129938-20-1
129938-20-1
Chemical Structure
Dapoxetine hydrochloride
Synonym(s): LY-210448 hydrochloride
- CAS No.: 129938-20-1
- Formula:C21H24ClNO
- Molecular Weight:341.87
IUPAC Name: (S)-N,N-dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride
InChIKey: IHWDIQRWYNMKFM-BDQAORGHSA-N
SMILES: CN(C)[C@H](C1=CC=CC=C1)CCOC2=C3C(C=CC=C3)=CC=C2.Cl
Biological Activity: Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine hydrochloride can be used for the research of premature ejaculation (PE)[1].
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Dapoxetine hydrochloride | 99.87% | Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine hydrochloride can be used for the research of premature ejaculation (PE). | ||||||||||||||||||||
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Dapoxetine hydrochloride (Standard) | ≥98% | Dapoxetine (hydrochloride) (Standard) is the analytical standard of Dapoxetine (hydrochloride). This product is intended for research and analytical applications. Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine hydrochloride can be used for the research of premature ejaculation (PE). | ||||||||||||||||||||
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Dapoxetine-d7 | Dapoxetine-d7 (LY-210448-d7) is the deuterium labeled Dapoxetine (HY-B0304). Dapoxetine (LY-210448) is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine can be used for the research of premature ejaculation (PE). | |||||||||||||||||||||
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Dapoxetine-d6 hydrochloride | 99.68% | Dapoxetine-d6 (LY-210448-d6) hydrochloride is the deuterium labeled Dapoxetine hydrochloride. Dapoxetine hydrochloride is a short-acting selective serotonin reuptake inhibitor (SSRI) | ||||||||||||||||||||
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(rac)-Dapoxetine-d6 hydrochloride | (rac)-Dapoxetine-d6 (hydrochloride) is the deuterium labeled (rac)-Dapoxetine hydrochloride. | |||||||||||||||||||||
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Dapoxetine-d7 hydrochloride | 99.96% | Dapoxetine-d7 (hydrochloride) is the deuterium labeled Dapoxetine hydrochloride. Dapoxetine hydrochloride is a short-acting selective serotonin reuptake inhibitor (SSRI). | ||||||||||||||||||||
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LY125180 | LY125180 is a serotonin uptake inhibitor. LY125180 competitively inhibits the uptake of serotonin and norepinephrine by cortical synaptosomes and of dopamine by striatal synaptosomes, with Ki values of 0.06 μM, 2.2 μM and 2.5 μM respectively. | |||||||||||||||||||||
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(Rac)-N-desmethyl Dapoxetine-d7 (hydrochloride) | (Rac)-N-desmethyl Dapoxetine-d7 hydrochloride is the deuterium labeled (Rac)-N-desmethyl Dapoxetine hydrochloride. | |||||||||||||||||||||
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Duloxetine-d7 | 97.30% | Duloxetine-d7 ((S)-Duloxetine-d7) is the deuterium labeled Duloxetine. Duloxetine is a serotonin-norepinephrine reuptake inhibitor with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD). | ||||||||||||||||||||
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Dapoxetine (Standard) | ≥98% | Dapoxetine (Standard) is the analytical standard of Dapoxetine. This product is intended for research and analytical applications. Dapoxetine (LY-210448) is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine can be used for the research of premature ejaculation (PE). | ||||||||||||||||||||
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Dapoxetine-d6 | Dapoxetine-d6 is the deuterium labeled Dapoxetine. Dapoxetine (LY-210448) is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine can be used for the research of premature ejaculation (PE). | |||||||||||||||||||||
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Phenoxybenzamine-d5 hydrochloride | Phenoxybenzamine-d5 (hydrochloride) is the deuterium labeled Phenoxybenzamine hydrochloride. Phenoxybenzamine hydrochloride is a nonselective, irreversible, orally active α-adrenoceptor antagonist that is commonly used for the research of hypertension, specifically caused by pheochromocytoma. Phenoxybenzamine hydrochloride also shows antitumor activity. | |||||||||||||||||||||
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Propranolol-d7 (ring-d7) | 99.71% | Propranolol-d7 (ring-d7) is the deuterium labeled Propranolol hydrochloride. Propranolol hydrochloride is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. Propranolol hydrochloride inhibits [3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM. Propranolol hydrochloride is used for study of hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy. | ||||||||||||||||||||
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(Rac)-Dapoxetine hydrochloride | 99.49% | (Rac)-Dapoxetine hydrochloride is a racemate of Dapoxetine hydrochloride (HY-B0304A). Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI). Dapoxetine hydrochloride can be used for the research of premature ejaculation (PE). | ||||||||||||||||||||
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Cinacalcet impurity 13 | Cinacalcet impurity 13 is an impurity of Cinacalcet. | |||||||||||||||||||||
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(S)-N-methyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride (Standard) | ≥98% | (S)-N-methyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride (Standard) is the analytical standard of (S)-N-methyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride. This product is intended for research and analytical applications. | ||||||||||||||||||||
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Duloxetine impurity 8 | Duloxetine impurity 8 is an impurity of Duloxetine. | |||||||||||||||||||||
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Duloxetine impurity 8 hydrochloride | Duloxetine impurity 8 hydrochloride is an impurity of Duloxetine hydrochloride. | |||||||||||||||||||||
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