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Details

Stereochemistry RACEMIC
Molecular Formula C13H16N2.ClH
Molecular Weight 236.74
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEDETOMIDINE HYDROCHLORIDE

SMILES

Cl.CC(C1=CN=CN1)C2=C(C)C(C)=CC=C2

InChI

InChIKey=VPNGEIHDPSLNMU-UHFFFAOYSA-N
InChI=1S/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H

HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C13H16N2
Molecular Weight 200.2795
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:06:41 UTC 2023
Edited
by admin
on Fri Dec 15 16:06:41 UTC 2023
Record UNII
BH210P244U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEDETOMIDINE HYDROCHLORIDE
MART.   MI   USAN  
USAN  
Official Name English
MEDETOMIDINE HYDROCHLORIDE [GREEN BOOK]
Common Name English
MEDETOMIDINE HCL
Common Name English
MEDETOMIDINE HYDROCHLORIDE [MI]
Common Name English
MEDETOMIDINE HYDROCHLORIDE [MART.]
Common Name English
MEDETOMIDINE HYDROCHLORIDE [USAN]
Common Name English
(±)-4-(.ALPHA.,2,3-TRIMETHYLBENZYL)IMIDAZOLE MONOHYDROCHLORIDE
Systematic Name English
4-(1-(2,3-DIMETHYLPHENYL)ETHYL)-, MONOHYDROCHLORIDE, (±)-
Common Name English
MPV-785
Code English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
CFR 21 CFR 522.1335
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
Code System Code Type Description
MERCK INDEX
m7128
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY Merck Index
FDA UNII
BH210P244U
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
USAN
Z-59
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
ChEMBL
CHEMBL77921
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
NCI_THESAURUS
C81368
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
PUBCHEM
68601
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
EPA CompTox
DTXSID3045691
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
CAS
86347-15-1
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
DRUG BANK
DBSALT002859
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
DAILYMED
BH210P244U
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
RXCUI
29428
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY RxNorm
SMS_ID
300000023831
Created by admin on Fri Dec 15 16:06:41 UTC 2023 , Edited by admin on Fri Dec 15 16:06:41 UTC 2023
PRIMARY
Related Record Type Details
Structure of MEDETOMIDINE
PARENT -> SALT/SOLVATE
Structure of LEVOMEDETOMIDINE HYDROCHLORIDE
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of MEDETOMIDINE
ACTIVE MOIETY
NIH
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