Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Sphingomonadaceae 3
Tricholomataceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (4)

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
C00007485 External link 512 Tetrachlorohydroquinone
/ 2,3,5,6-Tetrachlorohydroquinone
CHEMBL2074639
C044578
1 / 1 / 0 3 / 0
C00007486 External link 512 2,3,6-Trichloro-p-hydroquinone
C00007496 External link 512 Pentachlorophenol
CHEMBL75967
D010416
34 / 52 / 73 38 / 23
C00016089 External link 512 Tetrachloro-pyrocatechol
C423629
2 / 0

Human Protein / Gene in interactions

35 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00007496 7 / 37
P49798 Regulator of G-protein signaling 4 Unclassified protein C00007496 2 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00007496 0 / 0
P02545 Prelamin-A/C Unclassified protein C00007496 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00007496 3 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00007496 3 / 1
P08183 Multidrug resistance protein 1 drug C00007485 1 / 0
P11473 Vitamin D3 receptor NR1I1 C00007496 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00007496 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00007496 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007496 2 / 0
O75496 Geminin Unclassified protein C00007496 0 / 0
P10145 Interleukin-8 Secreted protein C00007496 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00007496 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00007496 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00007496 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00007496 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007496 5 / 3
Q96RI1 Bile acid receptor NR1H4 C00007496 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00007496 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00007496 2 / 2
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00007496 0 / 0
P03372 Estrogen receptor NR3A1 C00007496 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00007496 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00007496 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00007496 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00007496 0 / 0
P10275 Androgen receptor NR3C4 C00007496 3 / 4
P35869 Aryl hydrocarbon receptor Transcription Factor C00007496 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00007496 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007496 1 / 0
O00255 Menin Unclassified protein C00007496 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00007496 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00007496 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007496 1 / 1

41 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1434 CSE1L, CAS, CSE1, XPO2 CSE1 chromosome segregation 1-like (yeast) C00007485 C00007496
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00007496 C00016089
2071 ERCC3, BTF2, GTF2H, RAD25, TFIIH, XPB excision repair cross-complementing rodent repair deficiency, complementation group 3 (EC:3.6.4.12) C00007496
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00007485
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00016089
126 ADH1C, ADH3 alcohol dehydrogenase 1C (class I), gamma polypeptide (EC:1.1.1.1) C00007496
127 ADH4, ADH-2 alcohol dehydrogenase 4 (class II), pi polypeptide (EC:1.1.1.1) C00007496
128 ADH5, ADH-3, ADHX, FALDH, FDH, GSH-FDH, GSNOR alcohol dehydrogenase 5 (class III), chi polypeptide (EC:1.1.1.1 1.1.1.284) C00007496
131 ADH7, ADH4 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide (EC:1.1.1.1) C00007496
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00007496
1234 CCR5, CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5, CMKBR5, IDDM22 chemokine (C-C motif) receptor 5 (gene/pseudogene) C00007496
1583 CYP11A1, CYP11A, CYPXIA1, P450SCC cytochrome P450, family 11, subfamily A, polypeptide 1 (EC:1.14.15.6) C00007496
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00007496
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00007496
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00007496
1555 CYP2B6, CPB6, CYP2B, CYP2B7, CYP2B7P, CYPIIB6, EFVM, IIB1, P450 cytochrome P450, family 2, subfamily B, polypeptide 6 (EC:1.14.14.1) C00007496
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00007496
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) C00007496
1551 CYP3A7, CP37, CYPIIIA7, P450-HFLA cytochrome P450, family 3, subfamily A, polypeptide 7 (EC:1.14.14.1) C00007496
11080 DNAJB4, DNAJW, DjB4, HLJ1 DnaJ (Hsp40) homolog, subfamily B, member 4 C00007496
367 AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM androgen receptor C00007485
2072 ERCC4, ERCC11, FANCQ, RAD1, XPF excision repair cross-complementing rodent repair deficiency, complementation group 4 C00007496
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00007496
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00007496
3295 HSD17B4, DBP, MFE-2, MPF-2, PRLTS1, SDR8C1 hydroxysteroid (17-beta) dehydrogenase 4 (EC:4.2.1.107 4.2.1.119 1.1.1.n12) C00007496
3283 HSD3B1, 3BETAHSD, HSD3B, HSDB3, HSDB3A, I, SDR11E1 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 (EC:1.1.1.145 5.3.3.1) C00007496
3320 HSP90AA1, EL52, HSP86, HSP89A, HSP90A, HSP90N, HSPC1, HSPCA, HSPCAL1, HSPCAL4, HSPN, Hsp89, Hsp90, LAP2 heat shock protein 90kDa alpha (cytosolic), class A member 1 C00007496
59067 IL21, IL-21, Za11 interleukin 21 C00007496
4055 LTBR, CD18, D12S370, LT-BETA-R, TNF-R-III, TNFCR, TNFR-RP, TNFR2-RP, TNFR3, TNFRSF3 lymphotoxin beta receptor (TNFR superfamily, member 3) C00007496
9 NAT1, AAC1, MNAT, NAT-1, NATI N-acetyltransferase 1 (arylamine N-acetyltransferase) (EC:2.3.1.5) C00007496
5241 PGR, NR3C3, PR progesterone receptor C00007496
5447 POR, CPR, CYPOR, P450R P450 (cytochrome) oxidoreductase (EC:1.6.2.4) C00007496
5886 RAD23A, HHR23A, HR23A RAD23 homolog A (S. cerevisiae) C00007496
6462 SHBG, ABP, SBP, TEBG sex hormone-binding globulin C00007496
6770 STAR, STARD1 steroidogenic acute regulatory protein C00007496
6817 SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) C00007496
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00007496
8717 TRADD, Hs.89862 TNFRSF1A-associated via death domain C00007496
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00007496
6846 XCL2, SCM-1b, SCM1B, SCYC2 chemokine (C motif) ligand 2 C00007496
7518 XRCC4 X-ray repair complementing defective repair in Chinese hamster cells 4 C00007496

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (53)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#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
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%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 P84022
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#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
#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
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#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
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#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

KEGG DISEASE (73)

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)
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)
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)
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)
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)
H00036 Osteosarcoma P04637 (related)
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)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (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)
H00409 Type II diabetes mellitus P37231 (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)
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)

Diseases related to CTD interactions

23 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002759 Adenoma, Bile Duct C00007496
D018248 Adenoma, Liver Cell C00007496
D000310 Adrenal Gland Neoplasms C00007496
D002653 Child Behavior Disorders C00007496
D018281 Cholangiocarcinoma C00007496
D003072 Cognition Disorders C00007496
D056486 Drug-Induced Liver Injury C00007496
D006394 Hemangiosarcoma C00007496
D006529 Hepatomegaly C00007496
D006965 Hyperplasia C00007496
D015470 Leukemia, Myeloid, Acute C00007496
D008113 Liver Neoplasms C00007496
D008223 Lymphoma C00007496
D008659 Metabolic Diseases C00007496
D019957 Motor Skills Disorders C00007496
D018777 Multiple Chemical Sensitivity C00007496
D018301 Neoplasms, Mesothelial C00007496
D009422 Nervous System Diseases C00007496
D009845 Oligospermia C00007496
D011041 Poisoning C00007496
D011297 Prenatal Exposure Delayed Effects C00007496
D013160 Splenic Neoplasms C00007496
D013959 Thyroid Diseases C00007496