PCIDB

Solanum dulcamara

Family in NCBI taxonomy	Solanaceae
ID	4070

Kingdom (Superkingdom) in NCBI taxonomy	Viridiplantae
ID	33090

Plant class	asterids
ID	71274

KNApSAcK ID	name	ChEMBL link	CTD link	# of proteins in ChEMBL interaction / related OMIM / related KEGG DISEASE	KCF-S cluster	phytochemical cluster
C00003778	Lycoxanthin				No. 97	No. 59
C00022905	Lycophyll / psi,psi-Carotene-16,16'-diol				No. 97	No. 59
C00025533	Megacarpidin / Soladulcidine / Megacarpidine / 5alpha,25D-Solasodan-3b-ol	CHEMBL365417 CHEMBL1476096 CHEMBL1622974 CHEMBL1976775 CHEMBL1998601 CHEMBL2165711		10 / 15 / 14	No. 171	No. 11
C00002283	Calystegin B2 / Calystegine B2	CHEMBL526330 CHEMBL513797 CHEMBL1213469 CHEMBL1984376	C095613	1 / 6 / 4	No. 643	No. 1
C00002282	Calystegin A3 / Calystegine A3				No. 643	No. 1

accession	description	class description	KNApSAcK metabolite in interactions	# of diseases (OMIM / KEGG)
Q15125	3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase	Enzyme	C00025533	1 / 1
P10635	Cytochrome P450 2D6	Cytochrome P450 2D6	C00025533	1 / 0
P04062	Glucosylceramidase	Enzyme	C00002283	6 / 4
O75604	Ubiquitin carboxyl-terminal hydrolase 2	Enzyme	C00025533	0 / 0
P02545	Prelamin-A/C	Unclassified protein	C00025533	11 / 10
P11712	Cytochrome P450 2C9	Cytochrome P450 2C9	C00025533	0 / 1
P00352	Retinal dehydrogenase 1	Enzyme	C00025533	0 / 0
Q99720	Sigma non-opioid intracellular receptor 1	Membrane receptor	C00025533	1 / 0
P05177	Cytochrome P450 1A2	Cytochrome P450 1A2	C00025533	0 / 0
P33261	Cytochrome P450 2C19	Cytochrome P450 2C19	C00025533	1 / 1
P08684	Cytochrome P450 3A4	Cytochrome P450 3A4	C00025533	0 / 1

OMIM	preferred title	UniProt
#614373	Amyotrophic lateral sclerosis 16, juvenile; als16	Q99720
#115200	Cardiomyopathy, dilated, 1a; cmd1a	P02545
#212112	Cardiomyopathy, dilated, with hypergonadotropic hypogonadism	P02545
#605588	Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1	P02545
#302960	Chondrodysplasia punctata 2, x-linked dominant; cdpx2	Q15125
#609535	Drug metabolism, poor, cyp2c19-related	P33261
#608902	Drug metabolism, poor, cyp2d6-related	P10635
#181350	Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2	P02545
#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
#610140	Heart-hand syndrome, slovenian type	P02545
#176670	Hutchinson-gilford progeria syndrome; hgps	P02545
#151660	Lipodystrophy, familial partial, type 2; fpld2	P02545
#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
#168600	Parkinson disease, late-onset; pd	P04062
#275210	Restrictive dermopathy, lethal	P02545

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)
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)
H01205	Coumarin resistance	P11712 (related)
H01171	Poor drug metabolism (PM)	P33261 (related)
H01194	X-linked chondrodysplasia punctata	Q15125 (related)