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1978371-23-1

1978371-23-1 Structure

1978371-23-1 Structure
IdentificationBack Directory
[Name]

1H-Pyrrole-3-methanamine, 5-(2-fluorophenyl)-1-[[3-(3-methoxypropoxy)phenyl]sulfonyl]-N-methyl-
[CAS]

1978371-23-1
[Synonyms]

P-CAB agent 2
Ornidazole Impurity 46
1H-Pyrrole-3-methanamine, 5-(2-fluorophenyl)-1-[[3-(3-methoxypropoxy)phenyl]sulfonyl]-N-methyl-
[Molecular Formula]

C22H25FN2O4S
[MOL File]

1978371-23-1.mol
[Molecular Weight]

432.51
Chemical PropertiesBack Directory
[Boiling point ]

587.5±60.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[form ]

Oil
[pka]

9.18±0.10(Predicted)
[color ]

Light brown to brown
Hazard InformationBack Directory
[Uses]

P-CAB agent 2 is a potent and orally active potassium-competitive acid blocker and a gastric acid secretion inhibitor. P-CAB agent 2 inhibits H+/K+-ATPase activity with an IC50 value of <100 nM. P-CAB agent 2 inhibits the hERG potassium channel with an IC50 value of 18.69 M. P-CAB agent 2 shows no acute toxicity and inhibits histamine (HY-B1204)-induced gastric acid secretion[1].
[in vivo]

P-CAB agent 2 (example 1) inhibits histamine (HY-B1204)-induced gastric acid secretion in SD rats[1].
P-CAB agent 2 (600, 2000 mg/kg; p.o.; once) shows no acute toxicity and 600mg/kg shows no significant effect on animal body weight in SD rats[1].

Animal Model:180-220 g, SPF grade, male SD rats[1]
Dosage:2 mg/kg
Administration:P.o.; once
Result:Inhibited histamine-induced gastric acid secretion with the acid suppression rate of 55.4%.
[References]

[1] YinLin Qin, et al. Pyrrole sulfonyl derivative, and preparation method and medical use thereof. WO2016119505A1.
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