Basic information
- CAS
108316-83-2- Standard SMILES
CCCCCCCCCCOC(=O)C[N+](C)(C)CC[N+](C)(C)CC(=O)OCCCCCCCCCC.[Cl-].[Cl-]- InChIKey
UPCOSYBELNEQAU-UHFFFAOYSA-L- Molecular formula
- C30H62Cl2N2O4
- Average molar mass
- 585.7 g/mol
- Monoisotopic mass
- 584.4086639
Overview
Russian drug; RN given refers to dichloride
Names & identifiers
- Preferred name
- Ethonium
- IUPAC
- (2-decoxy-2-oxoethyl)-[2-[(2-decoxy-2-oxoethyl)-dimethylazaniumyl]ethyl]-dimethylazanium dichloride
Names & synonyms
EthoniumEtoniumAethoniumN,N'-Bis(2-(decyloxy)-2-oxoethyl)-N,N,N',N'-tetramethyl-1,2-ethanediaminiumetoniiRefChem:1384191,2-ethylenebis(N-dimethylcarbodecyloxymethyl)ammonium dichloridedichloride ethylene-1,2-bis(N-dimethylcarbodecyloxymethyl)ammonium21954-74-5SCHEMBL28175725DTXSID50910680Ethylenebis((carboxymethyl)dimethylammonium), dichloride, didecyl ester
Show more names
AKOS024399265N,N-Bis(carboxymethyl)-N,N,N',N'-tetramethylethylenediammonium chloride1,2-Ethanediaminium, N,N'-bis(2-(decyloxy)-2-oxoethyl)-N,N,N',N'-tetramethyl-, dichloride1,2-Ethylenediamine, N,N'-dicarboxymethyl-N,N'-dimethyl-, dimethochloride, didecyl esterAMMONIUM, ETHYLENEBIS((CARBOXYMETHYL)DIMETHYL-, DICHLORIDE, DIDECYL ESTERN,N'-Bis(decyloxycarbonylmethyl)-N,N,N',N'-tetramethylethylenediammonium chloride(2-decoxy-2-oxoethyl)-[2-[(2-decoxy-2-oxoethyl)-dimethylazaniumyl]ethyl]-dimethylazanium;dichloride108316-83-2
Database identifiers
- CAS
108316-83-2、21954-74-5- PubChem CID
- 30869
- DTXSID
DTXSID50910680
Properties
Computed structural properties
- Topological polar surface area
- 52.6 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 27
- Heavy atoms
- 38
- Formal charge
- 0
- Complexity
- 501
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection.
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Various agents with different action mechanisms used to treat or ameliorate PEPTIC ULCER or irritation of the gastrointestinal tract. This has included ANTIBIOTICS to treat HELICOBACTER INFECTIONS; HISTAMINE H2 ANTAGONISTS to reduce GASTRIC ACID secretion; and ANTACIDS for symptomatic relief.
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.
Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues.
Substances that inhibit or arrest DENTAL CARIES formation. (Boucher's Clinical Dental Terminology, 4th ed)
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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