Pralnacasan

DB04875ExperimentalSmall molecule

Pralnacasan is an orally bioavailable pro-drug of a potent, non-peptide inhibitor of interleukin-1beta converting enzyme (ICE).

Chemical structure of Pralnacasan
Mechanism
Curator reviewed
Primary indication
For the treatment of rheumatoid arthritis (RA).Curator reviewed
Formula / weight
C26H29N5O7 · 523.5378 g/mol (avg)
Code names
HMR-3480 · HMR-3480/VX-740 · VX-740

Resolves to

Structure
InChIKeyCXAGHAZMQSCAKJ-WAHHBDPQSA-NSMILESCCO[C@@H]1OC(=O)C[C@@H]1NC(=O)[C@@H]1CCCN2N1C(=O)[C@H](CCC2=O)NC(=O)C1=NC=CC2=CC=CC=C12

What you can answer from here — as of March 06, 2025

1Protein targetEach mapped to UniProt, with action and pharmacological action
Listed above
558Drug interactionsStructured to mechanism, not free text
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7+ReferencesStructured and connected to the statements they support
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Which drugs share a target with Pralnacasan, and which of those have an active Phase 3 trial?

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