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Details

Stereochemistry ACHIRAL
Molecular Formula C17H24N2O
Molecular Weight 272.3853
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMETHISOQUIN

SMILES

CCCCC1=NC(OCCN(C)C)=C2C=CC=CC2=C1

InChI

InChIKey=XNMYNYSCEJBRPZ-UHFFFAOYSA-N
InChI=1S/C17H24N2O/c1-4-5-9-15-13-14-8-6-7-10-16(14)17(18-15)20-12-11-19(2)3/h6-8,10,13H,4-5,9,11-12H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C17H24N2O
Molecular Weight 272.3853
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dimethisoquin (also known as Quinisocaine and QUOTANE) is a topical anesthetic used as an antipruritic. It was shown that dimethisoquin inhibits nicotinic acetylcholine receptors (alpha4/beta4 and alpha4/beta2) with the maximum inhibition potency occurring for the α4β4 subtype.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Synthetic antimalarials].
2005 Aug-Sep
Patents

Sample Use Guides

To the skin as a 0.5% oinment or lotion 2 to 4 times per day.
Route of Administration: Topical
In Vitro Use Guide
Various local anesthetics enhanced the incorporation of [3H]inositol into phosphoinositides in guinea pig cerebral cortical synaptoneurosomes. Dibucaine, QX-572 and dimethisoquin showed maximum stimulation at 100 microM. There was no correlation between local anesthetic activity, estimated by inhibition of the 22Na+ flux elicited by the sodium channel activator batrachotoxin, and the potency for stimulation of inositol incorporation.
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:48:25 GMT 2023
Edited
by admin
on Sat Dec 16 16:48:25 GMT 2023
Record UNII
772EN3BH6I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMETHISOQUIN
MI  
Common Name English
quinisocaine [INN]
Common Name English
Quinisocaine [WHO-DD]
Common Name English
ETHANAMINE, 2-((3-BUTYL-1-ISOQUINOLINYL)OXY)-N,N-DIMETHYL-
Systematic Name English
QUINISOCAINE
INN   WHO-DD  
INN  
Official Name English
3-BUTYL-1-(2-(DIMETHYLAMINO)ETHOXY)ISOQUINOLINE
Systematic Name English
NSC-39695
Code English
DIMETHISOQUIN [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
WHO-VATC QD04AB05
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
WHO-ATC D04AB05
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
Code System Code Type Description
MERCK INDEX
m1118
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY Merck Index
FDA UNII
772EN3BH6I
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID8048525
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
MESH
C009146
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
CAS
86-80-6
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
EVMPD
SUB10218MIG
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
WIKIPEDIA
QUINISOCAINE
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
INN
367
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
NSC
39695
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
DRUG BANK
DB13683
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
ChEMBL
CHEMBL127643
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
NCI_THESAURUS
C72169
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
PUBCHEM
6857
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
DRUG CENTRAL
3153
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-700-0
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY