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1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine - >99%, high purity , CAS No.19420-56-5, Agonist of GPR119

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1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine - >99%, high purity , CAS No.19420-56-5, Agonist of GPR119

1 Citations

COA

Grade & Purity:

Moligand™

≥99%

Cas Number: 19420-56-5
Molecular Weight: 521.67
Beilstein Registry Number: 4033747
MDL number: MFCD00133435
PubChem CID: 16081932

In stock

Item Number

O130376

Grouped product items
SKU	Size	Availability	Price
O130376-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$29.90
O130376-25mg	25mg	2	$99.90
O130376-100mg	100mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$275.90

View related series

GPR119 Agonist (40) Phospholipid (111)

Basic Description

Synonyms	FS74G26ZZ4 \| LMGP01050032 \| 1-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine \| butyldi-1 adamantylphosphine \| Q27088173 \| 18:1 Lyso PC, 1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine, powder \| 1-Oleoyllysophosphatidylcholine \| 1-Oleoyl-sn-glycero-3-phospho
Specifications & Purity	Moligand™, ≥99%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Grade	Moligand™
Action Type	AGONIST
Mechanism of action	Agonist of GPR119

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Glycerophospholipids
    - Subclass Glycerophosphocholines
      - Level5 Lysophosphatidylcholines
        Level6 1-acyl-sn-glycero-3-phosphocholines

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Glycerophospholipids
Subclass	Glycerophosphocholines
Intermediate Tree Nodes	Lysophosphatidylcholines
Direct Parent	1-acyl-sn-glycero-3-phosphocholines
Alternative Parents	Phosphocholines Fatty acid esters Dialkyl phosphates Tetraalkylammonium salts Secondary alcohols Carboxylic acid esters Monocarboxylic acids and derivatives Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines
Molecular Framework	Aliphatic acyclic compounds
Substituents	1-acyl-sn-glycero-3-phosphocholine - Phosphocholine - Fatty acid ester - Dialkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Tetraalkylammonium salt - Quaternary ammonium salt - Secondary alcohol - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic salt - Amine - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as 1-acyl-sn-glycero-3-phosphocholines. These are glycerophosphocholines in which the glycerol is esterified with a fatty acid at O-1 position, and linked at position 3 to a phosphocholine.
External Descriptors	Monoacylglycerophosphocholines
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

Associated Targets(Human)

GPR119 Tclin Glucose-dependent insulinotropic receptor (1 Activities)

Discover Target: GPR119

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	[(2R)-2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
INCHI	InChI=1S/C26H52NO7P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-26(29)32-23-25(28)24-34-35(30,31)33-22-21-27(2,3)4/h12-13,25,28H,5-11,14-24H2,1-4H3/b13-12-/t25-/m1/s1
InChIKey	YAMUFBLWGFFICM-PTGWMXDISA-N
Smiles	CCCCCCCCC=CCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O
Isomeric SMILES	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O
WGK Germany	3
Alternate CAS	19420-56-5
MeSH Entry Terms	Lysolecithin;Lysolecithins;Lysophosphatidylcholine;Lysophosphatidylcholines
Molecular Weight	521.67
Beilstein	4033747
Reaxy-Rn	4033747
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4033747&ln=

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

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

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number	Certificate Type	Date	Item
F2506642	Certificate of Analysis	May 28, 2025	O130376
F2506643	Certificate of Analysis	May 28, 2025	O130376
F2506649	Certificate of Analysis	May 28, 2025	O130376
F2506646	Certificate of Analysis	May 28, 2025	O130376
B2506076	Certificate of Analysis	Feb 10, 2025	O130376
K2218932	Certificate of Analysis	Sep 18, 2024	O130376
K22181024	Certificate of Analysis	Sep 18, 2024	O130376
G2209169	Certificate of Analysis	Apr 07, 2024	O130376
K2110141	Certificate of Analysis	Aug 15, 2023	O130376
K2110142	Certificate of Analysis	Aug 15, 2023	O130376
J2028187	Certificate of Analysis	Sep 12, 2022	O130376
G2209168	Certificate of Analysis	Jun 13, 2022	O130376

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Chemical and Physical Properties

Molecular Weight	521.700 g/mol
XLogP3	5.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	25
Exact Mass	521.348 Da
Monoisotopic Mass	521.348 Da
Topological Polar Surface Area	105.000 Å²
Heavy Atom Count	35
Formal Charge	0
Complexity	584.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Lei He, Qian Hu, Liyang Wei, Xuliyang Ge, Ning Yu, Ying Chen. (2023) Unravelling dynamic changes in non-volatile and volatile metabolites of pulses during soaking: An integrated metabolomics approach. FOOD CHEMISTRY, 422 (136231).

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