DIROCAFTOR

Dirocaftor is a CFTR modulator improving chloride transport in cystic fibrosis. Side effects include headache, abdominal pain, and elevated liver enzymes. Only GMP materials will be supplied, logistics all according to GDP.

SKU: f805a9d0bb5e Category: Tag:

Product Description


Mechanism of Action

Dirocaftor (VX561) is a nextgeneration CFTR potentiator designed to enhance the gating function of mutant CFTR channels at the cell surface. By increasing the open probability of CFTR, it improves chloride transport across epithelial membranes in cystic fibrosis models with specific gating mutations.

Benefits and Advantages

Used in CFTRmodulator research, ionchannel pharmacology studies, epithelialtransport modelling, combinationtherapy investigations with CFTR correctors, and precisionmedicine development for cystic fibrosis.

Side Effects and Risks

Risks (based on class effects) may include hepatic enzyme elevations, GI symptoms, headache and respiratory events; longterm safety is evaluated in controlled models. Handle as a targeted ionchannel modulator.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C22H28N2O3Si2

Molecular Weight

424.6 g/mol

CAS Number

2137932-23-9

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Dirocaftor; Dirocaftor [USAN]; PTI-808; 2137932-23-9; 2G3T6M1AS9

IUPAC/Chemical Name

N-[5-hydroxy-2,4-bis(trimethylsilyl)phenyl]-4-oxo-1H-quinoline-3-carboxamide

InChl Key

TYQIFWXBQYAKCR-UHFFFAOYSA-N

InChl Code

InChI=1S/C22H28N2O3Si2/c1-28(2,3)19-12-20(29(4,5)6)18(25)11-17(19)24-22(27)15-13-23-16-10-8-7-9-14(16)21(15)26/h7-13,25H,1-6H3,(H,23,26)(H,24,27)

References

https://pubchem.ncbi.nlm.nih.gov/compound/141671949;

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