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(2S)-3-{4-[2-(3,4,5,6-tetrahydropyrimidin-2-ylamino)ethoxy]benzoyl}-2-{2-[3-(tert-butoxycarbonylamino)-3-methylpropoxycarbonylamino]ethylsulfonylamino}propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

856244-25-2

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856244-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 856244-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,2,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 856244-25:
(8*8)+(7*5)+(6*6)+(5*2)+(4*4)+(3*4)+(2*2)+(1*5)=182
182 % 10 = 2
So 856244-25-2 is a valid CAS Registry Number.

856244-25-2Downstream Products

856244-25-2Relevant academic research and scientific papers

Integrin alpha-v beta-3 antagonists for use in imaging and therapy

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Page/Page column 5-6, (2008/06/13)

Integrin receptor antagonists whose molecular structure includes a tetrahydropyridimidinylaminoethyloxybenzoyl group on a sulfonylamino-β-alanine nucleus exhibit increased binding affinity for the αvβ3 receptor when further substituted on the sulfonyl moi

Synthesis, in vitro, and in vivo characterization of an integrin αvβ3-targeted molecular probe for optical imaging of tumor

Burnett, Christopher A.,Xie, Jianwu,Quijano, Jade,Shen, Zhimin,Hunter, Finie,Bur, Monica,Li, King C. P.,Danthi, S. Narasimhan

, p. 3763 - 3771 (2007/10/03)

Integrin αvβ3 is a widely-recognized target for the development of targeted molecular probes for imaging pathological conditions. αvβ3 is a cell-surface receptor protein that is upregulated in various pathological conditions including osteoporosis, rheumatoid arthritis, macular degeneration, and cancer. The synthesis of an αvβ3-targeted optical probe 7 from compound 1, and its in vitro and in vivo characterization is described. A series of aliphatic carbamate derivatives of the potent non-peptide integrin antagonist 1 was synthesized and the binding affinity to α vβ3 was determined in both enzyme linked immunosorbent assay (ELISA) and cell adhesion inhibition assays. The hydrophobic carbamate-linked appendages improved the binding affinity of the parent compound for αvβ3 by 2-20 times. A Boc-protected neopentyl derivative in the series is shown to have the best binding affinity to αvβ3 (IC50 = 0.72 nM) when compared to compound 1 as well as to c-RGDfV. Optical probe 7 utilizes the neopentyl linker and demonstrates increased binding affinity and significant tumor cell uptake in vitro as well as specific tumor accumulation and retention in vivo. These results illustrate the potential of employing integrin-targeted molecular probes based on 1 to image a multitude of diseases associated with αvβ3 overexpression.

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