Page last updated: 2024-11-07

lidorestat

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Description

lidorestat: might prove useful in treating chronic diabetic complications; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID157839
CHEMBL ID363387
SCHEMBL ID419032
MeSH IDM0485432

Synonyms (37)

Synonym
3na ,
{3-[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]-1h-indol-1-yl}acetic acid
bdbm16469
2-{3-[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]-1h-indol-1-yl}acetic acid
lidorestat
idd-676
chembl363387 ,
indoleacetic acid inhibitor 9
DB07063
idd 676
lidorestat anhydrous
eml 676
idd-000676
2-[3-[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]indol-1-yl]acetic acid
245116-90-9
3-((4,5,7-triflurobenzothiazol-2-yl)methyl)-1h-indol-1-yl)acetic acid
1h-indole-1-acetic acid, 3-((4,5,7-trifluoro-2-benzothiazolyl)methyl)-
r3734k0m7l ,
unii-r3734k0m7l
gtpl7411
(3-((4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl)-1h-indol-1-yl)acetic acid
lidorestat [inn]
SCHEMBL419032
3-(4,5,7-trifluorobenzothiazol-2-yl)methyl-indole-n-acetic acid
KYHVTMFADJNSGS-UHFFFAOYSA-N
1h-indole-1-acetic acid, 3-[(4,5,7-trifluoro-2-benzothiazolyl)methyl]-
FD10676
DTXSID40179264
AKOS028111328
AS-72624
'3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-n-acetic acid'
mfcd08067733
2-(3-((4,5,7-trifluorobenzo[d]thiazol-2-yl)methyl)-1h-indol-1-yl)acetic acid
Q27080524
HY-106198
CS-0025212
c18h11f3n2o2s

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
"45 mug equiv/g, respectively, when dosed with [(14)C]lidorestat at 10 mg/kg po)."( Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
Dicioccio, AT; Geraci, LS; Gunn, DE; Jacot, JL; Jones, JH; Jones, ML; Mitschler, A; Petrova, T; Podjarny, AD; Sawicki, DR; Sredy, J; Van Zandt, MC, 2005
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)IC50 (µMol)0.00500.00041.877310.0000AID1202885
Aldo-keto reductase family 1 member A1Homo sapiens (human)IC50 (µMol)18.00170.00502.78569.9000AID1797506; AID242605
Aldo-keto reductase family 1 member B1Homo sapiens (human)IC50 (µMol)10.80300.00101.191310.0000AID1797506; AID242668; AID309933; AID598104
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (21)

Processvia Protein(s)Taxonomy
lipid metabolic processAldo-keto reductase family 1 member A1Homo sapiens (human)
glucuronate catabolic process to xylulose 5-phosphateAldo-keto reductase family 1 member A1Homo sapiens (human)
L-ascorbic acid biosynthetic processAldo-keto reductase family 1 member A1Homo sapiens (human)
D-glucuronate catabolic processAldo-keto reductase family 1 member A1Homo sapiens (human)
negative regulation of apoptotic processAldo-keto reductase family 1 member A1Homo sapiens (human)
daunorubicin metabolic processAldo-keto reductase family 1 member A1Homo sapiens (human)
doxorubicin metabolic processAldo-keto reductase family 1 member A1Homo sapiens (human)
aldehyde catabolic processAldo-keto reductase family 1 member A1Homo sapiens (human)
cellular detoxification of aldehydeAldo-keto reductase family 1 member A1Homo sapiens (human)
glutathione derivative biosynthetic processAldo-keto reductase family 1 member A1Homo sapiens (human)
retinoid metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
epithelial cell maturationAldo-keto reductase family 1 member B1Homo sapiens (human)
renal water homeostasisAldo-keto reductase family 1 member B1Homo sapiens (human)
carbohydrate metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
prostaglandin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
C21-steroid hormone biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
L-ascorbic acid biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
regulation of urine volumeAldo-keto reductase family 1 member B1Homo sapiens (human)
retinol metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
negative regulation of apoptotic processAldo-keto reductase family 1 member B1Homo sapiens (human)
daunorubicin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
doxorubicin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
fructose biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
cellular hyperosmotic salinity responseAldo-keto reductase family 1 member B1Homo sapiens (human)
metanephric collecting duct developmentAldo-keto reductase family 1 member B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (16)

Processvia Protein(s)Taxonomy
all-trans-retinol dehydrogenase (NAD+) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
aldo-keto reductase (NADPH) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
protein bindingAldo-keto reductase family 1 member A1Homo sapiens (human)
allyl-alcohol dehydrogenase activityAldo-keto reductase family 1 member A1Homo sapiens (human)
L-glucuronate reductase activityAldo-keto reductase family 1 member A1Homo sapiens (human)
glucuronolactone reductase activityAldo-keto reductase family 1 member A1Homo sapiens (human)
glycerol dehydrogenase [NADP+] activityAldo-keto reductase family 1 member A1Homo sapiens (human)
S-nitrosoglutathione reductase (NADH) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
S-nitrosoglutathione reductase (NADPH) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
methylglyoxal reductase (NADPH) (acetol producing) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
aldose reductase (NADPH) activityAldo-keto reductase family 1 member A1Homo sapiens (human)
retinal dehydrogenase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
aldose reductase (NADPH) activityAldo-keto reductase family 1 member B1Homo sapiens (human)
protein bindingAldo-keto reductase family 1 member B1Homo sapiens (human)
electron transfer activityAldo-keto reductase family 1 member B1Homo sapiens (human)
prostaglandin H2 endoperoxidase reductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
glyceraldehyde oxidoreductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
allyl-alcohol dehydrogenase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
L-glucuronate reductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
glycerol dehydrogenase [NADP+] activityAldo-keto reductase family 1 member B1Homo sapiens (human)
all-trans-retinol dehydrogenase (NADP+) activityAldo-keto reductase family 1 member B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
extracellular spaceAldo-keto reductase family 1 member A1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member A1Homo sapiens (human)
synapseAldo-keto reductase family 1 member A1Homo sapiens (human)
extracellular exosomeAldo-keto reductase family 1 member A1Homo sapiens (human)
apical plasma membraneAldo-keto reductase family 1 member A1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member A1Homo sapiens (human)
extracellular spaceAldo-keto reductase family 1 member B1Homo sapiens (human)
nucleoplasmAldo-keto reductase family 1 member B1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member B1Homo sapiens (human)
extracellular exosomeAldo-keto reductase family 1 member B1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member B1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (53)

Assay IDTitleYearJournalArticle
AID249247Ability to lower elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 1.4 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252277Myo-inositol accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID242668In vitro inhibition of recombinant human aldose reductase expressed in Escherichia coli2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251202Improvement in motor nerve conduction velocity in 1 month diabetic rats (streptozotocin treated) at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID242605In vitro inhibition of recombinant human aldehyde reductase2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251594Motor nerve conduction velocity in 1 month diabetic rats (streptozotocin treated) measured by sciatic/tibialis-interosseous system at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236986Time require to reach maximum plasma concentration was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252120Inhibition of sciatic nerve sorbitol accumulation in diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251403Percent reduction in elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 1.4 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249250Ability to lower elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 0.48 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249248Ability to lower elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 1.9 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252279Improvement in sorbitol accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251595Motor nerve conduction velocity in 3 month diabetic rats (streptozotocin treated) measured by sciatic/tibialis-interosseous system at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249244Ability to lower elevated glucose levels in diabetic rats (streptozotocin treated) model at 4.8 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID598104Inhibition of human recombinant aldose reductase 1 after 10 mins by spectrophotometry analysis2009Bioorganic & medicinal chemistry letters, Apr-01, Volume: 19, Issue:7
Discovery of [3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyridin-1-yl]acetic acids as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249249Ability to lower elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 4.8 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251404Percent reduction in elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 1.9 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236537Total body clearance was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID309933Inhibition of aldose reductase2007Bioorganic & medicinal chemistry, Dec-15, Volume: 15, Issue:24
Validation of an automated procedure for the prediction of relative free energies of binding on a set of aldose reductase inhibitors.
AID251405Percent reduction in elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 4.8 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID598103Inhibition of human recombinant aldose reductase 2 expressed in Escherichia coli BL21 after 10 mins by spectrophotometry analysis2009Bioorganic & medicinal chemistry letters, Apr-01, Volume: 19, Issue:7
Discovery of [3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyridin-1-yl]acetic acids as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236659Maximum plasma concentration was determined in fasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249245Ability to lower elevated glucose levels in diabetic rats (streptozotocin treated) model at 0.48 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236985Time require to reach maximum plasma concentration was determined in fasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236536Total body clearance was determined in fasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252280Improvement in myo-inositol accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236433Area under the concentration time curve 0-24 hr was determined in fasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251596Motor nerve conduction velocity in 1 month diabetic rats (streptozotocin treated) measured by sciatic/tibialis-interosseous system at 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251203Improvement in motor nerve conduction velocity in 3 month diabetic rats (streptozotocin treated) at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251407Percent reduction in elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 0.48 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID1202885Inhibition of Wistar rat lens aldose reductase using D,L-glyceraldehyde as substrate incubated for 1 min measured for 4 mins by spectrophotometry2015Journal of medicinal chemistry, Mar-26, Volume: 58, Issue:6
Identification of novel aldose reductase inhibitors based on carboxymethylated mercaptotriazinoindole scaffold.
AID236298Volume of distribution was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251204Improvement in motor nerve conduction velocity in 1 month diabetic rats (streptozotocin treated) at 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID237158Half-life was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236538Total body clearance was determined in nonfasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252115Inhibition of sorbitol accumulation in lens of diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID237166Half-life was determined in nonfasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236442Area under the concentration time curve 0-24 h was determined in nonfasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249246Ability to lower elevated glucose levels in diabetic rats (streptozotocin treated) model at 0.95 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252276Fructose accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID251408Percent reduction in elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 0.95 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252278Improvement in fructose accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249251Ability to lower elevated plasma triglyceride levels in diabetic rats (streptozotocin treated) model at 0.95 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249243Ability to lower elevated glucose levels in diabetic rats (streptozotocin treated) model at 1.9 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID237157Half-life was determined in fasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236436Area under the concentration time curve 0-24 hr was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236662Maximum plasma concentration was determined in fasted rats after i.v. doses of 10 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236988Time require to reach maximum plasma concentration was determined in nonfasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID236666Maximum plasma concentration was determined in nonfasted rats after p.o. doses of 6 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID252281Sorbitol accumulation in 3 month diabetic rats (streptozotocin treated) done for 30 minutes at 22 degree C in dark by using sorbitol dehydrogenase at 5 mg/kg/day; BQL is Below quantifiable level2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID249242Ability to lower elevated glucose levels in diabetic rats (streptozotocin treated) model at 1.4 mg/kg/day2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID1797506Enzyme Inhibition Assay from Article 10.1021/jm0492094: \\Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabet2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
AID1346211Human aldo-keto reductase family 1 member B (1.-.-.- Oxidoreductases)2005Journal of medicinal chemistry, May-05, Volume: 48, Issue:9
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]