Plant Species


Cumulative plant class count

class name count
asterids 10
rosids 3
Spermatophyta 1

Cumulative family count

class name count
Asteraceae 4
Rutaceae 2
Lamiaceae 2
Gesneriaceae 2
Solanaceae 1
Pinaceae 1
Apocynaceae 1
Cucurbitaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (4)

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
C00002698 External link 512 Piceol
/ p-Hydroxyacetophenone
/ 4'-Hydroxyacetophenone
CHEMBL201083
C031335
5 / 3 / 3
C00029478 External link 512 3,4'-Dihydroxypropiophenone
/ 4-Hydroxy-(3-hydroxypropionyl)benzene
CHEMBL1417159
25 / 10 / 7
C00033557 External link 512 3,4'-Dihydroxypropiophenone
CHEMBL1417159
25 / 10 / 7
C00040821 External link 512 3'-Hydroxyacetophenone
CHEMBL404719

Human Protein / Gene in interactions

30 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00029478 C00033557 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00029478 C00033557 0 / 0
P06746 DNA polymerase beta Enzyme C00029478 C00033557 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00029478 C00033557 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00029478 C00033557 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00029478 C00033557 2 / 1
P54132 Bloom syndrome protein Enzyme C00029478 C00033557 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00029478 C00033557 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00029478 C00033557 0 / 0
P39748 Flap endonuclease 1 Enzyme C00029478 C00033557 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00029478 C00033557 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00029478 C00033557 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00029478 C00033557 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00029478 C00033557 3 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00029478 C00033557 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00029478 C00033557 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00029478 C00033557 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00029478 C00033557 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00029478 C00033557 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00029478 C00033557 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00029478 C00033557 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00029478 C00033557 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00029478 C00033557 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00029478 C00033557 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00029478 C00033557 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00002698 0 / 0
P37058 Testosterone 17-beta-dehydrogenase 3 Enzyme C00002698 1 / 1
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002698 1 / 1
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002698 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002698 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#264300 17-beta hydroxysteroid dehydrogenase iii deficiency P37058
#210900 Bloom syndrome; blm P54132
#114500 Colorectal cancer; crc Q14191
#613163 Gaba-transaminase deficiency P80404
#232300 Glycogen storage disease ii P10253
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (10)

KEGG name UniProt
H00213 Hypophosphatasia P05186 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00023 Testicular cancer P10696 (marker)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P37058 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)