Species

KNApSAcK Entry

Organism name Aconitum subcuneatum Nakai
Genus Aconitum
Family Ranunculaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aconitum
Linked NCBI taxonomy ID 49188
Linked level genus

Family

Family in NCBI taxonomy Ranunculaceae
ID 3440

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (5)

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
C00025683 External link 512 Penduline
/ (+)-Penduline
CHEMBL504323
CHEMBL507540
CHEMBL1198334
4 / 3 / 4 No. 10 No. 4
C00027680 External link 512 14-Acetyldelcosine
/ 4-O-Acetyldelcosine
CHEMBL399468
No. 31 No. 10
C00028671 External link 512 Neoline
CHEMBL1242346
No. 31 No. 10
C00038990 External link 512 Deoxyjesaconitine
CHEMBL247593
No. 138 No. 10
C00024912 External link 512 Ignavine
C035745
No. 317

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P54750 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A PDE_1A C00025683 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00025683 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00025683 3 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00025683 0 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (3)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (4)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
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)