80095-44-9 Usage
Uses
Used in Enzyme Activity Detection:
4-Nitrophenyl2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfatepotassiumsalt is used as a substrate for detecting and measuring the activity of certain enzymes. It serves as a marker for enzymatic reactions, allowing researchers to monitor the progress and efficiency of these reactions.
Used in Carbohydrate Metabolism Research:
In the field of biochemistry, 4-Nitrophenyl2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfatepotassiumsalt is used as a research tool for studying carbohydrate metabolism. Its interaction with enzymes involved in this metabolic pathway provides insights into the mechanisms and regulation of these processes.
Used in Medical Testing:
4-Nitrophenyl2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfatepotassiumsalt is utilized in medical testing to assess the functionality of enzymes related to carbohydrate metabolism. Its use in diagnostic assays helps in the identification of enzymatic deficiencies or abnormalities that may be associated with certain diseases or conditions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-Nitrophenyl2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfatepotassiumsalt is employed as a compound of interest for the development of drugs targeting carbohydrate metabolism. Its ability to interact with specific enzymes makes it a potential candidate for the creation of therapeutic agents that can modulate enzymatic activity for treating related disorders.
Used in Academic Research:
4-Nitrophenyl2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfatepotassiumsalt is also used in academic research settings to explore the fundamental aspects of enzyme-substrate interactions and the biochemical pathways involved in carbohydrate metabolism. This research contributes to a deeper understanding of biological systems and may lead to the discovery of new therapeutic targets or strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 80095-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,9 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80095-44:
(7*8)+(6*0)+(5*0)+(4*9)+(3*5)+(2*4)+(1*4)=119
119 % 10 = 9
So 80095-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O11S/c1-7(17)15-11-13(19)12(18)10(6-25-28(22,23)24)27-14(11)26-9-4-2-8(3-5-9)16(20)21/h2-5,10-14,18-19H,6H2,1H3,(H,15,17)(H,22,23,24)/t10-,11-,12-,13-,14-/m1/s1
80095-44-9Relevant academic research and scientific papers
Substrate Engineering and its Synthetic Utility in the Sulfation of Primary Aliphatic Alcohol Groups by a Bacterial Arylsulfotransferase
Hartog, Aloysius F.,Wever, Ron
supporting information, p. 2629 - 2632 (2015/09/01)
The use of substrate engineering allowed the enzymatic sulfation by an arylsulfotransferase from Desulfitobacterium hafniense of a number of carbohydrate derivatives. Specific sulfation of carbohydrates chemically or enzymatically is notoriously difficult
N-acetyl-6-sulfo-D-glucosamine as a promising mimic of N-acetyl neuraminic acid
Sasaki, Kenji,Nishida, Yoshihiro,Uzawa, Hirotaka,Kobayashi, Kazukiyo
, p. 2821 - 2823 (2007/10/03)
6-Sulfo-D-GlcNAc with a molecular geometry close to that of N-acetylneuraminic acid (Neu5Ac) was hypothesized to serve as a simple Neu5Ac mimic possessing high potential in biochemical and medicinal applications. The hypothesis was evidenced with a neuraminidase inhibition assay using p-nitrophenyl (pNP) 3-, 4-, and 6-sulfo-β-D-GlcNAc (4, 5 and 2a) and 6-sulfo-β-D-Glc 6, in which only pNP 6-sulfo-β-D-GlcNAc 2a was found to show substantial activity.
