Item 11 of 29 (back to results) previous next 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with Schistosoma haematobium and S. mansoni, but due to its toxicity and concern about possible carcinogenicity, it has been replaced by other drugs such as praziquantel.

Current search: 03. Biological Effects of Specific Chemicals: aetiopathogenetic uses [CHEBI:52209] > genotoxin [CHEBI:50902] > mutagen [CHEBI:25435] > alkylating agent [CHEBI:22333] × Select any link to see items in a related category. more general categories    information about this item 03. Biological Effects of Specific Chemicals  03. Biological Effects of Specific Chemicals  aetiopathogenetic uses [CHEBI:52209] (178)   genotoxin [CHEBI:50902] (78)   mutagen [CHEBI:25435] (74)   hycanthone mesylate [CHEBI:24624] (1)  alkylating agent [CHEBI:22333] (29)   hycanthone mesylate [CHEBI:24624] (1) 05. Industrial Uses  05. Industrial Uses  pharmaceutical [CHEBI:52217] (1978)   drug [CHEBI:23888] (1930)   antiinfective agent [CHEBI:35441] (82)   antiparasitic agent [CHEBI:35442] (30)   anthelminthic drug [CHEBI:35443] (20)   antiplatyhelmintic drug [CHEBI:35684] (8)   schistosomicide drug [CHEBI:38941] (7)   hycanthone mesylate [CHEBI:24624] (1) 08. Chemical Category  08. Chemical Category  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   chalcogen molecular entity [CHEBI:33304] (15225)   sulfur molecular entity [CHEBI:26835] (1541)   organosulfur compound [CHEBI:33261] (1005)   methanesulfonates [CHEBI:48544] (33)   methanesulfonate salt [CHEBI:38037] (28)   hycanthone mesylate [CHEBI:24624] (1)  organochalcogen compound [CHEBI:36962] (11874)   organosulfur compound [CHEBI:33261] (1005)   methanesulfonates [CHEBI:48544] (33)   methanesulfonate salt [CHEBI:38037] (28)   hycanthone mesylate [CHEBI:24624] (1)  carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   heteroorganic entity [CHEBI:33285] (15197)   organochalcogen compound [CHEBI:36962] (11874)   organosulfur compound [CHEBI:33261] (1005)   methanesulfonates [CHEBI:48544] (33)   methanesulfonate salt [CHEBI:38037] (28)   hycanthone mesylate [CHEBI:24624] (1)  polyatomic entity [CHEBI:36357] (18777)   heteroatomic molecular entity [CHEBI:37577] (13672)   salt [CHEBI:24866] (931)   organic salt [CHEBI:24868] (775)   organosulfonate salt [CHEBI:64382] (37)   methanesulfonate salt [CHEBI:38037] (28)   hycanthone mesylate [CHEBI:24624] (1) ChEBI Compound Accession Identifier:   [CHEBI:24624] ChEBI Compound Description:   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. ChEBI Compound Identification Number:   24624 ChEBI InChI Value:   "InChI=1S/C20H24N2O2S.CH4O3S/c1-3-22(4-2)12-11-21-16-10-9-14(13-23)20-18(16)19(24)15-7-5-6-8-17(15)25-20;1-5(2,3)4/h5-10,21,23H,3-4,11-13H2,1-2H3;1H3,(H,2,3,4)" ChEBI InChIKey Value:   LOEQGPPJCCUXEJ-UHFFFAOYSA-N ChEBI Compound Name:   hycanthone mesylate ChEBI SMILES Value:   CS(O)(=O)=O.CCN(CC)CCNc1ccc(CO)c2sc3ccccc3c(=O)c12 ChEBI Substance ID:   160644711 ChEBI URL:   ChEBI:24624 ChemSpider ID:   NS Ontomatica Chemical Accession Key (OnChAKey):   LOEQGPPJCCUXEJ_UHFFFAOYSA_N_000_000000 PubChem Compound ID:   285666