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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
19 Results for "
Glyoxalase (GLO)
" in MedChemExpress (MCE) Product Catalog:
Products (19)
19 Results for "Glyoxalase (GLO)" in MCE Product Catalog:
5
5 Cited Publications
Synonyms: S-p-Bromobenzylglutathione cyclopentyl diester
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BrBzGCp2 is a Glyoxalase 1 (GLO1) inhibitor, with a GC50 of 4.23 μM in HL-60 cells. BrBzGCp2 possesses antitumor and neuroprotective activity .
5
5 Cited Publications
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Glyoxalase I inhibitor free base (3(Et)2) is the inhibitor for glyoxalase I (GLO), and can be used in antitumor research .
1
1 Cited Publications
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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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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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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 .
Cat. No.: HY-15167
CAS No.: 221174-33-0
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Glyoxalase I inhibitor (3(Et)2) is the inhibitor for glyoxalase I (GLO), and can be used in antitumor research .
Cat. No.: HY-148216
CAS No.: 156727-62-7
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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 .
Cat. No.: HY-185057
CAS No.: 41656-56-8
Synonyms: S-Lactylglutathione; (R)-S-Lactoylglutathione
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Cat. No.: HY-146653
CAS No.: 1622952-07-1
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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.
Cat. No.: HY-146657
CAS No.: 828262-76-6
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4BAB (compound 29) is an irreversible glyoxalase I (GLO1) inhibitor. 4BAB has anticancer effects .
Cat. No.: HY-124824
CAS No.: 700870-56-0
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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 .
Cat. No.: HY-147649
CAS No.: 2455508-31-1
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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 .
Cat. No.: HY-146654
CAS No.: 2314467-61-1
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Glyoxalase I inhibitor 2 (compound 26) is a potent glyoxalase I (GLO1) inhibitor with an IC50 of 0.5 µM. Glyoxalase I inhibitor 2 has the potential for the research of depression and anxiety .
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Glyoxalase I inhibitor 3 (compound 22g) is a potent glyoxalase I (GLO1) inhibitor with an IC50 of 0.011 µM. Glyoxalase I inhibitor 3 has the potential for the research of depression and anxiety .
Cat. No.: HY-P71690
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HAGH; GLXII; Hydroxyacylglutathione Hydrolase; Hydroxyacylglutathione Hydroxylase; HAGH1; Hydroxyacyl Glutathione Hydrolase; GLO2; Glx II; Hydroxyacylglutathione Hydrolase, Mitochondrial; GLO2D; Glyoxalase II; GLX2
Species:
Human
Source:
E. coli
Cat. No.: HY-181980
CAS No.: 883054-47-5
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SPB07393SC is a glyoxalase-I (Glo-I) inhibitor with an IC50 of 11.1 μM. SPB07393SC is applicable for cancer research .
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2-Dimethylaminophenol is an inhibitor of human glyoxalase 1 (GLO1). 2-Dimethylaminophenol disrupts metal binding by substituting the pyridine nitrogen donor with a dimethylamino group .
Cat. No.: HY-P75162
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: GLO1; Aldoketomutase; Glyoxalase I; Glx I; Lactoylglutathione Lyase; Epididymis Secretory Protein Li 74; GLOD1; Glyoxalase Domain Containing 1; S-D-Lactoylglutathione Methylglyoxal Lyase; Lactoyl Glutathione Lyase; Ketone-Aldehyde Mutase; HEL-S-74; Methyl
Species:
Mouse
Source:
E. coli
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
