(S)-Omeprazole Sodium Salt

CAS: 161796-78-7

Ref. TR-O635011

Product Information

• Name: (S)-Omeprazole Sodium Salt
• Synonyms: Esomeprazole sodium salt, (S)-(-)-Omeprazole Sodium, Esomeprazole Sodium, (S)-5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole sodium salt, (S)-Omeprazole sodium, 1H-Benzimidazole, 5-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-, sodium salt, 1H-Benzimidazole, 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-, sodium salt, (S)-, 1H-Benzimidazole, 6-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-, sodium salt (1:1), 1H-benzimidazole, 5-Methoxy-2-[[(4-Methoxy-3,5-dimethyl-2-PYRIDINYL)methyl]sulfinyl]-, sodium salt, 5-Methoxy-2-((S)-((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinyl-1H-benzimidazole sodium salt, Bis[5-Methoxy-2-[(4-Methoxy-3,5-Dimethyl-2-Pyridyl)Methylsulfinyl]Benzimidazol-1-Yl]Magnesium, Esomeprazole Na, Esomeprazoleandsalts, H 199/18 sodium, Sodium 5-Methoxy-2-{[(4-Methoxy-3,5-Dimethylpyridin-2-Yl)Methyl]Sulfinyl}Benzimidazol-1-Ide, sodium 5-methoxy-2-{(S)-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-2,3-dihydrobenzimidazol-1-ide

Description

Stability Hygroscopic
Applications (S)-Omeprazole is the (S)-enantiomer of Omeprazole (O635000) a gastric proton-pump inhibitor. (S)-Omeprazole is more potent that its (R)-enantiomer and is used in the treatment of gastroesophageal reflux disease as well as gastrointestinal ulcers associated with Crohn's disease.
References Stedman, C.A.: Aliment. Pharmacol. Ther., 14, 963 (2000); Stenhoff, H., et al.: J. Chromatogr., 734, 191 (1999); Johnson, D.A., et al.: Expert Opin. Pharmacother., 4, 253 (2003);

• Brand: TRC

Chemical properties

• Molecular weight: 367.40
• Formula: C₁₇H₁₈N₃NaO₃S
• Color/Form: Neat
• InChI: InChI=1S/C17H18N3O3S.Na/c1-10-8-18-15(11(2)16(10)23-4)9-24(21)17-19-13-6-5-12(22-3)7-14(13)20-17;/h5-8H,9H2,1-4H3;/q-1;+1/t24-;/m0./s1
• InChI key: InChIKey=KEDWLCOPRDSQBB-MGPQQGTHSA-N
• SMILES: O=C(OCc1ccccc1)[C@H]1C[C@H]2CCC[C@H]2N1