KCF-S cluster No. 376 (17 metabolites)

Corresponding Phytochemical cluster No. 3


Plant Species


Cumulative plant class count

class name count
rosids 221
eudicotyledons 6
asterids 3

Cumulative family count

class name count
Fabaceae 219
Berberidaceae 5
Convolvulaceae 2
Viscaceae 1
Orobanchaceae 1
Anacardiaceae 1
Rosaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Quinolizidine alkaloids 3

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Quinolizidine alkaloids C10760 C00002216
Quinolizidine alkaloids C10763 C00002218
Quinolizidine alkaloids C10781 C00002234

Metabolite list (17)

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
C00002216 External link 512 Caulophylline
/ N-Methylcytisine
/ (-)-N-Methylcytisine
CHEMBL66191
CHEMBL1085045
C034245
C00002218 External link 512 Cytisine
/ (-)-Cytisine
CHEMBL47039
CHEMBL497939
CHEMBL1628606
C004712
27 / 36 / 33 6 / 1
C00002234 External link 512 Rhombifoline
/ (-)-Rhombifoline
CHEMBL1397610
C119591
C00007725 External link 512 Sophorasine A
C00007726 External link 512 Sophorasine B
C00007727 External link 512 Ethyl 12-cytisineacetate
C00007728 External link 512 12-Cytisineacetamide
CHEMBL508431
C00007735 External link 512 N-Formylcytisine
/ (-)-N-Formylcytisine
CHEMBL1396784
CHEMBL1433686
4 / 6 / 11
C00007736 External link 512 N-Acetylcytisine
CHEMBL1513538
CHEMBL1553838
2 / 3 / 7
C00007737 External link 512 Ethyl cytisine-12-carboxylate
/ 12-Carboxycytisine ethyl ester
C00007738 External link 512 N-Carbomethoxycytisine
/ 12-Carboxycytisine methyl ester
C00007742 External link 512 12-Hydroxycytisine
C00026275 External link 512 (-)-N-(3-Oxobutyl)cytisine
CHEMBL190851
4 / 3 / 1
C00026276 External link 512 (-)-N-(N-Acetylaminomethyl)cytisine
C00026325 External link 512 Dehydrocytisine A
/ (-)-Dehydrocytisine A
CHEMBL47039
CHEMBL497939
CHEMBL1628606
27 / 36 / 33
C00026326 External link 512 Dehydrocytisine B
/ (-)-Dehydrocytisine B
CHEMBL47039
CHEMBL497939
CHEMBL1628606
27 / 36 / 33
C00026339 External link 512 N-(3-Oxobutyl)cytisine
CHEMBL190851
4 / 3 / 1

Human Protein / Gene in interactions

28 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P32297 Neuronal acetylcholine receptor subunit alpha-3 CHRN alpha C00002218 C00026275 C00026325 C00026326 C00026339 1 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002218 C00007735 C00007736 C00026325 C00026326 1 / 2
O00255 Menin Unclassified protein C00002218 C00007735 C00007736 C00026325 C00026326 2 / 5
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00002218 C00026275 C00026325 C00026326 C00026339 0 / 0
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00002218 C00026275 C00026325 C00026326 C00026339 1 / 1
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00002218 C00026275 C00026325 C00026326 C00026339 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002218 C00007735 C00026325 C00026326 0 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00002218 C00026325 C00026326 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002218 C00026325 C00026326 1 / 0
P07510 Acetylcholine receptor subunit gamma CHRN gamma C00002218 C00026325 C00026326 2 / 1
P02545 Prelamin-A/C Unclassified protein C00002218 C00026325 C00026326 11 / 10
P02708 Acetylcholine receptor subunit alpha CHRN alpha C00002218 C00026325 C00026326 3 / 2
P11230 Acetylcholine receptor subunit beta CHRN beta C00002218 C00026325 C00026326 2 / 1
O75496 Geminin Unclassified protein C00002218 C00026325 C00026326 0 / 0
Q07001 Acetylcholine receptor subunit delta CHRN delta C00002218 C00026325 C00026326 3 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002218 C00026325 C00026326 0 / 0
P36544 Neuronal acetylcholine receptor subunit alpha-7 CHRN alpha C00002218 C00026325 C00026326 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002218 C00026325 C00026326 0 / 0
Q01196 Runt-related transcription factor 1 Unclassified protein C00002218 C00026325 C00026326 1 / 4
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002218 C00026325 C00026326 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002218 C00026325 C00026326 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002218 C00026325 C00026326 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002218 C00026325 C00026326 0 / 0
P04062 Glucosylceramidase Enzyme C00002218 C00026325 C00026326 6 / 4
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002218 C00026325 C00026326 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00002218 C00026325 C00026326 0 / 1
Q15822 Neuronal acetylcholine receptor subunit alpha-2 CHRN alpha C00002218 C00026325 C00026326 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00007735 3 / 3

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1135 CHRNA2 cholinergic receptor, nicotinic, alpha 2 (neuronal) C00002218
1136 CHRNA3, LNCR2, NACHRA3, PAOD2 cholinergic receptor, nicotinic, alpha 3 (neuronal) C00002218
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00002218
1139 CHRNA7, CHRNA7-2, NACHRA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) C00002218
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00002218
1143 CHRNB4 cholinergic receptor, nicotinic, beta 4 (neuronal) C00002218

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (39)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#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
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#610353 Epilepsy, nocturnal frontal lobe, 4; enfl4 Q15822
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#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
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#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
#265000 Multiple pterygium syndrome, escobar variant; evmps P07510
#253290 Multiple pterygium syndrome, lethal type; lmps P02708
P07510
Q07001
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#608931 Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency P11230
#608930 Myasthenic syndrome, congenital, fast-channel P02708
Q07001
#601462 Myasthenic syndrome, congenital, slow-channel; sccms P02708
P11230
Q07001
#168600 Parkinson disease, late-onset; pd P04062
#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
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (36)

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)
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)
H00770 Congenital myasthenic syndrome P02708 (related)
P11230 (related)
Q07001 (related)
H00986 Multiple pterygium syndrome P02708 (related)
P07510 (related)
Q07001 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00036 Osteosarcoma P08684 (marker)
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)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (related)
Q15822 (related)
H01171 Poor drug metabolism (PM) P33261 (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)
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

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D012640 Seizures C00002218