Basic information
- CAS
67704-50-1- Standard SMILES
CC(C)(CO)NCC(O)c1ccccc1.Cl- InChIKey
VJOOWJGUDMCBMI-UHFFFAOYSA-N- Molecular formula
- C12H20ClNO2
- Average molar mass
- 245.74 g/mol
- Monoisotopic mass
- 245.1182566
Names & identifiers
- Preferred name
- Fepradinol hydrochloride
- IUPAC
- 2-[(2-hydroxy-2-phenylethyl)amino]-2-methylpropan-1-ol;hydrochloride
Names & synonyms
fepradinol hydrochloride67704-50-147X845AK0JRefChem:140230EL-508UNII-47X845AK0Jalpha-(((1,1-Dimethyl-2-hydroxyethyl)amino)methyl)benzenemethanol hydrochlorideBenzenemethanol, alpha-(((1,1-dimethyl-2-hydroxyethyl)amino)methyl)-, hydrochlorideChlorhydrate de N-(hydroxy-2 dimethyl-1,1 ethyl)-amino-2 phenyl-1 ethanol [French]SCHEMBL29454386DTXSID109870502-[(2-hydroxy-2-phenylethyl)amino]-2-methylpropan-1-ol;hydrochloride
Show more names
Chlorhydrate de N-(hydroxy-2 dimethyl-1,1 ethyl)-amino-2 phenyl-1 ethanolFEPRADINOL HYDROCHLORIDE [WHO-DD]Q272590802-[(2-Hydroxy-2-phenylethyl)amino]-2-methylpropan-1-ol--hydrogen chloride (1/1)BENZENEMETHANOL, .ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDEBENZENEMETHANOL, .ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
Database identifiers
- CAS
67704-50-1- PubChem CID
- 3051696
- DTXSID
DTXSID10987050- UNII
- 47X845AK0J
Properties
Computed structural properties
- Topological polar surface area
- 52.5 Ų
- Hydrogen bond donors
- 4
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 5
- Heavy atoms
- 16
- Formal charge
- 0
- Complexity
- 176
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
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.
Related reactions
0 records
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Compound notes
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