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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9Cl2N3
Molecular Weight 230.094
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLONIDINE

SMILES

ClC1=CC=CC(Cl)=C1NC2=NCCN2

InChI

InChIKey=GJSURZIOUXUGAL-UHFFFAOYSA-N
InChI=1S/C9H9Cl2N3/c10-6-2-1-3-7(11)8(6)14-9-12-4-5-13-9/h1-3H,4-5H2,(H2,12,13,14)

HIDE SMILES / InChI
Molecular Formula C9H9Cl2N3
Molecular Weight 230.094
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:19:53 UTC 2023
Edited
by admin
on Sat Dec 16 16:19:53 UTC 2023
Record UNII
MN3L5RMN02
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLONIDINE
HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
CLONIDINE [VANDF]
Common Name English
ST-155-BS
Code English
CLONIDINE [HSDB]
Common Name English
CLONIDINE [USP-RS]
Common Name English
CLONIDINE EXTENDED RELEASE
Common Name English
CLONIDINE [MI]
Common Name English
CLONIDINE [USAN]
Common Name English
CLONIDINE [JAN]
Common Name English
Clonidine [WHO-DD]
Common Name English
CATARPRES-TTS
Brand Name English
CLONIDINE [MART.]
Common Name English
CLONIDINE [ORANGE BOOK]
Common Name English
2-[(2,6-Dichlorophenyl)imino]imidazolidine
Systematic Name English
clonidine [INN]
Common Name English
CLONIDINE [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
WHO-ATC C02LC51
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-ATC S01EA04
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
NDF-RT N0000009918
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-VATC QC02LC01
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-ATC N02CX02
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-VATC QC02LC51
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-VATC QN02CX02
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
NCI_THESAURUS C29709
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
FDA ORPHAN DRUG 425614
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
NDF-RT N0000175554
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
FDA ORPHAN DRUG 34388
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-VATC QC02AC01
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-VATC QS01EA04
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
LIVERTOX NBK548329
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-ATC C02AC01
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
WHO-ATC C02LC01
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C380
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID6022846
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
DRUG BANK
DB00575
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
RXCUI
2599
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY RxNorm
FDA UNII
MN3L5RMN02
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
CAS
4205-90-7
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
ECHA (EC/EINECS)
224-119-4
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
MESH
D003000
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
IUPHAR
516
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
DAILYMED
MN3L5RMN02
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
SMS_ID
100000084529
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
PUBCHEM
2803
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
LACTMED
Clonidine
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
INN
2624
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
WIKIPEDIA
CLONIDINE
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
USAN
U-77
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
ChEMBL
CHEMBL134
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
DRUG CENTRAL
704
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
MERCK INDEX
m3650
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY Merck Index
RS_ITEM_NUM
1140393
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
HSDB
3040
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
CHEBI
46631
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
EVMPD
SUB06730MIG
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
CHEBI
3757
Created by admin on Sat Dec 16 16:19:55 UTC 2023 , Edited by admin on Sat Dec 16 16:19:55 UTC 2023
PRIMARY
Related Record Type Details
Nischarin
TARGET -> AGONIST
Ki
ALPHA-2A ADRENERGIC RECEPTOR
TARGET -> AGONIST
SHORT-ACTING
ALPHA-2B ADRENERGIC RECEPTOR
TARGET -> AGONIST
OCT-3
TRANSPORTER -> INHIBITOR
OCT-1
TRANSPORTER -> INHIBITOR
OCT-2
TRANSPORTER -> INHIBITOR
ALPHA-2C ADRENERGIC RECEPTOR
TARGET -> AGONIST
Structure of CLONIDINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of N-ACETYLCLONIDINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of CLONIDINE DIMER
IMPURITY -> PARENT
Related Record Type Details
Structure of CLONIDINE
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
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