Lusaperidone - Moligand™, ≥99% , CAS No.214548-46-6

CAS: 214548-46-6 Cat. No.: L647620 Formule: C22H21N3O2 Poids moléculaire: 359.42 PubChem CID: 3045401
DISPONIBLE À COMMANDE
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%
Synonyms
EN300-19634530 | AKOS040733633 | MS-25665 | UNII-5KTD2O86CB | Lusaperidone | R107474 | 3-(2-(3,4-Dihydrobenzofuro[3,2-c]pyridin-2(1H)-yl)ethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | BDBM50403744
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Allemagne (EU)
USA*
Price
Qty
1mg
L647620-1mg
—
4 En stock
183,87€
5mg
L647620-5mg
—
3 En stock
550,06€
25mg
L647620-25mg
—
3 En stock
1 100,21€
100mg
L647620-100mg
—
2 En stock
2 256,03€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

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)

Specifications

Synonymes
EN300-19634530 | AKOS040733633 | MS-25665 | UNII-5KTD2O86CB | Lusaperidone | R107474 | 3-(2-(3,4-Dihydrobenzofuro[3,2-c]pyridin-2(1H)-yl)ethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | BDBM50403744
Spécifications et pureté
Moligand™, ≥99%
Mécanismes biochimiques et physiologiques
Lusaperidone (R107474) is an α2 adrenergic receptor antagonist with K i s of 0.13 and 0.15 nM for α2A and α2C, respectively.
Conditions de stockage 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
ANTAGONIST
Pureté
≥99%
Noms et identifiants
Pubchem Sid528765404
Sourires canoniquesCC1=C(C(=O)N2C=CC=CC2=N1)CCN3CCC4=C(C3)C5=CC=CC=C5O4
IUPAC Name3-[2-(3,4-dihydro-1H-[1]benzofuro[3,2-c]pyridin-2-yl)ethyl]-2-methylpyrido[1,2-a]pyrimidin-4-one
InChIKeyZYXHQIPQIKTEDI-UHFFFAOYSA-N
INCHI1S/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
Isomères SMILES CC1=C(C(=O)N2C=CC=CC2=N1)CCN3CCC4=C(C3)C5=CC=CC=C5O4
CAS alternatif 214548-46-6
PubChem CID 3045401
Termes d'entrée MeSH (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
Poids moléculaire 359.42

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassePyridopyrimidines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyridopyrimidines
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 FrameworkAromatic 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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
ADRA2B Tclin Alpha-2B adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2C Tclin Alpha-2C adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2A Tclin Alpha-2A adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
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.

4 results found

Lot NumberCertificate TypeDateArticle
I2524502Certificate of AnalysisJul 21, 2025 L647620
I2524503Certificate of AnalysisJul 21, 2025 L647620
I2524505Certificate of AnalysisJul 21, 2025 L647620
I2524506Certificate of AnalysisJul 21, 2025 L647620
Propriétés chimiques et physiques
SolubilitéDMSO : 3.45 mg/mL (9.60 mM; ultrasonic and warming and heat to 60°C)
Poids moléculaire359.400 g/mol
XLogP32.800
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass359.163 Da
Monoisotopic Mass359.163 Da
Topological Polar Surface Area49.100 Ų
Heavy Atom Count27
Formal Charge0
Complexity751.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculateurs de solution
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