Javascript est désactivé dans votre navigateur. Pour une meilleure expérience sur notre site, assurez-vous d’activer JavaScript dans votre navigateur.

Il s'agit d'un magasin de démonstration. Aucune commande ne sera honorée.

Appelez le +1 (833) 552-7181 ou contactez-nous

Allez au contenu

Devise

Langue

Basculer la navigation

Mon panier

Rechercher

Comparer des produits

Compte

Paramètres

Langue

Devise

྾

Accueil
Petites molécules bioactives
Signaling Pathways
Metabolic Enzyme/Protease
Endogenous Metabolite
1-Stearoyl-sn-glycero-3-phosphocholine - >99%, high purity , CAS No.19420-57-6, Agonist of GPR119

Skip to the end of the images gallery

Skip to the beginning of the images gallery

1-Stearoyl-sn-glycero-3-phosphocholine - >99%, high purity , CAS No.19420-57-6, Agonist of GPR119

COA

Grade & Purity:

Moligand™

≥99%

Cas Number: 19420-57-6
Poids moléculaire: 523.683
MDL number: MFCD00050427
PubChem CID: 497299
PubChem SID: 504758948

En stock

Item Number

S130495

Articles du produit groupé
SKU	Taille	Disponibilité	Prix
S130495-5mg	5mg	3	48,90$US
S130495-25mg	25mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	216,90$US
S130495-100mg	100mg	3	339,90$US
S130495-500mg	500mg	3	1 526,90$US

View related series

GPR119 Agonist (40) Metabolite (5307)

Description générale

Synonymes	S-LYSO-PC \| HY-15440 \| LPC 18:0/0:0 \| [(2R)-2-hydroxy-3-octadecanoyloxypropyl] 2-trimethylazaniumylethyl phosphate \| DB12129 \| 18:0 Lyso PC \| 1-18:0-lysoPC \| AC-30913 \| AKOS027323602 \| 1-Stearoyl-sn-3-phosphatidylcholine \| PC 18:0/0:0 \| (R)-2-Hydroxy-3-(s
Spécifications et pureté	Moligand™, ≥99%
Mécanismes biochimiques et physiologiques	1-Stearoyl-sn-glycero-3-phosphocholine (LPC, Lyso-PC) is used in the development of drug transdermal delivery devices such as liposomes and micelles.
Température de stockage	Store at -20°C
Expédié en	Ice chest + Ice pads Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade	Moligand™
Type d'action	AGONIST
Mécanisme d'action	Agonist of GPR119

Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Classe	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

Cibles associées (humaines)

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)

Mécanismes d'action

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

Noms et identifiants

Pubchem Sid	504758948
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504758948
IUPAC Name	[(2R)-2-hydroxy-3-octadecanoyloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
INCHI	InChI=1S/C26H54NO7P/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/h25,28H,5-24H2,1-4H3/t25-/m1/s1
InChIKey	IHNKQIMGVNPMTC-RUZDIDTESA-N
Smiles	CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O
Isomères SMILES	CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O
WGK Allemagne	3
CAS alternatif	19420-57-6
Termes d'entrée MeSH	1-octadecyl-glycero-3-phosphocholine;1-stearoyl-2-hydroxy-sn-glycero-3-phosphocholine;1-stearoyl-sn-glycero-3-phosphorylcholine;stearoyl alpha-lysolecithin;stearoyl alpha-lysolecithin, (+-)-isomer;stearoyl alpha-lysolecithin, (R)-isomer;stearoyl L-alpha-l
Poids moléculaire	523.683

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

7 results found

Lot Number	Certificate Type	Date	Article
G2115344	Certificate of Analysis	May 12, 2025	S130495
I2410249	Certificate of Analysis	Sep 14, 2024	S130495
E2413069	Certificate of Analysis	Nov 09, 2023	S130495
I2002100	Certificate of Analysis	Nov 08, 2023	S130495
I2002099	Certificate of Analysis	Nov 08, 2023	S130495
G2115343	Certificate of Analysis	Feb 10, 2023	S130495
G2115346	Certificate of Analysis	Feb 10, 2023	S130495

Propriétés chimiques et physiques

Sensibilité	heat sensitive
Poids moléculaire	523.700 g/mol
XLogP3	6.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	26
Exact Mass	523.364 Da
Monoisotopic Mass	523.364 Da
Topological Polar Surface Area	105.000 Å²
Heavy Atom Count	35
Formal Charge	0
Complexity	546.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Calculateurs de solution

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Avis

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.