Species

KNApSAcK Entry

Organism name Ferula tenuisecta
Genus Ferula
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Ferula tenuisecta
Linked NCBI taxonomy ID 82087
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 (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
KCF-S
cluster
phytochemical
cluster
figure
C00021388 External link 512 Teferin
CHEMBL464467
CHEMBL1552750
CHEMBL1967912
9 / 13 / 9 No. 327
C00020368 External link 512 Tenuferinin
No. 971
C00020367 External link 512 Tenuferin
No. 971
C00020366 External link 512 Tenuferidin
No. 971

Human Protein / Gene in interactions

9 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00021388 1 / 0
Q99700 Ataxin-2 Unclassified protein C00021388 1 / 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
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00021388 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00021388 3 / 3
P03372 Estrogen receptor NR3A1 C00021388 1 / 1
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)
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)