PeptideDB

LUF5771 1141802-49-4

LUF5771 1141802-49-4

CAS No.: 1141802-49-4

LUF5771 is a potent allosteric inhibitor of recombinant luteinizing hormone (recLH) and Org 43553. LUF5771 can partially
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LUF5771 is a potent allosteric inhibitor of recombinant luteinizing hormone (recLH) and Org 43553. LUF5771 can partially activate LH receptors and has low efficacy.

Physicochemical Properties


Molecular Formula C24H23NO2
Molecular Weight 357.44492650032
Exact Mass 357.172
CAS # 1141802-49-4
PubChem CID 44572264
Appearance Typically exists as solid at room temperature
LogP 6
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 5
Heavy Atom Count 27
Complexity 435
Defined Atom Stereocenter Count 0
InChi Key YNYOWRRXJIPCGX-UHFFFAOYSA-N
InChi Code

InChI=1S/C24H23NO2/c26-24(25-22-13-7-8-14-22)27-23-16-20(18-9-3-1-4-10-18)15-21(17-23)19-11-5-2-6-12-19/h1-6,9-12,15-17,22H,7-8,13-14H2,(H,25,26)
Chemical Name

(3,5-diphenylphenyl) N-cyclopentylcarbamate
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


Targets recLH and Org 43553[1]
ln Vitro Concentration-dependent allosteric inhibition is observed with LUF5771 (1 µM or 10 µM). LUF5771 causes radioligand dissociation to rise noticeably. Like Org 43553, LUF5771 most likely binds to the seven transmembrane domain. The LH receptor can be partially activated by 31 ±4% with just 10 µM of LUF5771[1].
References [1]. Laura H. Heitman, et al. Substituted Terphenyl Compounds as the First Class of Low Molecular Weight Allosteric Inhibitors of the Luteinizing Hormone Receptor. Journal of Medicinal Chemistry 2009 52 (7), 2036-2042

Solubility Data


Solubility (In Vitro) DMSO: 100 mg/mL (279.77 mM)
Solubility (In Vivo) Solubility in Formulation 1: ≥ 2.5 mg/mL (6.99 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.7977 mL 13.9884 mL 27.9767 mL
5 mM 0.5595 mL 2.7977 mL 5.5953 mL
10 mM 0.2798 mL 1.3988 mL 2.7977 mL
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.