56531-69-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(p-tolyl)-3-adamantanecarboxylic acid is used as a building block for the synthesis of pharmaceutical products due to its unique chemical structure and potential biological activities.
Used in Antiviral Applications:
1-(p-tolyl)-3-adamantanecarboxylic acid is used as an antiviral agent for its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Anti-inflammatory Applications:
1-(p-tolyl)-3-adamantanecarboxylic acid is used as an anti-inflammatory agent to reduce inflammation and alleviate pain associated with various inflammatory conditions.
Used in Analgesic Applications:
1-(p-tolyl)-3-adamantanecarboxylic acid is used as an analgesic agent to provide pain relief and improve the quality of life for patients suffering from chronic or acute pain.
Used in Drug Development:
1-(p-tolyl)-3-adamantanecarboxylic acid is used in the development of potential drug candidates for the treatment of various diseases, leveraging its biological activities and chemical properties to create novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 56531-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,3 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56531-69:
(7*5)+(6*6)+(5*5)+(4*3)+(3*1)+(2*6)+(1*9)=132
132 % 10 = 2
So 56531-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H22O2/c1-12-2-4-15(5-3-12)17-7-13-6-14(8-17)10-18(9-13,11-17)16(19)20/h2-5,13-14H,6-11H2,1H3,(H,19,20)
56531-69-2Relevant academic research and scientific papers
Discovery and biological evaluation of adamantyl amide 11β-HSD1 inhibitors
Webster, Scott P.,Ward, Peter,Binnie, Margaret,Craigie, Eilidh,McConnell, Kirsty M.M.,Sooy, Karen,Vinter, Andy,Seckl, Jonathan R.,Walker, Brian R.
, p. 2838 - 2843 (2008/02/05)
A series of adamantyl amide 11β-HSD1 inhibitors has been discovered and chemically modified. Selected compounds are selective for 11β-HSD1 over 11β-HSD2 and possess excellent cellular potency in human and murine 11β-HSD1 assays. Good pharmacodynamic characteristics are observed in ex vivo assays.
