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3',4',4-Tribenzyloxy-2'-hydroxy-chalkon is a complex organic compound with the molecular formula C33H31O5. It is a derivative of the parent compound chalkon, which is a type of chalcone, a class of organic compounds that are open-chain flavonoids. This specific derivative is characterized by the presence of three benzyloxy groups attached to the 3', 4', and 4 positions, as well as a hydroxyl group at the 2' position. The benzyloxy groups are derived from benzyl alcohol and are used to protect the hydroxyl groups during chemical reactions, which is a common strategy in organic synthesis to prevent unwanted side reactions. 3',4',4-Tribenzyloxy-2'-hydroxy-chalkon is of interest in the field of organic chemistry, particularly in the synthesis of more complex molecules and the study of chalcone derivatives, which have potential applications in pharmaceuticals and other industries due to their diverse biological activities.

2652-28-0

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2652-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2652-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2652-28:
(6*2)+(5*6)+(4*5)+(3*2)+(2*2)+(1*8)=80
80 % 10 = 0
So 2652-28-0 is a valid CAS Registry Number.

2652-28-0Relevant articles and documents

Studies on gambogic acid (IV): Exploring structure-activity relationship with IκB kinase-beta (IKKβ)

Sun, Haopeng,Chen, Feihong,Wang, Xiaojian,Liu, Zongliang,Yang, Qian,Zhang, Xiaojin,Zhu, Jia,Qiang, Lei,Guo, Qinglong,You, Qidong

experimental part, p. 110 - 123 (2012/07/28)

Previously we have reported a series of gambogic acid's analogs and have identified a compound that possessed comparable in vitro growth inhibitory effect as gambogic acid. However, their target protein as well as the key pharmacophoric motifs on the target have not been identified yet. Herein we report that gambogic acid and its analogs inhibit the activity of IκB Kinase-beta (IKKβ) through suppressing the activation of TNFα/NF-κB pathway, which in turn induces A549 and U251 cell apoptosis. IKKβ can serve as one of gambogic acid's targets. The preparation of the compounds was carefully discussed in the article. Caged 4-oxa-tricyclo[4.3.1.03,7]dec-2-one xanthone, which was identified as the pharmacophoric scaffold, represents a promising therapeutic agent for cancer and useful probe against NF-κB pathway.

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