balaglitazone: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
ID Source | ID |
---|---|
PubMed CID | 9889200 |
CHEMBL ID | 2103991 |
SCHEMBL ID | 242011 |
MeSH ID | M0481676 |
Synonym |
---|
nnc-61-2344 |
nn-2344 |
nnc-61-0645 |
balaglitazone |
drf-2593 |
nn 2344 |
5-(p-((3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)benzyl)-2,4-thiazolidinedione |
drf 2593 |
nn2344 |
4m1609828o , |
balaglitazone [inn] |
unii-4m1609828o |
199113-98-9 |
(+-)-5-(p-((3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)benzyl)-2,4-thiazolidinedione |
CHEMBL2103991 |
SCHEMBL242011 |
CS-1441 |
HY-16086 |
IETKPTYAGKZLKY-UHFFFAOYSA-N |
5-[4-[[3-methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione |
5-[4-[[-methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione |
5-((4-((3-methyl-4-oxo-3,4-dihydro-2-quinazolinyl)methoxy)phenyl)methyl)thiazolidine-2,4-dione |
(+/-)-5-(p-((3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)benzyl)-2,4-thiazolidinedione |
balaglitazone [who-dd] |
2,4-thiazolidinedione, 5-((4-((3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)phenyl)methyl)- |
AKOS030526698 |
5-({4-[(3-methyl-4-oxo-3,4-dihydroquinazolin-2-yl)methoxy]phenyl}methyl)-1,3-thiazolidine-2,4-dione |
AS-74629 |
5-(4-((3-methyl-4-oxo-3,4-dihydroquinazolin-2-yl)methoxy)benzyl)thiazolidine-2,4-dione |
A856108 |
DB12781 |
FT-0766930 |
BCP11371 |
SB16864 |
drf 2593;nn 2344 |
drf-2593;nn-2344;nnc-610645 |
2,4-thiazolidinedione, 5-[[4-[(3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy]phenyl]methyl]- |
Q27260063 |
F84947 |
5-[[4-[(3-methyl-4-oxoquinazolin-2-yl)methoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione |
ZHA11398 |
EX-A3756 |
2,4-thiazolidinedione,5-[[4-[(3,4-dihydro-3-methyl-4-oxo-2-quinazolinyl) methoxy]phenyl]methyl]- |
DTXSID30870213 |
Balaglitazone (DRF-2593) is a novel partial agonist of PPAR-gamma (γ) It is in clinical development for the treatment of type 2 diabetes.
Excerpt | Reference | Relevance |
---|---|---|
"Balaglitazone treated groups shown significantly reduce of HbA1c (%), FSG (mmol/L), postprandial glucose as comparison to pioglitazone." | ( Balaglitazone: a second generation peroxisome proliferator-activated receptor (PPAR) gamma (γ) agonist. Agrawal, R; Dikshit, SN; Jain, P, 2012) | 2.54 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (37.50) | 29.6817 |
2010's | 5 (62.50) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (25.51) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 3 (37.50%) | 5.53% |
Reviews | 1 (12.50%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (50.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |