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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14N4O2.ClH
Molecular Weight 258.705
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MORINAMIDE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=CQTFUUAUHIMFAJ-UHFFFAOYSA-N
InChI=1S/C10H14N4O2.ClH/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);1H

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
[Clinical findings on curative action of morphazinamide, administered intravenously, to patients with pulmonary tuberculosis].
1965 Sep 5
[Morphazinamide in antitubercular therapy. 2 years of clinical experimentation].
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 HYDROCHLORIDE
WHO-DD  
Common Name English
PIAZOFOLINA
Brand Name English
MORINAMIDE HCL
Common Name English
B-2311
Code English
Morinamide hydrochloride [WHO-DD]
Common Name English
2-PYRAZINECARBOXAMIDE, N-(4-MORPHOLINYLMETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
MORPHAZINAMIDE HYDROCHLORIDE [MI]
Common Name English
MORPHAZINAMIDE HYDROCHLORIDE
MI  
Common Name English
Code System Code Type Description
EVMPD
SUB03330MIG
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID50933091
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-013-1
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
CAS
1473-73-0
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
PUBCHEM
164837
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
MERCK INDEX
m7629
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY Merck Index
FDA UNII
2F6F46T9YC
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY
SMS_ID
100000086125
Created by admin on Fri Dec 15 18:37:44 GMT 2023 , Edited by admin on Fri Dec 15 18:37:44 GMT 2023
PRIMARY