Aldose reductase
Aldose reductase catalyzes the NADPH-dependent reduction of glucose to sorbitol. It is involved in the progression of diabetic and glactosemic complications.
Products Related to Aldose reductase(26)
- GC10001EpalrestatCAS: 82159-09-9Purity: >99.50%
Epalrestat is an orally active inhibitor of aldose reductases AKR1B1 and AKR1B10, with IC 50 values of 0.1µM and 0.33µM, respectively.
- GC250092-Chloro-1-(4-fluorobenzyl)benzimidazoleCAS: 84946-20-3Purity: >98%
2-Chloro-1-(4-fluorobenzyl)benzimidazole is an aldose reductase (ALR2) inhibitor which is used for preparation of disubstituted benzimidazole derivative.
- GC31359Ranirestat (AS-3201)CAS: 147254-64-6Purity: >98.00%
Ranirestat (AS-3201) (AS-3201) potent and orally active aldose reductase (AR) inhibitor with IC50s of 11 nM and 15 nM for rat lens AR and recombinant human AR, respectively, and a Ki of 0.38 nM for recombinant human AR.
- GC31376Aldose reductase-IN-1CAS: 1355612-71-3Purity: >99.50%
Aldose reductase-IN-1 (Aldose reductase-IN-1) is a inhibitor of aldose reductase with IC50 of 28.9 pM.
- GC31412Imirestat (AL 1576)CAS: 89391-50-4Purity: >99.50%
Imirestat (AL 1576) (AL 1576) is an aldose reductase inhibitor, used for the treatment of diabetes.
- GC31474Risarestat (CT 112)CAS: 79714-31-1Purity: >98.00%
Risarestat (CT 112) (CT-112), an aldose reductase inhibitor, is developed for the treatment of diabetic complications.
- GC31487Fidarestat (SNK 860)CAS: 136087-85-9Purity: >99.00%
Fidarestat (SNK 860) (SNK 860) is an inhibitor of aldose reductase, with IC50s of 26 nM, 33 μM, and 1.8 μM for aldose reductase, AKR1B10 and V301L AKR1B10, respectively; Fidarestat (SNK 860) (SNK 860) has the potential to treat diabetic disease.
- GC351796-MethoxytricinCAS: 76015-42-4Purity: >98%
6-Methoxytricin (Compound 6) is an flavonoid isolated from Artemisia iwayomogi.
- GC35309Alrestatin sodiumCAS: 51876-97-2Purity: >98%
Alrestatin sodium is an inhibitor of aldose reductase, an enzyme involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy.
- GC37053Quercetin 3-gentiobiosideCAS: 7431-83-6Purity: >98%
Quercetin 3-gentiobioside is isolated from A.
- GC38810LidorestatCAS: 245116-90-9Purity: >99.50%
Lidorestat (IDD-676) is a potent, selective and orally active aldose reductase inhibitor with an IC50 of 5 nM.
- GC63990ZenarestatCAS: 112733-06-9Purity: >98%
Zenarestat is a potent and orally active aldose reductase inhibitor.
- GC68633AKR1C3-IN-9Purity: >99.00%
AKR1C3-IN-9 is a selective inhibitor of aldo-keto reductase 1C3 (AKR1C3), with an IC50 of 8.92 nM. AKR1C3-IN-9 significantly reverses Doxorubicin (DOX) resistance in drug-resistant breast cancer cell lines.
- GC795592-(2-Chlorobenzamido)acetic acidCAS: 16555-60-5Purity: >98.00%
2-(2-Chlorobenzamido)acetic acid is an aldose reductase inhibitor with an IC 50 of 31 μM.
- GC79560CemtirestatCAS: 309283-89-4Purity: >98.00%
Cemtirestat (CMTI) is a carboxymethylated thiatriazinoindole inhibitor of aldose reductase ( ALR2 ).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10001 | Epalrestat | 82159-09-9 | >99.50% | |
Epalrestat is an orally active inhibitor of aldose reductases AKR1B1 and AKR1B10, with IC 50 values of 0.1µM and 0.33µM, respectively. | ||||
| GC10332 | EBPC | 4450-98-0 | >98% | |
aldose reductase inhibitor | ||||
| GC10958 | Statil | 72702-95-5 | >99.50% | |
Statil (ICI 128436) is an orally active, selective and noncompetitive aldose reductase (AKR1B1; ALR) inhibitor. | ||||
| GC11756 | Alrestatin | 51411-04-2 | >99.50% | |
aldose reductase inhibitor | ||||
| GC25009 | 2-Chloro-1-(4-fluorobenzyl)benzimidazole | 84946-20-3 | >98% | |
2-Chloro-1-(4-fluorobenzyl)benzimidazole is an aldose reductase (ALR2) inhibitor which is used for preparation of disubstituted benzimidazole derivative. | ||||
| GC31359 | Ranirestat (AS-3201) | 147254-64-6 | >98.00% | |
Ranirestat (AS-3201) (AS-3201) potent and orally active aldose reductase (AR) inhibitor with IC50s of 11 nM and 15 nM for rat lens AR and recombinant human AR, respectively, and a Ki of 0.38 nM for recombinant human AR. | ||||
| GC31376 | Aldose reductase-IN-1 | 1355612-71-3 | >99.50% | |
Aldose reductase-IN-1 (Aldose reductase-IN-1) is a inhibitor of aldose reductase with IC50 of 28.9 pM. | ||||
| GC31412 | Imirestat (AL 1576) | 89391-50-4 | >99.50% | |
Imirestat (AL 1576) (AL 1576) is an aldose reductase inhibitor, used for the treatment of diabetes. | ||||
| GC31474 | Risarestat (CT 112) | 79714-31-1 | >98.00% | |
Risarestat (CT 112) (CT-112), an aldose reductase inhibitor, is developed for the treatment of diabetic complications. | ||||
| GC31487 | Fidarestat (SNK 860) | 136087-85-9 | >99.00% | |
Fidarestat (SNK 860) (SNK 860) is an inhibitor of aldose reductase, with IC50s of 26 nM, 33 μM, and 1.8 μM for aldose reductase, AKR1B10 and V301L AKR1B10, respectively; Fidarestat (SNK 860) (SNK 860) has the potential to treat diabetic disease. | ||||
| GC35179 | 6-Methoxytricin | 76015-42-4 | >98% | |
6-Methoxytricin (Compound 6) is an flavonoid isolated from Artemisia iwayomogi. | ||||
| GC35309 | Alrestatin sodium | 51876-97-2 | >98% | |
Alrestatin sodium is an inhibitor of aldose reductase, an enzyme involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy. | ||||
| GC37053 | Quercetin 3-gentiobioside | 7431-83-6 | >98% | |
Quercetin 3-gentiobioside is isolated from A. | ||||
| GC37666 | Sorbinil | 68367-52-2 | >99.50% | |
Sorbinil, is an Aldose reductase inhibitor (ARI). | ||||
| GC37812 | Tolrestat | 82964-04-3 | >98.50% | |
Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM. | ||||
| GC38584 | AT-007 | 2170729-29-8 | >99.00% | |
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase inhibitor for treatment of Galactosemia with an IC50 value of 100 pM. | ||||
| GC38810 | Lidorestat | 245116-90-9 | >99.50% | |
Lidorestat (IDD-676) is a potent, selective and orally active aldose reductase inhibitor with an IC50 of 5 nM. | ||||
| GC63990 | Zenarestat | 112733-06-9 | >98% | |
Zenarestat is a potent and orally active aldose reductase inhibitor. | ||||
| GC68633 | AKR1C3-IN-9 | - | >99.00% | |
AKR1C3-IN-9 is a selective inhibitor of aldo-keto reductase 1C3 (AKR1C3), with an IC50 of 8.92 nM. AKR1C3-IN-9 significantly reverses Doxorubicin (DOX) resistance in drug-resistant breast cancer cell lines. | ||||
| GC68645 | ALR2-IN-1 | 2799695-54-6 | >98% | |
ALR2-IN-1 is a potent and selective inhibitor of ALR2 (IC50=1.42 μM). It exhibits antioxidant and antiglycation properties. ALR2-IN-1 can be used for research on complications related to diabetes. | ||||
| GC70493 | MK204 | 1959605-73-2 | - | |
MK204 is an aldose reductase (AR) inhibitor that can be used in diabetes research. | ||||
| GC70526 | IDD388 | 314297-26-2 | - | |
IDD388 is a selective aldose reductase (ALR2) inhibitor with an IC50 of 30 nM. | ||||
| GC79559 | 2-(2-Chlorobenzamido)acetic acid | 16555-60-5 | >98.00% | |
2-(2-Chlorobenzamido)acetic acid is an aldose reductase inhibitor with an IC 50 of 31 μM. | ||||
| GC79560 | Cemtirestat | 309283-89-4 | >98.00% | |
Cemtirestat (CMTI) is a carboxymethylated thiatriazinoindole inhibitor of aldose reductase ( ALR2 ). | ||||
