+ |
all-trans-retinoic acid | up-regulates activity
chemical activation
|
CYP26A1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265138 |
|
|
Homo sapiens |
|
pmid |
sentence |
31963453 |
Cytochrome P450 (CYP) subfamily 26 of enzymes degrade the excess of RA to avoid detrimental effects [17]. Among the three subtypes (CYP26A1, CYP26B1, and CYP26C1), CYP26A1 is particularly important during embryonic development |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Retinoic Acid Metabolism |
+ |
CYP26A1 | down-regulates quantity
chemical modification
|
all-trans-retinoic acid |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265139 |
|
|
Homo sapiens |
|
pmid |
sentence |
31963453 |
Cytochrome P450 (CYP) subfamily 26 of enzymes degrade the excess of RA to avoid detrimental effects [17]. Among the three subtypes (CYP26A1, CYP26B1, and CYP26C1), CYP26A1 is particularly important during embryonic development |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Retinoic Acid Metabolism |
+ |
CYP26A1 | down-regulates activity
chemical inhibition
|
all-trans-retinoic acid |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266425 |
|
|
Homo sapiens |
|
pmid |
sentence |
9716180 |
The RA-induced CYP26 was shown to be highly specific for the hydroxylation of all-trans-RA and did not recognize the 13-cis and 9-cis isomers. This substrate specificity is promising for finding retinoids that are not recognized by this enzyme and, therefore, could be more effective in growth inhibition of susceptible cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Retinoic Acid Metabolism |