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:63799 - 4-hydroxytolbutamide
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
4-hydroxytolbutamide
ChEBI ID
CHEBI:63799
Definition
A urea that consists of 1-butylurea having a 4-hydroxymethylbenzenesulfonyl group attached at the 3-position.
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
Formula
C12H18N2O4S
Net Charge
0
Average Mass
286.34700
Monoisotopic Mass
286.09873
InChI
InChI=1S/C12H18N2O4S/c1-
2-
3-
8-
13-
12(16)
14-
19(17,18)
11-
6-
4-
10(9-
15)
5-
7-
11/h4-
7,15H,2-
3,8-
9H2,1H3,(H2,13,14,16)
InChIKey
SJRHYONYKZIRPM-UHFFFAOYSA-N
SMILES
CCCCNC(=O)NS(=O)(=O)c1ccc(CO)cc1
Roles Classification
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
4-hydroxytolbutamide (
CHEBI:63799
)
has role
metabolite (
CHEBI:25212
)
4-hydroxytolbutamide (
CHEBI:63799
)
is a
benzyl alcohols (
CHEBI:22743
)
4-hydroxytolbutamide (
CHEBI:63799
)
is a
sulfonamide (
CHEBI:35358
)
4-hydroxytolbutamide (
CHEBI:63799
)
is a
ureas (
CHEBI:47857
)
IUPAC Name
N
-(butylcarbamoyl)-4-(hydroxymethyl)benzenesulfonamide
Synonyms
Sources
1-Butyl-3-(4-hydroxymethylphenyl)sulfonylurea
ChemIDplus
Hydroxymethyltolbutamide
ChemIDplus
Hydroxytolbutamide
ChemIDplus
Methylhydroxytolbutamide
ChemIDplus
Manual Xref
Database
HMDB0006408
HMDB
View more database links
Registry Numbers
Types
Sources
2867981
Reaxys Registry Number
Reaxys
5719-85-7
CAS Registry Number
ChemIDplus
Citation
Type
Source
16493553
PubMed citation
Europe PMC
Last Modified
01 February 2012