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6-N-(4-dimethylaminophenylcarbamoyl)hexanoic acid N'-benzoyloxyamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

251304-84-4

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251304-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251304-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,3,0 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 251304-84:
(8*2)+(7*5)+(6*1)+(5*3)+(4*0)+(3*4)+(2*8)+(1*4)=104
104 % 10 = 4
So 251304-84-4 is a valid CAS Registry Number.

251304-84-4Downstream Products

251304-84-4Relevant academic research and scientific papers

Amide analogues of trichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation

Jung, Manfred,Brosch, Gerald,K?lle, Doris,Scherf, Hans,Gerh?user, Clarissa,Loidl, Peter

, p. 4669 - 4679 (2007/10/03)

Inhibitors of histone deacetylase (HD) bear great potential as new drugs due to their ability to modulate transcription and to induce apoptosis or differentiation in cancer cells. We have described previously analogues of the complex natural HD inhibitors trapoxin B and trichostatin A with activities in the submicromolar range. Here we report structure-activity relationship analyses of further analogues of trichostatin A with respect to in vitro inhibition of maize HD-2 and their ability to induce terminal cell differentiation in Friend leukemic cells. This is the first report that shows the correlation between HD inhibitory activity and action on cancer cells on a larger series of similar compounds. Only the compounds that inhibit HD induce differentiation and/or exert antiproliferative activities in cell culture. Our studies support the use of in vitro systems as screening tools and provide structure-activity relationships that merit further investigation of this interesting target.

Inhibitors of histone deacetylase suppress the growth of MCF-7 breast cancer cells

Schmidt, Kathrin,Gust, Ronald,Jung, Manfred

, p. 353 - 357 (2007/10/03)

Inhibitors of histone deacetylase are attracting increasing interest due to their influence on transcription, differentiation, and apoptosis. We have investigated two synthetic inhibitors 3 and 4 of histone deacetylase and the natural product inhibitor tr

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