32 Results for "

Glyoxalase

" in MedChemExpress (MCE) Product Catalog:
Products (32)

32 Results for "Glyoxalase" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-136684
CAS No.: 166038-00-2
Purity:  99.00%
Synonyms: S-p-Bromobenzylglutathione cyclopentyl diester
Target:  

Glyoxalase (GLO)

Research Areas:  

Neurological Disease Cancer

BrBzGCp2 is a Glyoxalase 1 (GLO1) inhibitor, with a GC50 of 4.23 μM in HL-60 cells. BrBzGCp2 possesses antitumor and neuroprotective activity .
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4
4 Cited Publications
Cat. No.: HY-15167A
CAS No.: 174568-92-4
Purity:  98.52%
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor free base (3(Et)2) is the inhibitor for glyoxalase I (GLO), and can be used in antitumor research .
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1
1 Cited Publications
Cat. No.: HY-13634B
CAS No.: 152684-53-2
Purity:  99.89%
Synonyms: TER117
Research Areas:  

Inflammation/Immunology Cancer

TLK117, the active metabolite of TLK199, selective inhibits Glutathione S-transferase P1–1 (GSTP1-1) with a Ki of 0.4 μM for GSTP. TLK117 also competitively inhibits glyoxalase I with a Ki of 0.56 μM.
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1
1 Cited Publications
Cat. No.: HY-147648
CAS No.: 2455508-19-5
Purity:  99.26%
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 6 (Compound 9j) is a glyoxalase I (Glo-I) inhibitor with an IC50 of 1.13 μM. Glyoxalase I inhibitor 6 can be used as anticancer agent with low toxicity .
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Cat. No.: HY-126752
CAS No.: 495-27-2
Purity:  99.17%
Ophthalmic acid is a ubiquitous metabolite and glutathione modulator, with a Ki of 0.95 mM for glyoxalase I. Ophthalmic acid competitively inhibits glyoxalase I, glutathione S-transferase, glutaredoxin, glutamate-cysteine ligase, protein disulfide reductase (glutathione), as well as non-selective cation channels. Ophthalmic acid is applicable in diabetes-related research .
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Cat. No.: HY-W009177
CAS No.: 2922-56-7
Target:  

Glyoxalase (GLO)

Research Areas:  

Others

S-Methylglutathione is an S-substitued glutathione and a stronger nucleophile than GSH . S-Methylglutathione has inhibitory effect on glyoxalase 1 .
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Cat. No.: HY-P2774
CAS No.: 9033-12-9
Synonyms: Glo-I
Target:  

Glycosidase

Research Areas:  

Inflammation/Immunology Cancer

Glyoxalase I (Glo-I) is a glycosidase and a methylglyoxal (MOG) detoxification enzyme. Glyoxalase I can be used for the research of inflammation and cancer .
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Cat. No.: HY-147647
CAS No.: 2455508-17-3
Purity:  98.07%
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 5 (Compound 9h) is a glyoxalase I (Glo-I) inhibitor with an IC50 of 1.28 μM. Glyoxalase I inhibitor 5 can be used as anticancer agent .
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Cat. No.: HY-Y0785
CAS No.: 107-22-2
Glyoxal (40% w/w in water) is an α-oxoaldehyde that inhibits Aldose Reductase, Glutathione Reductase, and NADPH synthase. Glyoxal (40% w/w in water) exhibits cytotoxicity, triggers oxidative stress, induces ROS accumulation, lipid peroxidation, mitochondrial membrane potential collapse, DNA damage, apoptosis, and massive production of advanced glycation end products (AGEs). Glyoxal (40% w/w in water) depletes glutathione and activates MAPK phosphorylation. It has lower toxicity as a fixative than paraformaldehyde (PFA) and serves as a precursor for the synthesis of oxalates and dietary carcinogens. Glyoxal (40% w/w in water) is suitable for research related to calcium oxalate kidney stones, diabetes, atherosclerosis, cardiovascular diseases, retinopathy, and cataracts .
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Cat. No.: HY-P4277
CAS No.: 149438-56-2
Target:  

Glyoxalase (GLO)

Research Areas:  

Others

N,S-Bis-Fmoc-Glutathione is a potent glyoxalase II inhibitor with a Ki value of 0.75 μM and an IC50 of 2.5 μM .
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Cat. No.: HY-P4277A
Target:  

Glyoxalase (GLO)

Research Areas:  

Others

N,S-Bis-Fmoc-Glutathione TFA is a potent glyoxalase II inhibitor with a Ki value of 0.75 μM and an IC50 of 2.5 μM .
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Cat. No.: HY-15167
CAS No.: 221174-33-0
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor (3(Et)2) is the inhibitor for glyoxalase I (GLO), and can be used in antitumor research .
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Cat. No.: HY-185057
CAS No.: 41656-56-8
Synonyms: S-Lactylglutathione; (R)-S-Lactoylglutathione
S-D-Lactoylglutathione (S-Lactylglutathione; (R)-S-Lactoylglutathione) is a multifunctional metabolic intermediate of the glyoxalase system. S-D-Lactoylglutathione activates K + efflux in bacteria by displacing inhibitory glutathione from KefGB channels, thereby acidifying the cytoplasm. In eukaryotic cells, S-D-Lactoylglutathione mediates S-glutathionylation as a substrate of glyoxalase 2. S-D-Lactoylglutathione serves as a sensitive metabolic biomarker for neodymium nitrate neurotoxicity; when used in combination with MSCs-exo, it upregulates glutathione levels, downregulates lactate dehydrogenase and Glo2 levels, and inhibits cellular inflammatory responses and pyroptosis. S-D-Lactoylglutathione can be used in research related to prostate cancer, breast cancer, non-small cell lung cancer, sepsis-associated encephalopathy, and neurotoxicity .
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Cat. No.: HY-126752A
Research Areas:  

Inflammation/Immunology

Ophthalmic acid TFA, an analogue of GSH, is a marker of oxidative stress and hepatic GSH consumption. Ophthalmic acid TFA is an inhibitor of Glyoxalase I reaction .
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Cat. No.: HY-148216
CAS No.: 156727-62-7
Research Areas:  

Infection

HBPC-GSH is a glyoxalase (Glo) inhibitor (cGloI IC50=0.6 μM; cGloII IC50=1.6 μM), a glutathione derivative. HBPC-GSH can be used in antimalarial research .
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Cat. No.: HY-146653
CAS No.: 1622952-07-1
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 1 (compound 23) is a potent glyoxalase I (GLO1) inhibitor with an IC50 of 26 nM . Glyoxalase I inhibitor 1 is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-146657
CAS No.: 828262-76-6
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

4BAB (compound 29) is an irreversible glyoxalase I (GLO1) inhibitor. 4BAB has anticancer effects .
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Cat. No.: HY-124824
CAS No.: 700870-56-0
Target:  

Glyoxalase (GLO)

Research Areas:  

Others

Methyl gerfelin inhibits osteoclast differentiation by binding 3 major cellular proteins: glyoxalase 1 (GLO1), sterol binding protein 2 (SCP2), and small glutamine-rich tetratricopeptide repeat containing protein A (SGTA). Methyl gerfelin is a potent GLO1 inhibitor related to the flavonoid class .
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Cat. No.: HY-147649
CAS No.: 2455508-31-1
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 7 (Compound 6) is a glyoxalase I (Glo-I) inhibitor with an IC50 of 3.65 μM. Glyoxalase I inhibitor 7 can be used as anticancer agent .
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Cat. No.: HY-146656
CAS No.: 250155-72-7
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 4 (compound 14) is a potent glyoxalase I inhibitor with an Ki of 10 nM .
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