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2′-O-methyluridine CAS:2140-76-3
2′-O-Methyluridine is a naturally occurring nucleoside in which a methyl group is attached to the oxygen atom of the 2′ position of the ribose sugar in uridine. This modification enhances the stability and functionality of RNA molecules, making it a crucial component in various biological processes. 2′-O-Methyluridine plays significant roles in the structure and function of ribonucleic acids (RNAs), including messenger RNA (mRNA) and transfer RNA (tRNA). Its presence can influence RNA stability, translation efficiency, and interactions with proteins and other nucleic acids, making it an essential element in the study of molecular biology and therapeutic applications.
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adenosine 5′-monophosphate sodium*from yeast CAS:4578-31-8
Adenosine 5′-monophosphate sodium (AMP) is a nucleotide derived from adenosine that plays a crucial role in cellular metabolism. AMP is essential for various biological processes, including energy transfer, signal transduction, and as a precursor for the synthesis of ATP and other nucleotides. The sodium salt form of AMP can be derived from yeast, which is rich in nucleotides due to its active metabolic pathways. This compound is commonly used in biochemistry and pharmacology as a biochemical reagent, food additive, and dietary supplement, owing to its potential health benefits and applications in promoting energy metabolism.
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2′-Deoxycytidine CAS:951-77-9
2′-Deoxycytidine is a nucleoside composed of a deoxyribose sugar and cytosine, distinguished by the absence of a hydroxyl group at the 2′ position of the ribose. This modification makes it an essential component of DNA, where it pairs with guanine during base pairing. 2′-Deoxycytidine plays significant roles in cellular metabolism and DNA synthesis, serving as a building block for deoxycytidine triphosphate (dCTP), which is crucial for DNA replication and repair. Additionally, this nucleoside has important implications in molecular biology research, cancer therapy, and antiviral strategies, highlighting its relevance in both fundamental research and clinical applications.
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2,2′-cyclouridine CAS:3736-77-4
2,2′-Cyclouridine is a bicyclic nucleoside derivative of uridine, characterized by the formation of a unique cyclic structure involving the 2′ and 2” positions of the ribose moiety. This structural modification imparts distinct biochemical properties that influence its stability and biological activity. 2,2′-Cyclouridine has garnered interest in chemical biology and medicinal chemistry due to its potential applications as an antiviral agent and in RNA research. Its ability to modulate nucleic acid interactions makes it a valuable tool for studying RNA structure-function relationships, potentially leading to advancements in therapeutic strategies targeting viral infections and genetic diseases.
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2-Aminoadenosine CAS:2096-10-8
2-Aminoadenosine is a naturally occurring nucleoside derivative of adenosine, distinguished by the presence of an amino group at the 2-position of the ribose sugar. This modification significantly alters its biochemical properties and functions, making it an essential molecule in various physiological processes. 2-Aminoadenosine is involved in cellular signaling, metabolism, and regulatory pathways, including those related to energy homeostasis and neurotransmission. Its potential therapeutic applications span multiple fields, including neurobiology and cardiology, where it may influence cellular responses to stress and injury. As research continues, 2-aminoadenosine holds promise for developing novel bioactive compounds and therapeutic agents.
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2′-Deoxyuridine CAS:951-78-0
2′-Deoxyuridine is a nucleoside derived from uridine, with the distinguishing feature of having a hydrogen atom instead of a hydroxyl group at the 2′ position of the ribose sugar. This modification renders it a crucial building block in the synthesis of DNA, where it pairs with adenine during base pairing. 2′-Deoxyuridine plays a significant role in cellular metabolism and DNA replication. Additionally, it serves as a precursor for the synthesis of deoxythymidine and has applications in molecular biology research, cancer therapy, and antiviral strategies. Its unique properties make it an important compound in both fundamental and applied research.
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TERT-BUTYL ISOCYANIDE CAS:7188-38-7
tert-Butyl isocyanide (also known as 2-isocyanobutane) is an organic compound with the chemical formula C₄H₉N. It features a branched tert-butyl group attached to an isocyanide functional group (–N≡C). This unique structure imparts significant reactivity, making it a valuable intermediate in organic synthesis. tert-Butyl isocyanide is primarily utilized in the preparation of various nitrogen-containing compounds, including pharmaceuticals and agrochemicals. Its distinctive properties enable it to participate in several important reactions, making it a useful tool for chemists in the development of novel materials and bioactive molecules.
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p-Toluenesulfonyl Isocyanate CAS:4083-64-1
p-Toluenesulfonyl isocyanate (PTSI) is an organic compound with the chemical formula C₉H₉N₂O₂S. It features a p-toluenesulfonyl group attached to an isocyanate functional group, making it a valuable reagent in organic synthesis and material science. PTSI is known for its high reactivity and selectivity, particularly in coupling reactions and the synthesis of urea derivatives. Its applications extend to pharmaceuticals, agrochemicals, and polymer chemistry. The unique properties of p-toluenesulfonyl isocyanate make it an essential tool for chemists seeking to develop novel compounds with specific functionalities.
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sodium N-lauroylsarcosinate CAS:137-16-6;7631-98-3
Sodium N-lauroylsarcosinate is a sodium salt derived from the amino acid sarcosine and lauric acid. With the chemical formula C₁₂H₂₃NNaO₃S, it is recognized for its surfactant properties and is commonly used in personal care products, cosmetics, and cleaning formulations. As an amphiphilic compound, sodium N-lauroylsarcosinate exhibits excellent foaming, emulsifying, and cleansing abilities, making it suitable for a wide range of applications. Its mildness and compatibility with skin make it a preferred ingredient in formulations designed for sensitive skin. Understanding its properties and uses is essential for its effective application in various industries.
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![sodium 2-[methyl(1-oxododecyl)amino]ethanesulphonate CAS: 4337-75-1](https://cdn.globalso.com/xindaobiotech/14Z4YR3PJ6@V5_YM349.png)
sodium 2-[methyl(1-oxododecyl)amino]ethanesulphonate CAS: 4337-75-1
Sodium 2-[methyl(1-oxododecyl)amino]ethanesulphonate is a synthetic compound with both surfactant and amphiphilic properties, characterized by its unique structure that combines a sulfonate group with a long-chain fatty acid derivative. With applications in various sectors, particularly in biochemistry, pharmaceuticals, and cosmetic formulations, this compound serves as an effective emulsifier, stabilizer, and solubilizing agent. Its ability to interact with lipid membranes and proteins makes it valuable in drug delivery systems and formulations aimed at enhancing skin penetration. Understanding its chemical properties and functional applications is crucial for optimizing its use in specialized products.
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sodium hydrogen N-(1-oxododecyl)-L-glutamate CAS:29923-31-7;42926-22-7
Sodium hydrogen N-(1-oxododecyl)-L-glutamate is an amphiphilic compound that combines the properties of a fatty acid derivative with the amino acid L-glutamate. Its unique structure features a long-chain fatty acid, which enhances its surfactant properties, making it suitable for various applications in biochemistry, pharmaceuticals, and personal care products. This compound can act as an effective emulsifier, stabilizer, and solubilizing agent, promoting the mixing of oil and water phases. Understanding its chemical behavior and functional uses is essential for optimizing its application in specialized formulations.
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N4-Acetylcytosine CAS:14631-20-0
N4-Acetylcytosine (ac4C) is a modified nucleobase derived from cytosine, featuring an acetyl group attached to the nitrogen at the fourth position of the pyrimidine ring. This modification occurs naturally in RNA and has garnered significant research interest due to its role in regulating gene expression and influencing RNA metabolism. N4-acetylcytosine is involved in various biological processes, including mRNA stability, translation efficiency, and cellular stress responses. The study of ac4C provides insights into post-transcriptional regulation mechanisms and underscores the complexity of RNA modifications that contribute to cellular function and gene regulation.
