파록세틴

한글명:파록세틴

카스 번호61869-08-7

상품명:Paroxetine

CBNumberCB5178021

분자식C19H20FNO3

포뮬러 무게329.37

MOL 파일61869-08-7.mol

동의어(한글)

파록세틴

화학적 성질

녹는점	114-116°C
끓는 점	451.7±45.0 °C(Predicted)
밀도	1.1844 (estimate)
저장 조건	under inert gas (nitrogen or Argon) at 2–8 °C
산도 계수 (pKa)	pKa 9.51 (Uncertain)
CAS 데이터베이스	61869-08-7(CAS DataBase Reference)
NIST	Paroxetine(61869-08-7)
EPA	Paroxetine (61869-08-7)

위험 및 안전 성명

유엔번호(UN No.)	3249
위험 등급	6.1(b)
포장분류	III
유해 물질 데이터	61869-08-7(Hazardous Substances Data)

그림문자(GHS)

파록세틴 화학적 특성, 용도, 생산

개요
Paroxetine is a new highly selective serotonin reuptake inhibitor, mechanistically similar to fluoxetine, fluvoxamine and sertraline, introduced for the treatment of all types of depressive illnesses including depression associated with anxiety. It is reportedly non-sedating and non-stimulatory and compared to fluoxetine has a shorter duration of action (half-life of 24 hours versus 2 to 3 days). Paroxetine is also being investigated as a treatment for obesity, alcoholism and obsessive-compulsive disorders.
화학적 성질
White Solid
용도
A istopically labelled selective serotonin reuptake inhibitor. Used as an antidepressant
Biological Functions
Paroxetine (Paxil) has an elimination half-life of 21 hours and is also highly bound to plasma proteins, so it requires special attention when administered with drugs such as warfarin. Paroxetine is a potent inhibitor of the cytochrome P450 2D6 isoenzyme and can raise the plasma levels of drugs metabolized via this route. Of particular concern are drugs with a narrow therapeutic index, such as TCAs and the type 1C antiarrhythmics flecainide, propafenone, and encainide. Additionally, paroxetine itself is metabolized by this enzyme and inhibits its own metabolism, leading to nonlinear kinetics. Weight gain is higher with paroxetine than with the other SSRIs, and it tends to be more sedating, presumably because of its potential anticholinergic effects. Additionally, patients have had difficulty with abrupt discontinuation with this agent, reporting a flulike syndrome; this symptom can be avoided by tapering the medication.
일반 설명
In the structure of paroxetine (Paxil), an amino group, protonatedin vivo could H-bond with the–CH₂–O– unshared electrons.A β-arylamine–like structure with an extra aryl groupresults. The compound is a very highly selective SERT. Asexpected, it is an effective antidepressant and anxiolytic.
Clinical Use
In vitro binding studies suggest that paroxetine is a more selective and potent inhibitor of 5-HT reuptake than fluoxetine. The drug essentially has no effect on NE or dopamine reuptake, nor does it show affinity for other neuroreceptors. Its onset of action is 1 to 4 weeks.

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