89781-52-2 Usage
Description
8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID, also known as 5,6,7,8-Tetrahydro-8-oxo-2-naphthoic Acid, is a chemical compound with potential therapeutic applications. It is characterized by its unique molecular structure, which includes a naphthalene core with a carboxylic acid group and an oxo group at the 8-position. 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID has been identified for its potential role in treating cancer and other Pin1-associated conditions.
Uses
Used in Pharmaceutical Industry:
8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID is used as a therapeutic agent for treating cancer and other Pin1-associated conditions. Its application is based on its ability to target and modulate the activity of Pin1, a peptidyl-prolyl isomerase enzyme that plays a crucial role in cell cycle regulation and has been implicated in the development and progression of various cancers. By inhibiting Pin1, this compound may help to prevent the growth and spread of cancer cells, offering a potential treatment option for patients with cancer and other Pin1-associated diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 89781-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89781-52:
(7*8)+(6*9)+(5*7)+(4*8)+(3*1)+(2*5)+(1*2)=192
192 % 10 = 2
So 89781-52-2 is a valid CAS Registry Number.
89781-52-2Relevant articles and documents
Diastereoselective. synergistic dual-mode optical switch with integrated chirochromic helicene and photochromic bis-azobenzene moieties
Chen, Wen-Ching,Lee, Yi-Wei,Chen, Chien-Tien
, p. 1472 - 1475 (2010)
(Figure Presented) An unprecedented dual-mode optical switch by combining helicene and bis-azobenzene moieties in proximity allows for cooperative, highly diastereoselective chlrochromic (92/8 to 3/97) and photochromic (>99/1 to 19/81) switchings both in
Imidazolyl derivatives in medicinal chemistry
Carganico,Cozzi
, p. 209 - 231 (2007/10/02)
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