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S-(2,4-Dinitrophenyl)-cystein, also known as DNP-Cysteine, is a chemical compound derived from the amino acid cysteine. It is formed by the reaction of cysteine with 2,4-dinitrophenyl chloride, resulting in a conjugate that is often used in biochemical research. S-(2,4-Dinitrophenyl)-cystein is particularly useful for studying protein structure and function, as it can be used to modify proteins by attaching the DNP group to cysteine residues. The DNP group is a chromophore, which means it absorbs light in the ultraviolet region, making it a valuable tool for detecting and quantifying proteins in various assays. Additionally, the DNP-Cysteine conjugate can be used to investigate the role of cysteine in biological processes and to understand the effects of its modification on protein stability and activity.

3165-76-2

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3165-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3165-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3165-76:
(6*3)+(5*1)+(4*6)+(3*5)+(2*7)+(1*6)=82
82 % 10 = 2
So 3165-76-2 is a valid CAS Registry Number.

3165-76-2Downstream Products

3165-76-2Relevant academic research and scientific papers

Nile-red-based fluorescence probe for selective detection of biothiols, computational study, and application in cell imaging

Meng, Zhi-Zhong,Rong, Xiang,Xu, Zhong-Yong,Yan, Jin-Wu,Zhang, Lei,Zhu, Bin

, (2020)

A new colorimetric and fluorescence probe NRSH based on Nile-red chromophore for the detection of biothiols has been developed, exhibiting high selectivity towards biothiols over other interfering species. NRSH shows a blue shift in absorption peak upon reacting with biothiols, from 587 nm to 567 nm, which induces an obvious color change from blue to pink and exhibits a 35-fold fluorescence enhancement at 645 nm in red emission range. NRSH displays rapid (2S, which is faster than other biothiols (>5 min). The detection limits of probe NRSH towards biothiols are very low (22.05 nM for H2S, 34.04 nM for Cys, 107.28 nM for GSH and 113.65 nM for Hcy). Furthermore, NRSH is low cytotoxic and can be successfully applied as a bioimaging tool for real-time monitoring biothiols in HeLa cells. In addition, fluorescence mechanism of probe NRSH is further understood by theoretical calculations.

Two chemodosimeters for fluorescence recognition of biothiols in aqueous solution and their bioimaging application

Du, Wei,Liu, Rui-Juan,Fang, Jianguo,Gao, Hong,Wang, Ya-Wen,Peng, Yu

, (2019)

Two fluorescein derivatives containing 2,4-dinitrobenzenesulfonyl group have been developed as fluorescent probes to detect the biothiols (Cys, Hcy and GSH) in aqueous solution. Probes 1 and 2 can distinguish these biothiols in the presence of other amino

Thiol activated prodrugs of sulfur dioxide (SO2) as MRSA inhibitors

Pardeshi, Kundansingh A.,Malwal, Satish R.,Banerjee, Ankita,Lahiri, Surobhi,Rangarajan, Radha,Chakrapani, Harinath

, p. 2694 - 2697 (2015/06/08)

Drug resistant infections are becoming common worldwide and new strategies for drug development are necessary. Here, we report the synthesis and evaluation of 2,4-dinitrophenylsulfonamides, which are donors of sulfur dioxide (SO2), a reactive sulfur species, as methicillin-resistant Staphylococcus aureus (MRSA) inhibitors. N-(3-Methoxyphenyl)-2,4-dinitro-N-(prop-2-yn-1-yl)benzenesulfonamide (5e) was found to have excellent in vitro MRSA inhibitory potency. This compound is cell permeable and treatment of MRSA cells with 5e depleted intracellular thiols and enhanced oxidative species both results consistent with a mechanism involving thiol activation to produce SO2.

Stimuli-Responsive Polymer Film that Autonomously Translates a Molecular Detection Event into a Macroscopic Change in Its Optical Properties via a Continuous, Thiol-Mediated Self-Propagating Reaction

Mohapatra, Hemakesh,Kim, Hyungwoo,Phillips, Scott T.

, p. 12498 - 12501 (2015/10/19)

This Communication describes a chemically responsive polymer film that is capable of detecting low levels of a specific applied molecular signal (thiol) and subsequently initiating a self-propagating reaction within the material that converts the nonfluorescent film into a globally fluorescent material. We illustrate that the intensity of the resulting fluorescent material is independent of the quantity of the applied thiol, whereas the rate to reach the maximum level of signal is directly proportional to the quantity of the signal. In contrast, a control film, which lacks functionality for mediating the self-propagating reaction, provides a maximum change in fluorescence that is directly proportional to the quantity of the applied thiol. This level of nonamplified signal is 78% lower in intensity (when initiated with 100 μM of applied thiol) than is achieved when the material contains functionality that supports the self-powered, self-propagating amplification reaction.

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