222716-34-9 Usage
Description
SZL P1-41 is a compound with potential applications in various fields, particularly in the pharmaceutical industry. It is characterized by its unique chemical structure and properties that allow it to interact with specific biological targets.
Uses
Used in Pharmaceutical Industry:
SZL P1-41 is used as a pharmacological agent for the inactivation of Skp2 E3 ligase. This application is based on the compound's ability to interact with and inhibit the function of Skp2 E3 ligase, which plays a role in cell cycle regulation and has been implicated in various diseases, including cancer.
Used in Cancer Research:
SZL P1-41 is used as a research tool for studying the role of Skp2 E3 ligase in cancer development and progression. By inhibiting the activity of this ligase, researchers can gain insights into its contribution to cancer and potentially identify new therapeutic targets for cancer treatment.
Used in Drug Development:
SZL P1-41 serves as a lead compound in the development of new drugs targeting Skp2 E3 ligase. Its ability to inhibit the function of this ligase makes it a promising candidate for further optimization and development into a more potent and selective drug for cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 222716-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,7,1 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 222716-34:
(8*2)+(7*2)+(6*2)+(5*7)+(4*1)+(3*6)+(2*3)+(1*4)=109
109 % 10 = 9
So 222716-34-9 is a valid CAS Registry Number.
222716-34-9Relevant articles and documents
Chemistry of the hetero analogs of isoflavones. 22. Mannich reaction in the benzimidazole and benzothiazole analogs of isoflavones
Frasinyuk,Turov,Khilya
, p. 923 - 928 (1998)
New 3-(2-benzothiazolyl)chromones were obtained by the reaction of 2-(2,4-dihydroxy-5-ethylphenacyl)-benzothiazole with triethyl orthoformate or carboxylic acid anhydrides. Aminomethylation of the chromones and also of familiar 3-(2-benzimidazolyl) chromones by substituted 1,1-diaminomethanes gave Mannich bases. 1999 Kluwer Academic/Plenum Publishers.
