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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
Structure of BARNIDIPINE HYDROCHLORIDE

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

HIDE SMILES / InChI

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

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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Barnidipine.
2001
Patents

Patents

Sample Use Guides

single daily oral dose of 10 to 20 mg
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:50:14 GMT 2023
Edited
by admin
on Fri Dec 15 15:50:14 GMT 2023
Record UNII
7LZ6R3AEM1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BARNIDIPINE HYDROCHLORIDE
JAN   MART.   MI   WHO-DD  
Common Name English
Barnidipine hydrochloride [WHO-DD]
Common Name English
BARNIDIPINE HYDROCHLORIDE [MART.]
Common Name English
BARNIDIPINE HYDROCHLORIDE [MI]
Common Name English
(+)-(3'S,4S)-1-BENZYL-3-PYRROLIDINYL METHYL 1,4-DIHYDRO-2,6-DIMETHYL-4-(M-NITROPHENYL)-3,5-PYRIDINEDICARBOXYLATE HYDROCHLORIDE
Common Name English
LY-198561
Code English
BARNIDIPINE HCL
Common Name English
BARNIDIPINE HYDROCHLORIDE [JAN]
Common Name English
Code System Code Type Description
MERCK INDEX
m2268
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2103761
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
PUBCHEM
443868
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
CAS
104757-53-1
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
SMS_ID
100000084990
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
FDA UNII
7LZ6R3AEM1
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID8048654
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
RXCUI
283819
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY RxNorm
EVMPD
SUB00671MIG
Created by admin on Fri Dec 15 15:50:14 GMT 2023 , Edited by admin on Fri Dec 15 15:50:14 GMT 2023
PRIMARY
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ACTIVE MOIETY