U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C24H35NO5
Molecular Weight 417.5384
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DECOQUINATE

SMILES

CCCCCCCCCCOC1=CC2=C(O)C(=CN=C2C=C1OCC)C(=O)OCC

InChI

InChIKey=JHAYEQICABJSTP-UHFFFAOYSA-N
InChI=1S/C24H35NO5/c1-4-7-8-9-10-11-12-13-14-30-21-15-18-20(16-22(21)28-5-2)25-17-19(23(18)26)24(27)29-6-3/h15-17H,4-14H2,1-3H3,(H,25,26)

HIDE SMILES / InChI

Molecular Formula C24H35NO5
Molecular Weight 417.5384
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Decoquinate is a quinolone derivative that is used in the control of coccidiosis in domestic animals. Decoquinate treats and prevents coccidiosis in chickens, cattle, goats, sheep, etc. Decoquinate acts on sporozoites development and prevents their penetration of the gut epithelium. Decoquinate inhibits mitochondrial respiration and electron transport in Eimeria.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
DECCOX

Approved Use

For the prevention of coccidiosis.

Launch Date

1999
PubMed

PubMed

TitleDatePubMed
Decoquinate induces tissue cyst formation by the RH strain of Toxoplasma gondii.
1998 Jun 15
Treatment of dogs infected with Hepatozoon americanum: 53 cases (1989-1998).
2001 Jan 1
Efficacy of selected oral chemotherapeutants against Ichthyophthirius multifiliis (Ciliophora: Ophyroglenidae) infecting rainbow trout Oncorhynchus mykiss.
2003 Jun 20
Effect of the quinolone coccidiostat decoquinate on the rearrangement of chromosomes of Eimeria tenella.
2006 Dec
Relative virulences of a drug-resistant and a drug-sensitive strain of Eimeria acervulina, a coccidium of chickens.
2006 Jan 15
Tracing the emergence of drug-resistance in coccidia (Eimeria spp.) of commercial broiler flocks medicated with decoquinate for the first time in the United Kingdom.
2006 Jan 15
Field study of the efficacy of halofuginone and decoquinate in the treatment of cryptosporidiosis in veal calves.
2006 Nov 11
An Irish perspective on Cryptosporidium. Part 2.
2006 Sep 1
Oral pharmacokinetics and milk residues of decoquinate in milking cows.
2009 Aug
Multi-residue confirmatory method for the determination of twelve coccidiostats in chicken liver using liquid chromatography tandem mass spectrometry.
2009 Nov 13
Drug screen targeted at Plasmodium liver stages identifies a potent multistage antimalarial drug.
2012 Apr 15
In vitro determination of anticryptosporidial activity of phytogenic extracts and compounds.
2012 Jul
Nanoparticle formulations of decoquinate increase antimalarial efficacy against liver stage Plasmodium infections in mice.
2014 Jan
Patents

Sample Use Guides

22.7 mg/100 lb of body weight (0.5 mg/kg) per day (cattle, goats, sheep) or 0.003% (chicken). Feed for at least 28 days during periods of coccidiosis exposure or when experience indicates that coccidiosis is likely to be a hazard.
Route of Administration: Intragastric
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:03:28 GMT 2023
Edited
by admin
on Fri Dec 15 15:03:28 GMT 2023
Record UNII
534I52PVWH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DECOQUINATE
GREEN BOOK   INN   MART.   MI   USAN   USP   USP-RS  
INN   USAN  
Official Name English
M&B 15497
Code English
HC 1528
Code English
DECCOX
Brand Name English
M&B-15497
Code English
decoquinate [INN]
Common Name English
DECOQUINATE [USAN]
Common Name English
3-QUINOLINECARBOXYLIC ACID, 6-(DECYLOXY)-7-ETHOXY-4-HYDROXY-, ETHYL ESTER
Common Name English
DECOQUINATE [MI]
Common Name English
DECOQUINATE [USP MONOGRAPH]
Common Name English
NSC-339057
Code English
DECOQUINATE [USP-RS]
Common Name English
Ethyl 6-(decyloxy)-7-ethoxy-4-hydroxy-3-quinolinecarboxylate
Systematic Name English
DECOQUINATE [GREEN BOOK]
Common Name English
HC-1528
Code English
DECOQUINATE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C795
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
CFR 21 CFR 558.195
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
CFR 21 CFR 556.170
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
CFR 21 CFR 520.534
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
WHO-VATC QP51AX14
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
Code System Code Type Description
PUBCHEM
29112
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
NSC
339057
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
MERCK INDEX
m4127
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY Merck Index
RS_ITEM_NUM
1165408
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
INN
2592
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
DAILYMED
534I52PVWH
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
DRUG BANK
DB11394
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
WIKIPEDIA
DECOQUINATE
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
EVMPD
SUB06938MIG
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL416230
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
NCI_THESAURUS
C76919
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID5046851
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
SMS_ID
100000083494
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
FDA UNII
534I52PVWH
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
ECHA (EC/EINECS)
242-389-1
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
RXCUI
1314345
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY RxNorm
CAS
18507-89-6
Created by admin on Fri Dec 15 15:03:28 GMT 2023 , Edited by admin on Fri Dec 15 15:03:28 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY