Fosfolipase
As fosfolipases são um grupo de enzimas que hidrolisam fosfolipídios em ácidos graxos e outras substâncias lipofílicas, desempenhando um papel crítico na biologia das membranas e na geração de moléculas sinalizadoras. Inibidores de fosfolipases são usados para estudar seu papel em doenças inflamatórias, distúrbios cardiovasculares e neurodegeneração. Esses inibidores também são valiosos na exploração de vias de sinalização lipídica e suas implicações nos mecanismos de doenças. Na CymitQuimica, oferecemos uma variedade de inibidores de fosfolipases para apoiar sua pesquisa em inflamação, metabolismo lipídico e sinalização celular.
Foram encontrados 82 produtos de "Fosfolipase"
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Omeprazole
CAS:<p>Omeprazole (Losec) is a proton pump inhibitor (PPI), Omeprazole(Losec) is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor.</p>Fórmula:C17H19N3O3SPureza:98.43% - 98.48%Cor e Forma:White SolidPeso molecular:345.42ML349
CAS:<p>ML349 is an inhibitor of LYPLA2 (IC50: 144 nM). ML349 is an effective and specific acyl protein thioesterase 2 (APT-2) inhibitor (Ki: 120 nM).</p>Fórmula:C23H22N2O4S2Pureza:99.59% - 99.88%Cor e Forma:SolidPeso molecular:454.56Tris(2,4-di-tert-butylphenyl)phosphate
CAS:<p>Tris(2,4-di-tert-butylphenyl)phosphate (TDTBPP) inhibits secretory phospholipase A2 (sPLA2) with anti-inflammatory effect. Cost-effective and quality-assured.</p>Fórmula:C42H63O4PPureza:99.73%Cor e Forma:SolidPeso molecular:662.92Lp-PLA2-IN-1
CAS:<p>Lp-PLA2-IN-1 suppresses Lp-PLA2, aiding in treating atherosclerosis and Alzheimer's.</p>Fórmula:C21H17F5N4O3Pureza:99.60%Cor e Forma:SolidPeso molecular:468.38Lansoprazole
CAS:<p>Lansoprazole (A-65006) is a 2, 2, 2-trifluoroethoxypyridyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON</p>Fórmula:C16H14F3N3O2SPureza:99.18% - 99.84%Cor e Forma:White Crystalline PowderPeso molecular:369.36Niflumic acid
CAS:<p>Niflumic acid (Nifluril) is a Ca2+-activated Cl- channel blocker and an analgesic and anti-inflammatory agent used in the therapy of rheumatoid arthritis.</p>Fórmula:C13H9F3N2O2Pureza:99.47%Cor e Forma:SolidPeso molecular:282.22nSMase2-IN-1
<p>nSMase2-IN-1 is an orally active inhibitor of Neutral sphingomyelinase 2 (nSMase2) with a potent IC50 value of 0.13 ± 0.06 μM.</p>Fórmula:C12H17N5OPureza:98%Cor e Forma:SolidPeso molecular:247.3DPTIP hydrochloride
CAS:<p>DPTIP hydrochloride is a potent inhibitor of neutral sphingomyelinase (N-SMase 2) that can cross the blood-brain barrier. It acts as an exosome inhibitor with an IC50 value of 30 nM.</p>Fórmula:C21H19ClN2O3SCor e Forma:SolidPeso molecular:414.91A3373
CAS:<p>A3373 is a novel inhibitor targeting both Phospholipase D1 (PLD1) and Phospholipase D2 (PLD2), demonstrating half maximal inhibitory concentrations (IC50) of</p>Fórmula:C17H9F7N2OPureza:98%Cor e Forma:SoildPeso molecular:390.26BIRM 271
CAS:<p>BIRM 271 is a novel arachidonic acid release inhibitor that blocks leukotriene B4 and platelet-activating factor biosynthesis in human neutrophils.</p>Fórmula:C21H25N3OPureza:99.64%Cor e Forma:SoildPeso molecular:335.44AACOCF3
CAS:<p>AACOCF3 (Arachidonyl trifluoromethyl ketone) is a cell-permeable trifluoromethyl ketone analog of arachidonic acid.</p>Fórmula:C21H31F3OPureza:99% - 99%Cor e Forma:Yellow LiquidPeso molecular:356.47Compound 48/80 trihydrochloride
CAS:<p>Compound 48/80 trihydrochloride (C48/80 trihydrochloride) 是 N-甲基对甲氧基苯乙胺和甲醛发生缩合反应后的混合物。Compound 48/80 trihydrochloride 是一种肥大细胞 (mast cell) 脱颗粒剂和组胺 (histamine) 释放剂。Compound 48/80 trihydrochloride 对人血小板磷脂酰肌醇特异性磷脂酶 C (phosphatidylinositol-specific phospholipase C) 活性有抑制作用。</p>Fórmula:C32H48Cl3N3O3Pureza:98%Cor e Forma:SolidPeso molecular:629.11-Myristoyl-2-Linoleoyl-sn-glycero-3-PC
CAS:<p>1-Myristoyl-2-Linoleoyl-sn-glycero-3-PC is a phospholipid identified in human plasma, characterized by the presence of Myristic acid and Linoleic acid at the sn-1 and sn-2 positions, respectively.</p>Fórmula:C40H76NO8PCor e Forma:SolidPeso molecular:730.01A4333
<p>A4333, a biotinylated derivative of A3373, selectively inhibits Phospholipase D1 (PLD1) while sparing PLD2.</p>Pureza:98%Cor e Forma:Odour SolidDPTIP
CAS:<p>DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM.</p>Fórmula:C21H18N2O3SPureza:99.88%Cor e Forma:SolidPeso molecular:378.44PLA2-IN-1
<p>PLA2-IN-1 (Compound 7) is a potent and selective inhibitor of phospholipase A (PLA2) with an IC50 value of 1 nM. It effectively inhibits PLA2-induced coagulation disorders in vitro and shows potential for use as an antidote for snake bites caused by cobra venom.</p>Cor e Forma:Odour SolidVU533
CAS:<p>VU533 is a NAPE-PLD activator, EC50=0.30 µM, boosts macrophage activity, potential in cardiometabolic diseases.</p>Fórmula:C21H22FN3O3S2Pureza:99.08%Cor e Forma:SolidPeso molecular:447.55LEI110
CAS:<p>LEI110 inhibits PLA2G16 and HRASLS enzymes, Ki 20 nM, selectively targets related thiol hydrolases.</p>Fórmula:C25H23F3N2O3Pureza:98.66% - 98.8%Cor e Forma:SolidPeso molecular:456.46ASM-IN-3
CAS:<p>ASM-IN-3 (Compound 21b) is a selective acid sphingomyelinase (ASM) inhibitor that can penetrate the blood-brain barrier, with an IC50 of 3.37 μM against purified human ASM. By inhibiting ASM activity in the hippocampus and promoting neurogenesis, ASM-IN-3 alleviates depressive-like behavior in reserpine-induced depressive rats.</p>Fórmula:C17H13ClN2O4Cor e Forma:SolidPeso molecular:344.75SB-435495
CAS:<p>SB-435495 is a compound characterized by its potent, selective, reversible, and non-covalent inhibition of Lp-PLA2, demonstrating an IC50 value of 0.06 nM.</p>Fórmula:C38H40F4N6O2SPureza:99.07%Cor e Forma:SolidPeso molecular:720.82
