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N, N-bis(2-chloroethyl)-N-methyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl] methanaminium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1346936-27-3

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1346936-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346936-27-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,9,3 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1346936-27:
(9*1)+(8*3)+(7*4)+(6*6)+(5*9)+(4*3)+(3*6)+(2*2)+(1*7)=183
183 % 10 = 3
So 1346936-27-3 is a valid CAS Registry Number.

1346936-27-3Relevant academic research and scientific papers

ANTI-CANCER AGENTS

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Paragraph 0398, (2013/03/26)

Described herein are compounds that may be selectively activated to produce active anti-cancer agents in tumor cells. Also disclosed are pharmaceutical compositions comprising the compounds, and methods of treating cancer using the compounds.

Hydrogen peroxide inducible DNA cross-linking agents: Targeted anticancer prodrugs

Kuang, Yunyan,Balakrishnan, Kumudha,Gandhi, Varsha,Peng, Xiaohua

supporting information; experimental part, p. 19278 - 19281 (2012/01/15)

The major concern for anticancer chemotherapeutic agents is the host toxicity. The development of anticancer prodrugs targeting the unique biochemical alterations in cancer cells is an attractive approach to achieve therapeutic activity and selectivity. We designed and synthesized a new type of nitrogen mustard prodrug that can be activated by high level of reactive oxygen species (ROS) found in cancer cells to release the active chemotherapy agent. The activation mechanism was determined by NMR analysis. The activity and selectivity of these prodrugs toward ROS was determined by measuring DNA interstrand cross-links and/or DNA alkylations. These compounds showed 60-90% inhibition toward various cancer cells, while normal lymphocytes were not affected. To the best of our knowledge, this is the first example of H 2O2-activated anticancer prodrugs.

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