Species

KNApSAcK Entry

Organism name Ferula pallida
Genus Ferula
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Ferula pallida
Linked NCBI taxonomy ID 371378
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 (18)

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
C00033846 External link 512 Feselol
CHEMBL178485
CHEMBL1078138
CHEMBL1326960
CHEMBL1507262
CHEMBL2000585
13 / 14 / 10 No. 209
C00036927 External link 512 Conferol
CHEMBL1078139
CHEMBL1651079
No. 209
C00021395 External link 512 Pallinol
No. 1295
C00011697 External link 512 Angrendiol
No. 1547
C00047074 External link 512 Pallidone F
/ (+)-Pallidone F
No. 1806
C00047075 External link 512 Pallidone G
/ (+)-Pallidone G
No. 1806
C00047072 External link 512 Pallidone D
/ (+)-Pallidone D
No. 1806
C00047071 External link 512 Pallidone C
/ (+)-Pallidone C
No. 1806
C00047073 External link 512 Pallidone E
/ (+)-Pallidone E
No. 1806
C00011698 External link 512 Ferolin
CHEMBL2165591
No. 2685
C00021396 External link 512 Pallinin
CHEMBL1836963
No. 2936 No. 38
C00047070 External link 512 Pallidone B
/ (+)-Pallidone B
No. 3967
C00047076 External link 512 Pallidone I
/ (+)-Pallidone I
No. 3967
C00047077 External link 512 Pallidone J
/ (+)-Pallidone J
No. 3967
C00021383 External link 512 Pallidin (sesquiterpene)
No. 4156
C00047069 External link 512 Pallidone A
/ (+)-Pallidone A
No. 5492
C00021407 External link 512 Palliferin
No. 5534
C00021408 External link 512 Palliferinin
No. 5534

Human Protein / Gene in interactions

13 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 C00033846 0 / 0
Q99700 Ataxin-2 Unclassified protein C00033846 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00033846 0 / 0
P37840 Alpha-synuclein Unclassified protein C00033846 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00033846 3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00033846 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00033846 2 / 0
O75496 Geminin Unclassified protein C00033846 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00033846 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00033846 3 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00033846 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00033846 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00033846 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

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
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#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 (10)

KEGG name UniProt
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (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)