108 Results for "

S-Transferase

" in MedChemExpress (MCE) Product Catalog:
Products (108)

108 Results for "S-Transferase" in MCE Product Catalog:

10
10 Publications Verification
Cat. No.: HY-B1640
CAS No.: 58-54-8
Synonyms: Etacrynic acid
Ethacrynic acid has anti-inflammatory and anticancer activity. Ethacrynic acid is an orally active diuretic. Ethacrynic acid is an inhibitor of glutathione S-transferase (GSTs) and Wnt signaling pathways. Ethacrynic acid is a radiosensitizer. Ethacrynic acid can inhibit airway smooth muscle (ASM) contraction in mice. Ethacrynic acid can increase the outflow of aqueous humor from the eye for the study of glaucoma .
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8
8 Cited Publications
Cat. No.: HY-13634A
CAS No.: 168682-53-9
Purity:  99.71%
Synonyms: TER199free base; TLK199
Research Areas:  

Cancer

Ezatiostat (TER199 free base; TLK199) is a tripeptide analog of glutathione and is a selective and orally active glutathione S-transferase P1-1 (GSTP1) inhibitor. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. Ezatiostat has the potential for myelodysplastic syndrome (MDS) treatment .
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5
5 Cited Publications
Cat. No.: HY-P70270
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rSchGlutathione S-Transferase class-mu 26 kDa isozyme; Glutathione S-Transferase class-mu 26 kDa isozyme; GST 26; Sj26 antigen; SjGST
Species:  
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4
4 Cited Publications
Cat. No.: HY-111530
CAS No.: 568544-03-6
Purity:  99.11%
Research Areas:  

Cancer

GSTO1-IN-1 is a potent glutathione S-transferase omega 1 (GSTO1) inhibitor with an IC50 of 31 nM.
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2
2 Cited Publications
Cat. No.: HY-135318
CAS No.: 787634-60-0
Purity:  98.56%
Research Areas:  

Cancer

NBDHEX is a potent glutathione S-transferase P1-1 (GSTP1-1) inhibitor. NBDHEX induces apoptosis of tumor cells. NBDHEX acts as an anticancer agent by inhibiting GSTs catalytic activity, avoiding inconvenience of the inhibitor extrusion from the cell by specific pumps and disrupting the interaction between the GSTP1-1 and key signaling effectors. NBDHEX can also act as late-phase autophagy inhibitor .
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2
2 Cited Publications
Cat. No.: HY-112534
CAS No.: 1202710-57-3
Purity:  ≥98.0%
Research Areas:  

Cancer

GSTO-IN-2 is a glutathione S-transferase inhibitor with IC50s of 3.6, 16.3, and 1.4 μM for GSTA2, GSTM1, and GSTP1-1.
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1
1 Cited Publications
Cat. No.: HY-Y1147
CAS No.: 141-05-9
Synonyms: Maleic acid diethyl ester
Diethyl maleate (DEM) is an orally available, effective glutathione (GSH) depletor that crosses the blood-brain barrier. Diethyl maleate covalently binds irreversibly to GSH via glutathione S-transferase with an in vitro IC50 of 0.1-0.5 mM. Diethyl maleate selectively depletes GSH in liver, lung, and brain tissues, exacerbating oxidative stress and enhancing hyperbaric oxygen toxicity. Diethyl maleate promotes precursor amino acid uptake and in turn promotes GSH synthesis by upregulating the activity of the cystine-glutamate transporter XO -. Diethyl maleate can be used to study redox homeostasis and GSH protection mechanisms in oxidative stress-related diseases such as hyperbaric oxygen injury and metabolic diseases[1][2][3].
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1
1 Cited Publications
Cat. No.: HY-115673
CAS No.: 2362527-67-9
Purity:  97.46%
Research Areas:  

Cancer

LAS17 is a potent and selective tyrosine-directed irreversible inhibitor for glutathione S-Transferase Pi (GSTP1) . LAS17 inhibits GSTP1 activity with an IC50 of 0.5 μM . LAS17 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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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-N1916
CAS No.: 63644-62-2
Coniferyl ferulate is an orally active phenolic acid compound. Coniferyl ferulate is a potent inhibitor of glutathione S-transferase (GST) (IC50 = 0.3 μM), which downregulates P-gp expression, induces apoptosis in B-MD-C1 (ADR+/+) cells, and reverses multidrug resistance. Coniferyl ferulate blocks the NMDAR/NR2B-CaMKII-MAPKs signaling pathway, inhibits ROS production and mitochondrial apoptosis, while reshapes the intestinal microbiota and microbial metabolism, ameliorates colonic inflammation and alleviates depressive symptoms in mice. Coniferyl ferulate can alleviate the toxicity of xylene to hematopoietic stem and progenitor cells by targeting Mgst2. Coniferyl ferulate exhibits antibacterial activity against the Gram-positive Bacillus subtilis and Staphylococcus aureus .
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1
1 Cited Publications
Cat. No.: HY-126329
CAS No.: 2042347-69-1
Purity:  98.62%
Research Areas:  

Inflammation/Immunology

AZD9898 is an orally active leukotriene-C4 synthetase (LTC4S, glutathione S-transferase II) inhibitor, with an IC50 of 0.28 nM. AZD9898 mitigates the GABA binding and hepatic toxicity signal. AZD9898 has the potential to treat asthma .
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1
1 Cited Publications
Cat. No.: HY-P75153A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Glutathione S-Transferase A1; GST-epsilon; GSTA1-1; GTH1; GSTA1
Species:  
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1
1 Cited Publications
Cat. No.: HY-P75152A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Glutathione S-Transferase Mu 2; GST class-mu 2; GSTM2-2; GST4
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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-N2853
CAS No.: 7559-04-8
Synonyms: α-Tocopherylquinone
D-α-Tocopherylquinone (α-Tocopherylquinone) is a quinone, can be isolated from Phaeodactylum tricornutum. D-α-Tocopherylquinone is an oxidation product of α-Tocopherol (vitamin E). D-α-Tocopherylquinone can act as an anticoagulant and as an antioxidant. D-α-Tocopherylquinone reduces cellular oxidative damage produced by oxidized lipids. D-α-Tocopherylquinone binds to a liver cytosolic protein with a molecular mass of about 40 kDa. D-α-Tocopherylquinone binds to glurathione-S-transferase (GST) and can be transported to the site of metabolism or excreted in the bile .
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Cat. No.: HY-N2560
CAS No.: 130-01-8
Synonyms: Senecionan-11,16-dione, 12-hydroxy-; Aureine; Senecionin
Senecionine (Senecionan-11,16-dione, 12-hydroxy-) is a pyrrolizidine alkaloid could be isolated from Senecio vulgaris. Senecionine decreases the activities of glutathione S-transferase, aminopyrine demethylase and arylhydrocarbon hydroxylase (AHH) .
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Cat. No.: HY-P2961
CAS No.: 50812-37-8
Research Areas:  

Cancer

Glutathione S-transferase is a phase II metabolic enzyme consisting of three superfamilies: cytosolic, mitochondrial, and microsomal. Glutathione S-transferase possesses various catalytic activities such as catalytic detoxification and thiol transfer, as well as chaperone function. GSTP1, a subtype of Glutathione S-transferase, is highly expressed in malignant tissues and serves as a tumor marker .
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Cat. No.: HY-N9348A
CAS No.: 108844-81-1
Glucoraphenin potassium is an orally effective glucosinolate. Glucoraphenin potassium can be isolated from radish sprouts. Glucoraphenin potassium enhances the enzymatic activity of Glutathione S-transferase. Glucoraphenin potassium enhances the activity of cytochrome P450-related monooxygenase .
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Cat. No.: HY-147517
CAS No.: 2769963-24-6
Purity:  98.52%
Target:  

Keap1-Nrf2

Keap1-Nrf2-IN-9 (Compound 11) is a potent Keap1-Nrf2 PPI (Keap1-Nrf2 protein-protein interaction) inhibitor with an IC50 of 0.575 μM. Keap1-Nrf2-IN-9 increases the expression of Nrf2 target genes including heme oxygenase 1 (Hmox1), glutathione S-transferase P (GstP), and glutamate-cysteine ligase catalytic (Gclc) and modulatory (Gclm) subunits. Keap1-Nrf2-IN-9 shows no cytotoxic activity in ARPE19 cells .
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Cat. No.: HY-N7227
CAS No.: 1862-41-5
Anonaine is an antiparasitic agent. Anonaine also is a glutathione S-transferase (GST) inhibitor .
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