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Details

Stereochemistry ACHIRAL
Molecular Formula C17H21N6.CH4O4S.CH3O4S
Molecular Weight 532.591
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of QUINAPYRAMINE SULFATE

SMILES

COS(O)(=O)=O.COS([O-])(=O)=O.CN1C(C)=C\C(=N\C2=CC3=C(N)C=C(C)[N+](C)=C3C=C2)N=C1N

InChI

InChIKey=WZIPHSLUGLMTRU-UHFFFAOYSA-N
InChI=1S/C17H20N6.2CH4O4S/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;2*1-5-6(2,3)4/h5-9,18H,1-4H3,(H2,19,20,21);2*1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula CH4O4S
Molecular Weight 112.105
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 21:22:29 GMT 2025
Edited
by admin
on Mon Mar 31 21:22:29 GMT 2025
Record UNII
G83ZS9Z22U
Record Status Validated (UNII)
Record Version
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Name Type Language
ANTRYCIDE
Preferred Name English
QUINAPYRAMINE SULFATE
Common Name English
QUINAPYRAMINE METHYLSULFATE
Common Name English
QUINOLINIUM, 4-AMINO-6-((2-AMINO-1,6-DIMETHYL-4(1H)-PYRIMIDINYLIDENE)AMINO)-1,2-DIMETHYL-, METHYL SULFATE, MONO(METHYL SULFATE)
Common Name English
QUINAPYRAMINE DIMETHOSULFATE [MI]
Common Name English
M-7555
Code English
QUINALDINIUM, 4-AMINO-6-((2-AMINO-1,6-DIMETHYLPYRIMIDINIUM-4-YL)AMINO)-1-METHYL-, BIS(METHYL SULFATE)
Common Name English
QUINALDINIUM, 4-AMINO-6-((2-AMINO-1,6-DIMETHYLPYRIMIDINIUM- 4-YL)AMINO)-1-METHYL-, BIS(METHYL SULFATE)
Common Name English
ANTRYCIDE METHYL SULFATE
Common Name English
QUINAPYRAMINE METHOSULFATE
Common Name English
QUINOLINIUM, 4-AMINO-6-((1,2-DIHYDRO-2-IMINO-1,6-DIMETHYL-4-PYRIMIDINYL)AMINO)-1,2-DIMETHYL-, METHYL SULFATE, METHYL SULFATE (1:1:1)
Common Name English
4-AMINO-6-((2-AMINO-1,6-DIMETHYL-1H-PYRIMIDIN-4- YLIDENE)AMINO)-1,2-DIMETHYLQUINOLINIUM, METHYL SULPHATE, MONO(METHYL SULPHATE)
Common Name English
QUINAPYRAMINE METHYL SULFATE
Common Name English
SULFURIC ACID, MONOMETHYL ESTER, COMPD. WITH 4-AMINO-6-((2-AMINO-1,6-DIMETHYL-4(1H)-PYRIMIDINYLIDENE)AMINO)-1,2-DIMETHYLQUINOLINIUM METHYL SULFATE (1:1)
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
221-894-0
Created by admin on Mon Mar 31 21:22:29 GMT 2025 , Edited by admin on Mon Mar 31 21:22:29 GMT 2025
PRIMARY
CAS
3270-78-8
Created by admin on Mon Mar 31 21:22:29 GMT 2025 , Edited by admin on Mon Mar 31 21:22:29 GMT 2025
PRIMARY
MERCK INDEX
m9438
Created by admin on Mon Mar 31 21:22:29 GMT 2025 , Edited by admin on Mon Mar 31 21:22:29 GMT 2025
PRIMARY Merck Index
PUBCHEM
197022
Created by admin on Mon Mar 31 21:22:29 GMT 2025 , Edited by admin on Mon Mar 31 21:22:29 GMT 2025
PRIMARY
FDA UNII
G83ZS9Z22U
Created by admin on Mon Mar 31 21:22:29 GMT 2025 , Edited by admin on Mon Mar 31 21:22:29 GMT 2025
PRIMARY
Related Record Type Details
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