Name | [3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2-methyl-4-oxo-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidin-9-yl] hexadecanoate |
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Synonyms |
3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido-[1,2-a]pyrimidin-4-one palmitate ester
9-Hydroxyrisperidone palmitate Xeplion PALPERIDONE PALMITATE UNII-R8P8USM8FR Paliperidone Palmitate Invega Sustenna Paliperidone Palmitate [USAN] 3-[2-[4-(6-fluoro-1,2-benzoisoxazol-3-yl)-1-piperidyl]ethyl]-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one palmitate ester Hexadecanoic acid, 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-9-yl ester 3-{2-[4-(6-Fluoro-1,2-benzoxazol-3-yl)-1-piperidinyl]ethyl}-2-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-9-yl palmitate |
Description | Paliperidone palmitate (9-Hydroxyrisperidone palmitate), an atypical long-acting antipsychotic agent, is an ester prodrug of Paliperidone. Paliperidone is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class. Paliperidone palmitate shows efficacy against schizophrenia[1]. |
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Related Catalog | |
Target |
5-HT2A Receptor D2 Receptor |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 736.3±70.0 °C at 760 mmHg |
Molecular Formula | C39H57FN4O4 |
Molecular Weight | 664.893 |
Flash Point | 399.1±35.7 °C |
Exact Mass | 664.436401 |
PSA | 90.46000 |
LogP | 9.85 |
Vapour Pressure | 0.0±2.4 mmHg at 25°C |
Index of Refraction | 1.590 |
Storage condition | -20℃ |
~77% 199739-10-1 |
Literature: WO2012/164582 A1, ; Page/Page column 11-12 ; |
~90% 199739-10-1 |
Literature: WO2009/89076 A2, ; Page/Page column 15; 29 ; |
~81% 199739-10-1 |
Literature: WO2009/89076 A2, ; Page/Page column 28 ; |
~55% 199739-10-1 |
Literature: WO2009/89076 A2, ; Page/Page column 25-26 ; |
~10% 199739-10-1 |
Literature: WO2009/89076 A2, ; Page/Page column 9; 26 ; |
~% 199739-10-1 |
Literature: WO2012/164582 A1, ; |
~% 199739-10-1 |
Literature: WO2012/164582 A1, ; |
Precursor 6 | |
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DownStream 1 | |