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cyclo(-Gly-Asp-D-Phe-Lys(CO-COH)-Arg-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

343312-28-7

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343312-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343312-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,3,1 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 343312-28:
(8*3)+(7*4)+(6*3)+(5*3)+(4*1)+(3*2)+(2*2)+(1*8)=107
107 % 10 = 7
So 343312-28-7 is a valid CAS Registry Number.

343312-28-7Downstream Products

343312-28-7Relevant academic research and scientific papers

OPTIMISED MULTIVALENT TARGETING FLUORESCENT TRACER

-

, (2018/06/04)

A fluorescent tracer comprises: a RAFT template, comprising the residues: Glycine-Proline-Lysine-Alanine-Lysine-Glycine-Proline-Lysine-Lysine-Lysine and having a mean plane defining an upper face having four lysine residues and a lower face having one lysine residue, four identical targeting molecules comprising the amino acids: Arginine-Glycine-Aspartic acid-Phenylalanine-Lysine (RGDKf), each of the molecules being fixed to a different lysine residue of the first upper face via an oxime bond, and a fluorophore S0456 fixed to the lower face of the mean plane via a spacer arm connecting the central carbon of the sequence of double bonds of the fluorophore and the lysine amino acid of the lower face of the decapeptide via an amide bond, the spacer arm being 5-(4-hydroxyphenyl)pentanoic acid.

A convenient access to αVβ3/αVβ5 integrin ligand conjugates: Regioselective solid-phase functionalisation of an RGD based peptide

Boturyn, Didier,Dumy, Pascal

, p. 2787 - 2790 (2007/10/03)

The cyclopeptide (-RGDfK-) is a potent and selective αVβ3/αVβ5 integrin ligand. A methodology for the conjugation of cyclo(-RGDfK-) through the regioselective derivatisation of lysine side chains, either in solution or directly on the solid support, is described. This provides a rapid and flexible chemical entry to conjugated integrin ligands bearing reporter groups for biological investigations or reactive chemical functions for the preparation of new vector systems.

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