168 Results for "

Platelet activating factor

" in MedChemExpress (MCE) Product Catalog:
Products (168)

168 Results for "Platelet activating factor" in MCE Product Catalog:

Cat. No.: HY-P811810
Synonyms: Sphingomyelin phosphodiesterase 2, Lyso-Platelet-activating factor-phospholipase C, Neutral sphingomyelinase, Lyso-PAF-PLC, N-SMase, nSMase, nSMase1, SMPD2

Host:  

Rabbit

Application:  

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

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-180341
CAS No.: 179912-83-5
UR-12633 is a platelet-activating factor (PAF) antagonist. UR-12633 can effectively reverse hypotension, inhibit coagulation abnormalities, increased vascular permeability, and metabolic disorders in rodent models of endotoxic shock. UR-12633 can be used for research on endotoxic shock .
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Cat. No.: HY-W676872
CAS No.: 3791-76-2
Target:  

COX Parasite

Research Areas:  

Infection Inflammation/Immunology

Dihydroflavokawin B is a selective COX-1 inhibitor with an IC50 of 1.22 μM. Dihydroflavokawin B weakly inhibits COX-2 and 5-LOX. Dihydroflavokawin B inhibits promastigote forms of Leishmania panamensis and Leishmania braziliensis. Dihydroflavokawin B inhibits rabbit platelet aggregation induced by Arachidonic acid, platelet activating factor, and adenosine diphosphate. Dihydroflavokawin B exhibits in vitro anti-inflammatory activity. Dihydroflavokawin B can be used for the research of leishmaniasis .
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Cat. No.: HY-P70252
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: LCAT; Phosphatidylcholine--Sterol O-Acyltransferase; Lecithin-Cholesterol Acyltransferase; Platelet-activating factor Acetylhydrolase; Phosphatidylcholine-Sterol Acyltransferase; PAF Acetylhydrolase; Phospholipid-Cholesterol Acyltransferase; Testicular Se
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P77979
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: LCAT; Phosphatidylcholine--Sterol O-Acyltransferase; Lecithin-Cholesterol Acyltransferase; Platelet-activating factor Acetylhydrolase; Phosphatidylcholine-Sterol Acyltransferase; PAF Acetylhydrolase; Phospholipid-Cholesterol Acyltransferase; Testicular Se
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-P811810A
Synonyms: Sphingomyelin phosphodiesterase 2, Lyso-Platelet-activating factor-phospholipase C, Neutral sphingomyelinase, Lyso-PAF-PLC, N-SMase, nSMase, nSMase1, SMPD2

Host:  

Rabbit

Application:  

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

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-137257
CAS No.: 91575-58-5
Purity:  ≥99.0%
Synonyms: C-PAF
Carbamyl-PAF (C-PAF) is a metabolically stable platelet-activating factor analog and PAF receptor agonist that activates G protein-coupled PAF receptors, triggering calcium mobilization, NF-κB activation, and downstream signaling, thereby inducing neutrophil recruitment, inflammatory responses, and ROS generation. Carbamyl-PAF is used in research on obesity, pulmonary inflammation, Zellweger syndrome, and non-melanoma skin cancer .
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Cat. No.: HY-108908R
CAS No.: 122956-68-7
Synonyms: UK-74505 (Standard)
(Rac)-Modipafant (Standard) is the analytical standard of (Rac)-Modipafant (HY-108908). This product is intended for research and analytical applications. (Rac)-Modipafant (UK-74505) is an orally active, selective, long-acting irreversible platelet activating factor receptor (PAFR) antagonist. (Rac)-Modipafant prevents dengue infection .
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Cat. No.: HY-134101
CAS No.: 78858-42-1
2-O-Ethyl PAF C-16 is a homolog of PAF and a competitive ligand for PAF receptor (Platelet-activating Factor Receptor (PAFR)). 2-O-Ethyl PAF C-16 inhibits the binding of the PAF antagonist WEB 2086 (HY-108634) to the PAF receptor with an IC50 of 21 nM .
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Cat. No.: HY-48917
CAS No.: 15049-93-1
Target:  

Phospholipase Apoptosis

Research Areas:  

Inflammation/Immunology

C10 Bisphosphonate is an acid sphingomyelinase (aSMase) inhibitor with an IC50 of 0.02 μM in rats. C10 Bisphosphonate inhibits Dexamethasone (HY-14648)-induced cell apoptosis (apoptosis) and alleviates platelet-activating factor (PAF)-induced pulmonary edema. C10 Bisphosphonate can be used for the research of pulmonary edema .
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Cat. No.: HY-106899A
CAS No.: 143445-03-8
Synonyms: (rel)-L-680573
Research Areas:  

Others

(rel)-MK 287 ((rel)-L-680573) is a relative configuration of MK 287. MK 287 is a potent, selective and orally active antagonist of platelet-activating factor receptor (PAFR). MK 287 can inhibit [3H]C18-PAF binding to human platelet, polymorphonuclear leukocyte (PMN) and lung membranes with K1 values of 6.1, 3.2, and 5.49 nM, respectively. MK 287 can inhibit PAF-induced aggregation of platelets in plasma or gel-filtered platelets and elastase release from PMNs with ED50 values of 56, 1.5 and 4.4 nM. MK 287 can be used for the research of cardiovascular disease, such as thrombosis .
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Cat. No.: HY-102004R
CAS No.: 412950-08-4
Synonyms: SB 659032 (Standard)
Rilapladib (Standard) is the analytical standard of Rilapladib (HY-102004). This product is intended for research and analytical applications. Rilapladib (SB 659032) is a selective Lp-PLA2 (lipoprotein-associated phospholipase A2) inhibitor with an IC50 of 230 pM . Rilapladib (SB 659032) is also a PAFR (Platelet Activating Factor Receptor) antagonist .
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Cat. No.: HY-130345
CAS No.: 74389-69-8
Purity:  99.00%
C18-PAF, octadecane PAF, is the ligand of platelet-activating factor and PAF G protein-coupled receptor (PAFR). C18-PAF has renovasodilator properties and antihypertensive lipid properties. C18-PAF increases renal blood flow and causes dose-dependent systemic hypotension .
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Cat. No.: HY-134070
CAS No.: 78858-44-3
Synonyms: ET-18-O-OCH3
Target:  

TNF Receptor

Research Areas:  

Inflammation/Immunology

2-O-Methyl PAF C-16 (ET-18-O-OCH3), a structural analog of the mediator of inflammation platelet-activating factor (PAF), is a cytotoxic ether lipid. 2-O-Methyl PAF C-16 stimulates TNF-α release in murine macrophages .
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Cat. No.: HY-P992152
CAS No.: 897936-89-9
Synonyms: NN-1731

Research Areas:  

Cardiovascular Disease

Vatreptacog alfa is a recombinant hFVIIa analog, differing from native FVIIa by three amino acid substitutions (V158D, E296V and M298Q) in the protease domain. Vatreptacog alfa exhibits enhanced tissue factor-independent enzymatic activity toward activated platelets. Vatreptacog alfa can be used in the research of hemophilia .
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Cat. No.: HY-138053
CAS No.: 92989-99-6
Synonyms: Ristomycin III
Target:  

Antibiotic

Research Areas:  

Cardiovascular Disease Infection

Ristocetin A (sulfate) (Ristomycin III) is a glycopeptide antibiotic that binds to von Willebrand factor (VWF) and bacterial cell wall components. Ristocetin A (sulfate) interferes with the biosynthesis of bacterial peptidoglycan by inhibiting transpeptidation. As an inducer of platelet adhesion and aggregation, Ristocetin A (sulfate) drives conformational changes by binding to the A1 domain of VWF, thereby activating downstream signaling pathways and promoting cytoskeletal rearrangement. Ristocetin A (sulfate) not only enhances platelet adhesion and spreading on immobilized VWF, but also induces the formation of asymmetric dimers with anticooperativity between platelets and plasma VWF. Ristocetin A (sulfate) is widely used in studies related to thromboembolic diseases and bacterial infections .
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Cat. No.: HY-14162
CAS No.: 936349-47-2
Target:  

FLAP

Research Areas:  

Inflammation/Immunology

AM103 (free acid) is a selective FLAP inhibitor that can block the first step of the LT pathway, which is 5-LO activation. AM103 (free acid) can inhibit the production of LTB4 and cysteinyl leukotrienes (CysLT). AM103 (free acid) has anti-inflammatory activity in a mouse model of chronic lung inflammation and can extend the survival time of mice injected with platelet-activating factor. AM103 (free acid) can be used for research on respiratory diseases such as asthma .
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Cat. No.: HY-19125
CAS No.: 127279-06-5
BN-50726 is a potent platelet-activating factor (PAF) receptor antagonist. BN-50726 inhibits PAF-induced effects (e.g., [3H]-serotonin release and hypotension) (IC50=5.40 nM). BN-50726 is promising for research of PAF-mediated pathological processes (e.g., inflammation, anaphylaxis, hypotension) .
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Cat. No.: HY-182434
CAS No.: 97012-61-8
Target:  

Phosphatase FAP

Research Areas:  

Inflammation/Immunology

CL 118326 is a potent, selective, competitive inhibitor of mammalian pancreatic phospholipase A2 (PLA2) and a weak antagonist of platelet-activating factor receptor (PAF receptor). CL 118326 competitively inhibits mammalian pancreatic PLA2 (porcine: IC50 = 1.55 μg/mL), and shows no activity against snake venom or bee venom PLA2. CL 118326 inhibits PAF-induced and thrombin-induced platelet aggregation, as well as the release of leukotriene (LTC4) and histamine from basophil-enriched leukocytes. CL 118326 can be used for research on inflammation and allergic reactions .
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Cat. No.: HY-100164R
CAS No.: 114606-56-3
Synonyms: MKS 492 (Standard)
SDZ-MKS 492 (Standard) is the analytical standard of SDZ-MKS 492 (HY-100164). This product is intended for research and analytical applications. SDZ-MKS 492 (MKS 492) is a selective inhibitor of cyclic GMP-inhibited phosphodiesterase (type III PDE). SDZ-MKS 492 inhibits antigen- or platelet activating factor (PAF)-induced bronchoconstriction and allergic reactions in guinea pigs and rats .
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