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2-(piperidin-1-yl)-1-(2,4,6-trimethoxyphenyl)ethanone is a complex organic compound with the molecular formula C18H26N2O4. It features a piperidin-1-yl group attached to the 2-position of an ethanone (ketone) moiety, and a 2,4,6-trimethoxyphenyl group at the 1-position. The compound is characterized by its unique structure, which includes a six-membered piperidine ring and a methoxy-substituted phenyl ring. This chemical is primarily of interest in the field of organic chemistry, potentially for its pharmacological properties or as a synthetic intermediate in the preparation of more complex molecules. Its specific applications and properties would depend on further research and characterization, as the compound's behavior in various chemical reactions and its potential biological activity are not detailed in this summary.

4902-14-1

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4902-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4902-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4902-14:
(6*4)+(5*9)+(4*0)+(3*2)+(2*1)+(1*4)=81
81 % 10 = 1
So 4902-14-1 is a valid CAS Registry Number.

4902-14-1Upstream product

4902-14-1Downstream Products

4902-14-1Relevant academic research and scientific papers

A Novel Parkinson's Disease Drug Candidate with Potent Anti-neuroinflammatory Effects through the Src Signaling Pathway

Wang, Ya-Dan,Bao, Xiu-Qi,Xu, Song,Yu, Wen-Wen,Cao, Sheng-Nan,Hu, Jin-Ping,Li, Yan,Wang, Xiao-Liang,Zhang, Dan,Yu, Shi-Shan

, p. 9062 - 9079 (2016)

Numerous drug treatments are available for Parkinson's disease (PD), an age-related neurodegenerative disease, but most cause serious side effects. Therefore, novel therapeutic strategies that halt disease progression and allow for long-term administration are urgently needed. Neuroinflammation critically contributes to the pathogenesis of PD. Here, we report the discovery and optimization of phloroglucinol derivatives, a novel class of anti-neuroinflammatory compounds. Structural modifications of the hit compound 3-methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one produced 43 derivatives, including a preclinical candidate (compound 21), that exhibited potent in vitro anti-neuroinflammatory effects, good blood-brain barrier penetration, and desirable safety margins in mice at a median lethal dose (LD50) >5000 mg/kg. Its in vivo efficacy was demonstrated in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)- and MPTP/probenecid (prob)-induced subacute and chronic PD models, respectively, and α-synuclein transgenic mice. Mechanistic studies revealed neuroinflammation inhibition by targeting Src/phosphatase and tensin homologue deleted on chromosome 10 (PTEN)/Akt signaling might be promising. We highlighted the potential usefulness of phloroglucinol derivatives in PD treatment.

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