KCF-S cluster No. 502 (16 metabolites)

Corresponding Phytochemical cluster No. 4


Plant Species


Cumulative plant class count

class name count
asterids 55

Cumulative family count

class name count
Apocynaceae 55
Diclidophoridae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Indole alkaloids 3

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Indole alkaloids C09035 C00001688
Indole alkaloids C09146 C00001713
Indole alkaloids C09149 C00001714

Metabolite list (16)

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
C00001688 External link 512 Apovincamine
CHEMBL1163488
C063621
C00001713 External link 512 Eburnamine
/ (-)-Eburnamine
CHEMBL2104946
C00001714 External link 512 Eburnamonine
CHEMBL1318553
CHEMBL1553441
CHEMBL1733074
CHEMBL1892145
14 / 20 / 16
C00024535 External link 512 Goniomitine
/ (-)-Goniomitine
C00025041 External link 512 (-)-11-Methoxyeburnamonine
C00025047 External link 512 Vincamenine
/ (-)-Eburnamenine
/ cis-Vincamenine
CHEMBL1097688
C00025051 External link 512 O-Methyleburnamine
/ (-)-O-Methyleburnamine
/ O-Methyl-(-)-eburnamine
CHEMBL1097360
CHEMBL1164562
C00025061 External link 512 (+)-Eburnamenine
CHEMBL1097688
C00025062 External link 512 (+)-Isoeburnamine
CHEMBL2104946
C00025071 External link 512 16-Epivincanol
CHEMBL2104946
C00025075 External link 512 (+)-O-methylisoeburnamine
CHEMBL1097360
CHEMBL1164562
C00025079 External link 512 20-Oxoeburnamenine
C00027619 External link 512 (+)-19-Oxoeburnamine
C00027628 External link 512 (+)-Vincamone
/ d-Eburnamonine
/ (+)-Eburnamonine
/ (+)-cis-Vincamone
/ (+)-cis-Eburnamonine
CHEMBL1318553
CHEMBL1553441
CHEMBL1733074
CHEMBL1892145
C016422
14 / 20 / 16 2 / 0
C00042577 External link 512 Hecubine
C00047264 External link 512 Kopsiyunnanine D
/ (-)-Kopsiyunnanine D
CHEMBL564146

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001714 C00027628 1 / 0
Q99700 Ataxin-2 Unclassified protein C00001714 C00027628 1 / 1
P02545 Prelamin-A/C Unclassified protein C00001714 C00027628 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00001714 C00027628 3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001714 C00027628 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001714 C00027628 2 / 0
O75496 Geminin Unclassified protein C00001714 C00027628 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001714 C00027628 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00001714 C00027628 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001714 C00027628 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001714 C00027628 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001714 C00027628 0 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001714 C00027628 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001714 C00027628 1 / 0

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1129 CHRM2, HM2 cholinergic receptor, muscarinic 2 C00027628
1132 CHRM4, HM4, M4R cholinergic receptor, muscarinic 4 C00027628

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (16)

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)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)