id | C00002074 |
---|---|
Name | Stachydrine |
CAS RN | 471-87-4 |
Standard InChI | InChI=1S/C7H13NO2/c1-8(2)5-3-4-6(8)7(9)10/h6H,3-5H2,1-2H3/t6-/m0/s1 |
Standard InChI (Main Layer) | InChI=1S/C7H13NO2/c1-8(2)5-3-4-6(8)7(9)10/h6H,3-5H2,1-2H3 |
Phytochemical cluster | No. 1 |
---|---|
KCF-S cluster | No. 2627 |
By standard InChI | CHEMBL1456892 |
---|---|
By standard InChI Main Layer | CHEMBL394450 CHEMBL1456892 CHEMBL1986864 |
By LinkDB | C10172 |
---|
By CAS RN |
---|
class name | count |
---|---|
asterids | 14 |
rosids | 10 |
Liliopsida | 1 |
family name | count |
---|---|
Lamiaceae | 13 |
Capparaceae | 5 |
Fabaceae | 3 |
Combretaceae | 1 |
Asteraceae | 1 |
Xanthorrhoeaceae | 1 |
Rutaceae | 1 |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | CHEMBL1456892 |
CHEMBL1741321
(1)
|
1 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | CHEMBL1456892 |
CHEMBL1614361
(1)
|
3 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | CHEMBL1456892 |
CHEMBL1741325
(1)
|
0 / 1 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | CHEMBL1456892 |
CHEMBL1738606
(1)
|
0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | CHEMBL1456892 |
CHEMBL1794467
(1)
|
0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | CHEMBL1456892 |
CHEMBL1741322
(1)
|
0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | CHEMBL1456892 |
CHEMBL1741323
(1)
|
1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | CHEMBL1456892 |
CHEMBL1741324
(1)
|
0 / 1 |
O00255 | Menin | Unclassified protein | CHEMBL1456892 |
CHEMBL1614257
(1)
|
2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | CHEMBL1456892 |
CHEMBL1614257
(1)
|
1 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#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
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
KEGG | disease 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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(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)
|