+ |
3-isobutyl-1-methyl-7H-xanthine | down-regulates activity
chemical inhibition
|
PDE1C |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253017 |
|
|
Homo sapiens |
|
pmid |
sentence |
22014080 |
Until now, very few inhibitors of PDE1 were available for evaluating the contribution of PDE1 in tissue and cell function. Vinpocetine (Ahn et al., 1989) and 8-methoxymethyl-IBMX (Ahn et al., 1997) are common PDE1 inhibitors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDE1C | down-regulates quantity
chemical modification
|
3',5'-cyclic AMP |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253399 |
|
|
Homo sapiens |
|
pmid |
sentence |
22014080 |
PDE1A and PDE1B preferentially hydrolyse cGMP, whereas PDE1C hydrolyses cAMP and cGMP with similar Km values |
|
Publications: |
1 |
Organism: |
Homo Sapiens |