20267-87-2 Usage
General Description
Chelidonine monohydrate is a chemical compound found in the plants of the Papaveraceae family, particularly the greater celandine (Chelidonium majus). It is a benzophenanthridine alkaloid with potential analgesic, anti-inflammatory, and antitumor properties. Chelidonine monohydrate has been studied for its potential therapeutic applications, including its ability to inhibit the growth of cancer cells, induce apoptosis, and inhibit inflammation. It may also have potential in the treatment of various diseases, including neurodegenerative disorders and autoimmune diseases. Overall, chelidonine monohydrate is a compound of interest with diverse potential applications in medicine and research.
Check Digit Verification of cas no
The CAS Registry Mumber 20267-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20267-87:
(7*2)+(6*0)+(5*2)+(4*6)+(3*7)+(2*8)+(1*7)=92
92 % 10 = 2
So 20267-87-2 is a valid CAS Registry Number.
20267-87-2Relevant articles and documents
A NOVEL AND BIOMIMETIC SYNTHESIS OF (+/-)-CHELAMINE, (+/-)-CHELIDONINE, SANGUINARINE, AND DIHYDROSANGUINARINE FROM COPTISINE VIA A COMMON INTERMEDIATE
Hanaoka, Miyoji,Yoshida, Shuji,Annen, Masami,Mukai, Chisato
, p. 739 - 742 (1986)
(+/-)-Chelamine and (+/-)-chelidonine, B/C cis hexahydrobenzophenanthridine alkaloids were stereoselectively synthesized from coptisine via the key intermediate, which was also converted to fully aromatized benzophenanthridine alkaloids, sanguinarine and dihydrosanguinarine.
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Oppolzer,W.,Keller,K.
, p. 3836 - 3837 (1971)
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Total syntheses of chelidonine and norchelidonine via an enamide-benzyne-[2+2] cycloaddition cascade
Ma, Zhi-Xiong,Feltenberger, John B.,Hsung, Richard P.
, p. 2742 - 2745 (2012/08/07)
Total syntheses of chelidonine and norchelidonine featuring an enamide-benzyne-[2 + 2] cycloaddition initiated cascade is described. The cascade includes a pericyclic ring-opening and intramolecular Diels-Alder reaction.
