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1-Palmitoyl -2-pyrene decanoyl phosphatidyl choline-d9 is labelled 1-Palmitoyl -2-pyrene decanoyl phosphatidyl choline (P155100) which is a fluorescent phospholipid used to study the mechanism of spontaneous phospholipid transfer between single-walled phospholipid vesicles (liposomes) and other membrane interactions. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C50H67D9NO8P, Molecular Weight: 859.17. US Biological Life Sciences.
Requires divalent cations, with Mn2+ being more effective than Mg2+. Group: Enzymes. Synonyms: CDP-diglyceride-choline O-phosphatidyltransferase. Enzyme Commission Number: EC 2.7.8.24. CAS No. 243666-86-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3324; phosphatidylcholine synthase; EC 2.7.8.24; 243666-86-6; CDP-diglyceride-choline O-phosphatidyltransferase. Cat No: EXWM-3324.
1,2-Dimyristoyl-sn-glycero-3-phosphocholine
1,2-Dimyristoyl-sn-glycero-3-phosphocholine is used in the generation of micelles and liposomes.1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a phospholipid found in eukaryotes, but not most bacteria. It is used in lipid bilayer studies to analyze organelle and cell membranes. Its also been used to study molecules in membranes, such as the interaction between DMPC and proteins in lab-constructed dimyristoyl phosphatidyl choline vesicles.CAS Number:18194-24-6. Group: Biochemicals. Alternative Names: 3,5,9-Trioxa-4-phosphatricosan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxotetradecyl)oxy]-, hydroxide, inner salt, 4-oxide, (R)-; Choline, hydroxide, dihydrogen phosphate, inner salt, ester with 1,2-dimyristin, L- (8CI); Choline, phosphate, ester with L-1,2-dimyristin(6CI); 1,2-Bis(myristoyl)-sn-glycerophosphocholine; 1,2-Dimyristoyl-3-sn-phosphatidylcholine; 1,2-Dimyristoyl-3-sn-phosphatidylcholine; 1,2-Dimyristoyl-L-3-phosphatidylcholine; 1,2-Dimyristoyl-L-phosphatidylcholine; 1,2-Dimyristoyl-L-a-phosphatidylcholine; 1,2-Dimyristoyl-sn-3-glycerophosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphatidylcholine; 1,2-Dimyristoyl-sn-glycero-3-phosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphorylcholine; 1,2-Dimyristoyl-sn-glycerol-3. Grades: Highly Purified. CAS No. 18194-24-6. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences.
2-? [ [Hydroxy [ (2R) ?-?2-?oxiranylmethoxy] ?phosphinyl] ?oxy] ?-?N, ?N, ?N-?trimethyl-?ethanaminium Inner Salt is an intermediate in synthesizing sn-Glycero-3-phosphocholine-d9 (G598702), an isotope labelled analog of sn-Glycero-3-phosphocholine (G598700); a phospholipid and precursor in choline biosynthesis. sn-Glycero-3-phosphocholine is an intermediate in the catabolic pathway of phosphatidylcholine and is used as an nootropic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg. Molecular Formula: C8H9D9NO5P. US Biological Life Sciences.
Worldwide
2-(Methylamino)ethanol-[d9]
2-(Methylamino)ethanol-[d9] is the labelled analogue of 2-(Methylamino)Ethanol, which is a metabolite of Phosphatidylcholine. Phosphatidylcholines are a class of phospholipids that incorporate choline as a headgroup. Synonyms: Ethan-1,1,2,2-d4-ol-d, 2-(methyl-d3-amino-d)- (9CI). CAS No. 77504-94-0. Molecular formula: C3D9NO. Mole weight: 84.17.
2-((Methyl-d3)amino)
A metabolite of Phosphatidyl cholineadicals during methane production. Group: Biochemicals. Alternative Names: (2-Hydroxyethyl) methylamine-d3. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
5-Aminovaleric acid
5-Aminovaleric acid is used in the study of metabolic changes in male germ cells (toxins) after 24 hours of extinguishing cigarette smokes. Also used in the comprehensive characterization of the human saliva metabolome and in identification of different metabolites like sphingomyelins, phosphatidyl cholines, vitamins and trace elements in human saliva which showed diurnal variation. Uses: 5-aminovaleric acid, also known as 5-av or 5-ava, is a natural compound that has attracted increasing attention in drug discovery and pharmaceutical research due to its potential therapeutic applications. 5-aminovaleric acid is a structural analog of the amino acid lysine and is involved in various metabolic pathways in the human body. it plays a vital role in the biosynthesis of carnitine, a comp. Synonyms: 5-Ava-OH; 5-Amino-n-pentanoic acid; 5-Aminopentanoic acid; H-5-Ava-OH; delta-Aminovaleric acid; Homopiperidinic acid; 5-amino-pentanoic acid; Pentanoic acid, 5-amino-; Valeric acid, 5-amino-; delta-Amino-n-valeric acid; 5-aminopentanoate; 5-aminovalerate; 5-ammoniopentanoate; H 5 Ava OH. Grade: ≥ 98% (HPLC). CAS No. 660-88-8. Molecular formula: C5H11NO2. Mole weight: 117.15.
A cell-permeable, non-Hemicholinium-3 derivative and choline-competitive choline kinase-a inhibitor. It is demonstrated to inhibit endogenous choline kinase activity, dose-dependently, between 1-10uM, and dose-dependently decrease phosphocholine concentrations, as well as levels of downstream choline metabolites, including phosphatidylcholine and phosphatidic acid in HeLa cells. At 10uM, it is also shown to attenuate MAPK and PI3K/AKT signaling, and disrupt the actin cytoskeleton and membrane ruffling, consistent with siRNA choline kinase-a transfection. This compound exhibits dose-dependent suppression of cell growth in six tumor cell lines (IC50=5-10uM), in vitro. Furthermore, it is shown to suppress tumor growth in a mouse model by 48% at 0.08mg/g daily dose for 8 days without obvious toxicity, in vivo. Group: Biochemicals. Grades: Highly Purified. CAS No. 1001478-90-5. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Choline Kinase (Crude Enzyme)
Choline kinase (also known as CK,ChoK and choline phosphokinase) is an enzyme which catalyzes the first reaction in the choline pathway for phosphatidylcholine (PC) biosynthesis. This reaction involves the transfer of a phosphate group from adenosine triphosphate (ATP) to choline in order to form phosphocholine. Thus, the two substrates of this enzyme are ATP and choline, whereas its two products are adenosine diphosphate (ADP) and O-phosphocholine. Choline kinase requires magnesium ions (+2) as a cofactor for this reaction. This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol grou. CHKA and CHKB and are only active in their homodimeric, heterodimeric and oligomeric forms. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Biotechnology; diagnostics; drug development; medicine. Group: Enzymes. Synonyms: Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Enzyme Commission Number: EC 2.7.1.32. CAS No. 9026-67-9. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Pack: 100ml. Cat No: NATE-1825.
Citicoline
Citicoline is an endogenous intermediate in the synthesis of phosphatidylcholine which is a component of cell membranes. Citicoline inhibits reactive oxygen species (ROS) and apoptosis. Citicoline can be used for neurological disease and hearing loss study [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cytidine diphosphate-choline; CDP-Choline; Cytidine 5'-diphosphocholine. CAS No. 987-78-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0739.
Citicoline
Citicoline is an intermediate in the synthesis of phosphatidylcholine from choline. Citicoline exhibits neuroprotective activity thus can be used in dietary supplement for cognitive function. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Cytidine 5'-diphosphocholine; CDP-choline; Citicholine; Citidoline; Cytidoline. Grade: 95%. CAS No. 987-78-0. Molecular formula: C14H26N4O11P2. Mole weight: 488.327.
Citicoline sodium
Citicoline sodium is an endogenous intermediate in the synthesis of phosphatidylcholine which is a component of cell membranes. Citicoline sodium inhibits reactive oxygen species (ROS) and apoptosis. Citicoline sodium can be used for neurological disease and hearing loss study [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cytidine diphosphate-choline sodium; CDP-Choline sodium; Cytidine 5'-diphosphocholine sodium. CAS No. 33818-15-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0739A.
D609
D609, an antitumoural xanthate, is a specific and competitive phosphatidyl choline-specific phospholipase C (PC-PLC) inhibitor with a Ki of 6.4 ?M. D609 is an antioxidative protector and has antiviral and anti-inflammatory activity[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83373-60-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-70072.
D609
D609 is a selective competitive phosphatidyl choline-specific phospholipase C (PC-PLC) inhibitor and is antiviral and antitumor agent. It suppresses LPS- and IFNγ-induced NO production and blocks oxidative glutamate toxicity in nerve cells. Synonyms: D-609; D 609; D609; D-609 free. Grade: >98%. CAS No. 83373-60-8. Molecular formula: C11H15KOS2. Mole weight: 266.46.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Is an enzyme produced by microorganisms. this product shall be used for a diag.Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Mole weight: 60±5 kDa (TSK G-3000SW); 30±5 kDa (SDS-PAGE). Activity: > 1,500 U/mg. Appearance: White powder. Storage: -20°C. Form: Freeze dried powder. Source: Alcaligenes faecalis. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0005.
Native Bacillus cereus Phospholipase C
Phospholipase C is an enzyme with system name phosphatidylcholine cholinephosphohydrolase. This enzyme catalyses the following chemical reaction: a phosphatidylcholine + H2O<-> 1, 2-diacyl-sn-glycerol + phosphocholine. The bacterial enzyme is a zinc protein. It also acts on sphingomyelin and phosphatidylinositol. Native phospholipase c (ec 3.1.4.3) was purified from bacillus cereus. Applications: Useful for enzymatic determination of lecithin. Group: Enzymes. Synonyms: Phospholipase C; EC 3.1.4.3; lipophosphodiesterase I; Clostridium welchii alpha-toxin; Clostridium oedematiens beta-and gamma-toxins; lipophosphodiesterase C; phosphatidase C; heat-labile hemolysin; alpha-toxin. Enzyme Commission Number: EC 3.1.4.3. CAS No. 9001-86-9. Phospholipase C. Activity: > 30 U/mg. Appearance: White to brownish powder. Storage: Store in tightly closed containers, desiccated, protected from light, at-20°C. Form: Freeze dried powder. Source: Bacillus cereus. Phospholipase C; EC 3.1.4.3; lipophosphodiesterase I; Clostridium welchii alpha-toxin; Clostridium oedematiens beta-and gamma-toxins; lipophosphodiesterase C; phosphatidase C; heat-labile hemolysin; alpha-toxin. Cat No: DIA-163.
Native Cabbage Phospholipase D
Phospholipase D is a phospholipid hydrolyzing enzyme and an important component of receptor-mediated signal transduction responses and regulated secretion. Hydrolyzes the phosphate bonds of phospholipids and sphingomyelin to give the corresponding phosphatidic acid. Phospholipase D is involved in conferring drought susceptibility in peanuts, which increases the risk of aflatoxin contamination. Applications: Phospholipase d (pld) is used to hydrolyze the phosphate bonds of phospholipids and sphingomyelin to give the corresponding phosphatidic acid. it has also been used to study metabolic labeling and direct imaging of choline phospholipids in vivo by measuring propargyl-cho incorporation. furthermore, pld is used in purification and kinetic studies. the enzyme has been used for the preparation of bodipy-phosphatidylcholine during the preparation of fluorescently labelled lipids. Group: Enzymes. Synonyms: Phospholipase D; EC 3.1.4.4; lipophosphodiesterase II; lecithinase D; choline phosphatase; PLD; 9001-87-0. Enzyme Commission Number: EC 3.1.4.4. CAS No. 9001-87-0. PLD. Activity: > 100 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Cabbage. Phospholipase D; EC 3.1.4.4; lipophosphodiesterase II; lecithinase D; choline phosphatase; PLD; 9001-87-0. Cat No: NATE-0595.
Native Clostridium perfringens (C. welchII) Phospholipase C
Phospholipase C is induced by thrombin and platelet-activating factor, forming 1,2-diacylglycerol and phosphatidic acid. PLC hydrolyzes the phosphate bond on phosphatidylcholine and other glycerophospholipids yielding diacylglycerol; this enzyme will also hydrolyze the phosphate bonds of sphingomyelin, cardiolipin, choline plasmalogen and ceramide phospholipids. Group: Enzymes. Synonyms: Phospholipase C; PLC; 9001-86-9; lipophosphodiesterase I; lecithinase C; Clostridium welchii α-toxin; Clostridium oede. Enzyme Commission Number: EC 3.1.4.3. CAS No. 9001-86-9. Phospholipase C. Activity: Type I, > 150 units/mg protein; Type II, 10-50 units/mg protein; Type III, Type IV, > 1,000 units/mg protein (Lowry). Storage: -20°C. Form: Type I, Lyophilized powder in buffered salts; Type II, lyophilized powder; Type III, buffered aqueous glycerol solution; Solution in 60% (v/v) glycerol containing 10 mM Tris-HCl, pH 8.0 and 10 mM EDTA; Type IV, lyophilized powder, Contains phosphate buffer salts, EDTA and stabilizer. Source: Clostridium perfringens (C. welchII). Phospholipase C; PLC; 9001-86-9; lipophosphodiesterase I; lecithinase C; Clostridium welchii α-toxin; Clostridium oedematiens β-and γ-toxins; lipophosphodiesterase C; phosphatidase C; heat-labile hemolysin; α-toxin; EC 3.1.4.3. Cat No: NATE-0593.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Applications: Suitable for the determination of acetoacetate and d (-)-3-hy.1.1.30; 9028-38-0. Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Activity: > 200 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing sucrose, β-NAD and Tris buffer salts. Source: Pseudomonas lemoignei. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0003.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Applications: Suitable for the determination of acetoacetate and d (-)-3.nase; EC 1.1.1.30; 9028-38-0. Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Activity: 250-750 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing Tris buffer salts. Source: Rhodopseudomonas sphaeroides. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0004.
Native Streptomyces sp. Phospholipase D
Phospholipase D (PLD) is glycerophospholipid-specific. It is markedly less active on sphingomyelins and lysophospholipids. Phospholipase D hydrolyzes the phosphate bonds of phospholipids and sphingomyelin to give the corresponding phosphatidic acid. Applications: Phospholipase d (pld) has been used to hydrolyze the phosphate bonds of phospholipids and sphingomyelin to yield the corresponding phosphatidic acid. it has also been used to study metabolic labeling and direct imaging of choline phospholipids in vivo by measuring propargyl-cho incorporation. furthermore, pld has been used in purification and kinetic studies. the enzyme has been used in the translocation of sphingosine kinase 1 (sk1) to membrane fractions under in vitro conditions. it has also been used to produce phosphatidic acid (pa) from phosphatidylcholine (pc) in hl60 permeabilized cells. Group: Enzymes. Synonyms: phospholipase D; lipophosphodiesterase II; lecithinase D. Enzyme Commission Number: EC 3.1.4.4. CAS No. 9001-87-0. PLD. Activity: > 150 units/mg solid. Storage: -20°C. Form: Type VII, lyophilized powder. Source: Streptomyces sp. phospholipase D; lipophosphodiesterase II; lecithinase D; choline phosphatase; phosphatidylcholine phosphatidohydrolase; EC 3.1.4.4; 9001-87-0; PLD. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0597.
phospholipase A2
Also acts on phosphatidylethanolamine, choline plasmalogen and phosphatides, removing the fatty acid attached to the 2-position. Requires Ca2+. Group: Enzymes. Synonyms: lecithinase A; phosphatidase; phosphatidolipase; phospholipase A. Enzyme Commission Number: EC 3.1.1.4. CAS No. 9001-84-7. PLA2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3466; phospholipase A2; EC 3.1.1.4; 9001-84-7; lecithinase A; phosphatidase; phosphatidolipase; phospholipase A. Cat No: EXWM-3466.
phospholipase D
Also acts on other phosphatidyl esters. Group: Enzymes. Synonyms: lipophosphodiesterase II; lecithinase D; choline phosphatase. Enzyme Commission Number: EC 3.1.4.4. CAS No. 9001-87-0. PLD. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3723; phospholipase D; EC 3.1.4.4; 9001-87-0; lipophosphodiesterase II; lecithinase D; choline phosphatase. Cat No: EXWM-3723.
Propargylcholine bromide
Propargylcholine bromide is a choline analogue containing terminal propargyl that can be incorporated into all classes of Choline-containing phospholipids such as phosphatidylcholine and sphingomyelin, labeling Choline-containing phospholipids. Propargylcholine bromide-labeled phospholipid molecules can be visualized in cells with high sensitivity and spatial resolution. Propargylcholine bromide can be used as a molecular tool to study the biochemical and metabolic processes of Choline-containing phospholipids in cells[1][2]. Propargylcholine (bromide) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 111755-76-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129084.
RHC 80267
RHC 80267 (U-57908) is a potent and selective inhibitor of diacylglycerol lipase (DAGL) (with IC 50 of 4 μM in canine platelets). RHC-80267 inhibits cholinesterase activity with an IC 50 of 4 μM, thereby enhancing the relaxation evoked by acetylcholine. RHC 80267 also inhibits COX and the hydrolysis of phosphatidylcholine (PC) [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-57908. CAS No. 83654-05-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107416.
sn-Glycero-3-phosphocholine
sn-Glycero-3-phosphocholine (Choline Alfoscerate) is a phospholipid; precursor in choline biosynthesis. sn-Glycero-3-phosphocholine is an intermediate in catabolic pathway of phosphatidylcholine. sn-Glycero-3-phosphocholine is used as an Nootropic. Group: Biochemicals. Alternative Names: 2- [ [ [ (2R) -2, 3-Dihydroxypropoxy] hydroxyphosphinyl] oxy] -N, N, N-trimethylethanaminium Inner Salt; Brezal; Cereton; Cholicerin; Choline Alfoscerate; Cholitiline; Delecit; Glyceryl phosphocholine; Glyceryl phosphoryl choline; L-α-GPC; L-α-Glycerophosphocholine; L- α -Glycerophosphoryl choline; L- α -Glyceryl phosphoryl choline; O-(sn-glycero-3-Phosphoryl)choline; Sn-Glycerophosphocholine; sn-Glycero-3-phosphorylcholine; sn-glycero-3-phosphocholine; α -Glycerophosphoryl choline; α -Glyceryl phosphoryl choline. Grades: Highly Purified. CAS No. 28319-77-9. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
sn-Glycero-3-phosphocholine
sn-Glycero-3-phosphocholine is a nootropic phospholipid and acts as a precursor to choline biosynthesis. sn-Glycero-3-phosphocholine is an intermediate in catabolic pathway of phosphatidylcholine. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Choline alfoscerate; (R)-2-[[(2,3-Dihydroxypropoxy)hydroxyphosphinyl]oxy]-N,N,N-trimethylethanaminium Inner Salt; 2-[[[(2R)-2,3-Dihydroxypropoxy]hydroxyphosphinyl]oxy]-N,N,N-trimethylethanaminium Inner Salt; Brezal; Cereton; Cholicerin; Cholitiline; Delecit; Glycerylphosphocholine; L-α-GPC; L-α-Glycerophosphocholine; L-α-Glycerylphosphorylcholine; O-(sn-glycero-3-Phosphoryl)choline; Sn-Glycerophosphocholine; sn-Glycero-3-phosphorylcholine; α-Glycerophosphorylcholine; α-Glycerylphosphorylcholine. Grade: ≥95%. CAS No. 28319-77-9. Molecular formula: C8H20NO6P. Mole weight: 257.22.
Soybean phospholipids
Food-grade lecithin is obtained from soybeans and other plant sources. It is a complex mixture of acetone-insoluble phosphatides that consists chiefly of phosphatidyl choline, phosphatidyl etha nolamine, and phosphatidyl inositol, combined with various amounts of other substances such as triglycerides, fatty acids, and carbohydrates. CAS No. 8002-43-5. Product ID: PE-0113. Molecular formula: C42H80NO8P. Mole weight: 758.06. Category: Emulsifier & Suspending Agents. Product Keywords: Pharmaceutical Excipients; Injections & Sterile Formulation; Emulsifier & Suspending Agents; Soybean phospholipids; PE-0113; C42H80NO8P; 8002-43-5; 8002-43-5. Appearance: Pale Brown to Yellow. Purity: 0.99. EC Number: 232-307-2. Synonym(s): l-α-phosphatidylcholine solution; l-α -phosphatidylcholine, hydrogenated. Solubility: chloroform: 0.1 g/mL, slightly hazy, slightly yellow to deep orange. Storage: -20°C. Melting Point: >145°C (dec.). Density: 1.0305.
sphingomyelin phosphodiesterase D
Does not act on phosphatidylcholine, but hydrolyses 2-lysophosphatidylcholine to choline and 2-lysophosphatidate. Group: Enzymes. Synonyms: sphingomyelinase D. Enzyme Commission Number: EC 3.1.4.41. CAS No. 54992-31-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3725; sphingomyelin phosphodiesterase D; EC 3.1.4.41; 54992-31-3; sphingomyelinase D. Cat No: EXWM-3725.
sphingomyelin synthase
The reaction can occur in both directions. This enzyme occupies a central position in sphingolipid and glycerophospholipid metabolism. Up- and down-regulation of its activity has been linked to mitogenic and pro-apoptotic signalling in a variety of mammalian cell types. Unlike EC 2.7.8.3, ceramide cholinephosphotransferase, CDP-choline cannot replace phosphatidylcholine as the donor of the phosphocholine moiety of sphingomyelin. Group: Enzymes. Synonyms: SM synthase; SMS1; SMS2. Enzyme Commission Number: EC 2.7.8.27. CAS No. 58703-97-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3326; sphingomyelin synthase; EC 2.7.8.27; 58703-97-2; SM synthase; SMS1; SMS2. Cat No: EXWM-3326.
3-O-tert-Butyl di methyl silyl -D-Erythro-sphingosyl phosphoryl choline
Involved in cell regulation, and transmembrane signaling. A putative lipid second messenger, connected via Protein Kinase C to the phosphatidylinositol-derived second messengers for signal transduction. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
D-Erythro-Sphingosyl phosphoryl choline
Involved in cell regulation, and transmembrane signaling. A putative lipid second messenger, connected via Protein Kinase C to the phosphatidylinositol-derived second messengers for signal transduction. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences.
Worldwide
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