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Search Results for " aldose "

Targets

46

Compounds

31

Natural Products

3

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T14175 Aldose reductase-IN-1 AT-001,Caficrestat Others , Reductase
Aldose reductase-IN-1 (AT-001) is a aldose reductase inhibitor (IC50: 28.9 pM).
T75390 Aldose 1-epimerase
Aldose 1-epimerase (mutarotases), an essential enzyme for carbohydrate metabolism, facilitates the interconversion between α- and β-anomers of hexose sugars, including glucose and galactose. This enzyme plays a vital rol...
T61555 Aldose reductase-IN-6
Aldose reductase-IN-6 (Compound 3) is a competitive inhibitor of aldose reductase (AR), possessing an IC50 of 3.164 μM and a Ki of 0.018 μM. Notably, Aldose reductase-IN-6 demonstrates no cytotoxicity toward normal cells...
T60897 Aldose reductase-IN-5
Aldose reductase-IN-5 is an inhibitor of aldose reductase (ALR2) that enhances the combination of inhibitory excitability and antioxidant capacity, thereby delaying the diabetes complications progress.
T62951 Aldose reductase-IN-2
Aldose reductase-IN-2 (Compound 5f) is a potent inhibitor of aldose reductase (AR) with antioxidant properties. aldose reductase-IN-2 is a promising anti-diabetic complication drug.
T61957 Aldose reductase-IN-3
Aldose reductase-IN-3 (Compound 5) is an effective and moderately selective aldose reductase (AR) inhibitor (IC50=3.99 μ M). Aldose reductase is a molecular target involved in various inflammatory diseases (including sep...
T60601 Aldose reductase-IN-4
Aldose reductase-IN-4 (compund IIc) is an inhibitor of aldose reductase with IC50s of 11.70 μM and 0.98 μM for ALR1 and ALR2, respectively [1].
T16910 Sorbinil Reductase
Sorbinil is an Aldose reductase inhibitor. Sorbinil plays a therapeutic role in treating diabetes and diabetic complications decreases AR activity and inhibit the polyol pathway.
T22757 EBPC Reductase
EBPC is an inhibitor of aldose reductase.
T23403 Sulindac sulfone Reductase , COX
Sulindac sulfone is a metabolite of the nonsteroidal anti-inflammatory drug sulindac.
T10393 AT-007 Reductase
AT-007 is an orally active CNS penetrant Aldose Reductase inhibitor for the treatment of Galactosemia (IC50: 100 pM). It reduces toxic galactitol levels and prevents disease complications in GALT deficiency rats.
T35317 Zopolrestat CP 73850,CP73850,CP-73850,Zopolrestatum Reductase
Zopolrestat (CP 73850) is a potent inhibitor of aldose reductase (IC50 = 3.1 nM).
T2013 Ponalrestat Reductase
Ponalrestat is an aldose reductase inhibitor.
T17114 Tolrestat AY-27773 Reductase
Tolrestat (AY-27773) is a potent inhibitor of aldose reductase (IC50 = 35 nM).
T5195 Alrestatin AY-22284 Reductase
Alrestatin (AY-22284) is a specific inhibitor of aldose reductase and attenuates glucose-induced angiotensin II production in rat vascular smooth muscle in vitro.
T1458 Epalrestat ONO2235 Reductase
Epalrestat (ONO2235), an aldose reductase inhibitor, is well tolerated in Long-term therapy. It can effectually ameliorate the associated symptoms of diabetic neuropathy and delay the progression of the disease, particul...
T15568 Imirestat Alcon 1576,AL 1576,HOE 843 Reductase
Imirestat (HOE 843) is an aldose reductase inhibitor that can be used in diabetes research.
T33389 Minalrestat ARI509,WAY-121509,WAY121509,WAYARI-509,ARI-509,WAY-ARI-509 Reductase
Minalrestat(ARI-509) is an orally active and potent aldose reductase inhibitor for the study of impaired microvascular reactivity in diabetic patients.
T27583 IDD388 IDD-388,IDD 388 DNA/RNA Synthesis
IDD388 is a selective and potent aldose reductase (ALR2) inhibitor with antitumor activity that inhibits the ALR1 receptor.
T7478 2-Chloro-1-(4-fluorobenzyl)benzimidazole Reductase
2-Chloro-1-(4-fluorobenzyl)benzimidazole is an inhibitor of aldose reductase (ALR2).
T15756 Lidorestat IDD-676 Reductase
Lidorestat (IDD-676) is an aldose reductase inhibitor (IC50: 5 nM) with effective, selective and oral activity. Lidorestat improves nerve conduction and reduces the formation of cataracts. Lidorestat can be used to treat...
T67805 Oxepinac
oxepinac is an effective and well-tolerated compound for the treatment of painful osteoarthritis. oxepinac has no teratogenic effect on mouse and rabbit fetuses in animal experiments.
T15281 Fidarestat SNK 860 Reductase
Fidarestat is an aldose reductase inhibitor (IC50s: 26 nM, 33 μM, and 1.8 μM for aldose reductase, AKR1B10, and V301L AKR1B10, respectively). It has the potential to treat diabetic disease.
T16723 Ranirestat AS-3201 Others
Ranirestat effective and orally active aldose reductase inhibitor ( IC50s: 11 nM and 15 nM for rat lens AR and recombinant human AR, respectively and a Ki: 0.38 nM for recombinant human AR). Ranirestat has a neuroprotect...
T25019 AL 4114 Al4114,AL-4114
AL 4114 is used as an aldose reductase inhibitor.
T68630 M 79175
M 79175 is an aldose reductase inhibitor.
T68651 ICI-105552
ICI-105552 is an aldose reductase inhibitor.
T5195L Alrestatin Sodium AY 22284A,AY-22284A,Alrestatine sodium,AY22284A
Alrestatin is a specific inhibitor of the aldose reductase enzyme.
T71868 Cemtirestat
Cemtirestat is an aldose reductase inhibitor
T71052 M 16287
M 16287 is a potent aldose reductase inhibitor.
T70968 ICI-222155
ICI-222155 is an aldose reductase inhibitor.
T27362 FR 62765 FR62765,FR-62765
FR 62765 is a derivative of WF-3681, an aldose reductase inhibitor.
T31075 CP-744809 UNII-U63F8E95J1,CP 744809,ARI-809
CP-744809 is a highly selective oral small-molecule aldose reductase inhibitor.
T70579 SX 3202
SX 3202 is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.
T35299 Zenarestat CI1014,FR74366,FK-366,CI-1014,FR 74366,FR-74366
Zenarestat (CI-1014, FK-366, FR-74366) is an aldose reductase inhibitor being studied as a treatment for diabetic neuropathy and cataracts.
T71057 WF 2421
WF 2421 is an aldose reductase inhibitor produced by Humicola grisea.
T68929 Lidorestat monohydrate
Lidorestat monohydrate is an aldose reductase inhibitor potentially for the treatment of diabetic neuropathy and diabetic complications.
T70679 Spr 210
Spr 210 is an aldose reductase (AR) inhibitor with potential uses as a therapeutic agent for preventing and improving some diabetic complications.
T79005 6-Hydroxyluteolin
6-Hydroxyluteolin (Compound 17), a flavonoid, exhibits inhibition of aldose reductase (AR) [1].
T16756 Risarestat CT 112 Reductase
Risarestat (CT-112) is a potent aldose reductase inhibitor and thyroid hormone receptor (TR) antagonist for the treatment of hypoglycemia.
T62456 ALR1/2-IN-1
ALR1/2-IN-1 (Compound 6e) is an aldehyde reductase (ALR1) (IC50: 3.26 μM) and aldose reductase (ALR2) (IC50: 3.06 μM) inhibitor with anticancer effects.
T73305 ALR2-IN-3
ALR2-IN-2, a potent aldose reductase (ALR2) inhibitor, demonstrates IC50 values of 22 nM for rat ALR2 and 116 nM for ALR1, respectively. This compound is utilized in diabetic complications research.
T73304 ALR2-IN-2
ALR2-IN-2, a potent aldose reductase (ALR2) inhibitor, exhibits IC50 values of 27 nM for rat ALR2 and 228 nM for ALR1, respectively. This compound is utilized in the research of diabetic complications.
T78612 APPA Apoptosis
APPA, an aldose reductase inhibitor, demonstrates efficacy in preventing apoptosis and symptoms of Streptozotocin-induced diabetes in rats through inhibition of the polyol pathway. This compound shows promise for researc...
T13037 Sulindac sulfide cis-Sulindac sulfide Raf , Others , AChR
Sulindac sulfide (cis-Sulindac sulfide) is a non-steroidal anti-inflammatory compound that has a high affinity for COX-1 and acts as an inhibitor in Ras activation of Raf-1. Sulindac sulfide is a non-competitive inhibito...
T78702 PTP1B/AKR1B1-IN-1 Phosphatase
PTP1B/AKR1B1-IN-1 is a dual inhibitor targeting protein tyrosine phosphatase 1B (PTP1B) and aldose reductase (AKR1B1), exhibiting inhibitory potency with IC50s of 0.06 μM for PTP1B and 4.3 μM for AKR1B1. Additionally, it...

Compounds

Aldose reductase-IN-1
T14175
Synonym: AT-001,Caficrestat
Target: Others, Reductase
Aldose 1-epimerase
T75390
Synonym:
Target:
Aldose reductase-IN-6
T61555
Synonym:
Target:
Aldose reductase-IN-5
T60897
Synonym:
Target:
Aldose reductase-IN-2
T62951
Synonym:
Target:
Aldose reductase-IN-3
T61957
Synonym:
Target:
Aldose reductase-IN-4
T60601
Synonym:
Target:
Sorbinil
T16910
Synonym:
Target: Reductase
EBPC
T22757
Synonym:
Target: Reductase
Sulindac sulfone
T23403
Synonym:
Target: Reductase, COX
AT-007
T10393
Synonym:
Target: Reductase
Zopolrestat
T35317
Synonym: CP 73850,CP73850,CP-73850,Zopolrestatum
Target: Reductase
Ponalrestat
T2013
Synonym:
Target: Reductase
Tolrestat
T17114
Synonym: AY-27773
Target: Reductase
Alrestatin
T5195
Synonym: AY-22284
Target: Reductase
Epalrestat
T1458
Synonym: ONO2235
Target: Reductase
Imirestat
T15568
Synonym: Alcon 1576,AL 1576,HOE 843
Target: Reductase
Minalrestat
T33389
Synonym: ARI509,WAY-121509,WAY121509,WAYARI-509,ARI-509,WAY-ARI-509
Target: Reductase
IDD388
T27583
Synonym: IDD-388,IDD 388
Target: DNA/RNA Synthesis
2-Chloro-1-(4-fluorobenzyl)benzimidazole
T7478
Synonym:
Target: Reductase
Lidorestat
T15756
Synonym: IDD-676
Target: Reductase
Oxepinac
T67805
Synonym:
Target:
Fidarestat
T15281
Synonym: SNK 860
Target: Reductase
Ranirestat
T16723
Synonym: AS-3201
Target: Others
AL 4114
T25019
Synonym: Al4114,AL-4114
Target:
M 79175
T68630
Synonym:
Target:
ICI-105552
T68651
Synonym:
Target:
Alrestatin Sodium
T5195L
Synonym: AY 22284A,AY-22284A,Alrestatine sodium,AY22284A
Target:
Cemtirestat
T71868
Synonym:
Target:
M 16287
T71052
Synonym:
Target:
ICI-222155
T70968
Synonym:
Target:
FR 62765
T27362
Synonym: FR62765,FR-62765
Target:
CP-744809
T31075
Synonym: UNII-U63F8E95J1,CP 744809,ARI-809
Target:
SX 3202
T70579
Synonym:
Target:
Zenarestat
T35299
Synonym: CI1014,FR74366,FK-366,CI-1014,FR 74366,FR-74366
Target:
WF 2421
T71057
Synonym:
Target:
Lidorestat monohydrate
T68929
Synonym:
Target:
Spr 210
T70679
Synonym:
Target:
6-Hydroxyluteolin
T79005
Synonym:
Target:
Risarestat
T16756
Synonym: CT 112
Target: Reductase
ALR1/2-IN-1
T62456
Synonym:
Target:
ALR2-IN-3
T73305
Synonym:
Target:
ALR2-IN-2
T73304
Synonym:
Target:
APPA
T78612
Synonym:
Target: Apoptosis
Sulindac sulfide
T13037
Synonym: cis-Sulindac sulfide
Target: Raf, Others, AChR
PTP1B/AKR1B1-IN-1
T78702
Synonym:
Target: Phosphatase
Cat No. Product Name Synonyms Targets
T6S2384 Poliumoside Reductase
Poliumoside is a natural compound which exhibits significant inhibition of advanced glycation end product formation with IC50 value of 4.6-25.7 μM, it also exhibits great inhibitory effects on rat lens aldose reductase w...
T5S1131 Ganoderic acid C6 Others
1. Ganoderic acid C6 has antinociceptive activity.
T0725 Isoliquiritigenin ISL,Isoliquiritigen,GU17 Apoptosis , Influenza Virus , Reductase , Autophagy
Isoliquiritigenin (ISL), an anti-tumor flavonoid from the root of Glycyrrhiza glabra, suppresses aldose reductase (IC50=320 nM).
T3801 (Rac)-Byakangelicin Bjacangelicin,Bjakangelicin,Biacangelicin,7H-Furo[3,2-g][1]benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-,Byakangelicin Others
(Rac)-Byakangelicin (7H-Furo[3,2-g][1]benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-) is an antineoplastic agent.
TN5276 (Z)-Aldosecologanin (Centauroside) Others
(Z)-Aldosecologanin is a natural product from Lonicera japonica.
TN3908 (E)-Aldosecologanin Others
(E)-Aldosecologanin is a natural product from Lonicera japonica.
TN1661 Ganoderic acid C2 Reductase , Histamine Receptor , Immunology/Inflammation related
Ganoderic acid C2 has anti-inflammatory,and anti-tumor-promoting activities. Ganoderic acid C2 can inhibit histamine release, it also has inhibitory effects on the induction of Epstein-Barr Virus early antigen.
TN1975 Neosmitilbin Neoastilbin Others
Neosmitilbin (Neoastilbin) may have antioxidant and anti-inflammatory activities, it shows potent inhibition of lens aldose reductase.
TN1656 Ganoderenic acid A Others
Ganoderenic acid A has a potent hepatoprotective, and cytotoxic effects, it shows inhibitory activity on human aldose reductase in vitro.
T5S1026 Apigenin-7-glucuronide Apigenin 7-O-glucuronide MMP
Apigenin-7-glucuronide (Apigenin 7-O-glucuronide) possesses multiple activities, including antioxidant, anti-inflammatory, and aldose reductase inhibitory activities, it can inhibit MMP activities (IC50s: 12.87, 22.39, 1...
T6S0840 Engeletin Dihydrokaempferol 3-rhamnoside NF-κB , Reductase
1. Engeletin (Dihydrokaempferol 3-rhamnoside) may serve as a potential anti-inflammatory agent. 2. Engeletin possesses potent inhibition of PGE2 release with IC5 values of 19.6 μg/ml. 3. Engeletin inhibits a recombinant ...
T3665 Tectoridin Shekanin Estrogen Receptor/ERR , Reductase
Tectoridin (Shekanin) possesses an estrogenic and thyroid hormone-like agent by activating estrogen and thyroid hormone receptors. Tectoridin has anti-oxidant, anti-inflammatory and hypoglycemic activities; Tectoridin an...
TN2122 Quercetin 3-gentiobioside Quercetin-3-gentiobioside Reductase
Quercetin 3-gentiobioside (Quercetin-3-gentiobioside) is an inhibitor of AR and AGE formation and can be extracted from A. iwayomogi.Quercetin 3-gentiobioside inhibits the biological activity of aldose reductase (AR) and...
TN1037 Groenlandicine Topoisomerase
Groenlandicine is a protoberberine alkaloid from Coptidis Rhizoma. Groenlandicine exhibits moderate inhibitory effect with IC50 value of 154.2 μM for human recombinant aldose reductase (HRAR). Groenlandicine selectively ...
T4704 L-Anserine nitrate L-Anserine nitrate salt Others , Endogenous Metabolite
L-Anserine nitrate (L-Anserine nitrate salt) is a dipeptide found in most animal tissues. In model systems it is a potent Antioxidant and scavener of hydroxyl radicals. The compound inhibits nonenzymatic protein glycatio...
T5S1988 Isorhamnetin-3-O-glucoside Isorhamnetin-3-O-beta-D-Glucoside Others
Isorhamnetin-3-O-glucoside (Isorhamnetin-3-O-beta-D-Glucoside) inhibits the activity of alpha-glucosidase from rat intestine; it exhibits a potent rat lens aldose reductase (RLAR) inhibition in vitro, its IC(50) being 1....
T5813 BYAKANGELICIN Reductase
BYAKANGELICIN,a main furanocoumarin constituent isolated and characterized as an aldose reductase inhibitor,and is effective for the treatment of sugar cataracts and diabetic neuropathy and hence might be useful as a lea...
T2S1635 3-Isomangostin MTH1
3-Isomangostin is a potent human aldose reductase inhibitor with an IC50 of 3.48 uM; it is also an acetylcholinesterase selective inhibitor. 3-Isomangostin has free radical scavenging activity; it shows antiplasmodial ac...
T6102 2'-acetylacteoside Antioxidant , Reductase
2'-Acetylacteoside has antioxidative activity. It can significantly attenuate glutamate-induced neurotoxicity at concentrations ranging from 0.1 to 10 μM. 2'-Acetylacteoside shows antiproliferative effects on aortic smoo...
TL0008 Gigantol Wnt/beta-catenin , Glucosidase
Gigantol is a novel inhibitor of the Wnt/β-catenin pathway. It inhibits Wnt/β-catenin signaling through downregulation of phosphorylated LRP6 and cytosolic β-catenin in breast cancer cells. Gigantol may be developed as a...
T4918 DL-Glyceraldehyde Glyceric aldehyde Reductase
DL-Glyceraldehyde (Glyceric aldehyde) is produced from the action of the enzyme glyceraldehyde dehydrogenase, which converts glycerol to glyceraldehyde using NADP as a cofactor. When present at sufficiently high levels, ...
TN5183 Triptocalline A Others
Triptocalline A shows an inhibitory effect on rat lens aldose reductase.
T39435 Myrciacetin
Myrciacetin, a flavonoid derived from Rhododendron dauricum, exhibits inhibitory activity against rat lens aldose reductase, as demonstrated by an IC50 value of 13 μM.
TN3287 8-Lavandulylkaempferol Reductase , AChR
8-Lavandulylkaempferol exhibits significant inhibitory effects with IC(50) values of 7.10 and 8.11 microM for butyrylcholinesterase and acetylcholinesterase, respectively. It shows inhibitory activities against aldose re...
TN5672 Puerol A
Puerol A exhibits potent inhibitory effects on aldose reductase with IC50 values of 6.4 uM. dl-Puerol A has antioxdiant activity, it shows inhibitory effects on copper ion-induced protein oxidative modification of mouse ...
T75627 Ganoderic acid Df
Ganoderic acid Df, a lanostane-type triterpenoid isolated from the fruiting body of Ganoderma lucidum, potently inhibits aldose reductase with an IC 50 of 22.8 ± 0.6 μM [1].
T10183 6-Methoxytricin Others
6-Methoxytricin is a flavonoid isolated from Artemisia iwayomogi. It is an inhibitor on aldose reductase (AR) and advanced glycation endproduct (AGE) formation activities (IC50s: 30.29 μM and 134.88 μM). 6-Methoxytricin ...
TN6645 Lucidumol A
Lucidumol A has relatively good effect against aldose reductase with IC50 of 19.1uM. Lucidumol A has cytotoxic activity, it reduced cell growth in three human carcinoma cells (Caco-2, HepG2, and HeLa cells) dose dependen...
TMA0291 Dehydroglyasperin D GSK-3 , p38 MAPK , ROS , Akt , COX , PI3K , DNA/RNA Synthesis , Prostaglandin Receptor , JNK
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction wit...
TN3760 Danshenol A Reductase
Danshenol A has strong aldose reductase (AR) inhibitory activity, has IC50 of 0.10 microM which is comparable to that of epalrestat in clinical use. Danshenol A also has antitumor activity in T-24, QGY, K562, Me180 and B...
TN3692 Conduritol A TNF
Conduritol A has a hypoglycemic effect, can have an effect on regulating the metabolism of blood lipid, free-radical scavenging, enhancing the antioxidant ability, potentiating immune function; it also can markedly preve...

Natural Products

Poliumoside
T6S2384
Synonym:
Target: Reductase
Ganoderic acid C6
T5S1131
Synonym:
Target: Others
Isoliquiritigenin
T0725
Synonym: ISL,Isoliquiritigen,GU17
Target: Apoptosis, Influenza Virus, Reductase, Autophagy
(Rac)-Byakangelicin
T3801
Synonym: Bjacangelicin,Bjakangelicin,Biacangelicin,7H-Furo[3,2-g][1]benzopyran-7-one, 9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-,Byakangelicin
Target: Others
(Z)-Aldosecologanin (Centauroside)
TN5276
Synonym:
Target: Others
(E)-Aldosecologanin
TN3908
Synonym:
Target: Others
Ganoderic acid C2
TN1661
Synonym:
Target: Reductase, Histamine Receptor, Immunology/Inflammation related
Neosmitilbin
TN1975
Synonym: Neoastilbin
Target: Others
Ganoderenic acid A
TN1656
Synonym:
Target: Others
Apigenin-7-glucuronide
T5S1026
Synonym: Apigenin 7-O-glucuronide
Target: MMP
Engeletin
T6S0840
Synonym: Dihydrokaempferol 3-rhamnoside
Target: NF-κB, Reductase
Tectoridin
T3665
Synonym: Shekanin
Target: Estrogen Receptor/ERR, Reductase
Quercetin 3-gentiobioside
TN2122
Synonym: Quercetin-3-gentiobioside
Target: Reductase
Groenlandicine
TN1037
Synonym:
Target: Topoisomerase
L-Anserine nitrate
T4704
Synonym: L-Anserine nitrate salt
Target: Others, Endogenous Metabolite
Isorhamnetin-3-O-glucoside
T5S1988
Synonym: Isorhamnetin-3-O-beta-D-Glucoside
Target: Others
BYAKANGELICIN
T5813
Synonym:
Target: Reductase
3-Isomangostin
T2S1635
Synonym:
Target: MTH1
2'-acetylacteoside
T6102
Synonym:
Target: Antioxidant, Reductase
Gigantol
TL0008
Synonym:
Target: Wnt/beta-catenin, Glucosidase
DL-Glyceraldehyde
T4918
Synonym: Glyceric aldehyde
Target: Reductase
Triptocalline A
TN5183
Synonym:
Target: Others
Myrciacetin
T39435
Synonym:
Target:
8-Lavandulylkaempferol
TN3287
Synonym:
Target: Reductase, AChR
Puerol A
TN5672
Synonym:
Target:
Ganoderic acid Df
T75627
Synonym:
Target:
6-Methoxytricin
T10183
Synonym:
Target: Others
Lucidumol A
TN6645
Synonym:
Target:
Dehydroglyasperin D
TMA0291
Synonym:
Target: GSK-3, p38 MAPK, ROS, Akt, COX, PI3K, DNA/RNA Synthesis, Prostaglandin Receptor, JNK
Danshenol A
TN3760
Synonym:
Target: Reductase
Conduritol A
TN3692
Synonym:
Target: TNF

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPJ-01264 GALM Protein, Human, Recombinant (His) Human E. coli
Galactose Mutarotase (GALM) is a cytoplasmic enzyme that belongs to the Aldose Epimerase family. GALM is a Mutarotase that converts α-Aldose to the β-Anomer. GALM is active on D-Glucose, L-Arabinose, D-Xylose, D-Galactos...
TMPY-02438 AKR1B1 Protein, Human, Recombinant (His) Human E. coli
Aldose reductase (AKR1B1) belongs to the aldo/keto reductase superfamily. AKR1B1 is a NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Expression of AKR1B1 was the highest...
TMPJ-00524 SORD Protein, Human, Recombinant (His) Human Human Cells
Sorbitol dehydrogenase, also known as L-iditol 2-dehydrogenase and SORD, is a member of the zinc-containing alcohol dehydrogenase family. SORD exsits in a homotetramer and binds one zinc ion per subunit. SORD is expresse...
TargetMol