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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9N5O3
Molecular Weight 271.2316
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CIADOX

SMILES

[O-][N+]1=CC(C=NNC(=O)CC#N)=[N+]([O-])C2=C1C=CC=C2

InChI

InChIKey=MBCZYLSVSCJJJQ-AUWJEWJLSA-N
InChI=1S/C12H9N5O3/c13-6-5-12(18)15-14-7-9-8-16(19)10-3-1-2-4-11(10)17(9)20/h1-4,7-8H,5H2,(H,15,18)/b14-7-

HIDE SMILES / InChI

Molecular Formula C12H9N5O3
Molecular Weight 271.2316
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Ciadox is Quinoxaline 1,4-dioxide derivative with antimicrobial and promoting activities. Cyadox supplied as premix in the final feed in Eastern Europe and may be used in pigs up to four months of age. Some evidence demonstrated that the mechanism of Ciadox for improving pig growth performance was correlated with several metabolic hormones and growth factors. Cyadox also did not show any adverse effects in carcinogenicity tests with rats and long-term toxicity tests with mice and rats. Cyadox subchronic oral toxicity evaluation shows mild toxicity in non-rodents animals. Metabolic transformation of Ciadox leads to three major metabolites, including 1,4-bisdesoxycyadox, 4-desoxycyadox, and quinoxaline-2-carboxylic acid. Ciadox and metabolites shows virtually no toxic effects in the acute and subchronic oral toxicity study and no mutagenic, carcinogenic activivt.

Originator

Sources: Biologizace a Chemizace Vyzivy Zvirat (1977), 13, (4), 357-74.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

pigs: 20 mg/kg of body weight for five consecutive days. dogs: 100, 450 and 2500 mg/kg of cyadox, for 13 weeks.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:07:16 GMT 2023
Edited
by admin
on Sat Dec 16 17:07:16 GMT 2023
Record UNII
HX312O5UGN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CIADOX
INN  
INN  
Official Name English
CYADOX [MI]
Common Name English
CYANOACETIC ACID (2-QUINOXALINYLMETHYLENE)HYDRAZIDE, N1,N4-DIOXIDE
Common Name English
ciadox [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C52588
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
Code System Code Type Description
MERCK INDEX
m3941
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY Merck Index
FDA UNII
HX312O5UGN
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
INN
4857
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
SMS_ID
100000081898
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
CAS
65884-46-0
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
265-963-3
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID501014550
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
PUBCHEM
135565684
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
NCI_THESAURUS
C83622
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104068
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
EVMPD
SUB06222MIG
Created by admin on Sat Dec 16 17:07:16 GMT 2023 , Edited by admin on Sat Dec 16 17:07:16 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY