MedKoo Cat#: 574832 | Name: (R)-Omeprazole sodium salt
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

(R)-Omeprazole sodium salt is the inactive isomer of Omeprazole, a gastric proton-pump inhibitor. (R)-Omeprazole has been shown to act as a reversible direct-acting and metabolism-dependent inhibitor of CYP2C19 in pooled human liver microsomes.

Chemical Structure

(R)-Omeprazole sodium salt
(R)-Omeprazole sodium salt
CAS#161796-77-6

Theoretical Analysis

MedKoo Cat#: 574832

Name: (R)-Omeprazole sodium salt

CAS#: 161796-77-6

Chemical Formula: C17H18N3NaO3S

Exact Mass: 367.0967

Molecular Weight: 367.40

Elemental Analysis: C, 55.58; H, 4.94; N, 11.44; Na, 6.26; O, 13.06; S, 8.73

Price and Availability

Size Price Availability Quantity
1mg USD 400.00 2 Weeks
5mg USD 1,000.00 2 Weeks
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Related CAS #
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Synonym
(R)-Omeprazole sodium salt
IUPAC/Chemical Name
6-methoxy-2-[(R)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, monosodium salt
InChi Key
HVAJOLFRLWQQQL-GJFSDDNBSA-N
InChi Code
InChI=1S/C17H19N3O3S.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,(H,19,20);/t24-;/m1./s1
SMILES Code
COC1=CC=C2C(N=C([S@@](CC3=C(C)C(OC)=C(C)C=N3)=O)N2)=C1.[Na]
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 367.40 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Shi, S., and Klotz, U. Proton pump inhibitors: An update of their clinical use and pharmacokinetics. Eur. J. Clin. Pharmacol. 64(10), 935-951 (2008). 2. Lind, T., Rydberg, L., Kylebäck, A., et al. Esomeprazole provides improved acid control vs. omeprazole in patients with symptoms of gastro-oesophageal reflux disease. Alimentary Pharmacology and Therapeutics 14, 861-867 (2000). 3. Äbelö, A., Andersson, T.B., Antonsson, M., et al. Stereoselective metabolism of omeprazole by human cytochrome P450 enzymes. Drug Metab. Dispos. 28(8), 966-972 (2000). 4. Ogilvie, B.W., Yerino, P., Kazmi, F., et al. The proton pump inhibitor, omeprazole, but not lansoprazole or pantoprazole, is a metabolism-dependent inhibitor of CYP2C19: Implications for coadministration with clopidogrel. Drug Metab. Dispos. 39(11), 2020-2033 (2011). 5: Sørensen, A. M., Hansen, C. H., Bonomo, S., Olsen, L., Jørgensen, F. S., Weisser, J. J., ... & Styrishave, B. (2016). Enantioselective endocrine disrupting effects of omeprazole studied in the H295R cell assay and by molecular modeling. Toxicology in Vitro, 34, 71-80.