155593-75-2
Chemical Structure
Perphenazine-d4
- CAS No.: 155593-75-2
- Formula:C21H22D4ClN3OS
- Molecular Weight:407.99
IUPAC Name: 2-(4-(3-(2-chloro-10H-phenothiazin-10-yl-1,3,7,9-d4)propyl)piperazin-1-yl)ethan-1-ol
InChIKey: RGCVKNLCSQQDEP-WNJORUDBSA-N
SMILES: OCCN(CC1)CCN1CCCN2C3=C([2H])C(Cl)=C([2H])C=C3SC4=CC([2H])=CC([2H])=C42
Biological Activity: Perphenazine-d4 is the deuterium labeled Perphenazine. Perphenazine is a typical antipsychotic agent, inhibits 5-HT2Areceptor, Alpha-1A adrenergic receptor, Dopamine receptor D2/D3, D2L receptor, and Histamine H1 receptor, with Ki values of 5.6, 10, 0.765/0.13, 3.4, and 8 nM, respectively.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Perphenazine-d4 | 98.83% | Perphenazine-d4 is the deuterium labeled Perphenazine. Perphenazine is a typical antipsychotic agent, inhibits 5-HT2Areceptor, Alpha-1A adrenergic receptor, Dopamine receptor D2/D3, D2L receptor, and Histamine H1 receptor, with Ki values of 5.6, 10, 0.765/0.13, 3.4, and 8 nM, respectively. | ||||||||||||||||||||
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Perphenazine (Standard) | ≥98% | Perphenazine (Standard) is the analytical standard of Perphenazine. This product is intended for research and analytical applications. Perphenazine is an orally active dopamine receptor and histamine-1 receptor antagonist, with Ki values of 0.56 nM (D2), 0.43 nM (D3), 6 nM (5-HT2A), respectively. Perphenazine also binds to Alpha-1A adrenergic receptor. Perphenazine inhibits cancer cell proliferation, and induces apoptosis. Perphenazine can be used in the research of mental disease, cancer, inflammation. | ||||||||||||||||||||
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Perphenazine-d6 fumarate | Perphenazine-d6 (fumarate) is a deuterated labeled Perphenazine. Perphenazine is an orally active dopamine receptor and histamine-1 receptor antagonist, with Ki values of 0.56 nM (D2), 0.43 nM (D3), 6 nM (5-HT2A), respectively. Perphenazine also binds to Alpha-1A adrenergic receptor. Perphenazine inhibits cancer cell proliferation, and induces apoptosis. Perphenazine can be used in the research of mental disease, cancer, inflammation. | |||||||||||||||||||||
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Perphenazine | 99.81% | Perphenazine is an orally active dopamine receptor and histamine-1 receptor antagonist, with Ki values of 0.56 nM (D2), 0.43 nM (D3), 6 nM (5-HT2A), respectively. Perphenazine also binds to Alpha-1A adrenergic receptor. Perphenazine inhibits cancer cell proliferation, and induces apoptosis. Perphenazine can be used in the research of mental disease, cancer, inflammation. | ||||||||||||||||||||
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Similarity Score 0.97
HY-A0077APerphenazine dihydrochloride -
Similarity Score 0.83
![4-[3-(10H-Phenothiazin-10-yl)propyl]-1-piperazineethanol Chemical Structure](//file.medchemexpress.com/product_pic/hy-w587792.gif)
HY-W5877924-[3-(10H-Phenothiazin-10-yl)propyl]-1-piperazineethanol -
Similarity Score 0.80
HY-116916Acetophenazine -
Similarity Score 0.80
HY-133092Perphenazine sulfoxide -
Similarity Score 0.79
HY-119980Fluphenazine -
Similarity Score 0.79
HY-119980BFluphenazine hydrochloride -
Similarity Score 0.78
HY-137088Imiclopazine -
Similarity Score 0.78
HY-A0081RFluphenazine dihydrochloride (Standard) -
Similarity Score 0.78
HY-A0211Carphenazine -
Explore the MedChemAI to find more analogs
![4-[3-(10H-Phenothiazin-10-yl)propyl]-1-piperazineethanol Chemical Structure](http://file.medchemexpress.com/product_pic/hy-w587792.gif)
