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Details

Stereochemistry ACHIRAL
Molecular Formula C17H21N6
Molecular Weight 309.3888
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 1

SHOW SMILES / InChI
Structure of QUINAPYRAMINE

SMILES

CN1C(C)=C\C(=N\C2=CC=C3C(=C2)C(N)=CC(C)=[N+]3C)N=C1N

InChI

InChIKey=KMJWBVJQFGRCEB-UHFFFAOYSA-O
InChI=1S/C17H20N6/c1-10-7-14(18)13-9-12(5-6-15(13)22(10)3)20-16-8-11(2)23(4)17(19)21-16/h5-9,18H,1-4H3,(H2,19,20,21)/p+1

HIDE SMILES / InChI

Molecular Formula C17H20N6
Molecular Weight 308.3809
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Studies of quinapyramine-resistance of Trypanosoma brucei evansi in China.
2010-12
In vitro activity and preliminary toxicity of various diamidine compounds against Trypanosoma evansi.
2010-05-11
Proteomics of Trypanosoma evansi infection in rodents.
2010-03-22
Immunobiology of African trypanosomes: need of alternative interventions.
2010
Genotypic status of the TbAT1/P2 adenosine transporter of Trypanosoma brucei gambiense isolates from Northwestern Uganda following melarsoprol withdrawal.
2009-09-29
Development and application of an antibody-ELISA to follow up a Trypanosoma evansi outbreak in a dromedary camel herd in France.
2009-06-10
Health management of horses under high challenge from trypanosomes: a case study from Serengeti, Tanzania.
2008-07-04
The history of African trypanosomiasis.
2008-02-12
The effect of TAO expression on PCD-like phenomenon development and drug resistance in Trypanosoma brucei.
2006-06
Resistance to drug by different isolates Trypanosoma evansi in China.
2004-05
RNA-interference silencing of the adenosine transporter-1 gene in Trypanosoma evansi confers resistance to diminazene aceturate.
2003-10-22
Antibody levels by indirect ELISA test in Trypanosoma evansi infected horses following treatment with quinapyramine sulphate.
2003-01-20
New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii.
1995-11-24
Treatment of experimental pneumocystosis: review of 7 years of experience and development of a new system for classifying antimicrobial drugs.
1992-09
Cationic antitrypanosomal and other antimicrobial agents in the therapy of experimental Pneumocystis carinii pneumonia.
1988-06
Uridine 5'-diphosphate glucose analogues. Inhibitors of protein glycosylation that show antiviral activity.
1985-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:31:34 GMT 2025
Edited
by admin
on Mon Mar 31 21:31:34 GMT 2025
Record UNII
B2NT1100WR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-48223
Preferred Name English
QUINAPYRAMINE
MI  
Common Name English
QUINAPYRAMINE ION
Common Name English
QUINAPYRAMINE CATION
Common Name English
QUINOLINIUM, 4-AMINO-6-((1,2-DIHYDRO-2-IMINO-1,6-DIMETHYL-4-PYRIMIDINYL)AMINO)-1,2-DIMETHYL-
Systematic Name English
QUINAPYRAMINE [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AX20
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
Code System Code Type Description
FDA UNII
B2NT1100WR
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
PUBCHEM
122993
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
CAS
20493-41-8
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
MERCK INDEX
m9438
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY Merck Index
SMS_ID
100000141676
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
WIKIPEDIA
QUINAPYRAMINE
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
NSC
48223
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID90942667
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
CAS
64215-84-5
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
ALTERNATIVE
EVMPD
SUB96098
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
PRIMARY
CAS
1082114-38-2
Created by admin on Mon Mar 31 21:31:34 GMT 2025 , Edited by admin on Mon Mar 31 21:31:34 GMT 2025
ALTERNATIVE