Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H29N3O6.ClH |
Molecular Weight | 527.997 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC(=O)C1=C(C)NC(C)=C([C@H]1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)O[C@H]3CCN(CC4=CC=CC=C4)C3
InChI
InChIKey=XEMPUKIZUCIZEY-YSCHMLPRSA-N
InChI=1S/C27H29N3O6.ClH/c1-17-23(26(31)35-3)25(20-10-7-11-21(14-20)30(33)34)24(18(2)28-17)27(32)36-22-12-13-29(16-22)15-19-8-5-4-6-9-19;/h4-11,14,22,25,28H,12-13,15-16H2,1-3H3;1H/t22-,25-;/m0./s1
Molecular Formula | C27H29N3O6 |
Molecular Weight | 491.5357 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
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 |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/?term=11434453
Sources: http://www.ncbi.nlm.nih.gov/pubmed/?term=11434453
Bamidipine is an antihypertensive drug belonging to the dihydropyridine (DHP) group of calcium antagonists. The product was originally developed by Yamanouchi Pharmaceutical (Tokyo, Japan) and is currently marketed in Japan under the trade name of Hypoca (Astellas Pharma Inc, Tokyo, Japan). It is available in a modified-release formulation which has a gradual onset of action and is effective in a single daily oral dose of 10 to 20 mg. Bamidipine has selective action against cardiovascular calcium antagonist receptors and its antihypertensive action is related to the reduction of peripheral vascular resistance secondary to its vasodilatory action. The clinical antihypertensive efficacy of barnidipine is similar to that of other DHP calcium antagonists such as nitrendipine and amlodipine, and antihypertensives belonging to other drug classes such as atenolol and enalapril. Barnidipine has been found to be as efficacious and well tolerated as hydrochlorothiazide in the management of hypertension in elderly patients. Barnidipine is generally well tolerated. As with other DHP calcium antagonists, vasodilator adverse events such as headache, flushing and peripheral oedema account for most of the adverse events reported with its use and are usually transient. Oedema is less frequent than with amlodipine and nitrendipine. Its use is not associated with reflex tachycardia.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2363032 Sources: http://www.ncbi.nlm.nih.gov/pubmed/15853594 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/?term=11434453
single daily oral dose of 10 to 20 mg
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:10:26 GMT 2025
by
admin
on
Mon Mar 31 18:10:26 GMT 2025
|
Record UNII |
7LZ6R3AEM1
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
m2268
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | Merck Index | ||
|
CHEMBL2103761
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
443868
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
104757-53-1
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
100000084990
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
7LZ6R3AEM1
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
DTXSID8048654
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | |||
|
283819
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY | RxNorm | ||
|
SUB00671MIG
Created by
admin on Mon Mar 31 18:10:26 GMT 2025 , Edited by admin on Mon Mar 31 18:10:26 GMT 2025
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |