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Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Lusaperidone (R107474) is an α2 adrenergic receptor antagonist with K i s of 0.13 and 0.15 nM for α2A and α2C, respectively.
In Vitro
Lusaperidone has subnanomolar affinity for α2A and α2C adrenergic receptor (K i =0.13 and 0.15 nM, respectively) and shows nanomolar affinity for the hα2B adrenergic receptor and h5-HT7 receptors (K i =1 and 5 nM, respectively). Lusaperidone interacts weakly (K i values ranging between 81 and 920 nM) with dopamine-hD2L, -hD3 and -hD4, h5-HT1D-, h5-HT1F-, h5-HT2A-, h5-HT2C-, and h5-HT5A receptors. Lusaperidone, tested up to 10 μM, interacts only at micromolar concentrations or not at all with any of the other receptor or transporter binding sites tested in this study. Lusaperidone has been shown to reverse the clonidine-induced inhibition of cyclic AMP production mediated by human α2A and α2C adrenoceptors expressed in cell lines (K b is 2.8 and 4.4 nM, respectively) and is a full antagonist on both receptor subtypes. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
Lusaperidone occupies the α2A and α2C adrenergic receptor with an ED 50 of 0.014 mg/kg sc (0.009-0.019) and 0.026 mg/kg sc (0.022-0.030), respectively. The uptake of R107474 after in vivo intravenous administration is very rapid; in most tissues (including the brain) it reaches maximum concentration at 5 min after tracer injection . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Form:Solid
IC50& Target:Ki: 0.13 nM (α2A adrenergic receptor), 0.15 nM (α2C adrenergic receptor)
| Canonical Smiles | CC1=C(C(=O)N2C=CC=CC2=N1)CCN3CCC4=C(C3)C5=CC=CC=C5O4 |
|---|---|
| IUPAC Name | 3-[2-(3,4-dihydro-1H-[1]benzofuro[3,2-c]pyridin-2-yl)ethyl]-2-methylpyrido[1,2-a]pyrimidin-4-one |
| InChIKey | ZYXHQIPQIKTEDI-UHFFFAOYSA-N |
| INCHI | 1S/C22H21N3O2/c1-15-16(22(26)25-11-5-4-8-21(25)23-15)9-12-24-13-10-20-18(14-24)17-6-2-3-7-19(17)27-20/h2-8,11H,9-10,12-14H2,1H3 |
| Isomeric SMILES | CC1=C(C(=O)N2C=CC=CC2=N1)CCN3CCC4=C(C3)C5=CC=CC=C5O4 |
| Alternate CAS | 214548-46-6 |
| PubChem CID | 3045401 |
| MeSH Entry Terms | (11C)R107474;2-methyl-3-(2-(1,2,3,4-tetrahydrobenzo(4,5)furo(3,2-c)pyridin-2-yl)ethyl)-4H-pyrido(1,2-a)pyrimidin-4-one;R107474 |
| Molecular Weight | 359.42 |
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Pyridopyrimidines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridopyrimidines |
| Alternative Parents | Benzofurans Pyrimidones Aralkylamines Pyridines and derivatives Benzenoids Heteroaromatic compounds Furans Trialkylamines Lactams Oxacyclic compounds Azacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Pyridopyrimidine - Benzofuran - Aralkylamine - Pyrimidone - Pyridine - Pyrimidine - Benzenoid - Furan - Heteroaromatic compound - Lactam - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyridopyrimidines. These are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 21, 2025 | L647620 | |
| Certificate of Analysis | Jul 21, 2025 | L647620 | |
| Certificate of Analysis | Jul 21, 2025 | L647620 | |
| Certificate of Analysis | Jul 21, 2025 | L647620 |
| Solubility | DMSO : 3.45 mg/mL (9.60 mM; ultrasonic and warming and heat to 60°C) |
|---|---|
| Molecular Weight | 359.400 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 359.163 Da |
| Monoisotopic Mass | 359.163 Da |
| Topological Polar Surface Area | 49.100 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 751.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |
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