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

Details

Stereochemistry ACHIRAL
Molecular Formula C6H13N5O
Molecular Weight 171.2003
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOROXYDINE

SMILES

NC(=N)NC(=N)N1CCOCC1

InChI

InChIKey=KJHOZAZQWVKILO-UHFFFAOYSA-N
InChI=1S/C6H13N5O/c7-5(8)10-6(9)11-1-3-12-4-2-11/h1-4H2,(H5,7,8,9,10)

HIDE SMILES / InChI

Molecular Formula C6H13N5O
Molecular Weight 171.2003
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Moroxydine is an antiviral drug discovered in the 1950’s which was shown to be active against DNA and RNA viruses. Moroxydine analogues are potent anti-hepatitis C virus (HCV) agents.

Originator

Curator's Comment: reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9868507

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
VIRULEX FORTE

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Trisodium bis-{1-[iminio-(morpholino)meth-yl]guanidinium} bis-[hexa-hydrogen-hexa-molybdoaluminate(III)] chloride icosa-hydrate.
2008 Jul 26
Study of molecularly imprinted solid-phase extraction of diphenylguanidine and its structural analogs.
2009 Apr 20
Effect of N-[Imino(4-morpholyl)methyl]guanidine on the oxidative status in rats with toxic hepatitis.
2009 Oct
[The influense of guanidine derivatives on free radical oxidation intensity and aconitase activity at development of brain ischemia-reperfusion at rats].
2009 Sep-Oct
Patents

Sample Use Guides

Daily dose ranges from 25 to 5600 mg.
Route of Administration: Other
6.3 μg/mL Moroxydine suppresses apoptosis in grass carp reovirus (GCRV)-infected Ctenopharyngodon idella kidney (CIK) cells.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:11:09 GMT 2023
Edited
by admin
on Sat Dec 16 17:11:09 GMT 2023
Record UNII
O611591WAH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOROXYDINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
SKF-8898A
Code English
SKF-8898-A
Code English
MOROXYDINE [MI]
Common Name English
moroxydine [INN]
Common Name English
SKF 8898-A
Code English
N-CARBAMIMIDOYLMORPHOLINE-4-CARBOXIMIDAMIDE
Systematic Name English
N-(AMINOIMINOMETHYL)-4-MORPHOLINECARBOXIMIDAMIDE
Systematic Name English
ABOB
Common Name English
Moroxydine [WHO-DD]
Common Name English
4-MORPHOLINECARBOXIMIDOYLGUANIDINE
Systematic Name English
MOROXYDINE [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC J05AX01
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
NCI_THESAURUS C281
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
WHO-VATC QJ05AX01
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
Code System Code Type Description
INN
1220
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
DRUG BANK
DB13597
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
MERCK INDEX
m7628
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C66200
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
RXCUI
30227
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY RxNorm
ALANWOOD
moroxydine
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
SMS_ID
100000080390
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
DRUG CENTRAL
1844
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
CAS
3731-59-7
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
EVMPD
SUB09070MIG
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID3048526
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
PUBCHEM
71655
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-093-1
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
WIKIPEDIA
MOROXYDINE
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
FDA UNII
O611591WAH
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL1490434
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
MESH
C005267
Created by admin on Sat Dec 16 17:11:09 GMT 2023 , Edited by admin on Sat Dec 16 17:11:09 GMT 2023
PRIMARY
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SALT/SOLVATE -> PARENT
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