UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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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
selected terms: 5 page 1 of 1

1. N-(((3,4-Dichlorophenyl)amino)carbonyl)-2,3-dihydro-5-benzofuransulfonamide
(UMLS (NCI) C0299218) =Organic Chemical; Pharmacologic Substance ;
4. N-(2-Dimethylaminopropyl-1)phenothiazine Hydrochloride
[The hydrochloride salt form of promethazine, a phenothiazine derivative with antihistaminic, sedative and antiemetic properties. Promethazine hydrochloride selectively blocks peripheral H1 receptors thereby diminishing the effects of histamine on effector cells. Promethazine hydrochloride also blocks the central histaminergic receptors, thereby depressing the reticular system causing sedative and hypnotic effects. In addition, promethazine hydrochloride also has centrally acting anticholinergic properties and probably mediates nausea and vomiting by acting on the medullary chemoreceptive trigger zone. ( NCI )] (UMLS (NCI) C0546876) =Organic Chemical; Pharmacologic Substance =PROMETHAZINE;
=PROMETHAZINE HYDROCHLORIDE 25 MG;
PROMETHAZINE HYDROCHLORIDE 6.25 MG/5ML;
PROMETHAZINE HYDROCHLORIDE 625 MG/5ML;
PROMETHAZINE HYDROCHLORIDE 25 MG/ML;
PROMETHAZINE HYDROCHLORIDE 50 MG/ML;
PROMETHAZINE HYDROCHLORIDE 5 MG;
PROMETHAZINE HYDROCHLORIDE 6.25 MG;
PROMETHAZINE HYDROCHLORIDE 12.5 MG;
PROMETHAZINE HYDROCHLORIDE 50 MG;
PROMETHAZINE HYDROCHLORIDE 25 MG/5ML;
PROMETHAZINE HYDROCHLORIDE 5 MG/5ML;
PROMETHAZINE HYDROCHLORIDE 6.2 MG
2. 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 =N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine;
=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;
5. N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine
[N-2-(5-dimethylamino)methyl-2- furanylmethyl thioethyl-N'-methyl-2-nitro-1,1 -ethenediamine; cimetidine analog; H2 histamine receptor antagonist used to treat gastric ulcers. ( CSP )] (UMLS (NCI) C0034665) =Organic Chemical; Pharmacologic Substance ;
=[GA300] ANTIULCER AGENTS;
Furans;
[GA301] HISTAMINE ANTAGONISTS;
1,4-Epoxy-1,3-butadiene;
[GA303] H.PYLORI AGENTS;
=N-(2-((5-((Dimethylamino)methyl)furfuryl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, compound with bismuth(3(+)) citrate (1:1);
N-(2-(((5-((Dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, hydrochloride;
N-(2-((5-((Dimethylamino)methyl)furfuryl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, compound with bismuth(3(+)) citrate (1:1);
N-(2-(((5-((Dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, hydrochloride;
RANITIDINE 75 MG
3. N-(2-((5-((Dimethylamino)methyl)furfuryl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine, compound with bismuth(3(+)) citrate (1:1)
[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) C0139919) =Organic Chemical; Pharmacologic Substance =Bi element;
N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine =RANITIDINE BISMUTH CITRATE 400 MG

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