AJ-76 HCL - Moligand™, ≥98% , Antagonist of D 3 receptor, CAS No.85378-82-1, Antagonist of D 3 receptor

CAS: 85378-82-1 Cat. No.: A337224 Formula: C₁₅H₂₃NO•HCl Peso molecolare: 269.81

GRADE & PURITY Moligand™, ≥98%

Synonyms

SCHEMBL276252 | AJ76(+) | AJ76-(+) | 5-methoxy-1-methyl-2-(n-propylamino)tetralin | (1S,2R)-(5-Methoxy-1-methyl-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine | (1S,2R)-5-methoxy-1-methyl-2-(propylamino)tetralin | (1S,2R)-5-methoxy-1-methyl-N-propyl-1,2

Storage

Store at 2-8°C

Shipped In

Wet ice

Panoramica

AJ-76 HCL is a selective antagonist of dopamine autoreceptors, which displays a reduction in ventral firing rates of dopaminergic neurons. Studies indicate that AJ-76 HCL increases dopamine synthesis in the nigrostriatal system in neurons with partial lesions. It is known that the effects of AJ-76 HCL displays similar effects on dopamine receptors as cocaine. Based on these properties this compound is essential in studying the effects of cocaine on dopamine release from neurons.

Specifications

Sinonimi

SCHEMBL276252 | AJ76(+) | AJ76-(+) | 5-methoxy-1-methyl-2-(n-propylamino)tetralin | (1S,2R)-(5-Methoxy-1-methyl-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine | (1S,2R)-5-methoxy-1-methyl-2-(propylamino)tetralin | (1S,2R)-5-methoxy-1-methyl-N-propyl-1,2

Specifiche e purezza

Moligand™, ≥98%

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

ANTAGONIST

Meccanismo d'azione

Antagonist of D 3 receptor

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 528763064
• Sorrisi canonici: CCCNC1CCC2=C(C1C)C=CC=C2OC.Cl
• IUPAC Name: (1S,2R)-5-methoxy-1-methyl-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine;hydrochloride
• InChIKey: KIRYNZFMOLYYQB-YECZQDJWSA-N
• INCHI: 1S/C15H23NO.ClH/c1-4-10-16-14-9-8-13-12(11(14)2)6-5-7-15(13)17-3;/h5-7,11,14,16H,4,8-10H2,1-3H3;1H/t11-,14+;/m0./s1
• Isomeri SMILES: CCCN[C@@H]1CCC2=C([C@@H]1C)C=CC=C2OC.Cl
• Peso molecolare: 269.81
• Reaxy-Rn: 13515057
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13515057&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Tetralins

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Tetralins
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetralins
• Alternative Parents: Anisoles Aralkylamines Alkyl aryl ethers Dialkylamines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Tetralin - Anisole - Alkyl aryl ether - Aralkylamine - Secondary aliphatic amine - Ether - Secondary amine - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Aromatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.
• External Descriptors: hydrochloride

Data sources

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

Obiettivi associati (umani)

CYP2D6 Tclin Cytochrome P450 2D6 (1 Activities)

Discover Target: CYP2D6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

DRD2 Tclin D(2) dopamine receptor (1 Activities)

Discover Target: DRD2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

DRD3 Tclin D(3) dopamine receptor (4 Activities)

Discover Target: DRD3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Proprietà chimiche e fisiche

• Solubilità: Soluble in 50% aq. ethanol (20 mg/ml)
• Sensibilità: Moisture sensitive
• Peso molecolare: 269.810 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 269.155 Da
• Monoisotopic Mass: 269.155 Da
• Topological Polar Surface Area: 21.300 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 231.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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: 2

XLogP3