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methyl {(2S,3R,4S,5S)-3-[(1S)-1-benzyloxy-2-methylbutyl]-4-nitro-5-phenyl}prolyl-β-alaninate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1420778-34-2

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1420778-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1420778-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,0,7,7 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1420778-34:
(9*1)+(8*4)+(7*2)+(6*0)+(5*7)+(4*7)+(3*8)+(2*3)+(1*4)=152
152 % 10 = 2
So 1420778-34-2 is a valid CAS Registry Number.

1420778-34-2Downstream Products

1420778-34-2Relevant academic research and scientific papers

Design, synthesis, and functional evaluation of leukocyte function associated antigen-1 antagonists in early and late stages of cancer development

San Sebastián, Eider,Zimmerman, Tahl,Zubia, Aizpea,Vara, Yosu,Martin, Elyette,Sirockin, Finton,Dejaegere, Annick,Stote, Roland H.,Lopez, Xabier,Pantoja-Uceda, David,Valcárcel, María,Mendoza, Lorea,Vidal-Vanaclocha, Fernando,Cossío, Fernando P.,Blanco, Francisco J.

, p. 735 - 747 (2013/03/28)

The integrin leukocyte function associated antigen 1 (LFA-1) binds the intercellular adhesion molecule 1 (ICAM-1) by its αL-chain inserted domain (I-domain). This interaction plays a key role in cancer and other diseases. We report the structure-based design, small-scale synthesis, and biological activity evaluation of a novel family of LFA-1 antagonists. The design led to the synthesis of a family of highly substituted homochiral pyrrolidines with antiproliferative and antimetastatic activity in a murine model of colon carcinoma, as well as potent antiadhesive properties in several cancer cell lines in the low micromolar range. NMR analysis of their binding to the isolated I-domain shows that they bind to the I-domain allosteric site (IDAS), the binding site of other allosteric LFA-1 inhibitors. These results provide evidence of the potential therapeutic value of a new set of LFA-1 inhibitors, whose further development is facilitated by a synthetic strategy that is versatile and fully stereocontrolled.

NOVEL INHIBITORS OF THE LFA-1/ICAM-1 INTERACTION, AND USES THEREOF

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Page/Page column 13-14; 19, (2010/11/27)

The invention relates to the treatment of disorders or diseases mediated by LFA-1/ ICAM-1 molecular interaction. This is based on the use of novel chemical compounds capable of inhibiting said interaction, and more particularly, to pharmaceutical composit

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