U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C20H22N2S
Molecular Weight 322.467
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEQUITAZINE

SMILES

C(C1CN2CCC1CC2)N3C4=CC=CC=C4SC5=C3C=CC=C5

InChI

InChIKey=HOKDBMAJZXIPGC-UHFFFAOYSA-N
InChI=1S/C20H22N2S/c1-3-7-19-17(5-1)22(18-6-2-4-8-20(18)23-19)14-16-13-21-11-9-15(16)10-12-21/h1-8,15-16H,9-14H2

HIDE SMILES / InChI

Molecular Formula C20H22N2S
Molecular Weight 322.467
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 15:22:17 UTC 2023
Edited
by admin
on Fri Dec 15 15:22:17 UTC 2023
Record UNII
Y463242LY2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEQUITAZINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
MEQUITAZINE [MI]
Common Name English
MEQUITAZINE [JAN]
Common Name English
Mequitazine [WHO-DD]
Common Name English
NSC-303612
Code English
MEQUITAZINE [MART.]
Common Name English
KITAZEMIN
Brand Name English
mequitazine [INN]
Common Name English
10-(3-QUINUCLIDINYLMETHYL)PHENOTHIAZINE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QR06AD07
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
WHO-ATC R06AD07
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
Code System Code Type Description
MESH
C006069
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
MERCK INDEX
m7201
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID8023262
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
RXCUI
29528
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY RxNorm
CAS
29216-28-2
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
FDA UNII
Y463242LY2
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
NCI_THESAURUS
C170162
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
WIKIPEDIA
MEQUITAZINE
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
NSC
303612
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
DRUG BANK
DB01071
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
PUBCHEM
4066
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
INN
3672
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
ChEMBL
CHEMBL1908311
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
ECHA (EC/EINECS)
249-521-7
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
DRUG CENTRAL
1707
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
EVMPD
SUB08766MIG
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
SMS_ID
100000081707
Created by admin on Fri Dec 15 15:22:17 UTC 2023 , Edited by admin on Fri Dec 15 15:22:17 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
ENANTIOMER -> RACEMATE
METABOLIC ENZYME -> SUBSTRATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY