z P63316
#611880 Cardiomyopathy, dilated, 2a; cmd2a P19429
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#613243 Cardiomyopathy, familial hypertrophic, 13; cmh13 P63316
#115195 Cardiomyopathy, familial hypertrophic, 2; cmh2 P45379
#613690 Cardiomyopathy, familial hypertrophic, 7; cmh7 P19429
#115210 Cardiomyopathy, familial restrictive, 1; rcm1 P19429
#612422 Cardiomyopathy, familial restrictive, 3; rcm3 P45379
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
P84022
Q14191
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P18054
#615363 Estrogen resistance; estrr P03372
#612219 Ewing sarcoma; es P11308
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#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
#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
#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
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#613705 Orofacial cleft 10; ofc10 P63165
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#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
#190300 Tremor, hereditary essential, 1; etm1 P35462
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (55)

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)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
P19429 (related)
P45379 (related)
P63316 (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)
P45379 (related)
H00026 Endometrial Cancer P03372 (marker)
Q92731 (marker)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (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)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00292 Hypertrophic cardiomyopathy (HCM) P19429 (related)
P45379 (related)
P63316 (related)
H01219 Restrictive cardiomyopathy (RCM) P19429 (related)
P45379 (related)
H00295 Viral myocarditis P19429 (marker)
P45379 (marker)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00516 Isolated orofacial clefts P63165 (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)
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)
H01235 Bleeding disorder platelet-type Q9H244 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D005909 Glioblastoma C00002829
D010146 Pain C00002829