LY 2183240
Tocris Bioscience, part of Bio-Techne | Catalog # 2452
Highly potent anandamide uptake inhibitor; also inhibits FAAH
Discontinued Product
2452 has been discontinued.
View all Cannabinoid Transporter Inhibitors products.
Key Product Details
Description
Highly potent anandamide uptake inhibitor; also inhibits FAAH
Product Description
LY 2183240 is a novel and highly potent blocker of anandamide uptake (IC50 = 270 pM). Inhibits fatty acid amide hydrolase (FAAH) activity (IC50 = 12.4 nM). Following i.p. administration in rats, increases brain anandamide concentration and exerts antinociceptive effects in formalin model of pain.Licensing Information
Sold under license from Eli Lilly and CompanyProduct Specifications
Molecular Weight
307.35
Formula
C17H17N5O
Storage
Store at +4°C
Purity
≥98% (HPLC)
Chemical Name
5-[(1,1'-Biphenyl]-4-yl)methyl]-N,N-dimethyl-1H-tetrazole-1-carboxamide
CAS Number
874902-19-9
PubChem ID
11507802
InChI Key
GZNIYOXWFCDBBJ-UHFFFAOYSA-N
SMILES
CN(C)C(=O)N1N=NN=C1CC1=CC=C(C=C1)C1=CC=CC=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 30.74 | 100 | |
| Ethanol | 15.37 | 50 with gentle warming |
Preparing Stock Solutions
for LY 2183240
The following data is based on the product molecular weight 307.35
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.25 mL | 16.27 mL | 32.54 mL |
| 5 mM | 0.65 mL | 3.25 mL | 6.51 mL |
| 10 mM | 0.33 mL | 1.63 mL | 3.25 mL |
| 50 mM | 0.07 mL | 0.33 mL | 0.65 mL |
Calculators
Molarity Calculator
Dilution Calculator
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Background References
References are publications that support the biological activity of the product.
- Alexander and Cravat The putative endocannabinoid transport blocker LY2183240 is a potent inhibitor of FAAH and several other brain serine hydrolases. J.Am.Chem.Soc. 2006 PMID: 16866524
- Moore Identification of a high-affinity binding site involved in the transport of endocannabinoids. Proc.Natl.Acad.Sci.USA
- Dickason-Chesterfield Pharmacological characterization of endocannabinoid transport and fatty acid amide hydrolase inhibitors. Cell Mol.Neurobiol. 2006 PMID: 16736384
Product Specific Notices for LY 2183240
For research use only
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