Description:
Famotidine is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. Unlike cimetidine, the first H2 antagonist, famotidine has no effect on the cytochrome P450 enzyme system, and does not appear to interact with other drugs.
- Molecular Weight: 337.45
- Molecular Formula: C8H15N7O2S3
Purity: >98%
Canonical SMILES:
C1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N
InChI:
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)
InChIKey: XUFQPHANEAPEMJ-UHFFFAOYSA-N
- Melting Point: 166-168 °C
- Appearance: White Solid
Synonyms:
Famotidine, Famotidine Hydrochloride, MK-208, Pepcid, YM-11170, YM11170, YM 11170, MK 208, MK208
More details are to be found on supplier website
