Page last updated: 2024-08-01 20:07:36

l 643441

Description

L 643441: structure given in first source [MeSH]

Cross-References

ID SourceID
PubMed CID5486883
SCHEMBL ID4604981
MeSH IDM0113230

Synonyms (15)

Synonym
l-643441
1-oxo-3-n-[3-[3-(piperidin-1-ylmethyl)phenoxy]propyl]-1,2,5-thiadiazole-3,4-diamine
bdbm50404821
78442-39-4
l-643,441
3-n-(3-(3-(1-piperidinomethyl)phenoxy)propyl)amino-4-amino-1,2,5-thiadiazole-1-oxide
1,2,5-thiadiazole-3,4-diamine, n-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)-, 1-oxide
l 643441
SCHEMBL4604981
3-amino-4-[3-(3-piperidinomethylphenoxy)propylamino]-1,2,5-thiadiazole 1-oxide
DUPAVAVETJQPOR-UHFFFAOYSA-N
3-amino-4-((3-(3-(piperidin-1-ylmethyl)phenoxy)propyl)amino)-1,2,5-thiadiazole 1-oxide
DTXSID60999769
3-amino-4-[(3-{3-[(piperidin-1-yl)methyl]phenoxy}propyl)amino]-1h-1lambda~4~,2,5-thiadiazol-1-one
AKOS040752306

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19909 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
histaminearalkylamino compound;
imidazoles
human metabolite;
mouse metabolite;
neurotransmitter
1983198739.2medium050000
3-methylcholanthreneortho- and peri-fused polycyclic arenearyl hydrocarbon receptor agonist;
carcinogenic agent
1988198836.0low010000
cimetidinealiphatic sulfide;
guanidines;
imidazoles;
nitrile
adjuvant;
analgesic;
anti-ulcer drug;
H2-receptor antagonist;
P450 inhibitor
1983198839.2medium050000
dimapritimidothiocarbamic ester1983198540.0low020000
famotidine1,3-thiazoles;
guanidines;
sulfonamide
anti-ulcer drug;
H2-receptor antagonist;
P450 inhibitor
1985198837.3low030000
omeprazolearomatic ether;
benzimidazoles;
pyridines;
sulfoxide
1985198539.0low010000
phenobarbitalbarbituratesanticonvulsant;
drug allergen;
excitatory amino acid antagonist;
sedative
1988198836.0low010000
aminopyrinepyrazolone;
tertiary amino compound
antipyretic;
environmental contaminant;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug;
xenobiotic
1983198540.0low030000
methacholine chloridequaternary ammonium salt1987198737.0low010000
thiazoles1,3-thiazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene
1985198837.3low030000
loxtidinearomatic ether;
piperidines;
primary alcohol;
triazoles
H2-receptor antagonist1987198737.0low010000
triazoles1,2,3-triazole1987198737.0low010000
thioureaone-carbon compound;
thioureas;
ureas
antioxidant;
chromophore
1983198540.0low020000
ranitidineC-nitro compound;
furans;
organic sulfide;
tertiary amino compound
anti-ulcer drug;
drug allergen;
environmental contaminant;
H2-receptor antagonist;
xenobiotic
1983198739.3low030000
rubidiumalkali metal atom1985198539.0low010000
sk&f 934791983198540.0medium020000
pentagastrinorganic molecular entity1985198539.0low010000
bucladesine3',5'-cyclic purine nucleotide1984198738.5low020000
pyrimidinones1983198540.0low020000
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020

Dosage (1)

ArticleYear
Effects of H2-receptor antagonists upon physiological acid secretory states in animals.
The Journal of pharmacology and experimental therapeutics, , Volume: 233, Issue:1
1985

Interactions (1)

ArticleYear
Comparative effects of H2-receptor antagonists on drug interaction in rats.
Drug metabolism and disposition: the biological fate of chemicals, , Volume: 14, Issue:6