22324-83-0 Usage
General Description
(+/-)-Cryptostyline III is a natural product isolated from the marine sponge (Cryptotethia crypta) that has been investigated for its potential pharmaceutical and medicinal properties. It is a member of the alkaloid family and has a complex chemical structure with a unique pentacyclic ring system. Research has shown that (+/-)-Cryptostyline III has anti-inflammatory and anti-cancer activities, making it a potential candidate for the development of new drugs for the treatment of various diseases. It has also been found to have inhibitory effects on the enzyme casein kinase 1, which plays a role in regulating cellular processes and has implications for the treatment of neurodegenerative disorders. The compound has attracted interest from the scientific community due to its unique structure and promising biological activities, and further research is being conducted to explore its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 22324-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22324-83:
(7*2)+(6*2)+(5*3)+(4*2)+(3*4)+(2*8)+(1*3)=80
80 % 10 = 0
So 22324-83-0 is a valid CAS Registry Number.
22324-83-0Relevant articles and documents
A one-pot synthesis of (±) cryptostylines I, II, III
Ruchirawat, Somsak,Bhavakul, Vanida,Chaisupakitsin, Malinee
, p. 621 - 625 (2003)
A one-pot synthesis of cryptostylines I, II, III, via the Pictet-Spengler reaction is reported.
Transition-Metal-Free Arylation of N -Alkyl-tetrahydroisoquinolines under Oxidative Conditions: A Convenient Synthesis of C1-Arylated Tetrahydro-isoquinoline Alkaloids
Singh, Kamal Nain,Kessar, Satinder V.,Singh, Paramjit,Singh, Pushpinder,Kaur, Manjot,Batra, Aanchal
supporting information, p. 2644 - 2650 (2015/12/26)
A simple protocol for the C1 arylation of tetrahydroisoquinolines with aryl Grignard reagents via diethyl azodicarboxylate (DEAD) mediated oxidative C-H activation under metal-free conditions has been developed. The target compounds, including some natura
Synthesis of Racemic Cryptostylines I, II, and III by Radical Cyclization
Takano, Seiichi,Suzuki, Mahito,Kijima, Atsushi,Ogasawara, Kunio
, p. 315 - 316 (2007/10/02)
Three 1-phenyl-1,2,3,4-tetrahydroisoquinoline alkaloids, cryptostylines I, II, and III, have been synthesized in racemic forms via an aryl radical-initiated cyclization.