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1H-Thieno[3,4-d]iMidazole-4-pentanaMide, N-(5-aMinopentyl)hexahydro-2-oxo-, (3aS,4S,6aR)-, Mono(trifluoroacetate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

288259-39-2

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288259-39-2 Usage

Molecular Structure

The compound has a thienoimidazole ring, a pentanamide side chain, and a hexahydro-2-oxo group.

Stereochemistry

The compound has a (3aS, 4S, 6aR) stereochemistry.

Salt Form

It is found as a mono(trifluoroacetate) salt.

Potential Applications

The compound has potential applications in pharmaceutical research and drug development due to its possible biological activities and pharmacological properties.

Synthesis Building Block

The unique structure and functional groups make it a valuable building block for the synthesis of new compounds with potentially beneficial properties.

Further Research

Additional research and testing are required to fully understand the specific characteristics and potential uses of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 288259-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,2,5 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 288259-39:
(8*2)+(7*8)+(6*8)+(5*2)+(4*5)+(3*9)+(2*3)+(1*9)=192
192 % 10 = 2
So 288259-39-2 is a valid CAS Registry Number.

288259-39-2Downstream Products

288259-39-2Relevant academic research and scientific papers

An improved synthesis of a fluorophosphonate-polyethylene glycol-biotin probe and its use against competitive substrates

Xu, Hao,Sabit, Hairat,Amidon, Gordon L.,Showalter, H.D. Hollis

, p. 89 - 96 (2013)

The fluorophosphonate (FP) moiety attached to a biotin tag is a prototype chemical probe used to quantitatively analyze and enrich active serine hydrolases in complex proteomes in an approach called activity-based protein profiling (ABPP). In this study we have designed a novel synthetic route to a known FP probe linked by polyethylene glycol to a biotin tag (FP-PEG-biotin). Our route markedly increases the efficiency of the probe synthesis and overcomes several problems of a prior synthesis. As a proof of principle, FP-PEG-biotin was evaluated against isolated protein mixtures and different rat-tissue homogenates, showing its ability to specifically target serine hydrolases. We also assessed the ability of FP-PEG-biotin to compete with substrates that have high enzyme turnover rates. The reduced protein-band intensities resulting in these competition studies demonstrate a new application of FP-based probes seldom explored before.

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