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10-[(1S)-octahydro-2H-quinolizin-1-ylacetyl]-10H-phenothiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104960-17-0

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104960-17-0 Usage

Molecular structure

Contains a phenothiazine ring and a quinolizine ring

Stereochemistry

(1S)-configuration at the quinolizine ring

Antipsychotic effects

Potential to alleviate symptoms of schizophrenia and bipolar disorder

Antiemetic effects

Potential to treat nausea and vomiting

Mechanism of action

Believed to act on dopamine receptors in the brain

Usage

Should be used under the supervision of a healthcare professional

Potential side effects

Not specified, but caution is advised due to possible side effects and interactions with other medications

Derivative

Phenothiazine derivative

Organic compound

Yes, classified as an organic compound

Applications

Potential use in the treatment of psychiatric conditions and nausea/vomiting, but further research and clinical trials are needed to confirm its efficacy and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 104960-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104960-17:
(8*1)+(7*0)+(6*4)+(5*9)+(4*6)+(3*0)+(2*1)+(1*7)=110
110 % 10 = 0
So 104960-17-0 is a valid CAS Registry Number.

104960-17-0Upstream product

104960-17-0Downstream Products

104960-17-0Relevant academic research and scientific papers

N-Homolupinanoyl and N-(ω-lupinylthio)alkanoyl derivatives of some tricyclic systems as ligands for muscarinic M1 and M2 receptor subtypes

Tasso, Bruno,Sparatore, Anna,Sparatore, Fabio

, p. 669 - 676 (2003)

A set of N-homolupinanoyl- and N-(ω-lupinylthio)alkanoyl derivatives of tricyclic systems (as phenothiazine, iminodibenzyl and dihydropyridobenzodiazepinone) has been prepared and tested for affinity for rat muscarinic M1 and M2 receptor subtypes labeled with [3H]pirenzepine and [3H]AF-DX 384. Good affinity for both M1 and M2 subtypes was displayed by most compounds, often with nanomolar Ki values, which for lupinylthiopropionyl- and lupinylthiobutyryl-phenothiazines (13-16) were comparable to those of pirenzepine and methoctramine, respectively. However, only moderate selectivity for one or the other subtype was seen.

Preparation and pharmacological activities of 10-homolupinanoyl-2-R- phenothiazines

Sparatore,Sparatore

, p. 5 - 17 (2007/10/02)

Pursuing our researches on quinolizidinyl derivatives of phenothiazine and on the ground of antidepressive, diuretic, antianginal and antiarrhythmic activities of several 10-(3-dialkylamino) propionylphenothiazines (as chloracizine, moricizine, etc.), six

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