Page last updated: 2024-12-06

isometamidium chloride

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

isometamidium chloride: Samorin & Veridium are tradenames [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID92295
CHEMBL ID2107182
CHEBI ID6028
SCHEMBL ID1683216
SCHEMBL ID18006993
MeSH IDM0040784

Synonyms (38)

Synonym
isometamidium chloride
34301-55-8
m & b 4180a
a 4180
cloruro de isometamidio [inn-spanish]
chlorure d'isometamidium [inn-french]
phenanthridinium, 8-(3-(m-amidinophenyl)-2-triazeno)-3-amino-5-ethyl-6-phenyl-, chloride
isometamidii chloridum [inn-latin]
8-(3-(m-amidinophenyl)-2-triazeno)-3-amino-5-ethyl-6-phenylphenanthridinium chloride
einecs 251-926-9
phenanthridinium, 3-amino-8-(3-(3-(aminoiminomethyl)phenyl)-1-triazenyl)-5-ethyl-6-phenyl-, chloride
cloruro de isometamidio
a-4180 ,
chlorure d'isometamidium
7nh28i651f ,
isometamidii chloridum
unii-7nh28i651f
isometamidium chloride [inn:ban]
chebi:6028 ,
CHEMBL2107182
isometamidium chloride [mart.]
isometamidium chloride [inn]
isometamidium chloride [mi]
SCHEMBL1683216
3-[2-(3-amino-5-ethyl-6-phenyl-phenanthridin-5-ium-8-yl)iminohydrazino]benzamidine
SCHEMBL18006993
phenanthridinium,3-amino-8-[3-[3-(aminoiminomethyl)phenyl]-2-triazen-1-yl]-5-ethyl-6-phenyl-
(e)-3-amino-8-(3-(3-carbamimidoylphenyl)triaz-1-enyl)-5-ethyl-6-phenylphenanthridinium chloride
Q3155582
FT-0713692
3-(2-(3-amino-5-ethyl-6-phenylphenanthridin-5-ium-8-yl)iminohydrazinyl)benzenecarboxamidine chloride
BCP28657
phenanthridinium,3-amino-8-[3-[3-(aminoiminomethyl)phenyl]-1-triazenyl]-5-ethyl-6-phenyl-, chloride
isometamidium (chloride)
DTXSID10955855
3-amino-8-[3-(3-carbamimidoylphenyl)triaz-2-en-1-yl]-5-ethyl-6-phenylphenanthridin-5-ium chloride
3-[2-(3-amino-5-ethyl-6-phenylphenanthridin-5-ium-8-yl)iminohydrazinyl]benzenecarboximidamide;chloride
AKOS040744427

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"The effectiveness of atropine in blocking the acute toxic effects of the antitrypanosomal drug isometamidium (ISMM) was evaluated in mice and goats using lethality as the primary index."( Influence of atropine on the acute toxicity of isometamidium.
Gimbi, AA; Kinabo, LD, 1992
)
0.28
" Following randomised trypanocidal treatment (diminazene diaceturate, melarsomine dihydrochloride or isometamidium chloride), animals were observed for immediate adverse drug reactions and follow-up assessment was performed at 1 and 2 weeks."( Safety and efficacy of three trypanocides in confirmed field cases of trypanosomiasis in working equines in The Gambia: a prospective, randomised, non-inferiority trial.
Jallow, S; Raftery, AG; Rodgers, J; Sutton, DGM, 2019
)
0.51

Pharmacokinetics

ExcerptReferenceRelevance
" After intramuscular administration, there was considerable individual variability in Cmax (mean = 111 ng x ml(-1); range = 37-197) and other pharmacokinetic parameters."( Pharmacokinetics of the chemoprophylactic and chemotherapeutic trypanocidal drug isometamidium chloride (Samorin) in cattle.
Eisler, MC, 1996
)
0.29

Compound-Compound Interactions

ExcerptReferenceRelevance
"0 micrograms/ml in combination with diminazene aceturate or isometamidium chloride."( The effect of verapamil alone and in combination with trypanocides on multidrug-resistant Trypanosoma brucei brucei.
Kaminsky, R; Zweygarth, E, 1991
)
0.28

Bioavailability

ExcerptReferenceRelevance
" It therefore appears that drug bioavailability is altered or drug biotransformation occurs during the in vivo test."( In vivo and in vitro sensitivity of Trypanosoma evansi and T. equiperdum to diminazene, suramin, MelCy, quinapyramine and isometamidium.
Baltz, T; Giroud, C; Zhang, ZQ, 1991
)
0.28
" After intramuscular administration, the absolute bioavailability was low, averaging 27%."( Isometamidium in goats: disposition kinetics, mammary excretion and tissue residues.
Kinabo, LD; McKellar, QA,
)
0.13
"The bioavailability and potential toxicity of the residues of the antitrypanosomal drug isometamidium (ISMM) in bovine tissues were investigated in male Sprague-Dawley rats."( Relay bioavailability and toxicity of isometamidium residues: a model for human risk assessment.
Bogan, JA; Kinabo, LD; McKellar, QA; Murray, M, 1989
)
0.28
"In this paper, pharmacokinetics, bioavailability and tissue residues are reported in non-infected and Trypanosoma congolense-infected Boran steers following either intravenous or intramuscular injection of [14C]isometamidium at a dose rate of 1 mg kg-1 body weight."( Pharmacokinetics, bioavailability and tissue residues of [14C]isometamidium in non-infected and Trypanosoma congolense-infected Boran cattle.
Karanja, WM; Mdachi, RE; Murilla, GA, 1996
)
0.29
" The overall absolute bioavailability of intramuscular-administered isometamidium was 65."( Pharmacokinetics of the chemoprophylactic and chemotherapeutic trypanocidal drug isometamidium chloride (Samorin) in cattle.
Eisler, MC, 1996
)
0.29

Dosage Studied

ExcerptRelevanceReference
" The ratio of the slope of the dose-response curve for ISMM in non-atropinized mice to that in atropinized mice was about 4:1."( Influence of atropine on the acute toxicity of isometamidium.
Gimbi, AA; Kinabo, LD, 1992
)
0.28
" The activity of each drug was expressed as: 1) in vitro: the minimal effective concentration which killed trypanosome population by 100% within 24 h of drug exposure (MEC100); the maximum tolerated concentration in which trypanosomes could propagate at the same rate as the controls during 48 h of drug exposure (MTC100); 2) in vivo: the curative dosage in 100% of infected mice (CD100); the highest ineffective dosage: 100% of infected mice remain infected (ID100)."( In vivo and in vitro sensitivity of Trypanosoma evansi and T. equiperdum to diminazene, suramin, MelCy, quinapyramine and isometamidium.
Baltz, T; Giroud, C; Zhang, ZQ, 1991
)
0.28
" It was concluded that, under the experimental conditions employed, (1) there was a direct relationship between drug dosage and the duration of chemoprophylaxis, (2) the weight of metacyclic challenge did not affect the duration of chemoprophylaxis and (3) when used to treat an existing infection, isometamidium chloride exerted the same degree of chemoprophylactic activity."( Factors influencing the duration of isometamidium chloride (Samorin) prophylaxis against experimental challenge with metacyclic forms of Trypanosoma congolense.
Hirumi, H; Holmes, PH; Moloo, SK; Murray, M; Ogunyemi, O; Peregrine, AS; Urquhart, GM; Whitelaw, DD, 1988
)
0.27
" The drug has been used successfully at the dosage of 1mg/kg body weight by deep intramuscular injection, every two or three months."( Chemoprophylaxis and treatment of African canine trypanosomosis in French military working dogs: a retrospective study.
Cuny, G; Davoust, B; Herder, S; MariƩ, JL; Watier-Grillot, S, 2013
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
organic molecular entityAny molecular entity that contains carbon.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (219)

TimeframeStudies, This Drug (%)All Drugs %
pre-199066 (30.14)18.7374
1990's80 (36.53)18.2507
2000's36 (16.44)29.6817
2010's32 (14.61)24.3611
2020's5 (2.28)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials9 (4.05%)5.53%
Reviews8 (3.60%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other205 (92.34%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]