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Details

Stereochemistry RACEMIC
Molecular Formula C33H34N6O6
Molecular Weight 610.6597
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CANDESARTAN CILEXETIL

SMILES

CCOC1=NC2=C(N1CC3=CC=C(C=C3)C4=C(C=CC=C4)C5=NN=NN5)C(=CC=C2)C(=O)OC(C)OC(=O)OC6CCCCC6

InChI

InChIKey=GHOSNRCGJFBJIB-UHFFFAOYSA-N
InChI=1S/C33H34N6O6/c1-3-42-32-34-28-15-9-14-27(31(40)43-21(2)44-33(41)45-24-10-5-4-6-11-24)29(28)39(32)20-22-16-18-23(19-17-22)25-12-7-8-13-26(25)30-35-37-38-36-30/h7-9,12-19,21,24H,3-6,10-11,20H2,1-2H3,(H,35,36,37,38)

HIDE SMILES / InChI

Molecular Formula C33H34N6O6
Molecular Weight 610.6597
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 Fri Dec 15 16:16:03 UTC 2023
Edited
by admin
on Fri Dec 15 16:16:03 UTC 2023
Record UNII
R85M2X0D68
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CANDESARTAN CILEXETIL
USAN  
Official Name English
ATACAND
Brand Name English
CANDESARTAN CILEXETIL [VANDF]
Common Name English
CANDESARTAN 1-(((CYCLOHEXYLOXY)CARBONYL)OXY)ETHYL ESTER
MI  
Common Name English
CANDESARTAN CILEXETIL [USP-RS]
Common Name English
CANDESARTAN CILEXETIL [MART.]
Common Name English
TCV-116
Code English
1H-BENZIMIDAZOLE-7-CARBOXYLIC ACID, 2-ETHOXY-1-((2'-(1H-TETRAZOL-5-YL)(1,1'-BIPHENYL)-4-YL)METHYL)-, 1-(((CYCLOHEXYLOXY)CARBONYL)OXY)ETHYL ESTER, (±)-
Common Name English
CANDESARTAN CILEXETIL [USAN]
Common Name English
NSC-758697
Code English
CANDESARTAN CILEXETIL [ORANGE BOOK]
Common Name English
CANDESARTAN 1-(((CYCLOHEXYLOXY)CARBONYL)OXY)ETHYL ESTER [MI]
Common Name English
CANDESARTAN CILEXETIL [EP MONOGRAPH]
Common Name English
CANDESARTAN CILEXETIL [USP MONOGRAPH]
Common Name English
(±)-1-HYDROXYETHYL 2-ETHOXY-1-(P-(O-1H-TETRAZOL-5-YLPHENYL)BENZYL)-7-BENZIMIDAZOLECARBOXYLATE, CYCLOHEXYL CARBONATE (ESTER)
Common Name English
Candesartan cilexetil [WHO-DD]
Common Name English
CANDESARTAN CILEXETIL [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66930
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
Code System Code Type Description
NSC
758697
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
RS_ITEM_NUM
1087803
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
MERCK INDEX
m3012
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY Merck Index
DAILYMED
R85M2X0D68
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
DRUG CENTRAL
475
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
DRUG BANK
DB00796
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
NCI_THESAURUS
C28903
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
MESH
C077793
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
FDA UNII
R85M2X0D68
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
ChEMBL
CHEMBL1014
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
SMS_ID
100000091533
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
CAS
145040-37-5
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
RXCUI
135481
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID5020239
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
USAN
JJ-7
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
PUBCHEM
2540
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
EVMPD
SUB13222MIG
Created by admin on Fri Dec 15 16:16:03 UTC 2023 , Edited by admin on Fri Dec 15 16:16:03 UTC 2023
PRIMARY
Related Record Type Details
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
IMPURITY -> PARENT
For the calculation of content, multiply the peak area by 0.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
for the calculation of content, multiply the peak area by 0.7.
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
For the calculation of content, multiply the peak area by 1.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY