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
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)
Molecular Formula | C10H14N4O2 |
Molecular Weight | 222.2438 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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
PubMed
Title | Date | PubMed |
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[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 |
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[On therapeutic effects of morphazinamide, used alone and in association, in recent and chronic pulmonary tuberculosis]. | 1965 Sep 5 |
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[Intravenous morphazinamide. Tolerance of the drug and therapeutic effects]. | 1965 Sep 5 |
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[Morphazinamide in antitubercular therapy. 2 years of clinical experimentation]. | 1965 Sep 5 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4953657
Mice: 500 mg/kg every day for a period of 20 weeks.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10864178
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.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:21:59 GMT 2023
by
admin
on
Sat Dec 16 17:21:59 GMT 2023
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Record UNII |
8CFL28PA3W
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Record Status |
Validated (UNII)
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Record Version |
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-
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WHO-VATC |
QJ04AK04
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NCI_THESAURUS |
C280
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WHO-ATC |
J04AK04
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100000080369
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C66197
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DB13417
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70374
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SUB09067MIG
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m7629
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PRIMARY | Merck Index | ||
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MORINAMIDE
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952-54-5
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |