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hycanthone methanesulfonate

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Description

hycanthone methanesulfonate: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hycanthone mesylate : A methanesulfonate salt resulting from the reaction of equimolar amounts of hycanthone and methanesulfonic acid. It was formerly used as a schistosomicide for individual or mass treatement of infection with Schistosoma haematobium and S. mansoni, but due to its toxicity and concern about possible carcinogenicity, it has been replaced by other drugs such as praziquantel. [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]

Cross-References

ID SourceID
PubMed CID285666
CHEMBL ID1983709
CHEBI ID24624
SCHEMBL ID1152656
MeSH IDM0041507

Synonyms (27)

Synonym
etrenol
hycanthone methanesulphonate
hycanthone monomethanesulphonate
hycanthone mesylate
thioxanthen-9-one, monomethanesulfonate (salt)
9h-thioxanthen-9-one, monomethanesulfonate (salt)
hycanthone methane sulfate
23255-93-8
hycanthone methanesulfonate
nsc142982 ,
hycanthone monomethanesulfonate
C19432
CHEMBL1983709
CCG-35909
48830nw22a ,
CHEBI:24624 ,
n,n-diethyl-2-{[4-(hydroxymethyl)-10-oxo-10h-dibenzo[b,e]thiopyran-1-yl]amino}ethanaminium methanesulfonate
1-{[2-(diethylamino)ethyl]amino}-4-(hydroxymethyl)-10h-dibenzo[b,e]thiopyran-10-one methanesulfonate
hycanthone monomesylate
hycanthone mesylate [iarc]
hycanthone mesylate [hsdb]
hycanthone mesylate [mi]
9h-thioxanthen-9-one, 1-((2-(diethylamino)ethyl)amino)-4-(hydroxymethyl)-, methanesulfonate (1:1)
SCHEMBL1152656
Q27109846
1-[2-(diethylamino)ethylamino]-4-(hydroxymethyl)thioxanthen-9-one;methanesulfonic acid
n-[2-(diethylamino)ethyl]-4-methoxy-9-oxoxanthene-1-aminemonomethanesulphonate
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
alkylating agentHighly reactive chemical that introduces alkyl radicals into biologically active molecules and thereby prevents their proper functioning. It could be used as an antineoplastic agent, but it might be very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. It could also be used as a component of poison gases.
mutagenAn agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
schistosomicide drugDrugs that used to treat infestations by flukes (trematodes) of the genus Schistosoma.
[role 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]

Drug Classes (1)

ClassDescription
methanesulfonate salt
[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 (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (40.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)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 (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]