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Details

Stereochemistry RACEMIC
Molecular Formula C16H17N3
Molecular Weight 251.3263
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MIDAGLIZOLE

SMILES

C(C(C1=CC=CC=C1)C2=NC=CC=C2)C3=NCCN3

InChI

InChIKey=TYZQFNOLWJGHRZ-UHFFFAOYSA-N
InChI=1S/C16H17N3/c1-2-6-13(7-3-1)14(12-16-18-10-11-19-16)15-8-4-5-9-17-15/h1-9,14H,10-12H2,(H,18,19)

HIDE SMILES / InChI

Molecular Formula C16H17N3
Molecular Weight 251.3263
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Midaglizole (also known as DG 5128) is a α2 adrenoceptor antagonist. Daiichi Pharmaceutical developed this drug as an oral antidiabetic agent and to treat asthma. However, further study of this drug was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of an alpha 2-adrenoceptor antagonist, midaglizole, on bronchial responsiveness to histamine in patients with mild asthma.
1995
Pharmacological studies with the alpha 2-adrenoceptor antagonist midaglizole. Part I: Respiratory and cardiovascular systems.
1991-01
Metabolic fate of the oral hypoglycaemic agent, midaglizole, in rats.
1989-06

Sample Use Guides

Oral administration of DG-5128 (MIDAGLIZOLE) significantly (P less than .05) enhanced insulin secretion both 30 and 60 min after a mixed meal (550 kcal), with a concomitant decrease in postprandial plasma glucose levels at 60 and 120 min
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:26:04 GMT 2025
Edited
by admin
on Mon Mar 31 18:26:04 GMT 2025
Record UNII
44NWV6A237
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MIDAGLIZOLE [MART.]
Preferred Name English
MIDAGLIZOLE
INN   MART.  
INN  
Official Name English
(±)-2-(.ALPHA.-(2-IMIDAZOLIN-2-YLMETHYL)BENZYL)PYRIDINE
Systematic Name English
midaglizole [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C72900
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
Code System Code Type Description
CAS
66529-17-7
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
MESH
C032368
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
EVMPD
SUB08947MIG
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
INN
6064
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
ChEMBL
CHEMBL40611
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
NCI_THESAURUS
C66146
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
FDA UNII
44NWV6A237
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID30867229
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
SMS_ID
100000080605
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
PUBCHEM
68864
Created by admin on Mon Mar 31 18:26:04 GMT 2025 , Edited by admin on Mon Mar 31 18:26:04 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY