MedKoo Cat#: 461148 | Name: Ramixotidine

Description:

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

Ramixotidine is a competitive histamine H2-receptor antagonist.

Chemical Structure

Ramixotidine
Ramixotidine
CAS#84071-15-8

Theoretical Analysis

MedKoo Cat#: 461148

Name: Ramixotidine

CAS#: 84071-15-8

Chemical Formula: C16H21N3O3S

Exact Mass: 335.1304

Molecular Weight: 335.42

Elemental Analysis: C, 57.29; H, 6.31; N, 12.53; O, 14.31; S, 9.56

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Ramixotidine;
IUPAC/Chemical Name
3-((2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)carbamoyl)pyridine 1-oxide
InChi Key
HIVRCMFJEMKPDS-UHFFFAOYSA-N
InChi Code
InChI=1S/C16H21N3O3S/c1-18(2)11-14-5-6-15(22-14)12-23-9-7-17-16(20)13-4-3-8-19(21)10-13/h3-6,8,10H,7,9,11-12H2,1-2H3,(H,17,20)
SMILES Code
CN(C)Cc1oc(CSCCNC(c(ccc2)cn2=O)=O)cc1
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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 335.42 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: Molgora M, Basilisco G, Bozzani A, Camboni G, Bianchi PA. Intragastric and intraoesophageal pH monitoring in duodenal ulcerpatients: effect of the new histamine H2-receptor antagonist ramixotidine. Eur J Clin Pharmacol. 1989;37(4):405-7. PubMed PMID: 2574675. 2: Brassinne A, Dresse A, Basilisco G, Manara L. Inhibition of pentagastrin-stimulated gastric acid secretion and plasma levels of the new histamine H2-receptor antagonist ramixotidine dihydrochloride (CM 57755) in human volunteers. Eur J Clin Pharmacol. 1987;32(5):467-70. PubMed PMID: 2957210. 3: Soldani G, Lavezzo A, Bianchetti A, Manzoni L, Mengozzi G, Manara L. Comparison of the gastric antisecretory effects of ramixotidine dihydrochloride (CM 57755), a new H2 receptor antagonist, and cimetidine in dogs. Pharmacol Res Commun. 1988 Aug;20(8):663-72. PubMed PMID: 2974998. 4: Colle M, Ruedas E, Cazenave J, Auzerie J, Basilisco G, Camboni G, Manara L. Plasma prolactin, sex steroids and gastrin in human volunteers treated for 2 weeks with therapeutic doses of cimetidine or the new histamine H2-receptor antagonist ramixotidine (CM 57755A). Eur J Clin Pharmacol. 1988;35(5):529-34. PubMed PMID: 2906873. 5: Lin JH. Pharmacokinetic and pharmacodynamic properties of histamine H2-receptor antagonists. Relationship between intrinsic potency and effective plasma concentrations. Clin Pharmacokinet. 1991 Mar;20(3):218-36. Review. PubMed PMID: 1673880. 6: Wilson JA, Johnston D, Penston J, Wormsley KG. Gastric inhibitory effects of CM57755. A new histamine H2 receptor antagonist. Eur J Clin Pharmacol. 1986;30(1):33-6. PubMed PMID: 2872060. 7: Necciari J, Mery D, Garriot P, Escourrou J, Cautreels W. Pharmacokinetics of CM 57755, a new histamine H2-receptor antagonist, after single oral doses in man. Int J Clin Pharmacol Res. 1985;5(6):457-65. PubMed PMID: 2869002. 8: Lavezzo A, Manzoni L, Aureggi G, Nisato D, Bianchetti A, Carminati P. In vivo and in vitro effects of CM 57755, a new gastric antisecretory agent acting on histamine H2 receptors. Int J Tissue React. 1984;6(2):155-65. PubMed PMID: 6145676. 9: Lavezzo A, Manzoni L, Bianchetti A, Manara L. Inhibition of dimaprit- and pentagastrin-induced gastric acid secretion in cats by the new histamine H2 antagonist, CM 57755. J Pharm Pharmacol. 1986 Nov;38(11):853-6. PubMed PMID: 2879021.