Esters Phospholipase Suppliers USA
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Product | Description | |
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12:0 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
13:0 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
14:0 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
16:0 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
16:0 Diether PC Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
18:0 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
18:0 Diether PC Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
18:1 Diether PC:Chol (70:30) Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
18:1 Diether PC Liposomes Quick inquiry Where to buy Suppliers range | Ether lipids are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. One hand, the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH, one the other hand, stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions. Besides, the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases. Uses: Control liposomes, membrane biology. Group: Plain liposome. | |
2-Chloro-1,3,2-dioxaphospholane-2-oxide Quick inquiry Where to buy Suppliers range | 2-Chloro-1,3,2-dioxaphospholane-2-oxide is used in the synthesis of α -naphthyl phosphoryl choline as a method to detect phospholipase C activity. Group: Biochemicals. Alternative Names: Ethylene phosphorochloridate; Phosphorochloridic Acid, Cyclic Ethylene Ester; 2-Chloro-2-oxido-1,3,2-dioxaphospholane; 2-Chloro-2-oxo-1,3,2-dioxaphospholane; Cyclic ethylene phosphorochloridate; Ethylene Chlorophosphate. Grades: Highly Purified. CAS No. 6609-64-9. Pack Sizes: 5g, 25g. Molecular Formula: C?H?ClO?P, Molecular Weight: 142.48. US Biological Life Sciences. | Worldwide |
2-Nitro-4-carboxyphenyl N,N-Diphenylcarbamate Quick inquiry Where to buy Suppliers range | 2-Nitro-4-carboxyphenyl N,N-Diphenylcarbamate is an inhibitor of Phospholipase C. Also functions in the inhibition of blood coagulation factors II, VII, IX, and X, serine esterase inhibition, and plant-growth regulator. Group: Biochemicals. Grades: Highly Purified. CAS No. 10556-88-4. Pack Sizes: 100mg, 250mg. Molecular Formula: C20H14N2O6, Molecular Weight: 378.33. US Biological Life Sciences. | Worldwide |
all cis-5,8,11,14,17-Eicosapentaenoic Acid Ethyl Ester Quick inquiry Where to buy Suppliers range | all cis-5,8,11,14,17-Eicosapentaenoic Acid Ethyl Ester is an omega-3 fatty acid agent. It is important polyunsaturated fatty acid of the marine food chain. It serves as a precursor of the prostaglandin-3 and thromboxane-3 families. It differs from arachidonic acid by the extra double bond between the third and fourth carbons from the "methyl end" of the molecule. It reduces non-high-density lipoprotein cholesterol, lipoprotein-associated phospholipase A2, apolipoprotein B, very low-density lipoprotein cholesterol, and total cholesterol. It reduces the TG levels and improved other lipid parameters without significantly increasing the LDL cholesterol levels. It is used in combination with changes in diet to lower triglyceride levels in adults with severe (≥ 500 mg/dL) hypertriglyceridemia. It has anti-inflammatory and cardiovascular benefits. It may alter the expression of genes related to fatty acid metabolism. It was the second class of fish oil-based drug to be approved for use as a drug. It was developed by Amarin Corporation. It has been listed. Uses: All cis-5,8,11,14,17-eicosapentaenoic acid ethyl ester reduces non-high-density lipoprotein cholesterol, lipoprotein-associated phospholipase a2, apolipoprotein b, very low-density lipoprotein cholesterol, and total cholesterol. it has anti-inflammatory and cardiovascular benefits. Synonyms: Eicosapentaenoic Acid Ethyl Ester;(5Z,8Z,11Z,14Z,17Z)-5,8,11,14,17-Eicosapentaenoic Acid Ethyl Ester;(all-Z)-5,8,11,14,17-Eicosapentaenoic Acid Ethyl Ester;cis-Eicosapentaenoic Acid Ethyl Ester;Ethyl icosapentate; Epadel;Ethyl eicosapentaenoate;Vascepa;EPA ethyl ester;Ethyl (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoate. Grades: >98%. CAS No. 86227-47-6. Molecular formula: C22H34O2. Mole weight: 330.50. | |
AX 048 Quick inquiry Where to buy Suppliers range | Ethyl 4-[(2-oxohexadecanoyl)amino]butanoate (AX 048) is a PLA2 (Phospholipase A2) and PGE2 (Prostaglandin E2) inhibitor. PLA2 is known as calcium-dependent cytosolic PLA2 (cPLA2), which selectively releases arachidonic acid from membrane phospholipids. It plays a central role in initiating the synthesis of prostaglandins and leukotrienes. This compound also contains a specific affinity for group IVA cPLA2 which moderates antihyperalgesia effects. Synonyms: AX-048; AX 048; Butanoic acid, 4-((1,2-dioxohexadecyl)amino)-, ethyl ester; UNII-8782Z45DLV; 8782Z45DLV; Butanoic acid, 4-[(1,2-dioxohexadecyl)amino]-, ethyl ester; ethyl 4-(2-oxohexadecanoylamino)butanoate; ethyl 4-(2-oxohexadecanamido)butanoate; CHEMBL574723; SCHEMBL4781039; DTXSID60236282; AKOS040755666; ethyl 4-[(2-oxohexadecanoyl)amino] butanoate; Q27269809; 4- [(1, 2- dioxohexadecyl)amino]- butanoic acid, ethyl ester. Grades: ≥98%. CAS No. 873079-69-7. Molecular formula: C22H41NO4. Mole weight: 383.6. | |
Caloporoside Quick inquiry Where to buy Suppliers range | Caloporoside is a phospholipase C inhibitor produced by Caloporus dichrous. It has only weak antifungal and bacterial activity, and has the effect of selectively inhibiting phospholipase C. Synonyms: 2-O-Acetyl-5-O-(2-O-acetylhexopyranosyl)-2-C-[17-(2-carboxy-3-hydroxyphenyl)heptadecan-2-yl]hexonic acid; D-Mannonic acid, 5-O-(2-O-acetyl-beta-D-mannopyranosyl)-, 16-(2-carboxy-3-hydroxyphenyl)-1-methylhexadecyl ester, 2-acetate, (R)-. CAS No. 160471-36-3. Molecular formula: C40H64O17. Mole weight: 816.92. | |
CAY10650 Quick inquiry Where to buy Suppliers range | Cytosolic phospholipase A2α (cPLA2α) specifically catalyzes the hydrolysis of arachidonic acid from the sn-2-ester position of membrane phospholipids, playing a central role in initiating the synthesis of prostaglandins and leukotrienes, both important mediators of the inflammatory process. CAY10650 is a highly potent (IC50 = 12 nM) cPLA2α inhibitor. It demonstrates strong anti-inflammatory effects when applied topically at a dose of 0.1 mg/ear in a mouse model of acute irritant contact dermatitis. Synonyms: CAY 10650; CAY-10650. Grades: >98%. CAS No. 1233706-88-1. Molecular formula: C28H25NO6. Mole weight: 471.5. | |
Ethyl arachidonate Quick inquiry Where to buy Suppliers range | Arachidonic acid (AA) is an unsaturated omega-6 fatty acid constituent of the phospholipids of cell membranes. Phospholipase A2 releases AA from the membrane phospholipids in response to inflammation. Uses: Arachidonic acid (aa) is an unsaturated omega-6 fatty acid constituent of the phospholipids of cell membranes. phospholipase a2 releases aa from the membrane phospholipids in response to inflammation. Synonyms: Arachidonic acid ethyl ester. Grades: 95%. CAS No. 1808-26-0. Molecular formula: C22H36O2. Mole weight: 332.52. | |
Rilapladib Quick inquiry Where to buy Suppliers range | Rilapladib is the third genomics-derived small molecule drug as a lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor which is an enzyme associated with the formation of atherosclerotic plaques. Uses: 1-alkyl-2-acetylglycerophosphocholine esterase inhibitors. Synonyms: GSK 659032; GSK659032; GSK-659032; SB-659032; SB659032; SB 659032; GTPL7376; GTPL-7376; GTPL 7376; D05728. Grades: ≥98%. CAS No. 412950-08-4. Molecular formula: C40H38F5N3O3S. Mole weight: 735.81. |