phenpropamine

Small moleculeexperimental

Alverine is a smooth muscle relaxant used for the treatment irritable bowel syndrome. Alverine may increase calcium influx during action potentials due to inhibition of the inactivation of L-type calcium channels, but may also suppress evoked activity by inhibiting the sensitivity of contractile proteins to calcium. — NCATS

Clinical trial activity

3 trials · 2 clinical orgs · 0 marketing orgs

Phase 1
0
Phase 2
1
Phase 3
0
Phase 4
2

Earliest trial started Jul 1, 2007 (NCT00542295)

Timeline

2020s

  1. Jan 1, 2022

    Earliest Phase 2 Sponsor(trial)

Indications

Mechanism of action

  • HNF4A activator

    Alverine has been shown to bind to 5-HT1A receptors thereby acting as an antagonist that reduces the visceral pronociceptive effect of 5-HT. Alverine acts directly on the muscle in the gut, causing it to relax. This prevents the muscle spasms which occur in the gut in conditions such as irritable bowel syndrome and diverticular disease. It has also been reported that Alverine acts as HNF4¿ activator.

  • HTR1A antagonist

    Alverine has been shown to bind to 5-HT1A receptors thereby acting as an antagonist that reduces the visceral pronociceptive effect of 5-HT. Alverine acts directly on the muscle in the gut, causing it to relax. This prevents the muscle spasms which occur in the gut in conditions such as irritable bowel syndrome and diverticular disease. It has also been reported that Alverine acts as HNF4¿ activator.

Chemistry & pharmacology

Loading structure…

SMILES

CCN(CCCc1ccccc1)CCCc1ccccc1
Mol. weight
281.44 g/mol
Lipinski Ro5
Pass
Rule of 3
No
Chirality
Achiral Molecule
Inorganic
No
Polymer
No

Oral

No

Parenteral

No

Topical

No

Sources

Also known as

  • alverina
  • alverina
  • alverine
  • alverine
  • alverine
  • alverine
  • alverine
  • alverine
  • alverine citrate
  • alverine citrate
  • alverine citrate
  • alverine citrate
  • alverine citrate
  • alverine citrate salt
  • alverine hydrochloride
  • alverine hydrochloride
  • alverine hydrochloride
  • alverine hydrochloride
  • alverine hydrochloride
  • alverine hydrochloride
  • alverinum
  • alverinum
  • audmonal
  • bis(gamma-phenylpropyl)ethylamine
  • bis(gamma-phenylpropyl)ethylamine
  • di(phenylpropyl)ethylamine
  • di(phenylpropyl)ethylamine
  • dipropylin
  • dipropyline
  • gielism
  • n-ethyl-3,3'-diphenyldipropylamine
  • n-ethyl-3,3'-diphenyldipropylamine
  • n-ethyl-3-phenyl-n-(3-phenylpropyl)-1-propanamine
  • n-ethyl-3-phenyl-n-(3-phenylpropyl)-1-propanamine
  • n-ethyl-n-(3-phenylpropyl)benzenepropanamine
  • n-ethyl-n-(3-phenylpropyl)benzenepropanamine
  • n,n-bis(3-phenylpropyl)ethylamine
  • n,n-bis(3-phenylpropyl)ethylamine
  • n,n-bis(3-phenylpropyl)ethylamine
  • norgine brand of alverine citrate
  • phenopropamine
  • phenopropamine
  • phenopropamine
  • phenpropamine
  • phenpropamine
  • phenpropamine
  • phenpropamine citrate
  • phenpropamine citrate
  • relaxyl
  • relaxyl
  • spasmaverine
  • spasmonal
  • spasmonal
  • spasmonal
  • spasmonal fte
  • united drug brand of alverine citrate

Clinical trials

NCT IDPhaseStart dateSponsor(s)
NCT05508633Phase 2Aug 31, 2022Second Military Medical University
NCT01404923Phase 4Dec 1, 2009Laboratoires Mayoly Spindler
NCT00542295Phase 4Jul 1, 2007Laboratoires Mayoly Spindler
Showing 3 of 3 trials
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Organizations

Research & Development (2)

OrganizationOrg typeTrialsAs lead sponsorPhasesEarliest year
Laboratoires Mayoly SpindlerFor profit2212007
Second Military Medical UniversityGovernment1112022
2 organizations
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