UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
N N- N0 N3 NA NB NC ND NE NF NG NH NI NK NL NM NN NO NP NR NS NT NU NV NX NY NZ
ND NDC NDD NDI NDL NDN NDO NDR NDU NDV

N-(2-(((5-((Dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, hydrochloride

[A member of the class of histamine H2-receptor antagonists with antacid activity. Ranitidine is a competitive and reversible inhibitor of the action of histamine, released by enterochromaffin-like (ECL) cells, at the histamine H2-receptors on parietal cells in the stomach, thereby inhibiting the normal and meal-stimulated secretion of stomach acid. In addition, other substances that promote acid secretion have a reduced effect on parietal cells when the H2 receptors are blocked. ( NCI )]
UMLS (NCI) C0700466
 
Organic Chemical
Pharmacologic Substance
Relation/PAR: N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine
Relation/CHD: RANITIDINE HYDROCHLORIDE 300 MG
RANITIDINE HYDROCHLORIDE 50 MG
RANITIDINE HYDROCHLORIDE 25 MG/ML
RANITIDINE HYDROCHLORIDE 75 MG/5ML
RANITIDINE HYDROCHLORIDE 0.5 MG/ML
RANITIDINE HYDROCHLORIDE 150 MG

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