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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=CC3=C(N)C=C(C)[N+](C)=C3C=C2)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
Uridine 5'-diphosphate glucose analogues. Inhibitors of protein glycosylation that show antiviral activity.
1985 Jan
Cationic antitrypanosomal and other antimicrobial agents in the therapy of experimental Pneumocystis carinii pneumonia.
1988 Jun
New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii.
1995 Nov 24
Antibody levels by indirect ELISA test in Trypanosoma evansi infected horses following treatment with quinapyramine sulphate.
2003 Jan 20
The history of African trypanosomiasis.
2008 Feb 12
Health management of horses under high challenge from trypanosomes: a case study from Serengeti, Tanzania.
2008 Jul 4
Development and application of an antibody-ELISA to follow up a Trypanosoma evansi outbreak in a dromedary camel herd in France.
2009 Jun 10
Genotypic status of the TbAT1/P2 adenosine transporter of Trypanosoma brucei gambiense isolates from Northwestern Uganda following melarsoprol withdrawal.
2009 Sep 29
Immunobiology of African trypanosomes: need of alternative interventions.
2010
Studies of quinapyramine-resistance of Trypanosoma brucei evansi in China.
2010 Dec
Proteomics of Trypanosoma evansi infection in rodents.
2010 Mar 22
In vitro activity and preliminary toxicity of various diamidine compounds against Trypanosoma evansi.
2010 May 11
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:40:25 GMT 2023
Edited
by admin
on Sat Dec 16 05:40:25 GMT 2023
Record UNII
B2NT1100WR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
NSC-48223
Code English
QUINAPYRAMINE [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AX20
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
Code System Code Type Description
FDA UNII
B2NT1100WR
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
PUBCHEM
122993
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
CAS
20493-41-8
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
MERCK INDEX
m9438
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY Merck Index
SMS_ID
100000141676
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
WIKIPEDIA
QUINAPYRAMINE
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
NSC
48223
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID90942667
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
CAS
64215-84-5
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
ALTERNATIVE
EVMPD
SUB96098
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
PRIMARY
CAS
1082114-38-2
Created by admin on Sat Dec 16 05:40:25 GMT 2023 , Edited by admin on Sat Dec 16 05:40:25 GMT 2023
ALTERNATIVE