66 Results for "

CCL-2

" in MedChemExpress (MCE) Product Catalog:
Products (66)

66 Results for "CCL-2" in MCE Product Catalog:

92
92 Publications Verification
Cat. No.: HY-B0673
CAS No.: 53179-13-8
Synonyms: AMR69
Target:  

TGF-beta/Smad CCR

Research Areas:  

Inflammation/Immunology Cancer

Pirfenidone (AMR69) is an antifibrotic agent that attenuates CCL2 and CCL12 production in fibrocyte cells. Pirfenidone has growth-inhibitory effect and reduces TGF-β2 protein levels in human glioma cell lines. Pirfenidone also has anti-inflammatory activities [2] .
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29
29 Cited Publications
Cat. No.: HY-B0498
CAS No.: 130641-38-2
Synonyms: AF2838
Bindarit (AF2838) is a selective inhibitor of the monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, and no effect on other CC and CXC chemokines such as MIP-1α/CCL3, MIP-1β/CCL4, MIP-3/CCL23. Bindarit also has anti-inflammatory activity .
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9
9 Cited Publications
Cat. No.: HY-P7764
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuCCL2; C-C motif chemokine 2; Monocyte chemoattractant protein 1; Monocyte chemotactic protein 1; MCP-1; CCL2; Scya2
Species:  
Source:  
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9
9 Cited Publications
Cat. No.: HY-P7237
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuMCP-1/CCL2; C-C motif chemokine 2; MCAF; MCP-1; SCYA2
Species:  
Source:  
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4
4 Cited Publications
Cat. No.: HY-P99188
CAS No.: 915404-94-3
Synonyms: CNTO 888

Target:  

CCR

Research Areas:  

Cancer

Carlumab (CNTO 888) is a human anti-CCL2 (chemokine ligand 2) monoclonal antibody. Carlumab binds and neutralises profibrotic activities of human CCL2. Carlumab inhibits tumor growth by reducing macrophage infiltration and decreasing tumor microvascular density. Carlumab can be used for the research of cancer, suah as prostate cancer [2].
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2
2 Cited Publications
Cat. No.: HY-P7235
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuMCP-1/CCL2; C-C motif chemokine 2; MCAF; MCP-1; SCYA2
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P990297

Target:  

CCR HIV

Anti-Mouse/Rat/Human CCL2/MCP-1 Antibody (2H5) is an anti-mouse/rat/human CCL2/MCP-1 IgG monoclonal antibody. Anti-Mouse/Rat/Human CCL2/MCP-1 Antibody (2H5) can reverse the immunosuppressive microenvironment by blocking the CCL2 signaling pathway. Anti-Mouse/Rat/Human CCL2/MCP-1 Antibody (2H5) can reduce the secretion of IFN-γ and the infiltration of macrophages. CCL2/MCP-1 Antibody (2H5) can reduce the amount of HIV virus by increasing the proportion of T cells. Anti-Mouse/Rat/Human CCL2/MCP-1 Antibody (2H5) can be used for researches on inflammation conditions, virus infection and cancer such as inflammatory bowel disease (IBD), hepatocellular carcinoma (HCC) and HIV [2] .
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1
1 Cited Publications
Cat. No.: HY-148100
CAS No.: 1390630-22-4
Synonyms: NOX-E36
Target:  

CCR

Research Areas:  

Inflammation/Immunology Cancer

Emapticap pegol (NOX-E36) is a inhibitor of pro-inflammatory chemokine C-C motif-ligand 2 (CCL2). Emapticap pegol is a 40-nucleotide oligonucleotide aptamer, displays different Spiegelmers (L-RNA aptamer) isform in human (NOX-E36) and mouse (mNOX-E36). mNOX-E36 is a murine-specific analogue of NOX-E36, an anti-MCP-1 L-RNA aptamer that was previously shown to attenuate liver fibrosis in mice [2] .
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1
1 Cited Publications
Cat. No.: HY-B1076
CAS No.: 2668-66-8
Synonyms: HMS; 6α-Methyl-11β-hydroxyprogesterone
Target:  

VEGFR CCR STAT

Research Areas:  

Neurological Disease

Medrysone (HMS; 6α-Methyl-11β-hydroxyprogesterone) is a STAT6 modulator and M2 macrophage polarization inducer. Medrysone enhances IL-4-triggered STAT6 activation, upregulates the expression of M2 markers, and promotes the secretion of VEGF and CCL2. Medrysone also enhances the pro-migratory activity of M2-like macrophages toward endothelial cells. By regulating macrophage polarization and related repair pathways, Medrysone significantly promotes corneal wound repair in a rat mechanical injury model. Medrysone can be used for research related to corneal injury .
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1
1 Cited Publications
Cat. No.: HY-148100A
Purity:  91.38%
Synonyms: NOX-E36 sodium
Target:  

CCR

Research Areas:  

Cancer

Emapticap pegol sodium is a inhibitor of pro-inflammatory chemokine C-C motif-ligand 2 (CCL2). Emapticap pegol sodium is a 40-nucleotide oligonucleotide aptamer, displays different Spiegelmers (L-RNA aptamer) isform in human (NOX-E36) and mouse (mNOX-E36) [2] .
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1
1 Cited Publications
Cat. No.: HY-P78173
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: C-C motif chemokine 2; CCL2; HC11; MCAF; MCP-1; HSMCR30; MCP1; SCYA2; SMC-CF; GDCF-2
Species:  
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1
1 Cited Publications
Cat. No.: HY-P7236
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtMCP-1/CCL2; C-C motif chemokine 2; MCAF; MCP-1; SCYA2
Species:  
Rat
Source:  
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Cat. No.: HY-B1203
CAS No.: 127-31-1
Synonyms: 9α-Fludrocortisone; 9α-Fluorcortisol
Fludrocortisone (9α-Fludrocortisone) is an orally active mineralocorticoid and glucocorticoid receptor agonist. Fludrocortisone suppresses pro-inflammatory cytokine expression, reduces CCL2, IL-6, IL-8 levels, upregulates mineralocorticoid receptor (MR) expression, induces PI3K/Akt, GSK-3β, CREB, ERK1/2, mTOR phosphorylation, blocks Tau hyperphosphorylation, prevents apoptosis, promotes survival and proliferation, enhances renal sodium and water transport, increases plasma volume and blood pressure, reduces plasma potassium and renin activity, stimulates erythropoietin expression, modulates uterine receptivity genes, and reverses PP242-induced MUC1 upregulation. Fludrocortisone can be used for the research of congenital adrenal hyperplasia, postural hypotension, and adrenal insufficiency [2] .
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Cat. No.: HY-P99781
CAS No.: 1610761-46-0
Synonyms: MLN-1202

Target:  

CCR

Research Areas:  

Inflammation/Immunology Cancer

Plozalizumab (MLN-1202) is a humanized anti-CCR2 IgG1 monoclonal antibody. Plozalizumab blocks the recruitment of myeloid cells to the tumor microenvironment by inhibiting the CCL2/CCR2 axis. In addition, Plozalizumab also ameliorates synovial inflammation in rheumatoid arthritis. Plozalizumab can be used in the research of malignant melanoma and bone metastasis-related cancers. Recommended isotype control: Human IgG1 kappa, Isotype Control (HY-P99001) [2] .
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Cat. No.: HY-B0673R
CAS No.: 53179-13-8
Synonyms: AMR69 (Standard)
Pirfenidone (Standard) is the analytical standard of Pirfenidone. This product is intended for research and analytical applications. Pirfenidone (AMR69) is an antifibrotic agent that attenuates CCL2 and CCL12 production in fibrocyte cells. Pirfenidone has growth-inhibitory effect and reduces TGF-β2 protein levels in human glioma cell lines. Pirfenidone also has anti-inflammatory activities [2] .
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Cat. No.: HY-B0673S1
CAS No.: 1093951-85-9
Synonyms: LYT-100; AMR69-d3
Deupirfenidone-d3 is the deuterium labeled Pirfenidone (HY-B0673). Pirfenidone (AMR69) is an antifibrotic agent that attenuates CCL2 and CCL12 production in fibrocyte cells. Pirfenidone has growth-inhibitory effect and reduces TGF2 protein levels in human glioma cell lines. Pirfenidone also has anti-inflammatory activities [2] .
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Cat. No.: HY-B0673S
CAS No.: 1020719-62-3
Synonyms: AMR69-d5
Pirfenidone-d5 (AMR69-d5) is a deuterium labeled Pirfenidone. Pirfenidone is an antifibrotic agent that attenuates CCL2 and CCL12 production in fibrocyte cells. Pirfenidone has growth-inhibitory effect and reduces TGF2 protein levels in human glioma cell lines. Pirfenidone also has anti-inflammatory activities [2] .
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Cat. No.: HY-170415
CAS No.: 1700655-93-1
Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

EGR-1 IN-3 (Compound 36) is an early growth response 1 (EGR-1)-DNA binding disruptor. EGR-1-IN-3 inhibits TNFα-induced binding of EGR-1 to DNA and expression of genes associated with inflammation (such as TSLP, IL-31, IL-6 and CCL2). EGR-1-IN-3 can be used in the study of inflammatory diseases .
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Cat. No.: HY-W013675
CAS No.: 824-46-4
Target:  

HSP

Research Areas:  

Inflammation/Immunology

2-Methoxyhydroquinone is a phenolic compound that reduces TNF-α-induced production of chemokine (C-C motif) ligand 2 (CCL2) with an IC50 value of 64.3 µM. 2-Methoxyhydroquinone is also a precursor in the synthesis of the Hsp90 inhibitor Geldanamycin (HY-15230) [2].
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Cat. No.: HY-160552
CAS No.: 2956402-64-3
Target:  

Liposome

Research Areas:  

Others

244cis, a piperazine-containing ionizable cationic lipid, has been used to generate lipid nanoparticles (LNPs). LNPs containing 244cis and coated with mRNA reporter gene were specifically accumulated in mouse lungs compared with LNPs containing SM-102. Induces a decrease in serum chemokine (C-C motif) ligand 2 (CCL2) levels .
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