duloxetine

Duloxetine is an inhibitor of serotonin-norepinephrine reuptake(Ki of 4.6 nM),with treatment of major depressive disorder and generalized anxiety disorder.

Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a thiophene derivative and selective neurotransmitter uptake inhibitor for serotonin and noradrenaline (SNRI). It is an antidepressant agent and anxiolytic, also used for treating pain in patients with diabetes mellitus and fibromyalgia.

Duloxetine-D3 hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for the treatment of major depressive disorder and generalized anxiety disorder (GAD). Duloxetine D3 hydrochloride ( (S)-Duloxetine D3 hydrochloride) is a deuterium-labeled Duloxetine hydrochloride (TMSM-3429).

N-Methyl Duloxetine hydrochloride elicits both tonic and use-dependent block of neuronal Na+ channels. N-Methyl Duloxetine hydrochloride is an analgesic.

(R)-Duloxetine, an isomer of Duloxetine, induces tonic and use-dependent blockade of neuronal Na+ channels. This compound is utilized in pain research.

5-Hydroxy-6-methoxy (S)-duloxetine maleate is an orally bioavailable and brain-penetrant serotonin (5-HT) and norepinephrine (NE) reuptake inhibitor with antidepressant and analgesic properties. It holds potential for research in psychiatric and neurological disorders such as depression, diabetic neuropathic pain, generalized anxiety disorder, and fibromyalgia.

(±)-Duloxetine ((Rac)-Duloxetine) hydrochloride is the racemate of Duloxetine hydrochloride and is used in research for diabetic neuropathic pain, fibromyalgia, and major depressive disorder as a serotonin-norepinephrine reuptake inhibitor [1].

(R)-Duloxetine Hydrochloride is a napthalenyloxy-substituted amine used in binding studies of human serum albumin along with (S)-Duloxetine. Unlike its enantiomer, it is not a very effective dual serotonin and norepinephrine reuptake inhibitor (SNRI).

Duloxetine-D3 hydrochloride is a deuterated compound of Duloxetine hydrochloride. Duloxetine hydrochloride has a CAS number of 136434-34-9. Duloxetine hydrochloride (T1471) is a thiophene derivative and selective neurotransmitter uptake inhibitor for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.

rac-Duloxetine-D3 is a deuterated compound of rac-Duloxetine. rac-Duloxetine has a CAS number of 116817-13-1.

Duloxetine-D3 Hcl (Standard) is a reference standard of Duloxetine-D3 Hcl intended for quantitative analysis, quality control, and related biochemical research applications. Duloxetine-d3 HCl is a deuterated compound of Duloxetine HCl. Duloxetine HCl has a CAS number of 136434-34-9. Duloxetine hydrochloride is a thiophene derivative and selective neurotransmitter uptake inhibitor for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.

4-Hydroxy duloxetine β-D-glucuronide (4-Hydroxy duloxetine glucuronide) sodium is one of the main metabolites of Duloxetine. This compound holds potential for research involving impaired liver or kidney function.

Duloxetine impurity 1 is a type of Duloxetine impurity.

Duloxetine metabolite Para-Naphthol Duloxetine is an inactive metabolite of Duloxetine. Duloxetine is an antidepressant and a serotonin-norepinephrine reuptake inhibitor (SNRI).

5-hydroxy-6-methoxy (S)-Duloxetine is a metabolite of (S)-duloxetine . It is formed from (S)-duloxetine via a 5- or 6-hydroxy duloxetine intermediate, which is formed by the cytochrome P450 (CYP) isoforms CYP1A2 and CYP2D6, and a catechol duloxetine intermediate. 5-hydroxy-6-methoxy (S)-Duloxetine binds to the serotonin (5-HT), norepinephrine, and dopamine transporters with Ki values of 266, 920, and 2,814 nM, respectively.

(S)-5-hydroxy-6-methoxy Duloxetine, an active metabolite of the (S)-duloxetine, functions as a serotonin (5-HT) and norepinephrine reuptake inhibitor. Its formation occurs through the cytochrome P450 (CYP) isoforms CYP1A2 and CYP2D6 via a 5- or 6-hydroxy duloxetine intermediate, followed by a catechol duloxetine intermediate. This compound effectively inhibits the serotonin transporter (SERT), norepinephrine transporter (NET), and dopamine transporter (DAT) across lipid membranes, with inhibition constants (Kis) of 266, 920, and 2,814 nM, respectively, for human transporters.

Duloxetine-D7 is a deuterated compound of Duloxetine. Duloxetine (T7061) has a CAS number of 116539-59-4. Duloxetine (T7061) is an inhibitor of serotonin-norepinephrine reuptake (Ki of 4.6 nM),with treatment of major depressive disorder and generalized anxiety disorder.

Duloxetine-D7 Maleate is a deuterated compound of Duloxetine Maleate. Duloxetine Maleate has a CAS number of 116817-86-8.

Duloxetine hydrochloride (Standard) is a reference standard for research and analysis in studies involving Duloxetine hydrochloride. Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a thiophene derivative and selective neurotransmitter uptake inhibitor for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.

Duloxetine-[D3] Oxalate (Standard) is a reference standard of Duloxetine-[D3] Oxalate intended for quantitative analysis, quality control, and related biochemical research applications.