153666-19-4 Usage
Description
KETODEOXYNONULOSONIC ACID (KDN) is a naturally occurring deaminated sialic acid derivative, predominantly found at the non-reducing end of sialyl chains. It is a white to off-white solid with potential anticancer properties, particularly noted for its elevated levels in human prostate cancer cells.
Uses
Used in Pharmaceutical Industry:
KETODEOXYNONULOSONIC ACID is used as a pharmaceutical compound for its potential anticancer activity. The expression is: KETODEOXYNONULOSONIC ACID is used as an anticancer agent for its potential to target and treat cancer cells, particularly in prostate cancer.
Used in Research and Development:
KETODEOXYNONULOSONIC ACID is used as a research compound for studying the role of sialic acid derivatives in cancer cell biology and their potential applications in cancer treatment. The expression is: KETODEOXYNONULOSONIC ACID is used as a research tool for understanding the mechanisms behind its elevated levels in prostate cancer cells and its potential therapeutic effects.
Used in Drug Development:
KETODEOXYNONULOSONIC ACID is used as a starting material or intermediate in the development of novel anticancer drugs. The expression is: KETODEOXYNONULOSONIC ACID is used as a chemical building block for creating new drugs that target cancer cells, leveraging its inherent anticancer properties.
Check Digit Verification of cas no
The CAS Registry Mumber 153666-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,6,6 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153666-19:
(8*1)+(7*5)+(6*3)+(5*6)+(4*6)+(3*6)+(2*1)+(1*9)=144
144 % 10 = 4
So 153666-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O9/c10-2-4(12)6(14)7-5(13)3(11)1-9(17,18-7)8(15)16/h3-7,10-14,17H,1-2H2,(H,15,16)/p-1/t3-,4+,5+,6-,7-,9-/m0/s1
153666-19-4Relevant articles and documents
Diastereoselective One-Step Synthesis of 2-Keto-3-deoxy-d- glycero-d-galacto-nononic acid (KDN) Analogues as Templates for the Development of Influenza Drugs
Laborda, Pedro,Wang, Su-Yan,Lu, Ai-Min,He, Meng,Duan, Xu-Chu,Qian, Ying-Juan,Jung, Yong-Sam,Liu, Li,Voglmeir, Josef
, p. 3120 - 3125 (2017)
Novel sialic acid scaffolds have great significance in the development of influenza neuraminidase inhibitors. Here the enzymatic synthesis of a wide range of 2-keto-3-deoxy-d-glycero-d-galacto-nononic acid (KDN) analogues via aldol addition of pyruvate to d-mannose, d-glucose, d-galactose, 2-deoxy-d-glucose, d-arabinose, l-arabinose and l-rhamnose using a previously unstudied N-acetylneuraminic acid (Neu5Ac) aldolase derived from the bacterium Dyadobacter fermentas is exemplified. Several of the synthesized KDN analogues showed comparable or better inhibitory activity than unstudied Neu5Ac against the mutated influenza neuraminidases (A/California/04/2009 and A/Anhui/1/2005), which both show resistance to Neu5Ac-based neuraminidase inhibitors, demonstrating that these compounds are promising templates for the development of anti-influenza drugs. (Figure presented.).