Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H27NO4 |
Molecular Weight | 345.4327 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(CCNC[C@@H](O)COC2=CC(C)=CC=C2)C=C1OC
InChI
InChIKey=HXLAFSUPPDYFEO-QGZVFWFLSA-N
InChI=1S/C20H27NO4/c1-15-5-4-6-18(11-15)25-14-17(22)13-21-10-9-16-7-8-19(23-2)20(12-16)24-3/h4-8,11-12,17,21-22H,9-10,13-14H2,1-3H3/t17-/m1/s1
Molecular Formula | C20H27NO4 |
Molecular Weight | 345.4327 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Atypical cardiostimulant beta-adrenoceptor in the rat heart: stereoselective antagonism by bupranolol but lack of effect by some bupranolol analogues. | 2003 Aug |
|
Determination of bevantolol in human plasma by high performance liquid chromatography using solid phase extraction technique. | 2007 Jul |
|
Different changes of plasma membrane beta-adrenoceptors in rat heart after chronic administration of propranolol, atenolol and bevantolol. | 2007 Jul 12 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:49:02 GMT 2023
by
admin
on
Sat Dec 16 10:49:02 GMT 2023
|
Record UNII |
34P43RW460
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
135531-40-7
Created by
admin on Sat Dec 16 10:49:02 GMT 2023 , Edited by admin on Sat Dec 16 10:49:02 GMT 2023
|
PRIMARY | |||
|
34P43RW460
Created by
admin on Sat Dec 16 10:49:02 GMT 2023 , Edited by admin on Sat Dec 16 10:49:02 GMT 2023
|
PRIMARY | |||
|
36690919
Created by
admin on Sat Dec 16 10:49:02 GMT 2023 , Edited by admin on Sat Dec 16 10:49:02 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
RACEMATE -> ENANTIOMER |