41506-62-1 Usage
Uses
Used in Pharmaceutical Industry:
AHNAK is utilized as a potential therapeutic agent for cancer treatment and prevention. Its unique chemical structure allows it to interact with biological targets, potentially modulating cellular processes and pathways associated with cancer development and progression. N-(4-Acetylaminophenyl)-3-hydroxynaphthalene-2-carboxamide is under investigation for its ability to inhibit tumor growth and metastasis, as well as to enhance the effectiveness of existing cancer therapies.
Used in Dermatology:
In the field of dermatology, AHNAK is explored for its potential role in treating and managing skin disorders. Its chemical properties may contribute to the regulation of skin cell functions, offering a novel approach to addressing various dermatological conditions. N-(4-Acetylaminophenyl)-3-hydroxynaphthalene-2-carboxamide's potential to modulate skin inflammation, promote healing, and protect against harmful environmental factors makes it a valuable candidate for dermatological applications.
Used in Biochemical Research:
AHNAK's distinctive structure and functional properties also make it a valuable tool in biochemical research. It can be employed as a probe or modifier in studies aimed at understanding the molecular mechanisms underlying various biological processes. N-(4-Acetylaminophenyl)-3-hydroxynaphthalene-2-carboxamide's potential to interact with specific proteins, enzymes, or other biomolecules may provide insights into the development of new therapeutic strategies and diagnostic tools in medicine and biochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 41506-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41506-62:
(7*4)+(6*1)+(5*5)+(4*0)+(3*6)+(2*6)+(1*2)=91
91 % 10 = 1
So 41506-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H16N2O3/c1-12(22)20-15-6-8-16(9-7-15)21-19(24)17-10-13-4-2-3-5-14(13)11-18(17)23/h2-11,23H,1H3,(H,20,22)(H,21,24)
41506-62-1Relevant academic research and scientific papers
Fluorescent substrates for potential use in enzyme-linked immunosorbent assay of membrane-bound nucleic acids
Fujita, Satoshi,Momiyama, Masayoshi,Kondo, Yasumitsu,Kagiyama, Naoto,Hori, Samuel H.,Toru, Takeshi
, p. 1347 - 1353 (2007/10/02)
A number of phosphorylated fluorochromes were synthesized and tested for the alkaline phosphatase-linked fluorescence assay of membrane-bound nucleic acids. 3-Hydroxy-N-2′-biphenyl-2-naphthalenecarboxamide phosphate ester (HBNP) was found to be the most suitable for the assay. Nonfluorescent HBNP is hydrolyzed by phospholipase bound to the probe DNA to the highly fluorescent 3-hydroxy-N,2′-biphenyl-2-naphthalenecarboxamide (HBN). HBN is insoluble enough in aqueous medium to precipitate on the nylon membrane. Spots containing as little as 5 fg of λ DNA can be successfully detected on the membrane with HBNP.
