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3β-Hydroxyurs-12-en-23-oic acid is a naturally occurring triterpenoid compound, which belongs to the ursane class of triterpenoids. It is characterized by the presence of a hydroxyl group at the 3β position, a double bond at the 12 position, and a carboxylic acid group at the 23 position. This chemical is derived from plants and has been found in various species, such as the bark of the tree Antrodia camphorata. It exhibits various biological activities, including anti-inflammatory, anti-tumor, and anti-viral properties. Due to its potential therapeutic applications, 3β-Hydroxyurs-12-en-23-oic acid has been a subject of interest in the field of natural product chemistry and pharmacology.

3877-93-8

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3877-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3877-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3877-93:
(6*3)+(5*8)+(4*7)+(3*7)+(2*9)+(1*3)=128
128 % 10 = 8
So 3877-93-8 is a valid CAS Registry Number.

3877-93-8Relevant 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

supporting information, 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.

Acyl derivatives of boswellic acids as inhibitors of NF-κB and STATs

Kumar, Ajay,Shah, Bhahwal A.,Singh, Samar,Hamid, Abid,Singh, Shashank K.,Sethi, Vijay K.,Saxena, Ajit K.,Singh, Jaswant,Taneja, Subhash C.

supporting information; experimental part, p. 431 - 435 (2012/03/11)

Boswellic acid acylates including their epimers were synthesized and screened against a panel of human cancer cell lines. They exhibited a range of cytotoxicity against various human cancer cell lines thereby leading to the development of a possible SAR. One of the identified lead compounds was found to be an inhibitor of the NF-κB and STAT proteins, warranting further investigations to be developed into a potential anticancer lead.

Cytotoxic and apoptotic activities of novel amino analogues of boswellic acids

Shah, Bhahwal A.,Kumar, Ajay,Gupta, Pankaj,Sharma, Madhunika,Sethi, Vijay K.,Saxena, Ajit K.,Singh, Jaswant,Qazi, Ghulam N.,Taneja, Subhash C.

, p. 6411 - 6416 (2008/09/17)

4-Amino analogues prepared from β-boswellic acid and 11-keto-β-boswellic acid, wherein the carboxyl group in ursane nucleus was replaced by an amino function via Curtius reaction, displayed improved cytotoxicity than the parent molecules. The same molecules also exhibited apoptotic activity by inducing DNA fragmentation.

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