ChemSpider 2D Image | Hycanthone mesylate | C21H28N2O5S2

Hycanthone mesylate

  • Molecular FormulaC21H28N2O5S2
  • Average mass452.587 Da
  • Monoisotopic mass452.143951 Da
  • ChemSpider ID29457

More details:

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

Hycanthone mesylate
1-((2-(diethylamino)ethyl)amino)-4-(hydroxymethyl)- 9H-Thioxanthen-9-one monomethanesulfonate (salt)
1-((2-(Diethylamino)ethyl)amino)-4-(hydroxymethyl)-9H-thioxanthen-9-one Monomethanesulfonate (Salt)
1-{[2-(Diethylamino)ethyl]amino}-4-(hydroxymethyl)-9H-thioxanthen-9-one methanesulfonate (1:1) [ACD/IUPAC Name]
9H-Thioxanthen-9-one, 1-[[2- (diethylamino)ethyl]amino]-4-(hydroxymethyl)-, monomethanesulfonate (salt)
9H-Thioxanthen-9-one, 1-[[2-(diethylamino)ethyl]amino]-4-(hydroxymethyl)-, methanesulfonate (1:1)
9H-Thioxanthen-9-one, 1-[[2-(diethylamino)ethyl]amino]-4-(hydroxymethyl)-, methanesulfonate (1:1) (salt) [ACD/Index Name]
9H-Thioxanthen-9-one, 1-[[2-(diethylamino)ethyl]amino]-4-(hydroxymethyl)-, monomethanesulfonate
Acide méthanesulfonique - 1-{[2-(diéthylamino)éthyl]amino}-4-(hydroxyméthyl)-9H-thioxanthén-9-one (1:1) [French] [ACD/IUPAC Name]
Etrenol [Trade name]
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

48830NW22A [DBID]
UNII:48830NW22A [DBID]
AI3-61987 [DBID]
CCRIS 333 [DBID]
HSDB 7094 [DBID]
NSC142982 [DBID]
UNII-48830NW22A [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Appearance:

      yellow to orange powder OU Chemical Safety Data (No longer updated) More details

    • Stability:

      Stable, but light sensitive. Decomposes rapidly in the presence of acid. OU Chemical Safety Data (No longer updated) More details

    • Toxicity:

      ORL-MUS LD50 565 mg kg-1, IVN-MUS LD50 79 mg kg-1, SCU-MUS LD50 204 mg kg-1 OU Chemical Safety Data (No longer updated) More details

    • Safety:

      Safety glasses. OU Chemical Safety Data (No longer updated) More details

    • Chemical Class:

      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 infectio n with <ital>Schistosoma haematobium</ital> and <ital>S. mansoni</ital>, but due to its toxicity and concern about possible carcinogenicity, it has been replaced by other drugs such as praziquantel. ChEBI CHEBI:24624
      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 infectio n 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 CHEBI:24624

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


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