26400-25-9 Usage
Chemical class
Canthin-6-one alkaloids
Natural occurrence
Found in a variety of plant species, including those in the genus Eurycoma
Anti-inflammatory properties
Exhibits anti-inflammatory effects
Anti-cancer properties
Demonstrates anti-cancer properties
Anti-microbial properties
Shows anti-microbial activity
Potential pharmaceutical applications
Due to its various biological activities, it is a potential candidate for the development of new pharmaceutical drugs
Neuroprotective effects
Studies suggest that it may have neuroprotective effects
Treatment of neurodegenerative diseases
Could be beneficial in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's
Promising compound for research
Its diverse range of biological activities makes it a promising compound for further research and potential therapeutic applications
Check Digit Verification of cas no
The CAS Registry Mumber 26400-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,0 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26400-25:
(7*2)+(6*6)+(5*4)+(4*0)+(3*0)+(2*2)+(1*5)=79
79 % 10 = 9
So 26400-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2O/c17-13-6-5-11-14-10(7-8-15-11)9-3-1-2-4-12(9)16(13)14/h1-4,11,15H,5-8H2
26400-25-9Relevant articles and documents
Cantffln - 6 - quaternary ammonium salt and its preparation method and application
-
, (2017/12/02)
The invention relates to a canthium dicoccum-6-one quaternary ammonium salt and a preparation method and an application thereof. The structural formula of the compound is shown in a formula (1) in the specification, wherein R is ethyl, propyl, isopropyl, allyl, normal-butyl, isobutyl, normal-amyl, normal-octyl, unsubstituted benzyl or substituted benzyl substituted by a hydrogen atom, methyl, bromomethyl, trifluoromethyl, benzyloxyl, a fluorine atom or a chlorine atom; X is chlorine, bromine or iodine. The application is that of the compound for preparing antibacterial drugs.
An improved synthesis of canthin-6-one
Czerwinski, Kevin M.,Zificsak, Craig A.,Stevens, John,Oberbeck, Melissa,Randlett, Christopher,King, Melissa,Mennen, Steve
, p. 1225 - 1231 (2007/10/03)
An improved route has been devised which provides canthin-6-one in the highest yield from tryptamine to date. Tryptamine is converted to Nb-benzyltryptamine via reaction with benzoylchloride and reduction using LAH. Pictet-Spengler condensation with 2-ketoglutaric acid, removal of the protecting group by CTH, and aromatization with MnO2 affords canthin-6-one in 48% overall yield.
