Glycerolipids

Cat. No.

A74337

CAS No.

109796-58-9

1,3-Capryloyl-2-oleoylglycerol

1,3-Capryloyl-2-oleoylglycerol is a triglyceride characterized by caprylic acid acylating the hydroxyl groups at the 1 and 3 positions of glycerol, while oleic acid modifies the 2 position. This compound exhibits key biological activity in lipid metabolism and serves as an important substrate in various biochemical assays. Its applications extend to studies involving lipogenesis, energy metabolism, and the modulation of lipid profiles in cellular models.

Cat. No.

A75894

CAS No.

139979-77-4

1,3-Dioleoyl-2-octanoyl glycerol

Synonyms: 1,3-Olein-2-caprylin; 1,3-Oleoyl-2-capryloyl glycerol; TG(18:1/8:0/18:1)

1,3-Dioleoyl-2-octanoyl glycerol is a triacylglycerol that serves as a substrate for the characterization of lipase activity, particularly in relation to the regioselective distribution of medium- and short-chain fatty acids. This compound can be utilized in biochemical assays to assess the enzymatic functionality of Rhizopus oryzae lipase, providing insights into lipid metabolism and enzymatic properties. It is particularly valuable for research focusing on lipid digestion and transesterification processes.

Cat. No.

A75915

CAS No.

17598-93-5

1,3-Didecanoylglycerol

Synonyms: 1,3-Dicaprin

1,3-Didecanoylglycerol, also known as 1,3-Dicaprin, functions as a triglyceride analog that serves as a substrate in pancreatic lipase hydrolysis reactions. Its key biological activity involves the modeling of triglyceride metabolism, making it a valuable tool for studies on lipid digestion and absorption. This compound is particularly useful in research applications focusing on enzyme kinetics and the biochemical pathways of lipid metabolism.

Cat. No.

A89355

CAS No.

869990-13-6

15:0-18:1-15:0 TG

Synonyms: 1,3-Dipentadecanoyl-2-oleoyl-glycerol

15:0-18:1-15:0 TG, also known as 1,3-Dipentadecanoyl-2-oleoyl-glycerol, is a triglyceride that is essential in lipid metabolism studies. This compound serves as a model substrate for investigating the biochemical pathways involved in triglyceride synthesis and hydrolysis. Its unique structure, featuring both saturated and unsaturated fatty acid chains, makes it relevant for research in metabolic disorders, obesity, and cardiovascular diseases.

Cat. No.

A89844

CAS No.

99483-10-0

Trimyristolein

Synonyms: 1,2,3-Trimyristoleoyl glycerol

Trimyristolein is a triacylglycerol that primarily targets lipid metabolism. Comprising three myristoleic acid moieties, this compound serves as a valuable substrate for studying lipid trafficking and storage in biological systems. It is utilized in research related to energy metabolism, obesity, and related metabolic disorders.

Cat. No.

A89909

CAS No.

20358-82-1

1-Palmitoyl-3-butyryl-rac-glycerol

1-Palmitoyl-3-butyryl-rac-glycerol is a diacylglycerol derivative formed from palmitic acid and butyric acid. This compound serves as an important substrate in studies of lipid metabolism and signaling pathways. Its unique structure allows for exploration of its role in cellular processes and potential implications in metabolic disorders and cancer research.

Cat. No.

A92601

CAS No.

2438-40-6

Triheptadecanoin

Synonyms: Glycerol triheptadecanoate; Trimargarin

Triheptadecanoin is a triacylglycerol composed of heptadecanoic acid at the sn-1, sn-2, and sn-3 positions. This compound serves as a key substrate for studying lipid metabolism and the biological roles of triacylglycerols. Its unique structure allows for applications in research related to energy storage, signaling pathways, and the synthesis of complex lipids.

Cat. No.

A93238

CAS No.

88286-44-6

1,2-Dioctanoyl-3-linoleoyl-rac-glycerol

1,2-Dioctanoyl-3-linoleoyl-rac-glycerol is a triacylglycerol characterized by the presence of octanoic acid and linoleic acid. This compound serves as a valuable substrate in biochemical research involving lipid metabolism and cellular energy storage. Its unique structure makes it useful for studies focused on the interplay between fatty acids and cellular signaling pathways.

Cat. No.

A93854

CAS No.

100732-08-9

1-Myristoyl-3-butyryl-rac-glycerol

1-Myristoyl-3-butyryl-rac-glycerol is a diacylglycerol that features myristic acid at the sn-1 position and butyric acid at the sn-3 position. This compound is primarily involved in lipid signaling pathways and acts as a substrate for diacylglycerol kinases. It serves as an important reagent for research into cellular signaling mechanisms, metabolism, and the physiological roles of diacylglycerols in various biological processes.

Cat. No.

A94111

CAS No.

799812-77-4

1,2-Dioleoyl-sn-glycero-3-(cytidine diphosphate) ammonium

Synonyms: 18:1 CDP DG

1,2-Dioleoyl-sn-glycero-3-(cytidine diphosphate) ammonium is a diacylglycerol derivative that functions primarily as a substrate for various enzymatic reactions. This compound is crucial in studies related to lipid metabolism and membrane biology, where it can serve as a key player in the synthesis of phospholipids and signaling molecules. Additionally, it is used in research focused on cellular signaling pathways and the regulation of lipid-based signaling networks.

Cat. No.

A94120

CAS No.

152914-63-1

1-Palmitoyl-2-stearoyl-3-butyryl-rac-glycerol

1-Palmitoyl-2-stearoyl-3-butyryl-rac-glycerol is a triacylglycerol composed of palmitic acid, stearic acid, and butyric acid at the sn-1, sn-2, and sn-3 positions, respectively. This compound serves as an important substrate for studying the stereospecificity and typoselectivity of lipases in biochemical research. It is particularly useful for understanding lipase reaction mechanisms and lipid metabolism.

Cat. No.

A94127

CAS No.

88286-47-9

1,2-Dioleoyl-3-caprin

Synonyms: 1,2-Dioleoyl-3-decanoyl-rac-glycerol; TG(18:1/18:1/10:0)

1,2-Dioleoyl-3-caprin is a triacylglycerol esterified with oleic acid and decanoic acid. This compound serves as a lipid substrate for studying lipid metabolism and energy homeostasis. Its applications include investigations into membrane dynamics, signaling pathways, and the regulation of metabolic diseases.

Cat. No.

A94813

CAS No.

91539-55-8

1,2-Dioleoyl-3-arachidonoyl-rac-glycerol

Synonyms: 1,2-Olein-3-arachidonin; TG(18:1/18:1/20:4)

1,2-Dioleoyl-3-arachidonoyl-rac-glycerol is a triacylglycerol composed of oleic and arachidonic acids. This compound serves as a significant substrate in lipid metabolism studies and can be utilized in research applications focusing on cell signaling and inflammatory responses. Its unique fatty acid composition makes it a valuable reagent for investigating the roles of triacylglycerols in various biological processes.

Cat. No.

B20821

CAS No.

17364-00-0

1,3-Dibutyrin

1,3-Dibutyrin is a glycerolipid that acts as a model compound for studying lipid metabolism and storage. It serves as a substrate for lipases and is utilized in research focusing on triglyceride synthesis and breakdown. Additionally, this reagent has applications in understanding the role of lipids in cell signaling and membrane dynamics.

Cat. No.

B20929

CAS No.

3443-83-2

2-Monomyristin

2-Monomyristin is an acylglycerol that primarily interacts with lipid structures within biological membranes. It serves as a substrate for various enzymatic reactions, playing a critical role in lipid metabolism and cellular signaling pathways. This compound is valuable for research applications in studying lipid biochemistry, membrane dynamics, and metabolic processes.

Cat. No.

B21033

CAS No.

55320-04-2

1-Linolein-2,3-acetyl

1-Linolein-2,3-acetyl is an acylglycerol that serves as a lipid compound. It plays a significant role in various lipid metabolism studies and can be utilized as a substrate in the investigation of enzymatic activity related to lipid processing. This reagent is valuable for research applications involving lipid signaling pathways and metabolic regulation.

Cat. No.

B21153

CAS No.

55268-70-7

1-Palmitin-2,3-acetyl

1-Palmitin-2,3-acetyl is an acylglycerol involved in lipid metabolism. This compound can serve as a substrate for studying fatty acid synthesis and storage, as well as exploring the structure-function relationship of lipid molecules. Its applications extend to bioenergetics, membrane dynamics, and the investigation of lipid-related metabolic disorders.