58100-26-8 Usage
Description
Cysteine, hydrazide, Lis a chemical compound derived from the amino acid cysteine, commonly utilized in bioconjugation and chemical modification reactions. It is frequently incorporated into proteins or other biomolecules for labeling or modification purposes, serving various applications in biotechnology and pharmaceutical research.
Uses
Used in Bioconjugation and Chemical Modification:
Cysteine, hydrazide, Lis used as a bioconjugation agent for the attachment of proteins or other biomolecules, facilitating their labeling or modification for research and development in biotechnology and pharmaceuticals.
Used in Pharmaceutical Research:
Cysteine, hydrazide, Lis used as a component in the production of antibody-drug conjugates, which are targeted cancer therapies that deliver cytotoxic drugs directly to cancer cells, enhancing the specificity and efficacy of treatment.
Used in Drug Delivery Systems Development:
Cysteine, hydrazide, Lis used as a key component in the development of novel drug delivery systems, potentially improving the delivery, bioavailability, and therapeutic outcomes of various medications.
Used in Diagnostic Tool Development:
Cysteine, hydrazide, Lhas potential applications in the creation of diagnostic tools for a range of diseases, contributing to advancements in medical diagnostics and treatment strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 58100-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,0 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58100-26:
(7*5)+(6*8)+(5*1)+(4*0)+(3*0)+(2*2)+(1*6)=98
98 % 10 = 8
So 58100-26-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H9N3OS/c4-2(1-8)3(7)6-5/h2,8H,1,4-5H2,(H,6,7)/t2-/m0/s1
58100-26-8Relevant articles and documents
Generation of Multicomponent Molecular Cages using Simultaneous Dynamic Covalent Reactions
Dro?d?, Wojciech,Bouillon, Camille,Kotras, Clément,Richeter, Sébastien,Barboiu, Mihail,Clément, Sébastien,Stefankiewicz, Artur R.,Ulrich, Sébastien
supporting information, p. 18010 - 18018 (2017/11/29)
Cage compounds are very attractive structures for a wide range of applications and there is ongoing interest in finding effective ways to access such kinds of complex structures, particularly those possessing dynamic adaptive features. Here we report the accessible synthesis of new type of organic cage architectures, possessing two different dynamic bonds within one structure: hydrazones and disulfides. Implementation of three distinct functional groups (thiols, aldehydes and hydrazides) in the structure of two simple building blocks resulted in their spontaneous and selective self-assembly into aromatic cage-type architectures. These organic cages contain up to ten components linked together by twelve reversible covalent bonds. The advantage provided by the presented approach is that these cage structures can adaptively self-sort from a complex virtual mixture of polymers or macrocycles and that dynamic covalent chemistry enables their deliberate disassembly through controlled component exchange.
