Plant Species


Cumulative plant class count

class name count
asterids 28

Cumulative family count

class name count
Apiaceae 28

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (21)

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
C00021386 External link 512 Teferidin
CHEMBL516694
CHEMBL1999942
1 / 1 / 1
C00021387 External link 512 Akiferidin
CHEMBL464462
1 / 1 / 1
C00021388 External link 512 Teferin
CHEMBL464467
CHEMBL1552750
CHEMBL1967912
9 / 13 / 9
C00021389 External link 512 Ferutinin
/ Jaeschkeanadiol p-hydroxybenzoate
CHEMBL465040
C111068
3 / 1 / 1
C00021390 External link 512 Ferutin
C00021397 External link 512 Feruginidin
/ 14-Hydroxyferutinin
C00021399 External link 512 Ferugin
CHEMBL1836964
C00021401 External link 512 Lancerodiol 6-(4-hydroxybenzoate)
CHEMBL1836966
C00021402 External link 512 Lancerodiol 6-(4-methoxybenzoate)
CHEMBL1836965
C00021403 External link 512 Lancerodiol vanillate
C00033573 External link 512 6-(p-Hydroxybenzoyl)lancerotriol
/ Lancerotriol 6-(p-hydroxybenzoate)
C00033804 External link 512 Elaeochytrin A
/ (+)-Elaeochytrin A
C00033805 External link 512 Elaeochytrin B
/ (+)-Elaeochytrin B
C00036567 External link 512 4beta,8alpha-Dihydroxy-6alpha-vanilloyloxydauc-9-ene
C00037144 External link 512 Ferutidin
/ Jaeschkeanadiol p-methoxybenzoate
CHEMBL465265
1 / 1 / 1
C00037397 External link 512 Kuhistanicaol B
/ (+)-Kuhistanicaol B
C00037398 External link 512 Kuhistanicaol C
/ (+)-Kuhistanicaol C
C00037399 External link 512 Kuhistanicaol D
/ (+)-Kuhistanicaol D
C00037400 External link 512 Kuhistanicaol E
/ (+)-Kuhistanicaol E
C00037401 External link 512 Kuhistanicaol F
/ (+)-Kuhistanicaol F
C00037402 External link 512 Kuhistanicaol G
/ (-)-Kuhistanicaol G

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P03372 Estrogen receptor NR3A1 C00021386 C00021387 C00021388 C00021389 C00037144 1 / 1
Q92731 Estrogen receptor beta NR3A2 C00021389 0 / 1
P37840 Alpha-synuclein Unclassified protein C00021388 4 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00021388 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00021388 2 / 0
Q99700 Ataxin-2 Unclassified protein C00021388 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00021388 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00021388 3 / 3
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00021389 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00021388 1 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00021388 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (9)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
Q92731 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)