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Details

Stereochemistry RACEMIC
Molecular Formula C14H17Cl2N3O
Molecular Weight 314.21
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PICLONIDINE

SMILES

ClC1=CC=CC(Cl)=C1N(C2CCCCO2)C3=NCCN3

InChI

InChIKey=NYQGJEQCYOJBPV-UHFFFAOYSA-N
InChI=1S/C14H17Cl2N3O/c15-10-4-3-5-11(16)13(10)19(14-17-7-8-18-14)12-6-1-2-9-20-12/h3-5,12H,1-2,6-9H2,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C14H17Cl2N3O
Molecular Weight 314.21
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Piclonidine is imidazoline derivative. Piclonidine has a relative specificity for the hypotensive action and thus indicate that the compound differs from the chemical congener clonidine which has other pharmacological effects involving several peripheral or centrally regulated autonomic functions. Unlike clonidine, this chemically related compound did not evoke hypertensive episodes or cause sedation in animals up to the oral dose of 1 mg/kg.

Approval Year

PubMed

PubMed

TitleDatePubMed
New centrally acting antihypertensive drugs related to methyldopa and clonidine.
1984-09-01
Comparative pharmacological profile of two imidazoline derivatives endowed with strong hypotensive activity: LR 99853 and clonidine.
1981-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:10:37 GMT 2025
Edited
by admin
on Mon Mar 31 18:10:37 GMT 2025
Record UNII
R7P4D56J1Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LR-99853
Preferred Name English
PICLONIDINE
INN  
INN  
Official Name English
N-(2,6-DICHLOROPHENYL)-4,5-DIHYDRO-N-(TETRAHYDRO-2H-PYRAN-2-YL)-1H-IMIDAZOL-2-AMINE
Common Name English
LR99853
Code English
piclonidine [INN]
Common Name English
1H-IMIDAZOL-2-AMINE, N-(2,6-DICHLOROPHENYL)-4,5-DIHYDRO-N-(TETRAHYDRO-2H-PYRAN-2-YL)-
Systematic Name English
(±)-2-(2,6-DICHLORO-N-(TETRAHYDRO-2H-PYRAN-2-YL)ANILINO-2-IMIDAZOLINE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
Code System Code Type Description
FDA UNII
R7P4D56J1Z
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
INN
4869
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
CAS
72467-44-8
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
EVMPD
SUB09811MIG
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
SMS_ID
100000082474
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
PUBCHEM
68914
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
ECHA (EC/EINECS)
276-672-6
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID00868142
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
NCI_THESAURUS
C66381
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106921
Created by admin on Mon Mar 31 18:10:37 GMT 2025 , Edited by admin on Mon Mar 31 18:10:37 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY