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Details

Stereochemistry ACHIRAL
Molecular Formula C16H16O3
Molecular Weight 256.2964
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PARVAQUONE

SMILES

OC1=C(C2CCCCC2)C(=O)C3=CC=CC=C3C1=O

InChI

InChIKey=JBFUOGRCSLVENL-UHFFFAOYSA-N
InChI=1S/C16H16O3/c17-14-11-8-4-5-9-12(11)15(18)16(19)13(14)10-6-2-1-3-7-10/h4-5,8-10,19H,1-3,6-7H2

HIDE SMILES / InChI
Parvaquone, an antitheilerial compound that was developed for the treatment of East Coast fever. Experiments on animals have shown that this drug was effective in the treatment of cattle infected with Theileria annulata.

Approval Year

PubMed

PubMed

TitleDatePubMed
Activity of 10 naphthoquinones, including parvaquone (993C) and menoctone, in cattle artificially infected with Theileria parva.
1983 Nov
Effectiveness of parvaquone in cattle infected with Theileria annulata.
1988 Nov
Treatment of East Coast fever of cattle with a combination of parvaquone and frusemide.
2004 Apr
Patents

Patents

Name Type Language
PARVAQUONE
INN   MART.   MI  
INN  
Official Name English
NSC-278
Code English
PARVAQUONE [MI]
Common Name English
PARVAQUONE [MART.]
Common Name English
2-CYCLOHEXYL-3-HYDROXYNAPHTHOQUINONE
Systematic Name English
parvaquone [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AX21
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
NCI_THESAURUS C271
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
Code System Code Type Description
EVMPD
SUB09634MIG
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
NSC
278
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
SMS_ID
100000083019
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-734-5
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
CAS
4042-30-2
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID00877991
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
MESH
C028032
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
INN
5223
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
NCI_THESAURUS
C66327
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
FDA UNII
A2BH18685W
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
ChEMBL
CHEMBL103124
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY
MERCK INDEX
m8424
Created by admin on Sat Dec 16 17:13:20 GMT 2023 , Edited by admin on Sat Dec 16 17:13:20 GMT 2023
PRIMARY Merck Index