Plant Species


Cumulative plant class count

class name count
asterids 29

Cumulative family count

class name count
Ericaceae 29

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Grayanoids 2

metabolites link (2)

br08003 Category KEGG ID KNApSAcK ID
Grayanoids C09103 C00003434
Grayanoids C09180 C00003479

KCF-S cluster (2)

KCF-S ID # of metabolite
No. 320 21
No. 1513 6

Metabolite list (27)

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
figure
C00003434 External link 512 Rhodojaponin II
No. 320
C00003479 External link 512 Rhodojaponin II
No. 320
C00040879 External link 512 Rhodojaponin V
No. 320
C00041086 External link 512 Rhodomollein III
No. 320
C00041087 External link 512 Rhodomollein XI
/ (-)-Rhodomollein XI
No. 320
C00042569 External link 512 Rhodomollein XVI
/ (+)-Rhodomollein XVI
No. 320
C00042909 External link 512 Rhodomollein XIII
/ (-)-Rhodomollein XIII
No. 320
C00042910 External link 512 Grayanotoxin I
CHEMBL169387
CHEMBL490705
CHEMBL1971906
C001311
No. 320
C00042911 External link 512 Pierisformosin B
CHEMBL169864
No. 320
C00050196 External link 512 Rhodomollein XIX
/ (+)-Rhodomollein XIX
No. 320
C00042913 External link 512 Asebotoxin V
CHEMBL1610188
4 / 15 / 11 No. 320
C00042915 External link 512 Pierisformosin D
/ (+)-Pierisformosin D
No. 320
C00042916 External link 512 Asebotoxin IV
No. 320
C00043869 External link 512 Rhodomollein XVII
/ (+)-Rhodomollein XVII
No. 320
C00050006 External link 512 Rhodomollein IX
/ (-)-Rhodomollein IX
No. 320
C00043625 External link 512 Rhodojaponin VI
No. 320
C00043865 External link 512 Grayanotoxin III
CHEMBL352732
CHEMBL454313
CHEMBL1567880
CHEMBL1981629
C020751
1 / 0 / 0 No. 320
C00043866 External link 512 Rhodojaponin III
CHEMBL517302
C069461
No. 320
C00043872 External link 512 Rhodomollein I
No. 320
C00043871 External link 512 Grayanotoxin II
CHEMBL453542
CHEMBL1484331
C020750
3 / 2 / 0 No. 320
C00042917 External link 512 Pierisformosin C
/ (-)-Pierisformosin C
No. 320
C00043870 External link 512 Rhodomollein XII
/ (-)-Rhodomollein XII
No. 1513
C00043868 External link 512 Rhodomollein XIV
/ (-)-Rhodomollein XIV
No. 1513
C00043867 External link 512 Kalmanol
No. 1513
C00043873 External link 512 Rhodomollein X
No. 1513
C00043548 External link 512 Rhodomollein XVIII
/ (-)-Rhodomollein XVIII
No. 1513
C00042912 External link 512 Rhodojaponin IV
No. 1513

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00050006 4 / 1
P02545 Prelamin-A/C Unclassified protein C00050006 11 / 10
P00352 Retinal dehydrogenase 1 Enzyme C00043548 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00043548 2 / 0
O75496 Geminin Unclassified protein C00050006 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00050006 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00042569 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00043548 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

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
#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
#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
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637

KEGG DISEASE (11)

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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)