16 Results for "

xc-

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "xc-" in MCE Product Catalog:

52
52 Publications Verification
Cat. No.: HY-114481
CAS No.: 1801530-11-9
Purity:  99.77%
Synonyms: IKE
Target:  

Ferroptosis

Research Areas:  

Cancer

Imidazole ketone erastin is a potent, selective, and metabolically stable inhibitor of the cystine-glutamate antiporter, system xc - and an activator of ferroptosis. Imidazole ketone erastin has anti-tumor activity .
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6
6 Cited Publications
Cat. No.: HY-139087
CAS No.: 1695533-44-8
Purity:  98.55%
Target:  

Ferroptosis

Research Areas:  

Metabolic Disease

Erastin2, an Erastin (HY-15763) analog, is a ferroptosis inducer and a potent, selective inhibitor of the system xc(-) cystine/glutamate transporter
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4
4 Cited Publications
Cat. No.: HY-B0774
CAS No.: 112665-43-7
Synonyms: AA 2414
Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
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1
1 Cited Publications
Cat. No.: HY-P702444
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Cystine/glutamate transporter; Amino acid transport system xc-; Calcium channel blocker resistance protein CCBR1; Solute carrier family 7 member 11; xcT
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P80523
Synonyms: Cystine/glutamate transporter, Amino acid transport system xc-, Calcium channel blocker resistance protein CCBR1, Solute carrier family 7 member 11, xcT, SLC7A11

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC

Reactivity:  

Human, Mouse

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Cat. No.: HY-W402682
CAS No.: 1695562-36-7
Research Areas:  

Neurological Disease Cancer

SXC2023 is a glutamatergic reagent and cystine-glutamate antiporter (System xc ) activator. SXC2023 can affect SLC7A11. SXC2023 is applicable to the research of colorectal cancer and trichotillomania .
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Cat. No.: HY-B0774R
CAS No.: 112665-43-7
Synonyms: AA 2414 (Standard)
Seratrodast (Standard) is the analytical standard of Seratrodast. This product is intended for research and analytical applications. Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
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Cat. No.: HY-176203
Target:  

CD73

Research Areas:  

Cancer

XC-12 is an orally active and potent small-molecule CD73 inhibitor (an immune checkpoint) with IC50 values of 12.36 nM and 1.29 nM against soluble and membrane-bound CD73 forms, respectively. XC-12 is promising for research of cancers .
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Cat. No.: HY-162785
Target:  

CDK

Research Areas:  

Infection

XC219 (compound 43) is a cyclin-dependent kinase CDK) inhibitor, that covalently binds to CDK active site Lys. XC219 can be used in antifungal research .
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Cat. No.: HY-165528
CAS No.: 1464897-15-1
Synonyms: xc8
Target:  

CCR

Research Areas:  

Inflammation/Immunology

Histamine glutarimide (XC8) is an orally active anti-asthma agent. Histamine glutarimide blocks the maturation of chemokines (CCL2, CCL7, CCL8, CCL13) and inhibits the migration of eosinophils and the degranulation of mast cells. In asthma models induced by carrageenan and rat ovalbumin, Histamine glutarimide can reduce airway resistance and the count of eosinophils in bronchoalveolar lavage fluid. Histamine glutarimide can be used in asthma research .
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Cat. No.: HY-14986
CAS No.: 936091-56-4
Target:  

JAK

Research Areas:  

Others

JAK-IN-32 (XC) is a bi-aryl meta-pyrimidine inhibitor of JAK kinase .
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Cat. No.: HY-111137
CAS No.: 916890-10-3
Synonyms: xc-302 free base
Target:  

Akt

Research Areas:  

Cancer

Puquitinib (XC-302 free base) is a multi-target inhibitor with the activity of inducing autophagy in nasopharyngeal carcinoma cells by inhibiting the PI3K/AKT/mTOR signaling pathway. Puquitinib was able to inhibit the proliferation of CNE-2 cells, showing a dose-dependent antiproliferative effect. Puquitinib induced the formation of autophagosomes and autolysosomes in CNE-2 cells, which were observed by fluorescence microscopy and electron microscopy. Puquitinib promoted the formation of LC3-II and increased the expression of beclin 1, while reducing the level of p62. Puquitinib inhibited the PI3K/AKT/mTOR pathway by reducing the expression of p-AKT and p-mTOR. Puquitinib also induced apoptosis in CNE-2 cells, and when autophagy was inhibited, the apoptosis rate was reduced, which means that autophagy may interact with apoptosis to induce cell death .
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Cat. No.: HY-174506
Target:  

mRNA

Research Areas:  

Cancer

Human XCR1 mRNA encodes the human X-C motif chemokine receptor 1 (XCR1) protein, a G protein-coupled receptor that belongs to the CXC chemokine receptor family. XCR1 can transduce a signal by increasing the intracellular calcium ions level.
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Cat. No.: HY-122006
CAS No.: 384361-79-9
Research Areas:  

Cancer

NPD926 is a small molecule that targets glutathione and induces cancer cell death. NPD926 causes cellular glutathione depletion and subsequent generation of reactive oxygen species (ROS), thereby sensitizing fibroblasts to Xc- system inhibitors. NPD926 is a ROS inducer with anticancer activity. .
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Cat. No.: HY-P86499
Synonyms: Cystine/glutamate transporter; Amino acid transport system xc-; Calcium channel blocker resistance protein CCBR1; Solute carrier family 7 member 11; xcT;

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P71434
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Lymphotactin; ATAC; C motif chemokine 1; Cytokine SCM-1; Lymphotaxin; SCM-1-alpha; Small-inducible cytokine C1; xc chemokine ligand 1; LTN; SCYC1 and xcL1
Species:  
Source:  
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