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2-(2-(2-(2-(pyridin-2-yldisulfanyl)ethoxy)ethoxy)ethoxy)ethan-1-ol, also known as (2-pyridyldithio)-PEG2-alcohol, is a PEG linker that contains a pyridyl disulfide moiety and an alcohol group. The pyridyl disulfide group can react with thiol groups of proteins over a wide range of pH levels, while the hydroxyl group allows for further derivatization of the compound. The hydrophilic PEG linker increases the water solubility of the compound, making it a versatile molecule for various applications.

851961-99-4

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851961-99-4 Usage

Uses

Used in Bioconjugation Applications:
2-(2-(2-(2-(pyridin-2-yldisulfanyl)ethoxy)ethoxy)ethoxy)ethan-1-ol is used as a bioconjugation agent for the selective attachment of proteins, peptides, and other biomolecules. The pyridyl disulfide group forms stable linkages with thiol groups, enabling the formation of well-defined bioconjugates with minimal disruption to the biological activity of the attached molecules.
Used in Drug Delivery Systems:
In the pharmaceutical industry, 2-(2-(2-(2-(pyridin-2-yldisulfanyl)ethoxy)ethoxy)ethoxy)ethan-1-ol is used as a component in drug delivery systems to improve the solubility, stability, and bioavailability of therapeutic agents. The PEG linker enhances the hydrophilicity of the drug, reducing aggregation and increasing circulation time in the body, while the pyridyl disulfide group allows for targeted delivery to specific cells or tissues.
Used in Analytical Chemistry:
2-(2-(2-(2-(pyridin-2-yldisulfanyl)ethoxy)ethoxy)ethoxy)ethan-1-ol is used as a reagent in analytical chemistry for the detection and quantification of thiol-containing compounds. The selective reaction between the pyridyl disulfide group and thiol groups allows for the specific labeling and separation of target molecules in complex samples.
Used in Materials Science:
In materials science, 2-(2-(2-(2-(pyridin-2-yldisulfanyl)ethoxy)ethoxy)ethoxy)ethan-1-ol is used as a building block for the development of functional polymers and materials with tailored properties. The pyridyl disulfide group can be used to create reversible cross-links or to attach functional groups to polymer chains, while the PEG linker provides enhanced solubility and stability.

Check Digit Verification of cas no

The CAS Registry Mumber 851961-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 851961-99:
(8*8)+(7*5)+(6*1)+(5*9)+(4*6)+(3*1)+(2*9)+(1*9)=204
204 % 10 = 4
So 851961-99-4 is a valid CAS Registry Number.

851961-99-4Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR INDUCING IMMUNE TOLERANCE

-

, (2019/01/08)

Several embodiments provided in the present disclosure relate to compositions that carry an antigen to which tolerance is desired, the antigen being coupled, bound, or otherwise joined to a targeting moiety, the targeting moiety configured to direct the composition to the liver of a subject. In several embodiments, the antigen in coupled to the targeting moiety by way of a polymeric linker. In several embodiments, the polymeric linker is configured to liberate the antigen in vivo. Methods of using the compositions to reduce and/or prevent unwanted immune responses against an antigen of interest are also provided.

Kinetic stabilization of an oligomeric protein by a single ligand binding event

Wiseman, R. Luke,Johnson, Steven M.,Kelker, Matthew S.,Foss, Ted,Wilson, Ian A.,Kelly, Jeffery W.

, p. 5540 - 5551 (2007/10/03)

Protein native state stabilization imposed by small molecule binding is an attractive strategy to prevent the misfolding and misassembly processes associated with amyloid diseases. Transthyretin (TTR) amyloidogenesis requires rate-limiting tetramer dissociation before misassembly of a partially denatured monomer ensues. Selective stabilization of the native TTR tetramer over the dissociative transition state by small molecule binding to both thyroxine binding sites raises the kinetic barrier of tetramer dissociation, preventing amyloidogenesis. Assessing the amyloidogenicity of a TTR tetramer having only one amyloidogenesis inhibitor (I) bound is challenging because the two small molecule binding constants are generally not distinct enough to allow for the exclusive formation of TTR·I in solution to the exclusion of TTR·I2 and unliganded TTR. Herein, we report a method to tether one fibril formation inhibitor to TTR by disulfide bond formation. Occupancy of only one of the two thyroxine binding sites is sufficient to inhibit tetramer dissociation in 6.0 M urea and amyloidogenesis under acidic conditions by imposing kinetic stabilization on the entire tetramer. The sufficiency of single occupancy for stabilizing the native state of TTR provides the incentive to search for compounds displaying striking negative binding cooperativity (e.g., Kd1 in nanomolar range and Kd2 in the micromolar to millimolar range), enabling lower doses of inhibitor to be employed in the clinic, mitigating potential side effects.

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