Species

KNApSAcK Entry

Organism name Anthriscus cerefolium
Genus Anthriscus
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Anthriscus cerefolium
Linked NCBI taxonomy ID 40888
Linked level species

Family

Family in NCBI taxonomy Apiaceae
ID 4037

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (1)

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
phytochemical
cluster
figure
C00002491 External link 512 Peucedanin
CHEMBL1410943
10 / 8 / 6 No. 4483 No. 25

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002491 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002491 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002491 2 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002491 2 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002491 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002491 3 / 3
O15118 Niemann-Pick C1 protein Unclassified protein C00002491 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002491 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002491 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002491 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#114500 Colorectal cancer; crc P84022
#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
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118

KEGG DISEASE (6)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (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)