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