Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C12H18FNO.ClH |
| Molecular Weight | 247.737 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)(C)NCC(O)C1=C(F)C=CC=C1
InChI
InChIKey=NXNFXCMJTRKWFF-UHFFFAOYSA-N
InChI=1S/C12H18FNO.ClH/c1-12(2,3)14-8-11(15)9-6-4-5-7-10(9)13;/h4-7,11,14-15H,8H2,1-3H3;1H
| Molecular Formula | C12H18FNO |
| Molecular Weight | 211.2758 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of CRL 40827 and salbutamol on exocrine pancreatic secretion in rats. | 1988 Jan 27 |
|
| Flerobuterol, a beta-adrenoceptor agonist, enhances serotonergic neurotransmission: an electrophysiological study in the rat brain. | 1991 |
|
| Flerobuterol: a potential antidepressant drug related to beta-adrenergic agonists. Experimental profile in mice. | 1991 |
|
| Evidence for different interactions between beta(1)- and beta(2)-adrenoceptor subtypes with adenylyl cyclase in the rat brain: a concentration-response study using forskolin. | 2000 Apr |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:30:27 UTC 2023
by
admin
on
Sat Dec 16 01:30:27 UTC 2023
|
| Record UNII |
48CC8WJ3WM
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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48CC8WJ3WM
Created by
admin on Sat Dec 16 01:30:27 UTC 2023 , Edited by admin on Sat Dec 16 01:30:27 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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RACEMATE -> ENANTIOMER | |||
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ENANTIOMER -> ENANTIOMER |
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