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

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

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
[On therapeutic effects of morphazinamide, used alone and in association, in recent and chronic pulmonary tuberculosis].
1965 Sep 5
[Intravenous morphazinamide. Tolerance of the drug and therapeutic effects].
1965 Sep 5
[Morphazinamide in antitubercular therapy. 2 years of clinical experimentation].
1965 Sep 5
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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:21:59 GMT 2023
Edited
by admin
on Sat Dec 16 17:21:59 GMT 2023
Record UNII
8CFL28PA3W
Record Status Validated (UNII)
Record Version
  • Download
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
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
NCI_THESAURUS
C66197
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
DRUG BANK
DB13417
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
EPA CompTox
DTXSID4046159
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
ECHA (EC/EINECS)
213-460-4
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
DRUG CENTRAL
1843
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
INN
1361
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
FDA UNII
8CFL28PA3W
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
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
PRIMARY
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
PRIMARY
EVMPD
SUB09067MIG
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
MERCK INDEX
m7629
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 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
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY