(H-Cys-pNA)2 is a bis-thioether amino acid derivative in which cysteine residues are linked to p-nitroanilide (pNA) groups, forming a conjugated disulfide-free scaffold with two cysteinyl functional units. The molecule contains amino and carboxyl functionalities characteristic of cysteine-derived backbones while presenting p-nitroanilide moieties that act as chromogenic leaving-group analogs, and its sulfur side chains provide thiol-derived chemical handles for cysteine chemistry. As a peptide- or amino-acid-related substrate mimic, (H-Cys-pNA)2 is used in biochemical and analytical workflows to monitor cysteine-reactive transformations and to generate measurable colorimetric readouts associated with pNA release under appropriate assay conditions.
CAT No: CP27029
CAS No:34199-07-0
Synonyms/Alias:34199-07-0;L-Cystinyl-bis-4-nitroanilide;(H-Cys-pNA)2;SCHEMBL10103954;ZINC13532293;FT-0639166
(H-Cys-pNA)2 is a cysteine-containing, p-nitroanilide (pNA) functional amino acid derivative designed for thiol-reactive biochemical workflows where controlled release or monitoring of pNA is useful. The presence of cysteine provides a nucleophilic thiol handle, while the pNA chromophore enables convenient spectrophotometric readout in assay formats. This reagent format is commonly leveraged in chemical biology and protein chemistry to build or evaluate cysteine-dependent labeling, conjugation, or cleavage-responsive systems.
1. Cysteine-Responsive Assays
(H-Cys-pNA)2 is used in assay development and screening workflows that rely on cysteine reactivity and chromogenic pNA reporting. Researchers employ it to generate measurable signal changes in reaction mixtures where thiol-dependent processes are being compared across conditions, reagent sets, or time courses. The pNA group supports straightforward spectrophotometric monitoring, making the compound a practical choice for method development in protein chemistry and chemical biology labs that need a cysteine-linked readout rather than a purely fluorescent system.
2. Cleavable Conjugate Probes
(H-Cys-pNA)2 is applied as a building block for constructing cysteine-triggered, cleavage-responsive conjugates used to interrogate chemical reactivity in complex biomolecular environments. In these workflows, the cysteine functionality serves as the reactive motif, while the pNA moiety provides an analytical handle that can report on bond disruption or release events after treatment with selected reagents. Protein engineers and chemical biologists use such designs to evaluate how cysteine accessibility, microenvironment, or reaction conditions influence downstream signal generation in conjugate-based studies.
3. Protein Labeling Evaluation
(H-Cys-pNA)2 is also used to benchmark cysteine-labeling strategies and to compare thiol-reactive chemistries in protein-focused experimental pipelines. Laboratories use the reagent to test labeling efficiency under controlled conditions and to assess whether thiol availability or competing nucleophiles affect the extent of modification, using pNA as the measurable output. This makes (H-Cys-pNA)2 a practical reagent for optimizing labeling protocols prior to applying more complex or resource-intensive labeling reagents to proteins or peptide substrates.
4. Chromogenic Reagent Development
(H-Cys-pNA)2 supports the development of chromogenic reagent systems where cysteine functionality is required alongside a stable, measurable reporter group. Formulators in chemical biology and analytical method development use it to prototype reaction-responsive materials and solution-phase reagents that translate chemical change into a quantifiable absorbance signal. The dual presence of a cysteine-derived reactive motif and the pNA reporter makes it particularly useful when assay readout simplicity and reproducible optical response are key selection criteria.
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