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Details

Stereochemistry RACEMIC
Molecular Formula C20H24N2O6
Molecular Weight 388.4144
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NISOLDIPINE

SMILES

COC(=O)C1=C(C)NC(C)=C(C1C2=C(C=CC=C2)[N+]([O-])=O)C(=O)OCC(C)C

InChI

InChIKey=VKQFCGNPDRICFG-UHFFFAOYSA-N
InChI=1S/C20H24N2O6/c1-11(2)10-28-20(24)17-13(4)21-12(3)16(19(23)27-5)18(17)14-8-6-7-9-15(14)22(25)26/h6-9,11,18,21H,10H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C20H24N2O6
Molecular Weight 388.4144
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:51:42 UTC 2023
Edited
by admin
on Sat Dec 16 17:51:42 UTC 2023
Record UNII
4I8HAB65SZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NISOLDIPINE
INN   JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
NISOLDIPINE [MART.]
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-4-(2-NITROPHENYL)-, METHYL 2-METHYLPROPYL ESTER, (±)-
Common Name English
NISOLDIPINE [ORANGE BOOK]
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-4-(2-NITROPHENYL)-, 3-METHYL 5-(2-METHYLPROPYL) ESTER
Systematic Name English
NISOLDIPIN
Brand Name English
BAYMYCARD
Brand Name English
SULAR
Brand Name English
NISOCOR
Brand Name English
(±)-NISOLDIPINE
Common Name English
NISOLDIPINE [JAN]
Common Name English
nisoldipine [INN]
Common Name English
NISOLDIPINE [USAN]
Common Name English
METHYL 2-METHYLPROPYL-1,4-DIHYDRO-2,6-DIMETHYL-4-(2-NITROPHENYL)-3,5-PYRIDINEDICARBOXYLATE, DL-
Common Name English
(±)-BAY-K-5552
Common Name English
NISOLDIPINE [VANDF]
Common Name English
NSC-759106
Code English
NISOLDIPINE (STN)
Brand Name English
NISOLDIPINE [USP-RS]
Common Name English
Nisoldipine [WHO-DD]
Common Name English
NISOLDIPINE [MI]
Common Name English
BAY-K-5552
Code English
GEOMATRIX 16E
Brand Name English
BAY K 5552
Code English
3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-4-(2-NITROPHENYL)-, METHYL 2-METHYLPROPYL ESTER
Common Name English
Classification Tree Code System Code
WHO-VATC QC08CA07
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
NCI_THESAURUS C333
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
NDF-RT N0000175421
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
WHO-ATC C08CA07
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
LIVERTOX NBK548364
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
Code System Code Type Description
MERCK INDEX
m7921
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY Merck Index
SMS_ID
100000092490
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
ECHA (EC/EINECS)
264-407-7
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
CHEBI
7577
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
MESH
D015737
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
LACTMED
Nisoldipine
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
INN
4753
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
NDF-RT
N0000178477
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY Decreased Blood Pressure [PE]
DRUG BANK
DB00401
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
ChEMBL
CHEMBL1726
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
EVMPD
SUB09307MIG
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
EPA CompTox
DTXSID0023371
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
RS_ITEM_NUM
1463927
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
NSC
759106
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
RXCUI
7435
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY RxNorm
DRUG CENTRAL
1942
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
IUPHAR
2524
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
FDA UNII
4I8HAB65SZ
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
NCI_THESAURUS
C29291
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
PUBCHEM
4499
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
WIKIPEDIA
NISOLDIPINE
Created by admin on Sat Dec 16 17:51:43 UTC 2023 , Edited by admin on Sat Dec 16 17:51:43 UTC 2023
PRIMARY
DAILYMED
4I8HAB65SZ
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
CAS
63675-72-9
Created by admin on Sat Dec 16 17:51:42 UTC 2023 , Edited by admin on Sat Dec 16 17:51:42 UTC 2023
PRIMARY
Related Record Type Details
METABOLITE -> PARENT
Dehydrogenation step is catalyzed by the cytochrome P450 (CYP) 3A4 enzyme
PLASMA
METABOLITE -> PARENT
Dehydrogenation step is catalyzed by the cytochrome P450 (CYP) 3A4 enzyme
PLASMA; URINE
METABOLITE -> PARENT
Although M9 showed small pharmacological activity ? qualitatively similar to nisoldipine ? in animal models, it does not contribute significantly to the haemodynamic effects of the drug in humans.
PLASMA
METABOLITE -> PARENT
Dehydrogenation step is catalyzed by the cytochrome P450 (CYP) 3A4 enzyme
PLASMA; URINE
METABOLITE -> PARENT
PLASMA
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
Dehydrogenation step is catalysed by the cytochrome P450 (CYP) 3A4 enzyme
URINE
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Excretion PHARMACOKINETIC Urine
BIOLOGICAL
Biological Half-life PHARMACOKINETIC