Application
Famotidine has been used to test its effect on the human ether-a-go-go-related gene (hERG) binding transfected in HEK293 membrane. It has also been used in polycaprolactone based drug delivery studies.
Biochem/physiol Actions
Famotidine is not effective on muscarinic and nicotinic receptors. It competitively inhibits the secretion of gastric acid and elicits mucosal injury protection.
H2 histamine receptor antagonist; anti-ulcer agent
Features and Benefits
This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
Molecular Weight: 337.45. Empirical Formula: C8H15N7O2S3. Quality Level: 100. originator: Johnson &. Johnson. SMILES string: N\C(N): N\c1nc(CSCCC(: N)NS(N)(: O): O)cs1. InChI: 1S/C8H15N7O2S3/c9-6(15-20(12,16)17)1-2-18-3-5-4-19-8(13-5)14-7(10)11/h4H,1-3H2,(H2,9,15)(H2,12,16,17)(H4,10,11,13,14). InChI key: XUFQPHANEAPEMJ-UHFFFAOYSA-N. Gene Information: human ... HRH2(3274). Storage Class Code: 11 - Combustible Solids. WGK: WGK 2. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).- UPC:
- 51171902
- Condition:
- New
- HazmatClass:
- No
- MPN:
- F6889-500MG
- CAS:
- 76824-35-6
akash.verma@cenmed.com
(732) 447-1115





