Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H5F3O |
| Molecular Weight | 126.0771 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(F)(F)COC=C
InChI
InChIKey=DLEGDLSLRSOURQ-UHFFFAOYSA-N
InChI=1S/C4H5F3O/c1-2-8-3-4(5,6)7/h2H,1,3H2
| Molecular Formula | C4H5F3O |
| Molecular Weight | 126.0771 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
CNS Activity
Approval Year
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://pubmed.ncbi.nlm.nih.gov/25763/ |
yes |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Cross-approximate entropy of cortical local field potentials quantifies effects of anesthesia--a pilot study in rats. | 2010-09-23 |
|
| General anesthetic actions on GABA(A) receptors. | 2010-03 |
|
| A calorimetric study on the binding of six general anesthetics to the hydrophobic core of a model protein. | 2005-02-01 |
|
| Cardiovascular effects of pancuronium in patients anaesthetized with enflurane and fluroxene. | 1981-01 |
|
| The effect of enflurane, isoflurane, fluroxene, methoxyflurane and diethyl ether anesthesia on ouabain tolerance in the dog. | 1976-05-01 |
|
| Electroencephalographic seizure activity in dogs during anaesthesia. | 1971-08 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:48:39 GMT 2025
by
admin
on
Mon Mar 31 17:48:39 GMT 2025
|
| Record UNII |
FO7JHA3G03
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Official Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Brand Name | English | ||
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Common Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C245
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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FO7JHA3G03
Created by
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PRIMARY | |||
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9844
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | |||
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C084587
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admin on Mon Mar 31 17:48:39 GMT 2025 , Edited by admin on Mon Mar 31 17:48:39 GMT 2025
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PRIMARY | |||
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760364
Created by
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PRIMARY | |||
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100000080951
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | |||
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m5502
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | Merck Index | ||
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C75097
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | |||
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Fluroxene
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | |||
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206-977-1
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY | |||
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CHEMBL141446
Created by
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PRIMARY | |||
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1278
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PRIMARY | |||
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3242
Created by
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PRIMARY | |||
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SUB07751MIG
Created by
admin on Mon Mar 31 17:48:39 GMT 2025 , Edited by admin on Mon Mar 31 17:48:39 GMT 2025
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PRIMARY | |||
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406-90-6
Created by
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PRIMARY | |||
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DTXSID5059957
Created by
admin on Mon Mar 31 17:48:40 GMT 2025 , Edited by admin on Mon Mar 31 17:48:40 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |