KCF-S cluster No. 3405 (3 metabolites)

Corresponding Phytochemical cluster No. 1


Plant Species


Cumulative plant class count

class name count
Liliopsida 3

Cumulative family count

class name count
Arecaceae 3

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Pyridine alkaloids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Pyridine alkaloids C10129 C00002020

Metabolite list (3)

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
C00002020 External link 512 Arecoline
CHEMBL7303
D001115
15 / 22 / 18 64 / 21
C00044165 External link 512 Ethyl N-methyl-1,2,5,6-tetrahydro-pyridine-3-carboxylate
C00044191 External link 512 Guvacoline
CHEMBL268808
C094105
1 / 1 / 0

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00002020 C00044191 1 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00002020 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002020 11 / 10
P10828 Thyroid hormone receptor beta NR1A2 C00002020 3 / 1
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00002020 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002020 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00002020 2 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00002020 2 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002020 1 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002020 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00002020 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002020 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002020 0 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00002020 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002020 1 / 4

64 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
57491 AHRR, AHH, AHHR, bHLHe77 aryl-hydrocarbon receptor repressor C00002020
10327 AKR1A1, ALDR1, ALR, ARM, DD3 aldo-keto reductase family 1, member A1 (aldehyde reductase) (EC:1.1.1.2) C00002020
223 ALDH9A1, ALDH4, ALDH7, ALDH9, E3, TMABADH aldehyde dehydrogenase 9 family, member A1 (EC:1.2.1.3 1.2.1.19 1.2.1.47) C00002020
328 APEX1, APE, APE1, APEN, APEX, APX, HAP1, REF1 APEX nuclease (multifunctional DNA repair enzyme) 1 (EC:4.2.99.18) C00002020
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002020
672 BRCA1, BRCAI, BRCC1, BROVCA1, IRIS, PNCA4, PPP1R53, PSCP, RNF53 breast cancer 1, early onset C00002020
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002020
6352 CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP chemokine (C-C motif) ligand 5 C00002020
902 CCNH, CAK, p34, p37 cyclin H C00002020
995 CDC25C, CDC25, PPP1R60 cell division cycle 25C (EC:3.1.3.48) C00002020
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00002020
10036 CHAF1A, CAF-1, CAF1, CAF1B, CAF1P150, P150 chromatin assembly factor 1, subunit A (p150) C00002020
8208 CHAF1B, CAF-1, CAF-IP60, CAF1, CAF1A, CAF1P60, MPHOSPH7, MPP7 chromatin assembly factor 1, subunit B (p60) C00002020
1131 CHRM3, EGBRS, HM3 cholinergic receptor, muscarinic 3 C00002020
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002020
56603 CYP26B1, CYP26A2, P450RAI-2, P450RAI2, RHFCA cytochrome P450, family 26, subfamily B, polypeptide 1 C00002020
64858 DCLRE1B, APOLLO, SNM1B, SNMIB DNA cross-link repair 1B C00002020
54541 DDIT4, Dig2, REDD-1, REDD1 DNA-damage-inducible transcript 4 C00002020
3301 DNAJA1, DJ-2, DjA1, HDJ2, HSDJ, HSJ2, HSPF4, NEDD7, hDJ-2 DnaJ (Hsp40) homolog, subfamily A, member 1 C00002020
9521 EEF1E1, AIMP3, P18 eukaryotic translation elongation factor 1 epsilon 1 C00002020
2068 ERCC2, COFS2, EM9, TTD, XPD excision repair cross-complementing rodent repair deficiency, complementation group 2 (EC:3.6.4.12) C00002020
2189 FANCG, FAG, XRCC9 Fanconi anemia, complementation group G C00002020
9518 GDF15, GDF-15, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB growth differentiation factor 15 C00002020
2937 GSS, GSHS glutathione synthetase (EC:6.3.2.3) C00002020
2966 GTF2H2, BTF2, BTF2P44, T-BTF2P44, TFIIH, p44 general transcription factor IIH, polypeptide 2, 44kDa C00002020
404672 GTF2H5, C6orf175, TFB5, TFIIH, TGF2H5, TTD, TTD-A, TTDA, bA120J8.2 general transcription factor IIH, polypeptide 5 C00002020
51182 HSPA14, HSP70-4, HSP70L1 heat shock 70kDa protein 14 C00002020
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00002020
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002020
51451 LCMT1, LCMT, PPMT1 leucine carboxyl methyltransferase 1 (EC:2.1.1.233) C00002020
4128 MAOA, MAO-A monoamine oxidase A (EC:1.4.3.4) C00002020
100302175 MIR1207, MIRN1207, hsa-mir-1207 microRNA 1207 C00002020
100188847 MIR1225, MIRN1225 microRNA 1225 C00002020
100302142 MIR1246, MIRN1246, hsa-mir-1246 microRNA 1246 C00002020
100302233 MIR1268A, MIR1268, MIRN1268, hsa-mir-1268, hsa-mir-1268a microRNA 1268a C00002020
100302276 MIR1290, MIRN1290, hsa-mir-1290 microRNA 1290 C00002020
100302270 MIR1305, MIRN1305, hsa-mir-1305 microRNA 1305 C00002020
406927 MIR136, MIRN136, miRNA136 microRNA 136 C00002020
406935 MIR143, MIRN143 microRNA 143 C00002020
406937 MIR145, MIRN145, miR-145, miRNA145 microRNA 145 C00002020
100302137 MIR1914, MIRN1914, hsa-mir-1914 microRNA 1914 C00002020
100302129 MIR1915, MIRN1915, hsa-mir-1915 microRNA 1915 C00002020
406978 MIR199B, MIRN199B, mir-199b microRNA 199b C00002020
407010 MIR23A, MIRN23A, hsa-mir-23a, miRNA23A microRNA 23a C00002020
407015 MIR26A1, MIR26A, MIRN26A1 microRNA 26a-1 C00002020
407017 MIR26B, MIRN26B, hsa-mir-26b, miR-26b microRNA 26b C00002020
407026 MIR29C, MIRN29C, miRNA29C microRNA 29c C00002020
407029 MIR30A, MIRN30A microRNA 30a C00002020
693215 MIR630, MIRN630, hsa-mir-630 microRNA 630 C00002020
4292 MLH1, COCA2, FCC2, HNPCC, HNPCC2, hMLH1 mutL homolog 1 C00002020
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00002020
4436 MSH2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2 mutS homolog 2 C00002020
4489 MT1A, MT1, MT1S, MTC metallothionein 1A C00002020
9027 NAT8, ATase2, CML1, GLA, Hcml1, TSC501, TSC510 N-acetyltransferase 8 (GCN5-related, putative) C00002020
5591 PRKDC, DNA-PKcs, DNAPK, DNPK1, HYRC, HYRC1, XRCC7, p350 protein kinase, DNA-activated, catalytic polypeptide (EC:2.7.11.1) C00002020
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) C00002020
5810 RAD1, HRAD1, REC1 RAD1 homolog (S. pombe) (EC:3.1.11.2) C00002020
10111 RAD50, NBSLD, RAD502, hRad50 RAD50 homolog (S. cerevisiae) C00002020
6283 S100A12, CAAF1, CAGC, CGRP, ENRAGE, MRP-6, MRP6, p6 S100 calcium binding protein A12 C00002020
8243 SMC1A, CDLS2, DXS423E, SB1.8, SMC1, SMC1L1, SMC1alpha, SMCB structural maintenance of chromosomes 1A C00002020
7076 TIMP1, CLGI, EPA, EPO, HCI, TIMP TIMP metallopeptidase inhibitor 1 C00002020
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002020
56886 UGGT1, HUGT1, UGCGL1, UGT1 UDP-glucose glycoprotein glucosyltransferase 1 C00002020
100126299 VTRNA2-1, CBL-3, CBL3, MIR886, MIRN886, VTRNA2, hsa-mir-886, hvg-5, nc886 vault RNA 2-1 C00002020

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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

KEGG DISEASE (18)

KEGG name UniProt
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)
H00036 Osteosarcoma P08684 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)

Diseases related to CTD interactions

21 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00002020
D001919 Bradycardia C00002020
D002277 Carcinoma C00002020
D002280 Carcinoma, Basal Cell C00002020
D002375 Catalepsy C00002020
D020820 Dyskinesias C00002020
D006965 Hyperplasia C00002020
D007022 Hypotension C00002020
D007153 Immunologic Deficiency Syndromes C00002020
D009062 Mouth Neoplasms C00002020
D009127 Muscle Rigidity C00002020
D009374 Neoplasms, Experimental C00002020
D019954 Neurobehavioral Manifestations C00002020
D009914 Oral Submucous Fibrosis C00002020
D010212 Papilloma C00002020
D010243 Paralysis C00002020
D020734 Parkinsonian Disorders C00002020
D011470 Prostatic Hyperplasia C00002020
D013226 Status Epilepticus C00002020
D014062 Tongue Neoplasms C00002020
D014202 Tremor C00002020