19 Results for "

C5a Receptor

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "C5a Receptor" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-110136
CAS No.: 514814-49-4
Purity:  99.54%
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

PMX 205 is a potent complement C5a receptor (C5aR; CD88) antagonist.
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9
9 Cited Publications
Cat. No.: HY-138161
CAS No.: 2411440-41-8
Purity:  99.59%
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

JR14a is a potent thiophene antagonist of human complement C3a receptor. JR14a shows selectivity for the human C3a receptor over C5a receptor. JR14a can suppress C3aR-mediated inflammation .
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9
9 Cited Publications
Cat. No.: HY-106178
CAS No.: 219639-75-5
Purity:  99.98%
Synonyms: 3D53
PMX-53 (3D53) is a synthetic peptidic and a potent and orally active complement C5a receptor (CD88) antagonist with an IC50 of 20 nM. PMX-53 is also a low-affinity MrgX2 agonist that stimulates MrgX2-mediated mast cell degranulation. PMX-53 specifically binds to C5aR1 and does not bind to the second C5aR (C5L2) and C3aR. PMX-53 has anti-inflammatory, anticancer and antiatherosclerotic effects .
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6
6 Cited Publications
Cat. No.: HY-16992A
CAS No.: 405098-33-1
W-54011 is a potent and orally active non-peptide C5a receptor antagonist. W-54011 inhibits the binding of 125I-labeled C5a to human neutrophils with a Ki value of 2.2 nM. W-54011 also inhibits C5a-induced intracellular Ca 2+ mobilization, chemotaxis, and generation of ROS in human neutrophils with IC50s of 3.1 nM, 2.7 nM, and 1.6 nM, respectively .
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5
5 Cited Publications
Cat. No.: HY-148141
CAS No.: 1254036-23-1
Purity:  99.96%
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

JPE-1375 is a complement C5a receptor 1 (C5aR1) antagonist. JPE-1375 effectively inhibits polymorphonuclear leukocyte mobilization (EC50=6.9 μM) and reduces TNF levels (EC50=4.5 μM) in mice. JPE-1375 can be used in studies of autoimmune and inflammatory diseases .
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Cat. No.: HY-P5506
CAS No.: 144555-23-7
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

C5a Receptor agonist, W5Cha (Peptide 1) is a synthetic C5a receptor hexapeptide agonist. C5a Receptor agonist, W5Cha exhibits a IC50 of 0.07 μM for binding to C5a receptor on human neutrophil membranes. C5a Receptor agonist, W5Cha activates wild-type C5a receptor and induces Ca 2+ flux. C5a Receptor agonist, W5Cha can be used in studies related to neutrophil activation and inflammation .
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Cat. No.: HY-P99450
CAS No.: 2226393-85-5
Synonyms: IPH 5401; Anti-C5aR1 mAb

Target:  

Complement System

Research Areas:  

Inflammation/Immunology Cancer

Avdoralimab (IPH 5401) is a fully human IgGκ monoclonal antibody that targets the complement C5a receptor 1 (C5aR1) that prevents its binding to C5a. Avdoralimab can be used for complement-driven inflammatory diseases and solid tumours research .
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Cat. No.: HY-110060
CAS No.: 439571-48-9
Purity:  99.35%
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

NDT 9513727 is a potent, selective, orally active and competitive inverse agonist of the human C5aR (C5a receptor), with an IC50 of 11.6 nM. NDT 9513727 can be used for the research of human inflammatory diseases .
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Cat. No.: HY-160901
CAS No.: 1349637-14-4
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

CP-289,503 is an inhibitor of the complement C5a receptor with an IC50 of 1 μM. C5a acts as an activator of leukocytes and phagocytes during complement system activation. The C5a receptor can bind to C5a, which can stimulate the upregulation of cell surface integrins and degranulation of inflammatory cells, leading to endothelial cell damage. C5a receptor inhibitors can block C5a signaling and inhibit a variety of inflammatory diseases .
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Cat. No.: HY-112199
CAS No.: 1092847-21-6
Purity:  99.70%
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

CP-447697 is a lipophilic C5a receptor antagonist with an IC50 value of 31 nM. CP-447697 can be used for the research of inflammation .
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Cat. No.: HY-177094
CAS No.: 2489430-53-5
Synonyms: INF056
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

Izicopan (INF056) is a complement factor C5a receptor (C5aR1) antagonist. Izicopan inhibits C5a-induced calcium mobilization with an IC50 of 10-100 nM. Izicopan is applicable for the research of complement-mediated inflammatory responses .
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Cat. No.: HY-16384
CAS No.: 125228-51-5
Synonyms: Antibiotic L 156602; PD 124966
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

L-156602 is a C5a receptor antagonist. L-156602 inhibits inflammation, and the migration of monocytes and neutrophils to the infiltrating site in mouse inflammatory models. L-156602 suppresses the efferent phase of delayed-type hypersensitivity (DTH) .
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Cat. No.: HY-W130878
CAS No.: 1806-26-4
4-Octylphenol is a hormone disruptor that has gender-specific effects on male reproductive cells, significantly reducing the mitotic index and the number of spermatogonia. 4-Octylphenol can cause inflammatory damage to fish gills by activating the complement system through the C3a/C3aR axis and the C5a/C5aR1 axis, this leads to complement activation and causes immune suppression due to the imbalance between Th1/Th2 cells and regulatory T cells (Treg)/Th17 cells, as well as inflammatory damage via the Toll-like receptor 7 (Toll-like Receptor (TLR))/IκBα/NF-κB pathway .
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Cat. No.: HY-163379
CAS No.: 2365161-92-6
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

C5aR1 antagonist 2 (Compound 6a) is an orally active C5a receptor 1 (C5aR1) antagonist that shows efficacy in inhibiting the C5a-induced neutrophil count increase. C5aR1 antagonist 2 is potent in the DISCO and migration assays, with IC50 values of 21 and 3 nM, respectively. C5aR1 antagonist 2 can be used for the research of acute and chronic inflammatory diseases .
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Cat. No.: HY-163378
CAS No.: 2365325-67-1
Target:  

Complement System

Research Areas:  

Inflammation/Immunology

C5aR1 antagonist 1 (Compound 7e) is an orally active C5a receptor 1 (C5aR1) antagonist. C5aR1 antagonist 1 is active in DISCO and migration assays, with IC50 values of 38 nM and 17 nM, respectively. C5aR1 antagonist 1 can be used for the research of acute and chronic inflammatory diseases .
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Cat. No.: HY-P5509
CAS No.: 230968-98-6
Target:  

Peptides

Research Areas:  

Others

C5aR1 antagonist peptide is a biological active peptide. (This linear peptide is derived from the C-terminus of the chemokine, complement fragment 5 anaphylatoxin (C5a). This peptide functions to inhibit C5a binding and function at human and rat C5a receptors. C5a is crucial to triggering cellular immune responses and its overexpression is involved in arthritis, Alzheimer’s disease, cystic fibrosis, systemic lupus erythematosus, and other immunoinflammatory diseases.)
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Cat. No.: HY-P700398
Purity:  Purity analysis by SDS-PAGE is not available for VLP proteins.
Synonyms: complement component 5a Receptor 1; C5R1, complement component 5 Receptor 1 (C5a ligand); C5a anaphylatoxin chemotactic Receptor; C5a; C5aR; CD88; C5a-R; C5a ligand; C5a anaphylatoxin Receptor; complement component 5 Receptor 1; C5R1;
Species:  
Source:  
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Cat. No.: HY-183414
CAS No.: 1257868-45-3
Target:  

Complement System

Research Areas:  

Endocrinology

C5aR antagonist-1 is a potent C5aR antagonist with an IC50 of < 5 nM. C5aR antagonist-1 is applicable to the research of crescentic and necrotizing glomerular lesions .
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Cat. No.: HY-180411
CAS No.: 146461-98-5
Target:  

Leukotriene Receptor

Research Areas:  

Inflammation/Immunology

SM-15178 is a potent, orally active and selective leukotriene B4 (LTB4) receptor antagonist with an IC50 of 0.30 μM. SM-15178 attenuates LTB4 (HY-107608)-induced neutrophil accumulation in mouse skin and bronchoconstriction in guinea pigs. SM-15178 emonstrates significant anti-inflammatory efficacy across multiple animal models of inflammation. SM-15178 can be used for the research of chronic inflammatory diseases such as inflammatory bowel disease, psoriasis, and asthma .
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