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1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid is a complex organic compound characterized by the presence of a piperidine ring with a carboxylic acid group, a naphthalene group with a methyl substituent, and a cyclohexyl group attached to it. The molecule also features a tert-butyl group, which adds to its structural complexity. 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid is likely to possess pharmaceutical or biological activity due to the presence of the piperidine ring and carboxylic acid group, which are common in drugs and natural products. The cyclohexyl and naphthalene groups may further contribute to the compound's physical and chemical properties.

1621065-22-2

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1621065-22-2 Usage

Uses

1. Used in Pharmaceutical Industry:
1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid is used as a potential pharmaceutical agent for its possible biological activity. The presence of the piperidine ring and carboxylic acid group suggests that it may interact with biological targets, making it a candidate for drug development.
2. Used in Chemical Research:
1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid can be utilized in chemical research for studying the effects of its unique structural features on its physical and chemical properties. The cyclohexyl and naphthalene groups, along with the tert-butyl group, may provide insights into the compound's behavior in various chemical reactions and interactions.
3. Used in Material Science:
The complex structure of 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid may offer unique properties that can be exploited in the development of new materials for various applications, such as in the fields of electronics, coatings, or polymers.
4. Used in Drug Delivery Systems:
Similar to gallotannin, 1-((2-(((trans)-4-(tert-butyl)cyclohexyl)oxy)-4-methylnaphthalen-1-yl)methyl)piperidine-4-carboxylic acid could potentially be employed in drug delivery systems to improve the delivery, bioavailability, and therapeutic outcomes of other pharmaceutical agents. The specific structural features of the compound may allow for targeted or controlled release of drugs, enhancing their efficacy and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1621065-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,0,6 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1621065-22:
(9*1)+(8*6)+(7*2)+(6*1)+(5*0)+(4*6)+(3*5)+(2*2)+(1*2)=122
122 % 10 = 2
So 1621065-22-2 is a valid CAS Registry Number.

1621065-22-2Downstream Products

1621065-22-2Relevant academic research and scientific papers

Novel Potent Selective Orally Active S1P5 Receptor Antagonists

Ma, Bin,Guckian, Kevin M.,Liu, Xiao-Gao,Yang, Chunhua,Li, Bing,Scannevin, Robert,Mingueneau, Micha?l,Drouillard, Annabelle,Walzer, Thierry

, (2021/02/01)

S1P5 is one of the five sphingosine-1-phosphate (S1P) receptors which play important roles in immune and CNS cell homeostasis, growth, and differentiation. Little is known about the effect of modulation of S1P5 due to the lack of S1P5 specific modulators with suitable druglike properties. Here we describe the discovery and optimization of a novel series of potent selective S1P5 antagonists and the identification of an orally active brain-penetrant tool compound 15.

S1P MODULATING AGENTS

-

, (2014/08/19)

Compounds of formula (I) can modulate the activity of one or more S 1P receptors. Sphingosine 1-phosphate (S IP) is a lysophospholipid mediator that evokes a variety of cellular responses by stimulation of five members of the endothelial cell differentiation gene (EDG) receptor family, namely S1P1, S1P2, S1P3, S1P4, and S1P5 (formerly EDG1, EDG5, EDG3, EDG6 and EDG8). The EDG receptors are G-protein coupled receptors (GPCRs) and on stimulation propagate second messenger signals via activation of heterotrimeric G-protein alpha (Ga.) subunits and beta-gamma (G()y) dimers.

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