19794-48-0 Usage
Description
H-D-SER(SO3H)-OH is a synthetic chemical compound derived from the amino acid serine, featuring a unique sulfo group on its side chain. This modification endows it with distinctive chemical properties, making it valuable for applications in biochemistry, organic synthesis, and potentially as a drug candidate or research tool.
Uses
Used in Biochemistry and Organic Synthesis:
H-D-SER(SO3H)-OH serves as a building block for peptide synthesis, contributing to the creation of complex biologically active molecules. Its sulfo group enhances its reactivity and solubility, facilitating its incorporation into various chemical structures.
Used in Pharmaceutical Research and Development:
As a derivative of serine, H-D-SER(SO3H)-OH may have potential medicinal uses. Its modified chemical structure could be explored for drug development, particularly in targeting specific biological pathways or as a component of therapeutic agents.
Used in the Preparation of Sulfo-Derivatives:
H-D-SER(SO3H)-OH can be utilized as a precursor for the synthesis of other sulfo-derivatives of amino acids. These derivatives may have specialized applications in various industries, such as pharmaceuticals, where they could be used to develop new drugs or improve existing ones.
Used in Research Tools Development:
Due to its unique chemical properties, H-D-SER(SO3H)-OH may also be employed as a research tool in scientific studies. It could be used to probe biological mechanisms, test hypotheses, or as a component in experimental models.
Check Digit Verification of cas no
The CAS Registry Mumber 19794-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19794-48:
(7*1)+(6*9)+(5*7)+(4*9)+(3*4)+(2*4)+(1*8)=160
160 % 10 = 0
So 19794-48-0 is a valid CAS Registry Number.
19794-48-0Relevant articles and documents
Mechanism and Stereochemistry of the Activation of (2S)- and (2R)-Serine O-Sulfate as Suicide Inhibitors for Escherichia coli Glutamic Acid Decarboxylase
Rose, Janet E.,Leeson, Paul D.,Gani, David
, p. 3089 - 3094 (2007/10/02)
E. coli glutamic acid decarboxylase is inactivated by both enantiomers of the suicide inhibitor serine O-sulfate; inactivation by the (2S)-enantiomer involves Cα-H bond cleavage while inactivation by the (2R)-isomer involves Cα-decarboxylation.Both processes occur on the 4'-Re-face of the coenzyme, the opposite face to that utilised in physiological decarboxylation.
