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Details

Stereochemistry RACEMIC
Molecular Formula C13H19N5
Molecular Weight 245.3235
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of PINACIDIL ANHYDROUS

SMILES

CC(NC(NC1=CC=NC=C1)=NC#N)C(C)(C)C

InChI

InChIKey=IVVNZDGDKPTYHK-UHFFFAOYSA-N
InChI=1S/C13H19N5/c1-10(13(2,3)4)17-12(16-9-14)18-11-5-7-15-8-6-11/h5-8,10H,1-4H3,(H2,15,16,17,18)

HIDE SMILES / InChI

Molecular Formula C13H19N5
Molecular Weight 245.3235
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:57:05 UTC 2023
Edited
by admin
on Fri Dec 15 18:57:05 UTC 2023
Record UNII
BB4UGO5K0D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PINACIDIL ANHYDROUS
Common Name English
(±)-PINACIDIL
Common Name English
GUANIDINE, N-CYANO-N'-4-PYRIDINYL-N''-(1,2,2-TRIMETHYLPROPYL)-
Systematic Name English
(R,S)-PINACIDIL
Common Name English
PINACIDIL [MI]
Common Name English
P-1134
Code English
1-(3,3-DIMETHYLBUTAN-2-YL)-2-CYANO-3-(PYRIDIN-4-YL)GUANIDINE
Systematic Name English
pinacidil [INN]
Common Name English
Pinacidil [WHO-DD]
Common Name English
S-1230
Code English
GUANIDINE, N''-CYANO-N-4-PYRIDINYL-N'-(1,2,2-TRIMETHYLPROPYL)-,(±)-
Common Name English
Classification Tree Code System Code
WHO-ATC C02DG01
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
NCI_THESAURUS C270
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
Code System Code Type Description
MERCK INDEX
m8819
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY Merck Index
PUBCHEM
4826
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
FDA UNII
BB4UGO5K0D
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
INN
5013
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
CAS
113563-69-2
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
SUPERSEDED
EPA CompTox
DTXSID7048249
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
CAS
60560-33-0
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
ECHA (EC/EINECS)
262-294-9
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
NCI_THESAURUS
C143025
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
EVMPD
SUB09848MIG
Created by admin on Fri Dec 15 18:57:05 UTC 2023 , Edited by admin on Fri Dec 15 18:57:05 UTC 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY