IPDMA
CFTR corrector and potentiator
General information
IPDMA is an experimental substance used in studies and not yet available as a human pharmaceutical. It was created as a derivate of a triple-acting compound TMA, which shows anti-inflammatory activity in addition to CFTR corrector and potentiator properties, but is mutagenic. In relation to cystic fibrosis, our AIM tool found the data that IPDMA can be effective in both correcting F508del-CFTR and potentiating CFTR-dependent chloride transport in G551D mutants.
Synonyms
4-isopropyl-6,4′-dimethylangelicin
Marketed as
N/A
Dietary sources
N/A
Structure image not available
N/A
Drug-Mutation Relation
results for D1152H / F508del
See all data on IPDMATreats
| Mutation | Link | Tested on | Impact factor | Notes |
|---|---|---|---|---|
| F508del | Molecular Mechanism of Action of Trimethylangelicin Derivatives as CFTR Modulators | human cell cultures | 3.85 | Less effective than TMA or lumacaftor. |
Does not treat
| Mutation | Link | Tested on | Impact factor | Notes |
|---|