41744-39-2 Usage
Description
Acuminatin, a benzophenanthridine alkaloid, is a naturally occurring chemical compound found predominantly in the bark and roots of Zanthoxylum acanthopodium, a plant belonging to the Zanthoxylum genus. It has been recognized for its potential anti-inflammatory, anti-bacterial, and anti-cancer properties, making it a biologically active compound with significant potential for pharmaceutical and therapeutic applications.
Uses
Used in Pharmaceutical Industry:
Acuminatin is used as a therapeutic agent for its potential anti-inflammatory properties, offering a natural alternative for the treatment of inflammatory diseases.
Used in Cancer Treatment:
Acuminatin is used as an anti-cancer agent, particularly for its inhibitory effects on the growth of certain cancer cells, indicating its potential in the development of new cancer therapies.
Used in Antibacterial Applications:
Acuminatin is used as an antimicrobial agent, showing promise as a natural ingredient in the development of new antibiotics to combat bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 41744-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,4 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41744-39:
(7*4)+(6*1)+(5*7)+(4*4)+(3*4)+(2*3)+(1*9)=112
112 % 10 = 2
So 41744-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H24O4/c1-6-7-14-10-16-13(2)20(25-21(16)19(11-14)24-5)15-8-9-17(22-3)18(12-15)23-4/h6-13,20H,1-5H3/b7-6+/t13-,20-/m1/s1
41744-39-2Relevant articles and documents
2,3-dihydrobenzofuran neolignans from Aristolochia pubescens
Nascimento, Isabele R.,Lopes, Lucia M.X.
, p. 345 - 350 (1999)
From a hexane extract of stems and roots of Aristolochia pubescens, the new neolignans (2S,3S,1'R,2'R)- and (2S,3S,1'S,2'R)-2,3-dihydro-5-(1',2'- dihydroxypropyl)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-methylbenzofuran and (2S,3S,1'R,2'R)- and (2S,3S,1
Cerium ammonium nitrate-mediated the oxidative dimerization of p-alkenylphenols: A new synthesis of substituted (±)-trans- dihydrobenzofurans
Chen, Po-Yuan,Wu, Yi-Hua,Hsu, Mon-Huei,Wang, Tzu-Pin,Wang, Eng-Chi
, p. 653 - 657 (2013/07/27)
A new method for the preparation of substituted dihydrobenzofurans is described. The p-alkenylphenols, mediated by cerium ammonium nitrate (CAN), undergo the oxidative dimerization to generate substituted dihydrobenzofurans including (±)-conocarpan, (±)-licarin A, (±)-acuminatin, as well as their related substituted dihydrobenzofurans.
Synthesis of (±)-licarin B and eupomatenoids-1 and -12: A general approach to 2-aryl-7-alkoxy-benzofuranoid neolignans
Engler, Thomas A.,Chai, Wenying
, p. 6969 - 6970 (2007/10/03)
New synthesis of the title compounds are described using Lewis acid-promoted reactions of styrenes with N-phenylsulfonyl-1,4-benzoquinone monoimines to regioselectively form the 2-arylbenzofuranoid ring system followed by conversion of the aromatic N-phenylsulfonyl moiety into a propenyl substituent.
