Species

KNApSAcK Entry

Organism name Lophophora williamsii
Genus Lophophora
Family Cactaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lophophora williamsii
Linked NCBI taxonomy ID 130138
Linked level species

Family

Family in NCBI taxonomy Cactaceae
ID 3593

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Natural Activity

List (47)

Species Activity
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Analgesic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Analgesic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Anorective
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Antiseptic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Antiseptic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Antispasmodic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Antispasmodic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Asthmatic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Asthmatic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Bradycardiac
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Bradycardic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Cardiotonic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Cardiotonic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. CNS Deressant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. CNS-Depressant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Emetic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Emetic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hallucinogen
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hallucinogen
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hypoglycemic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hypoglycemic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hypotensive
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Hypotensive
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Intoxicant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Intoxicant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Lactagogue
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Lactagogue
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Narcotic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Narcotic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Panacea
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Panacea
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Poison
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Poison
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Psychedelic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Psychedelic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Respiradepressant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Respirodepressant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Sedative
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Sedative
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Stimulant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Stimulant
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Sympathicomimetic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Sympathomimetic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Tonic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Tonic
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Vasodilator
Lophophora williamsii (Lem. Ex Salm-Dyck) J. M. Coult. Vasodilator

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
KCF-S
cluster
phytochemical
cluster
figure
C00001421 External link 512 N-Methylmescaline
CHEMBL100531
No. 723 No. 6
C00001419 External link 512 Mescaline
CHEMBL26687
D008635
3 / 0 / 0 0 / 1 No. 723 No. 6
C00001435 External link 512 Tyramine
CHEMBL11608
D014439
23 / 11 / 6 6 / 9 No. 936 No. 6
C00001408 External link 512 Dopamine
CHEMBL59
D004298
69 / 40 / 56 51 / 52 No. 1114 No. 6
C00042228 External link 512 Anhalamine
No. 1943 No. 4
C00001901 External link 512 Pellotine
CHEMBL1186202
C016645
No. 1943 No. 4
C00001881 External link 512 Lophophorine
C008296
No. 4329 No. 4

Human Protein / Gene in interactions

81 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001408 C00001435 1 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001408 C00001435 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001408 C00001435 0 / 0
O15245 Solute carrier family 22 member 1 Drug uniporter C00001408 C00001435 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001408 C00001435 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001408 C00001435 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001408 C00001435 0 / 0
P14679 Tyrosinase Oxidoreductase C00001408 C00001435 4 / 2
P21728 D(1A) dopamine receptor Dopamine receptor C00001408 C00001435 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001408 C00001435 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001408 C00001435 0 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00001408 C00001435 2 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001408 C00001435 0 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001408 C00001435 0 / 0
P49286 Melatonin receptor type 1B Melatonin receptor C00001408 0 / 1
O43704 Sulfotransferase family cytosolic 1B member 1 Enzyme C00001408 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00001408 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00001408 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001435 1 / 1
Q01959 Sodium-dependent dopamine transporter Dopamine C00001408 1 / 0
P21918 D(1B) dopamine receptor Dopamine receptor C00001408 1 / 0
P06241 Tyrosine-protein kinase Fyn Src C00001408 0 / 0
O95622 Adenylate cyclase type 5 Enzyme C00001408 1 / 0
P43166 Carbonic anhydrase 7 Lyase C00001408 0 / 0
P16662 UDP-glucuronosyltransferase 2B7 Enzyme C00001408 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00001408 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00001408 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00001408 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00001408 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00001408 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00001408 1 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001408 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001408 0 / 0
O75496 Geminin Unclassified protein C00001435 0 / 0
P50225 Sulfotransferase 1A1 Enzyme C00001408 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00001408 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001408 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00001435 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00001408 1 / 0
P46098 5-hydroxytryptamine receptor 3A NS C00001435 0 / 0
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001419 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00001408 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001435 0 / 0
P50224 Sulfotransferase 1A3/1A4 Enzyme C00001408 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001435 2 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001408 2 / 0
P48039 Melatonin receptor type 1A Melatonin receptor C00001408 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001408 0 / 0
P56817 Beta-secretase 1 A1A C00001435 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001408 1 / 1
Q16790 Carbonic anhydrase 9 Lyase C00001408 0 / 1
Q16853 Membrane primary amine oxidase Enzyme C00001408 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001408 3 / 3
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00001408 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001419 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001419 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00001408 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001408 0 / 0
O15244 Solute carrier family 22 member 2 Drug uniporter C00001408 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001408 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00001408 7 / 37
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001408 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00001408 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00001408 4 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein C00001408 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00001408 1 / 1
P07451 Carbonic anhydrase 3 Lyase C00001408 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00001408 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00001408 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00001408 3 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001408 0 / 0
P40225 Thrombopoietin Unclassified protein C00001408 1 / 1
P42345 Serine/threonine-protein kinase mTOR Enzyme C00001408 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001408 1 / 1
O75751 Solute carrier family 22 member 3 Unclassified protein C00001435 0 / 0
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001408 0 / 0
P35368 Alpha-1B adrenergic receptor Adrenergic receptor C00001408 0 / 0
P35348 Alpha-1A adrenergic receptor Adrenergic receptor C00001408 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00001408 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00001408 0 / 0
Q96RJ0 Trace amine-associated receptor 1 Trace amine receptor C00001435 0 / 0

52 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
6530 SLC6A2, NAT1, NET, NET1, SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 2 C00001408 C00001435
134864 TAAR1, RP11-295F4.9, TA1, TAR1, TRAR1 trace amine associated receptor 1 C00001408 C00001435
6818 SULT1A3, HAST, HAST3, M-PST, ST1A3/ST1A4, ST1A5, STM, TL-PST sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 (EC:2.8.2.1) C00001408 C00001435
6532 SLC6A4, 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT solute carrier family 6 (neurotransmitter transporter), member 4 C00001408 C00001435
6531 SLC6A3, DAT, DAT1, PKDYS solute carrier family 6 (neurotransmitter transporter), member 3 C00001408 C00001435
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00001408
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00001408
847 CAT catalase (EC:1.11.1.6) C00001408
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00001408
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001408
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00001408
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) C00001408
1812 DRD1, DADR, DRD1A dopamine receptor D1 C00001408
1813 DRD2, D2DR, D2R dopamine receptor D2 C00001408
2152 F3, CD142, TF, TFA coagulation factor III (thromboplastin, tissue factor) C00001408
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00001408
2668 GDNF, ATF1, ATF2, HFB1-GDNF, HSCR3 glial cell derived neurotrophic factor C00001408
2938 GSTA1, GST2, GSTA1-1, GTH1 glutathione S-transferase alpha 1 (EC:2.5.1.18) C00001408
2944 GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 glutathione S-transferase mu 1 (EC:2.5.1.18) C00001408
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00001408
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00001408
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00001408
3359 HTR3A, 5-HT-3, 5-HT3A, 5-HT3R, 5HT3R, HTR3 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic C00001408
9177 HTR3B, 5-HT3B 5-hydroxytryptamine (serotonin) receptor 3B, ionotropic C00001408
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001408
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00001408
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001408
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00001408
4137 MAPT, DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, TAU microtubule-associated protein tau C00001408
2475 MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) C00001408
4548 MTR, HMAG, MS, cblG 5-methyltetrahydrofolate-homocysteine methyltransferase (EC:2.1.1.13) C00001408
5071 PARK2, AR-JP, LPRS2, PDJ, PRKN parkin RBR E3 ubiquitin protein ligase C00001408
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00001408
5617 PRL prolactin C00001408
5998 RGS3, C2PA, RGP3 regulator of G-protein signaling 3 C00001408
6198 RPS6KB1, PS6K, S6K, S6K-beta-1, S6K1, STK14A, p70_S6KA, p70(S6K)-alpha, p70-S6K, p70-alpha ribosomal protein S6 kinase, 70kDa, polypeptide 1 (EC:2.7.11.1) C00001408
6343 SCT secretin C00001408
6570 SLC18A1, CGAT, VAT1, VMAT1 solute carrier family 18 (vesicular monoamine transporter), member 1 C00001408
6571 SLC18A2, SVAT, SVMT, VAT2, VMAT2 solute carrier family 18 (vesicular monoamine transporter), member 2 C00001408
85413 SLC22A16, CT2, FLIPT2, OAT6, OCT6, OKB1, dJ261K5.1 solute carrier family 22 (organic cation/carnitine transporter), member 16 C00001408
9016 SLC25A14, BMCP1, UCP5 solute carrier family 25 (mitochondrial carrier, brain), member 14 C00001408
183 AGT, ANHU, SERPINA8 angiotensinogen (serpin peptidase inhibitor, clade A, member 8) C00001408
664 BNIP3, NIP3 BCL2/adenovirus E1B 19kDa interacting protein 3 C00001408
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001408
6622 SNCA, NACP, PARK1, PARK4, PD1 synuclein, alpha (non A4 component of amyloid precursor) C00001408
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) C00001408
27113 BBC3, JFY-1, JFY1, PUMA BCL2 binding component 3 C00001408
581 BAX, BCL2L4 BCL2-associated X protein C00001408
7054 TH, DYT14, DYT5b, TYH tyrosine hydroxylase (EC:1.14.16.2) C00001408
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00001408
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00001408
4128 MAOA, MAO-A monoamine oxidase A (EC:1.4.3.4) C00001435

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (43)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P14416
P31645
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#606798 Blepharospasm, benign essential P21918
#300615 Brunner syndrome P21397
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#606703 Dyskinesia, familial, with facial myokymia; fdfm O95622
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#159900 Myoclonic dystonia P14416
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#607276 Resting heart rate, variation in P08588
#600852 Retinitis pigmentosa 17; rp17 P22748
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#190300 Tremor, hereditary essential, 1; etm1 P35462

KEGG DISEASE (57)

KEGG name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (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)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
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)
H00079 Asthma P07550 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00409 Type II diabetes mellitus P49286 (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)

Diseases related to CTD interactions

59 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006973 Hypertension C00001408
C00001435
D013610 Tachycardia C00001408
C00001435
D007022 Hypotension C00001408
C00001435
D017202 Myocardial Ischemia C00001408
D002303 Cardiac Output, Low C00001408
D002375 Catalepsy C00001408
D002389 Catatonia C00001408
D002493 Central Nervous System Diseases C00001408
D019970 Cocaine-Related Disorders C00001408
D004342 Drug Hypersensitivity C00001408
D062787 Drug Overdose C00001408
D004409 Dyskinesia, Drug-Induced C00001408
D004417 Dyspnea C00001408
D004802 Eosinophilia C00001408
D006323 Heart Arrest C00001408
D006331 Heart Diseases C00001408
D006333 Heart Failure C00001408
D006556 Heroin Dependence C00001408
D006930 Hyperalgesia C00001408
D006948 Hyperkinesis C00001408
D058186 Acute Kidney Injury C00001408
D007008 Hypokalemia C00001408
D018476 Hypokinesia C00001408
D001145 Arrhythmias, Cardiac C00001408
D007024 Hypotension, Orthostatic C00001408
D007859 Learning Disorders C00001408
D008133 Long QT Syndrome C00001408
D020149 Manganese Poisoning C00001408
D048629 Micronuclei, Chromosome-Defective C00001408
D001480 Basal Ganglia Diseases C00001408
D009205 Myocarditis C00001408
D009336 Necrosis C00001408
D009410 Nerve Degeneration C00001408
D009422 Nervous System Diseases C00001408
D009846 Oliguria C00001408
D010300 Parkinson Disease C00001408
D020734 Parkinsonian Disorders C00001408
D010547 Persistent Fetal Circulation Syndrome C00001408
D011595 Psychomotor Agitation C00001408
D012127 Respiratory Distress Syndrome, Newborn C00001408
D012640 Seizures C00001408
D012769 Shock C00001408
D012770 Shock, Cardiogenic C00001408
D012772 Shock, Septic C00001408
D013226 Status Epilepticus C00001408
D013375 Substance Withdrawal Syndrome C00001408
D000788 Angina Pectoris, Variant C00001408
D013616 Tachycardia, Sinus C00001408
D016171 Torsades de Pointes C00001408
D014202 Tremor C00001408
D020301 Vasospasm, Intracranial C00001408
D018487 Ventricular Dysfunction, Left C00001408
D011605 Psychoses, Substance-Induced C00001419
D009202 Cardiomyopathies C00001435
D002543 Cerebral Hemorrhage C00001435
D002637 Chest Pain C00001435
D008881 Migraine Disorders C00001435
D015878 Mydriasis C00001435
D011041 Poisoning C00001435