MedKoo Cat#: 573489 | Name: Sufotidine

Description:

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

Sufotidine is a long-acting competitive H2 receptor antagonist which was under development as an antiulcerant. It was planned to be a follow-up compound to ranitidine (Zantac). When taken in doses of 600 mg twice daily it induced virtually 24-hour gastric anacidity thus closely resembling the antisecretory effect of the proton pump inhibitor omeprazole. Its development was terminated based on the appearance of carcinoid tumors in long-term toxicity testing in rodents.

Chemical Structure

Sufotidine
Sufotidine
CAS#80343-63-1

Theoretical Analysis

MedKoo Cat#: 573489

Name: Sufotidine

CAS#: 80343-63-1

Chemical Formula: C20H31N5O3S

Exact Mass: 421.2148

Molecular Weight: 421.56

Elemental Analysis: C, 56.98; H, 7.41; N, 16.61; O, 11.39; S, 7.61

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.
Bulk Inquiry
Related CAS #
No Data
Synonym
Sufotidine; AH 25352X; AH25352X; AH-25352X;
IUPAC/Chemical Name
1H-1,2,4-Triazol-5-amine, 1-methyl-3-((methylsulfonyl)methyl)-N-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)-
InChi Key
JEYKZWRXDALMNG-UHFFFAOYSA-N
InChi Code
1S/C20H31N5O3S/c1-24-20(22-19(23-24)16-29(2,26)27)21-10-7-13-28-18-9-6-8-17(14-18)15-25-11-4-3-5-12-25/h6,8-9,14H,3-5,7,10-13,15-16H2,1-2H3,(H,21,22,23)
SMILES Code
n1(c(NCCCOc2cc(ccc2)CN2CCCCC2)nc(n1)CS(=O)(=O)C)C
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 421.56 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: Mela GS, Caputo E, Villa G, Savarino V, Zentilin P. Intragastric acidity and serum gastrin after sufotidine. Gut. 1990 Sep;31(9):1087-8. PubMed PMID: 1976577; PubMed Central PMCID: PMC1378679. 2: Smith JT, Pounder RE. Sufotidine 600 mg bd virtually eliminates 24 hour intragastric acidity in duodenal ulcer subjects. Gut. 1990 Mar;31(3):291-3. PubMed PMID: 1969833; PubMed Central PMCID: PMC1378269. 3: Rogers MJ, Holmfield JH, Primrose JN, Johnston D. The effects of 15 days of dosing with placebo, sufotidine 600 mg nocte or sufotidine 600 mg twice daily upon 24-hour intragastric acidity and 24-hour plasma gastrin. Aliment Pharmacol Ther. 1990;4 Suppl 1:65-74. PubMed PMID: 1983347. 4: Smith JT, Gavey C, Nwokolo CU, Pounder RE. Tolerance during 8 days of high-dose H2-blockade: placebo-controlled studies of 24-hour acidity and gastrin. Aliment Pharmacol Ther. 1990;4 Suppl 1:47-63. PubMed PMID: 1983346. 5: Johnston DA, Wormsley KG. Inhibition of gastric secretion following single morning or twice daily oral administration of sufotidine to volunteers. Br J Clin Pharmacol. 1989 Oct;28(4):403-7. PubMed PMID: 2574050; PubMed Central PMCID: PMC1379989.