phenpropamine
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
Earliest trial started Jul 1, 2007 (NCT00542295)
Timeline
2020s
- Jan 1, 2022
Earliest Phase 2 Sponsor(trial)
Indications
Approved for
Mechanism of action
- Hepatocyte nuclear factor 4-alphaACTIVATOR
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.
- Serotonin 1a (5-HT1a) receptorANTAGONIST
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
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
- ChEMBLCHEMBL253371 ↗
- NCATS46TIR1560O ↗
- ChEMBLCHEMBL1408594 ↗
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 ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT05508633 | Phase 2 | Aug 31, 2022 | Second Military Medical University |
| NCT01404923 | Phase 4 | Dec 1, 2009 | Laboratoires Mayoly Spindler |
| NCT00542295 | Phase 4 | Jul 1, 2007 | Laboratoires Mayoly Spindler |
Organizations
Research & Development (2)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| Laboratoires Mayoly Spindler | For profit | 2 | 2 | 1 | 2007 |
| Second Military Medical University | Government | 1 | 1 | 1 | 2022 |