diphenidol
CHEBI:CHEBI_4638
Definition
A tertiary alcohol that is butan-1-ol substituted by two phenyl groups at position 1 and a piperidin-1-yl group at position 4.
Chemical Information
- Molecular Formula
- C21H27NO
- Molecular Mass
- 309.44522
- Charge
- 0
- SMILES
- OC(CCCN1CCCCC1)(c1ccccc1)c1ccccc1
- InChI
- InChI=1S/C21H27NO/c23-21(19-11-4-1-5-12-19,20-13-6-2-7-14-20)15-10-18-22-16-8-3-9-17-22/h1-2,4-7,11-14,23H,3,8-10,15-18H2
- InChIKey
- OGAKLTJNUQRZJU-UHFFFAOYSA-N
Alternative Names
- 1,1-diphenyl-4-piperidin-1-ylbutan-1-ol
- alpha,alpha-Diphenyl-1-piperidinebutanol
- difenidol
- difenidolum
- Diphenidol
- Diphenyl(3-(1-piperidyl)propyl)carbinol
Drug Classification
-
tertiary alcoholView Class →
CHEBI:26878
-
benzenesView Class →
CHEBI:22712
-
piperidinesView Class →
CHEBI:26151
-
t223774
Important Medical Information
⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.
- Always consult with a healthcare professional before starting, stopping, or modifying any medication.
- Side effects may vary and this list may not be comprehensive.
- Drug interactions may occur with other medications.
Additional Identifiers
- DRON_00010000
- 23370
- oboInOwl#hasDbXref
- Wikipedia:Diphenidol
- core#notation
- CHEBI:4638
Additional References
🔍 Click on any linked disease name to learn more about the conditions this medication is used to treat, or explore related drug classifications for more information about similar medications.
Additional Attributes
- oboInOwl#hasOBONamespace
- chebi_ontology
- DRON_00010000
- 23370
- oboInOwl#hasDbXref
- Wikipedia:Diphenidol
- oboInOwl#id
- CHEBI:4638
- core#notation
- CHEBI:4638
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/chebi#3_STAR
- RO_0000087
- http://purl.obolibrary.org/obo/CHEBI_50919
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_side_effect24743
- owl#annotatedSource
- t224943
- owl#someValuesFrom
- t821286