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2-Arachidonoyl-1-stearoyl-sn-glycero-3-phosphocholine solution - 10mg/mL in Ethanol, high purity , CAS No.35418-59-8

COA

Grade & Purity:

≥98%
10mg/mL in Ethanol

Cas Number: 35418-59-8
Molecular Weight: 810.13
Beilstein Registry Number: 6090084
MDL number: MFCD00082436
PubChem CID: 16219824

In stock

Item Number

A769857

Grouped product items
SKU	Size	Availability	Price
A769857-0.5ml	0.5ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$349.90
A769857-1ml	1ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$539.90
A769857-2.5ml	2.5ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$999.90

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Carbohydrate (76) Metabolite (5307)

Basic Description

Synonyms	PC(18:0/20:4(5Z,8Z,11Z,14Z)) \| 18:0-20:4 PC \| 1-octadecanoyl-2-arachidonyl-sn-glycero-3-phosphocholine \| SAPC
Specifications & Purity	≥98%, 10mg/mL in Ethanol
Storage Temp	Store at -20°C,Desiccated
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	2-Arachidonoyl-1-stearoyl-sn-glycero-3-phosphocholine is a phospholipid molecule characterized by a glycerophospholipid backbone where the first position of the glycerol unit is esterified with a stearic acid (saturated fatty acid), and the second position is esterified with arachidonic acid (a polyunsaturated fatty acid). This specific molecular arrangement makes it a critical component in the study of lipid rafts and membrane fluidity within cellular models. Arachidonic acid, known for its role in the biosynthesis of eicosanoids, imparts a particular interest in 1-Stearoyl-2-Arachidonoyl PC for investigating signaling pathways related to inflammation and cellular signaling. In research, this lipid is predominantly utilized to explore the dynamics of cellular membranes, especially the effects of fatty acid composition on membrane properties such as fluidity, phase behavior, and lipid domain formation. The presence of both saturated and unsaturated fatty acids allows for nuanced studies of how these lipids affect the structural and functional aspects of cell membranes, including their interactions with proteins and the activation of specific signaling cascades. Furthermore, this phospholipid serves as a model compound in the study of lipid metabolism and its implications in cellular processes, offering insights into the molecular mechanisms that underlie cell functionality and communication.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Glycerophospholipids
    - Subclass Glycerophosphocholines

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Glycerophospholipids
Subclass	Glycerophosphocholines
Intermediate Tree Nodes	Not available
Direct Parent	Phosphatidylcholines
Alternative Parents	Phosphocholines Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Tetraalkylammonium salts Carboxylic acid esters Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines
Molecular Framework	Aliphatic acyclic compounds
Substituents	Diacylglycero-3-phosphocholine - Phosphocholine - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Amine - Organic salt - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
External Descriptors	Diacylglycerophosphocholines
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	[(2R)-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyl]oxy-3-octadecanoyloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
INCHI	InChI=1S/C46H84NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-37-39-46(49)55-44(43-54-56(50,51)53-41-40-47(3,4)5)42-52-45(48)38-36-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h14,16,20,22,25,27,31,33,44H,6-13,15,17-19,21,23-24,26,28-30,32,34-43H2,1-5H3/b16-14-,22-20-,27-25-,33-31-/t44-/m1/s1
InChIKey	PSVRFUPOQYJOOZ-QNPWAGBNSA-N
Smiles	CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCC=CCC=CCC=CCC=CCCCCC
Isomeric SMILES	CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
WGK Germany	3
PubChem CID	16219824
UN Number	1888
Molecular Weight	810.13
Beilstein	6090084

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Molecular Weight	810.100 g/mol
XLogP3	13.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	42
Exact Mass	809.593 Da
Monoisotopic Mass	809.593 Da
Topological Polar Surface Area	111.000 Å²
Heavy Atom Count	56
Formal Charge	0
Complexity	1090.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	4
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	4
Covalently-Bonded Unit Count	1

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