Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:64043 - desmethyl loperamide
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
desmethyl loperamide
ChEBI ID
CHEBI:64043
Definition
A monocarboxylic acid amide that is the methylamide of 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-2,2-diphenylbutanoic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
more structures >>
Molfile
Formula
C28H31ClN2O2
Net Charge
0
Average Mass
463.01100
Monoisotopic Mass
462.20741
InChI
InChI=1S/C28H31ClN2O2/c1-
30-
26(32)
28(23-
8-
4-
2-
5-
9-
23,24-
10-
6-
3-
7-
11-
24)
18-
21-
31-
19-
16-
27(33,17-
20-
31)
22-
12-
14-
25(29)
15-
13-
22/h2-
15,33H,16-
21H2,1H3,(H,30,32)
InChIKey
ZMOPTLXEYOVARP-UHFFFAOYSA-N
SMILES
CNC(=O)C(CCN1CCC(O)(CC1)c1ccc(Cl)cc1)(c1ccccc1)c1ccccc1
Roles Classification
Biological Role
(s):
drug metabolite
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
desmethyl loperamide (
CHEBI:64043
)
has role
drug metabolite (
CHEBI:49103
)
desmethyl loperamide (
CHEBI:64043
)
is a
monocarboxylic acid amide (
CHEBI:29347
)
desmethyl loperamide (
CHEBI:64043
)
is a
monochlorobenzenes (
CHEBI:83403
)
desmethyl loperamide (
CHEBI:64043
)
is a
piperidines (
CHEBI:26151
)
desmethyl loperamide (
CHEBI:64043
)
is a
tertiary alcohol (
CHEBI:26878
)
IUPAC Name
4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-
N
-methyl-2,2-diphenylbutanamide
Synonyms
Sources
monodesmethyl loperamide
ChEBI
N
-desmethyl loperamide
ChEBI
Manual Xref
Database
US2009274624
Patent
View more database links
Registry Number
Type
Source
1517638
Reaxys Registry Number
Reaxys
Citations
Types
Sources
18783208
PubMed citation
Europe PMC
19091890
PubMed citation
Europe PMC
19372478
PubMed citation
Europe PMC
20212014
PubMed citation
Europe PMC
20237038
PubMed citation
Europe PMC
20346873
PubMed citation
Europe PMC
20645912
PubMed citation
Europe PMC
21262843
PubMed citation
Europe PMC
21958857
PubMed citation
Europe PMC
7109845
PubMed citation
Europe PMC
Last Modified
24 October 2014