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(R)-2-[(4-Methoxy-benzenesulfonyl)-pyridin-3-ylmethyl-amino]-4-methyl-pentanoic acid tert-butoxy-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1026045-87-3

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1026045-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026045-87-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,0,4 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1026045-87:
(9*1)+(8*0)+(7*2)+(6*6)+(5*0)+(4*4)+(3*5)+(2*8)+(1*7)=113
113 % 10 = 3
So 1026045-87-3 is a valid CAS Registry Number.

1026045-87-3Downstream Products

1026045-87-3Relevant academic research and scientific papers

SMALL MOLECULE INHIBITORS OF BACTERIAL TOXINS

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, (2022/04/03)

Described herein are compounds and compositions for use in treatment or prevention of an inflammatory bowel disease, gastrointestinal cancer, or a systemic bacterial infection in a subject in need thereof. The subject may be colonized by one or more pathogenic bacterial strains such as B. fragilis, E. faecalis, or C. perfringens. In certain aspects, the disclosure provides a method of diminishing the pathogenic effects of these bacterial strains by administering a compound that binds to and/or inhibits one or more toxins produced thereby.

Discovery of CGS 27023A, a non, peptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits

MacPherson, Lawrence J.,Bayburt, Erol K.,Capparelli, Michael P.,Carroll, Brian J.,Goldstein, Robert,Justice, Michael R.,Zhu, Lijuan,Hu, Shou-Ih,Melton, Richard A.,Fryer, Lynn,Goldberg, Ron L.,Doughty, John R.,Spirito, Salvatore,Blancuzzi, Vincent,Wilson, Doug,O'Byrne, Elizabeth M.,Ganu, Vishwas,Parker, David T.

, p. 2525 - 2532 (2007/10/03)

Structure-activity relationships of a lead hydroxamic acid inhibitor of recombinant human stromelysin were systematically defined by taking advantage of a concise synthesis that allowed diverse functionality to be explored at each position in a template. An ex vivo rat model and an in vivo rabbit model of stromelysin-induced cartilage degradation were used to further optimize these analogs for oral activity and duration of action. The culmination of these modifications resulted in CGS 27023A, a potent, orally active stromelysin inhibitor that blocks the erosion of cartilage matrix.

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