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Details

Stereochemistry RACEMIC
Molecular Formula C19H29N3O
Molecular Weight 315.4531
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAMAQUINE

SMILES

CCN(CC)CCCC(C)NC1=CC(OC)=CC2=CC=CN=C12

InChI

InChIKey=QTQWMSOQOSJFBV-UHFFFAOYSA-N
InChI=1S/C19H29N3O/c1-5-22(6-2)12-8-9-15(3)21-18-14-17(23-4)13-16-10-7-11-20-19(16)18/h7,10-11,13-15,21H,5-6,8-9,12H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C19H29N3O
Molecular Weight 315.4531
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

The discovery of pamaquine, developed by replacing one of the methyl groups of methylene blue by a dialkylaminoalkyl chain, was a landmark in the design of drugs for malaria. It is closely related to primaquine. The administration of pamaquine during the incubation period delayed but did not prevent primary attacks of a New Guinea strain of Plasmodium vivax malaria. Hemolytic anemia after administration of the antimalarial drug pamaquine was reported in patients with Glucose-6-phosphate dehydrogenase (G6PD) deficiency. Pamaquine itself could not be used clinically due to high toxicity.

Approval Year

Doses

Doses

DosePopulationAdverse events​
10 mg 3 times / day multiple, oral
Recommended
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
quinine(650 mg; 3/day for 2 days)
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 10000
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 10000
Sources:
Other AEs: Haemoglobinuria...
Other AEs:
Haemoglobinuria (5 patients)
Sources:
10 mg 3 times / day multiple, oral
Recommended
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 10000
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 10000
Sources:
Other AEs: Haemoglobinuria...
Other AEs:
Haemoglobinuria (13 patients)
Sources:
40 mg 1 times / day multiple, oral
Recommended
unhealthy
n = 56
Other AEs: Abdominal pain...
60 mg 1 times / day multiple, oral
Recommended
unhealthy
n = 40
Other AEs: Abdominal pain, Cardiac disorder NOS...
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Other AEs: Abdominal pain, Urine discoloration...
Other AEs:
Abdominal pain (69%)
Urine discoloration (58%)
Anorexia (45%)
Jaundice (45%)
Headache (39%)
Nausea and vomiting (34%)
Fever (25%)
Weakness (23%)
Backache (22%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Haemoglobinuria 5 patients
10 mg 3 times / day multiple, oral
Recommended
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
quinine(650 mg; 3/day for 2 days)
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 10000
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 10000
Sources:
Haemoglobinuria 13 patients
10 mg 3 times / day multiple, oral
Recommended
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 10000
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 10000
Sources:
Abdominal pain 3 patients
40 mg 1 times / day multiple, oral
Recommended
unhealthy
n = 56
Abdominal pain 10%
60 mg 1 times / day multiple, oral
Recommended
unhealthy
n = 40
Cardiac disorder NOS 5%
60 mg 1 times / day multiple, oral
Recommended
unhealthy
n = 40
Backache 22%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Weakness 23%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Fever 25%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Nausea and vomiting 34%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Headache 39%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Anorexia 45%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Jaundice 45%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Urine discoloration 58%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Abdominal pain 69%
10 mg 3 times / day multiple, oral
Dose: 10 mg, 3 times / day
Route: oral
Route: multiple
Dose: 10 mg, 3 times / day
Co-administed with::
mepacrine(100 mg; 3/day for 5 days)
Sources:
unhealthy
n = 258
Health Status: unhealthy
Condition: malaria
Sex: M
Population Size: 258
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
likely
PubMed

PubMed

TitleDatePubMed
The relationship of physico-chemical properties and structure to the differential antiplasmodial activity of the cinchona alkaloids.
2003 Sep 1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:42:36 GMT 2023
Edited
by admin
on Fri Dec 15 15:42:36 GMT 2023
Record UNII
99QVL5KPSU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAMAQUINE
INN   MI  
INN  
Official Name English
PAMAQUINE [MI]
Common Name English
QUINOLINE, 6-METHOXY-8-(1-METHYL-4-DIETHYLAMINO)BUTYLAMINO-
Common Name English
PAMAQUINE, (±)-
Common Name English
PAMAQUIN
Common Name English
NSC-167382
Code English
(±)-PAMAQUINE
Common Name English
pamaquine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C271
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3416
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
NCI_THESAURUS
C73003
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
SMS_ID
100000082763
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
WIKIPEDIA
Pamaquine
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
CAS
491-92-9
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
EVMPD
SUB09595MIG
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID90862331
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
NSC
167382
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
MERCK INDEX
m8372
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY Merck Index
PUBCHEM
10290
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
FDA UNII
99QVL5KPSU
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
MESH
C004331
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
INN
408
Created by admin on Fri Dec 15 15:42:36 GMT 2023 , Edited by admin on Fri Dec 15 15:42:36 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY