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3-α-acetoxy-4-β-isocyanato-11-oxo-24-norurs-12-ene is a complex organic compound belonging to the triterpenoid class, characterized by its unique molecular structure. 3-α-acetoxy-4-β-isocyanato-11-oxo-24-norurs-12-ene features an acetoxy group at the 3-α position, an isocyanato group at the 4-β position, and an oxo group at the 11 position. The 24-norurs-12-ene part of the name indicates that it is a derivative of the ursane triterpenoid skeleton, with a nor (nor) group at the 24 position and a double bond at the 12 position. This chemical is known for its potential biological activities and applications in pharmaceutical research, particularly in the development of anti-inflammatory and anti-cancer agents. Its structure and properties make it an interesting target for further investigation in the field of natural product chemistry and drug discovery.

3022-80-8

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3022-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3022-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3022-80:
(6*3)+(5*0)+(4*2)+(3*2)+(2*8)+(1*0)=48
48 % 10 = 8
So 3022-80-8 is a valid CAS Registry Number.

3022-80-8Downstream Products

3022-80-8Relevant academic research and scientific papers

Analogues of boswellic acids as inhibitors of pro-inflammatory cytokines TNF-α and IL-6

Sharma, Simmi,Gupta, Shilpa,Khajuria, Vidushi,Bhagat, Asha,Ahmed, Zabeer,Shah, Bhahwal Ali

, p. 695 - 698 (2016/01/09)

A library of boswellic acid analogues were synthesized and tested for their anti-inflammatory potential on key inflammatory mediators, TNF-α and IL-6. The study led to the identification of lead compounds showing significant inhibition of the cytokines, TNF-α and IL-6 both in vitro and in vivo.

Design, synthesis and biological evaluation of β-boswellic acid based HDAC inhibitors as inducers of cancer cell death

Sharma, Simmi,Ahmad, Mudassier,Bhat, Javeed Ahmad,Kumar, Arvind,Kumar, Manjeet,Zargar, Mohmmad Afzal,Hamid, Abid,Shah, Bhahwal Ali

, p. 4729 - 4734 (2015/01/08)

The synthesis and bio-evaluation of naturally occurring boswellic acids (BAs) as an alternate CAP for the design of new HDAC inhibitors is described. All the compounds were screened against a panel of human cancer cell lines to identify leads, which were subsequently examined for their potential to inhibit HDACs. The identified lead compound showed IC50value of 6 μm for HDACs, found to induce G1cell cycle arrest at significantly low concentration (1 μM) and caused significant loss in mitochondrial membrane potential at 5 and 10 μM. Furthermore, specific interactions of the lead molecule inside the catalytic domain were also studied through in silico molecular modeling.

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