ChemicalBook--->CAS DataBase List--->1239729-06-6

1239729-06-6

1239729-06-6 Structure

1239729-06-6 Structure
IdentificationBack Directory
[Name]

RP-5063
[CAS]

1239729-06-6
[Synonyms]

RP-5063
Brilaroxazine
[Molecular Formula]

C22H25Cl2N3O3
[MDL Number]

MFCD34469282
[MOL File]

1239729-06-6.mol
[Molecular Weight]

450.36
Chemical PropertiesBack Directory
[Boiling point ]

643.0±55.0 °C(Predicted)
[density ]

1.301±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, protect from light
[solubility ]

DMSO : 100 mg/mL (222.04 mM; Need ultrasonic)
[form ]

Solid
[pka]

12.36±0.20(Predicted)
[color ]

Off-white to light yellow
[InChI]

InChI=1S/C22H25Cl2N3O3/c23-17-4-3-5-19(22(17)24)27-11-9-26(10-12-27)8-1-2-13-29-16-6-7-20-18(14-16)25-21(28)15-30-20/h3-7,14H,1-2,8-13,15H2,(H,25,28)
[InChIKey]

PMKMNTBZJOXTJW-UHFFFAOYSA-N
[SMILES]

O1C2=CC=C(OCCCCN3CCN(C4=CC=CC(Cl)=C4Cl)CC3)C=C2NC(=O)C1
Hazard InformationBack Directory
[Uses]

Brilaroxazine was developed as a antipsychotic which may be effective in the treatment of schizophrenia and bipolar disorder.
[in vivo]

Brilaroxazine (oral gavage; 10 mg/kg; twice daily; 28 days) limits the functional and structural effects of pulmonary arterial hypertension (PAH), with significant improvements in pulmonary hemodynamics, right ventricular (RV) hypertrophy, SO2, and pulmonary blood vessel structural changes[1].

Animal Model:SD-rats[2]
Dosage:10 mg/kg
Administration:Oral gavage; twice daily; 28 days
Result:Had the efficacy in PAH, and mitigated the functional and structural effects of MCT-induced PAH.
[IC 50]

5-HT1A Receptor: 1.5 nM (Ki); 5-HT2A Receptor: 2.5 nM (Ki); 5-HT2B Receptor: 0.19 nM (Ki); 5-HT7 Receptor: 2.7 nM (Ki); D2 Receptor; D3 Receptor; D4 Receptor
Spectrum DetailBack Directory
[Spectrum Detail]

RP-5063(1239729-06-6)1HNMR
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