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 |
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|||
C00034029
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Leonticin D
|
CHEMBL554128
|
No. 4 | No. 51 |
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|||
C00033710
![]() |
Cauloside D
|
CHEMBL538919
|
2 / 0 / 3 | No. 4 | No. 51 |
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||
C00033712
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Cauloside H
|
No. 4 | No. 51 |
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||||
C00034217
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Saponin PE
|
CHEMBL540220
CHEMBL1997061 |
No. 9 | No. 51 |
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|||
C00033709
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Cauloside C
/ (+)-Cauloside C |
CHEMBL537960
|
C018245
|
No. 9 | No. 51 |
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||
C00003527
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Cauloside A
/ (+)-Cauloside A / Hederagenin 3-O-arabinoside / Hederagenin 3-O-alpha-L-arabinopyranoside |
CHEMBL452911
CHEMBL538200 |
C036411
|
No. 50 | No. 51 |
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||
C00033708
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Cauloside B
/ (+)-Cauloside B |
CHEMBL555897
|
No. 50 | No. 51 |
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|||
C00002225
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Lupanine
/ (+)-Lupanine |
CHEMBL459396
CHEMBL520093 CHEMBL2008918 |
C008298
|
No. 85 | No. 3 |
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||
C00002216
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Caulophylline
/ N-Methylcytisine / (-)-N-Methylcytisine |
CHEMBL66191
CHEMBL1085045 |
C034245
|
No. 376 | No. 3 |
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||
C00007724
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O-Acetylbaptifolin
|
No. 384 | No. 3 |
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||||
C00002207
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Anagyrine
/ (-)-Anagyrine |
CHEMBL203399
CHEMBL509692 CHEMBL1324708 CHEMBL1454284 |
C012736
|
7 / 8 / 11 | No. 384 | No. 3 |
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|
C00033706
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Caulophyllumine A
/ (-)-Caulophyllumine A |
No. 5324 |
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|||||
C00033707
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Caulophyllumine B
/ (-)-Caulophyllumine B |
No. 8579 |
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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)
|