1986
DOI: 10.1016/s0099-5428(08)60423-2
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Ranitidine

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Cited by 21 publications
(11 citation statements)
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“…The UV spectra of 6.3 × 10 −5 M (1), 4.33 × 10 −5 M (2) and 5.7 × 10 −5 M (3) in ethanol (Table 1) showed characteristic bands and molar absorptivities, which were in agreement with previous studies [4,10,11]. A very slight, negligible, hypsochromic shift occurred on buffering 1 with acid or alkali.…”
Section: Ultraviolet Spectrasupporting
confidence: 90%
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“…The UV spectra of 6.3 × 10 −5 M (1), 4.33 × 10 −5 M (2) and 5.7 × 10 −5 M (3) in ethanol (Table 1) showed characteristic bands and molar absorptivities, which were in agreement with previous studies [4,10,11]. A very slight, negligible, hypsochromic shift occurred on buffering 1 with acid or alkali.…”
Section: Ultraviolet Spectrasupporting
confidence: 90%
“…It is a histamine H 2 -receptor antagonist with a furan ring structure that increases its potency to inhibit gastric acid secretion induced by various stimuli, while lacking the anti-androgenic and hepatic microsomal enzyme inhibiting effects [3]. IR analysis confirmed 3 to being a tautomer, with the enol form dominating [4]; as follows: The question of whether or not these three drugs may interact was the basis of this study. Kamath et al [5] stated that paracetamol interfered with the determination of diclofenac sodium studied by flow-injection analysis.…”
Section: Introductionmentioning
confidence: 80%
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“…Monographs in the "Analytical Profile of Drug Substances" series were also published for diltiazem [11], cimetidine [12], and ranitidine [13]. Eur Ph 2002 [14] recommends an HPLC assay for diltiazem in its dosage forms.…”
Section: Official and Compendial Methods Of Analysismentioning
confidence: 99%
“…RAN‐HCl works by blocking histamine H 2 receptor in the gut 1. The chemical formula of RAN‐HCl is C 13 H 22 N 4 O 3 S · HCl and the structure of one of the possible tautomers is shown in Scheme 2…”
Section: Introductionmentioning
confidence: 99%