Drug intelligence / Profile preview

Reytense-P

Development stage
Unknown
Lead developer
Sanrey Therapeutics
Modality
Small Molecules
Administration
Oral
01

Overview

Reytense-P is a fixed-dose combination analgesic developed by Sanrey Therapeutics, containing flupirtine (100 mg) and paracetamol (325 mg). Flupirtine is a selective neuronal potassium channel opener (SNEPCO) that acts as a non-opioid, non-NSAID analgesic with muscle-relaxant properties by opening Kv7 (KCNQ) channels and indirectly antagonizing NMDA receptors. Paracetamol (acetaminophen) provides complementary analgesic and antipyretic effects, likely through the inhibition of cyclooxygenase enzymes in the central nervous system. This combination is utilized for the management of moderate to severe acute and chronic pain, including musculoskeletal conditions such as rheumatoid arthritis and osteoarthritis, as well as post-surgical pain, cancer-related pain, and tension headaches.

Brand names
Reytense-P
Other names
Flupirtine + ParacetamolFlupirtine maleate + Acetaminophen
02

Targets

NMDAR (Glutamate receptor ionotropic, NMDA)KCNQ3 (Potassium voltage-gated channel subfamily Q member 3)KCNQ2 (Potassium voltage-gated channel subfamily KQT member 2)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)

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