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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
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
Resistance to drug by different isolates Trypanosoma evansi in China.
2004 May
RNA-interference silencing of the adenosine transporter-1 gene in Trypanosoma evansi confers resistance to diminazene aceturate.
2004 May-Jun
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
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:31:31 GMT 2023
Edited
by admin
on Sat Dec 16 04:31:31 GMT 2023
Record UNII
G83ZS9Z22U
Record Status Validated (UNII)
Record Version
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Name Type Language
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
ANTRYCIDE
Brand 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 Sat Dec 16 04:31:31 GMT 2023 , Edited by admin on Sat Dec 16 04:31:31 GMT 2023
PRIMARY
CAS
3270-78-8
Created by admin on Sat Dec 16 04:31:31 GMT 2023 , Edited by admin on Sat Dec 16 04:31:31 GMT 2023
PRIMARY
MERCK INDEX
m9438
Created by admin on Sat Dec 16 04:31:31 GMT 2023 , Edited by admin on Sat Dec 16 04:31:31 GMT 2023
PRIMARY Merck Index
PUBCHEM
197022
Created by admin on Sat Dec 16 04:31:31 GMT 2023 , Edited by admin on Sat Dec 16 04:31:31 GMT 2023
PRIMARY
FDA UNII
G83ZS9Z22U
Created by admin on Sat Dec 16 04:31:31 GMT 2023 , Edited by admin on Sat Dec 16 04:31:31 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY