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methyl 2-(N,4-dimethylphenylsulfonam ido)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28126-01-4

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28126-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28126-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,2 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28126-01:
(7*2)+(6*8)+(5*1)+(4*2)+(3*6)+(2*0)+(1*1)=94
94 % 10 = 4
So 28126-01-4 is a valid CAS Registry Number.

28126-01-4Relevant academic research and scientific papers

Substituted 2-hydroxy-4-(2-(phenylsulfonamido)acetamido)benzoic acid analogs as inhibitors of STAT protein

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Page/Page column 226-227; 231, (2019/02/14)

In one aspect, the invention relates to substituted 2-hydroxy-4-(2-(phenylsulfonamido)acetamido)benzoic acid analogs, derivatives thereof, and related compounds, which are useful as inhibitors of STAT protein activity; synthetic methods for making the com

STAT3 DIMERIZATION INHIBITORS

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Page/Page column 39, (2014/05/24)

The subject matter disclosed herein relates to compositions and methods of making and using the compositions. In a further aspect, the subject matter disclosed herein relates to inhibitors of STAT3 dimerization. Methods of making these compositions as wel

Development of new N-arylbenzamides as STAT3 dimerization inhibitors

Urlam, Murali K.,Pireddu, Roberta,Ge, Yiyu,Zhang, Xiaolei,Sun, Ying,Lawrence, Harshani R.,Guida, Wayne C.,Sebti, Said M.,Lawrence, Nicholas J.

supporting information, p. 932 - 941 (2013/07/27)

The O-tosylsalicylamide S3I-201 (10) was used as a starting point for design and synthesis of novel STAT-3 dimerization inhibitors with improved drug-like qualities. The phosphonic acid 12d and salicylic acids 13f, 13g with a shorter amide linker lacking

Antagonism of the Stat3-Stat3 Protein Dimer with Salicylic Acid Based Small Molecules

Fletcher, Steven,Page, Brent D.G.,Zhang, Xialoei,Yue, Peibin,Li, Zhi Hua,Sharmeen, Sumaiya,Singh, Jagdeep,Zhao, Wei,Schimmer, Aaron D.,Trudel, Suzanne,Turkson, James,Gunning, Patrick T.

scheme or table, p. 1459 - 1470 (2012/07/01)

More than 50 new inhibitors of the oncogenic Stat3 protein were identified through a structure-activity relationship (SAR) study based on the previously identified inhibitor S3I-201 (IC50=86μM, Ki>300μM). A key structural feature of

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