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2'-Hydroxy-4-methoxy-4'-methyl-trans-chalcone is a naturally occurring organic compound belonging to the chalcone family, characterized by its unique chemical structure. 2'-hydroxy-4-methoxy-4'-methyl-trans-chalcone is derived from the condensation of 4-hydroxy-3-methoxyacetophenone and 4'-methylbenzaldehyde, resulting in a flavonoid-like structure. It exhibits a yellow crystalline appearance and is known for its potential antioxidant, anti-inflammatory, and anticancer properties. The compound's molecular formula is C17H16O4, and it has a molecular weight of 284.31 g/mol. Due to its promising biological activities, 2'-hydroxy-4-methoxy-4'-methyl-trans-chalcone has been the subject of various scientific studies, with potential applications in the pharmaceutical and nutraceutical industries.

895-10-3

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895-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 895-10-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 895-10:
(5*8)+(4*9)+(3*5)+(2*1)+(1*0)=93
93 % 10 = 3
So 895-10-3 is a valid CAS Registry Number.

895-10-3Relevant academic research and scientific papers

4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity

De Meyer,Haemers,Mishra,Pandey,Pieters,Vanden Berghe,Vlietinck

, p. 736 - 746 (2007/10/02)

4'-Hydroxy-3-methoxyflavones are natural compounds with known antiviral activities against picornaviruses such as poliomyelitis and rhinoviruses. In order to establish a structure-activity relationship a series of analogues were synthesized, and their antiviral activities and cytotoxicities were compared with those of flavones from natural origin. The 4'-hydroxyl and 3-methoxyl groups, a substitution in the 5 position and a polysubstituted A ring appeared to be essential requirements for a high activity. The most interesting compound was 4',7-dihydroxy-3-methoxy-5,6-dimethylflavone possessing in vitro TI99 values of > 1000 and > 200 against poliovirus type 1 and rhinovirus type 15, respectively. This compound was also active against other rhinovirus serotypes (2, 9, 14, 29, 39, 41, 59, 63, 70, 85, and 89) tested, having MIC50 values ranging from 0.016 to 0.5 μg/mL. Finally in contrast to quercetin it showed to be not mutagenic in concentrations up to 2.5 mg in the Ames test.

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