General
Preferred name
URETHANE
Synonyms
Ethyl carbamate ()
Ethylurethane ()
Carbamic acid ethyl ester ()
Carbamic acid ethyl ester, Ethyl carbamate, Ethylurethane ()
Urethan ()
Carbamic acid, ethyl ester ()
Leucethane ()
Uretano ()
Pracarbamine ()
NSC-746 ()
O-ethylurethane ()
P&D ID
PD001002
CAS
51-79-6
121382-27-2
26680-22-8
Tags
available
drug
Drug Status
approved
withdrawn
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure
P&D probe-likeness score
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Urethane (Ethyl carbamate), the ethyl ester of carbamic acid, is a byproduct of fermentation found in various food products. Urethane has the ability to suppress bacterial, protozoal, sea urchin egg, and plant tissue growth in vitro[1].
PRICE
29
DESCRIPTION
Urethane is an ethyl ester of carbamic acid, that has been found in many fermented food products and alcoholic beverages. It has a potential to inhibit the growth of bacteria, plant tissue, and rat carcinoma. Urethane has been used for many years as an antineoplastic agent for medical purposes but this application ended after it was discovered to be carcinogenic.
(Enamine Bioactive Compounds)
DESCRIPTION
Urethane (Ethylurethane) was an antineoplastic agent .Now is used for other medicinal purposes.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
12
ChEMBL Approved Drugs
ChEMBL Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugMatrix
Enamine Bioactive Compounds
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
Withdrawn 2.0
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
40
Molecular Weight
89.05
Hydrogen Bond Acceptors
2
Hydrogen Bond Donors
1
Rotatable Bonds
1
Ring Count
0
Aromatic Ring Count
0
cLogP
0.1
TPSA
52.32
Fraction CSP3
0.67
Chiral centers
0.0
Largest ring
0.0
QED
0.5
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Target
AMPA
Bacterial
GABAR
Glycine receptor
NMDA Receptor
Parasite
α4β2 nAChR
MOA
local anesthetic
ATC
L
Toxicity type
carcinogenicity
Pathway
Membrane Transporter/Ion Channel
Microbiology/virology
Neuroscience
Anti-infection
Source data
