| Organism name | Caulophyllum thalictroides L. Michx. |
|---|---|
| Genus | Caulophyllum |
| Family | Berberidaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Caulophyllum |
|---|---|
| Linked NCBI taxonomy ID | 46962 |
| Linked level | genus |
| Family in NCBI taxonomy | Berberidaceae |
|---|---|
| ID | 41773 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | eudicotyledons |
|---|---|
| ID | 71240 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00033711
|
Cauloside G
/ (+)-Cauloside G |
CHEMBL550487
|
No. 4 | No. 51 |
|
|||
|
C00034029
|
Leonticin D
|
CHEMBL554128
|
No. 4 | No. 51 |
|
|||
|
C00033710
|
Cauloside D
|
CHEMBL538919
|
2 / 0 / 3 | No. 4 | No. 51 |
|
||
|
C00033712
|
Cauloside H
|
No. 4 | No. 51 |
|
||||
|
C00034217
|
Saponin PE
|
CHEMBL540220
CHEMBL1997061 |
No. 9 | No. 51 |
|
|||
|
C00033709
|
Cauloside C
/ (+)-Cauloside C |
CHEMBL537960
|
C018245
|
No. 9 | No. 51 |
|
||
|
C00003527
|
Cauloside A
/ (+)-Cauloside A / Hederagenin 3-O-arabinoside / Hederagenin 3-O-alpha-L-arabinopyranoside |
CHEMBL452911
CHEMBL538200 |
C036411
|
No. 50 | No. 51 |
|
||
|
C00033708
|
Cauloside B
/ (+)-Cauloside B |
CHEMBL555897
|
No. 50 | No. 51 |
|
|||
|
C00002225
|
Lupanine
/ (+)-Lupanine |
CHEMBL459396
CHEMBL520093 CHEMBL2008918 |
C008298
|
No. 85 | No. 3 |
|
||
|
C00002216
|
Caulophylline
/ N-Methylcytisine / (-)-N-Methylcytisine |
CHEMBL66191
CHEMBL1085045 |
C034245
|
No. 376 | No. 3 |
|
||
|
C00007724
|
O-Acetylbaptifolin
|
No. 384 | No. 3 |
|
||||
|
C00002207
|
Anagyrine
/ (-)-Anagyrine |
CHEMBL203399
CHEMBL509692 CHEMBL1324708 CHEMBL1454284 |
C012736
|
7 / 8 / 11 | No. 384 | No. 3 |
|
|
|
C00033706
|
Caulophyllumine A
/ (-)-Caulophyllumine A |
No. 5324 |
|
|||||
|
C00033707
|
Caulophyllumine B
/ (-)-Caulophyllumine B |
No. 8579 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002207 | 1 / 0 |
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00033710 | 0 / 3 |
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00033710 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002207 | 0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002207 | 3 / 3 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002207 | 1 / 1 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002207 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00002207 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002207 | 1 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| KEGG | name | UniProt |
|---|---|---|
| H00033 | Adrenal carcinoma |
O00255
(related)
|
| H00034 | Carcinoid |
O00255
(related)
|
| H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
| H00246 | Primary hyperparathyroidism |
O00255
(related)
|
| H01102 | Pituitary adenomas |
O00255
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00017 | Esophageal cancer |
P35354
(related)
|
| H00025 | Penile cancer |
P35354
(related)
|
| H00046 | Cholangiocarcinoma |
P35354
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(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)
|