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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H14N4O2
Molecular Weight 222.2438
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MORINAMIDE

SMILES

O=C(NCN1CCOCC1)C2=NC=CN=C2

InChI

InChIKey=GVTLAVKAVSKBKK-UHFFFAOYSA-N
InChI=1S/C10H14N4O2/c15-10(9-7-11-1-2-12-9)13-8-14-3-5-16-6-4-14/h1-2,7H,3-6,8H2,(H,13,15)

HIDE SMILES / InChI
Morinamide is a second line anti-tuberculous agent. In vitro morinamide demonstrated clear dose-dependent bacteriostatic and bactericidal activities. The anti-mycobacterial effect of morinamide was the same as pyrazinamide and was dependent on the acidity of medium (pH 5.6). Liver function test abnormalities following morinamide therapy are usually mild, and onset of jaundice is extremely uncommon. It has been given orally as the hydrochloride in the treatment of tuberculosis.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Piazofolina

Approved Use

Unknown

Launch Date

1991
PubMed

PubMed

TitleDatePubMed
[Behavior of some hematochemical data and of the most important biological indexes of disease and of phase in subjects affected by pulmonary tuberculosis treated with morphazinamide].
1965 Sep 1
[Morphazinamide in antitubercular therapy. 2 years of clinical experimentation].
1965 Sep 5
[Clinical experience with morphazinamide].
1965 Sep 5
[Morphazinamide by venous perfusion in therapy of pulmonary tuberculosis].
1965 Sep 5
New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method.
2004 Jan
Patents

Patents

Sample Use Guides

Mice: 500 mg/kg every day for a period of 20 weeks.
Route of Administration: Other
Monocytes separated from human blood were incubated in plastic plates for seven days to mature into macrophage monolayers. After activation with TNF-alpha or IFN-gamma or without prior treatment, the macrophages were infected with M. tuberculosis. Morinamide exhibited a very clear dose-dependent bacteriostatic and bactericidal effect in experiments with ‘normal’ macrophages at concentrations 64, 128 and 256 ug/ml.
Name Type Language
MORINAMIDE
INN   MART.   WHO-DD  
INN  
Official Name English
Morinamide [WHO-DD]
Common Name English
morinamide [INN]
Common Name English
MORINAMIDE [MART.]
Common Name English
MORPHAZINAMIDE [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ04AK04
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
NCI_THESAURUS C280
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
WHO-ATC J04AK04
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
Code System Code Type Description
SMS_ID
100000080369
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PRIMARY
NCI_THESAURUS
C66197
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DRUG BANK
DB13417
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EPA CompTox
DTXSID4046159
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ECHA (EC/EINECS)
213-460-4
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DRUG CENTRAL
1843
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INN
1361
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FDA UNII
8CFL28PA3W
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ChEMBL
CHEMBL1697759
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
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PUBCHEM
70374
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
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EVMPD
SUB09067MIG
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MERCK INDEX
m7629
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PRIMARY Merck Index
WIKIPEDIA
MORINAMIDE
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
PRIMARY
CAS
952-54-5
Created by admin on Sat Dec 16 17:21:59 GMT 2023 , Edited by admin on Sat Dec 16 17:21:59 GMT 2023
PRIMARY