15266-38-3 Usage
Uses
Used in Anti-inflammatory Applications:
Evocarpine is used as an anti-inflammatory agent for its potential to reduce inflammation, which can be beneficial in treating various inflammatory conditions.
Used in Anticancer Applications:
Evocarpine is used as an anticancer agent for its ability to inhibit tumor growth, making it a potential candidate for cancer treatment and prevention.
Used in Neuroprotective Applications:
Evocarpine is used as a neuroprotective agent for its potential to protect against neurodegenerative diseases such as Alzheimer's, offering a natural approach to managing these conditions.
Used in Psychiatric Disorder Treatment:
Evocarpine is used as a therapeutic agent in the treatment of psychiatric disorders due to its ability to modulate neurotransmitter activity, which can help alleviate symptoms associated with these conditions.
Used in Pharmaceutical Industry:
Evocarpine is used as a key ingredient in the development of pharmaceutical products for its diverse pharmacological properties, including anti-inflammatory, anti-cancer, neuroprotective, and potential psychiatric disorder treatment applications.
Used in Traditional Chinese Medicine:
Evocarpine is used as a component in traditional Chinese medicine formulations, leveraging its various pharmacological benefits for the treatment of different ailments and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 15266-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,6 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15266-38:
(7*1)+(6*5)+(5*2)+(4*6)+(3*6)+(2*3)+(1*8)=103
103 % 10 = 3
So 15266-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H33NO/c1-3-4-5-6-7-8-9-10-11-12-13-15-20-16-14-17-21-22(25)18-19-24(2)23(20)21/h12-14,16-19H,3-11,15H2,1-2H3/b13-12+
15266-38-3Relevant academic research and scientific papers
The Chemistry of 2H-3,1-Benzoxazine-2,4(1H)-dione (Isatoic Anhydride). 17. Synthesis of 2-Alkyl-4-quinolone Alkaloids via a One-step Reaction of N-Methylisatoic Anhydride with Methyl Ketone Enolates
Coppola, Gary M.
, p. 491 - 494 (2007/10/02)
Lithium enolates derived from aliphatic methyl ketones react with N-methylisatoic anhydride (5) at -78 deg C to give 2-alkyl-4-quinolone alkaloids 7 in a single step.The method was used to synthesize both double bond isomers of 1-methyl-2-(8-tridecenyl)-4(1H)-quinolinone (8) thereby showing that the alkaloid evocarpine possesses the Z-olefin stereochemistry 8a.Reduction of 8a provided the alkaloid dihydroevocarpine (16).Compound 16 was also directly prepared from the reaction of 5 with the lithium enolate of 2-pentadecanone.
