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N-{2-[2-(2-(2-Aminoethoxy)ethoxy)ethoxy]ethyl}biotinamide trifluoroacetate salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

945462-84-0

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945462-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945462-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,4,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 945462-84:
(8*9)+(7*4)+(6*5)+(5*4)+(4*6)+(3*2)+(2*8)+(1*4)=200
200 % 10 = 0
So 945462-84-0 is a valid CAS Registry Number.

945462-84-0 Well-known Company Product Price

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  • Sigma

  • (38801)  N-Biotinyl-3,6,9-trioxaundecane-1,11-diamine trifluoroacetate salt solution  ≥95.0% (TLC), 25 mg/mL in DMSO

  • 945462-84-0

  • 38801-25MG-F

  • 383.76CNY

  • Detail
  • Sigma

  • (38801)  N-Biotinyl-3,6,9-trioxaundecane-1,11-diamine trifluoroacetate salt solution  ≥95.0% (TLC), 25 mg/mL in DMSO

  • 945462-84-0

  • 38801-100MG-F

  • 1,253.07CNY

  • Detail

945462-84-0Relevant academic research and scientific papers

A cell-permeable inhibitor and activity-based probe for the caspase-like activity of the proteasome

van Swieten, Paul F.,Samuel, Emlyn,Hernandez, Rosa Orient,van den Nieuwendijk, Adrianus M.C.H.,Leeuwenburgh, Michiel A.,van der Marel, Gijsbert A.,Kessler, Benedikt M.,Overkleeft, Herman S.,Kisselev, Alexei F.

, p. 3402 - 3405 (2007)

The ubiquitin-proteasome pathway degrades the majority of proteins in mammalian cells and plays an essential role in the generation of antigenic peptides presented by major histocompatibility class I molecules. Proteasome inhibitors are of great interest

Thrombin-Inhibiting Anticoagulant Liposomes: Development and Characterization

Endreas, Wegderes,Brüssler, Jana,Vornicescu, Doru,Keusgen, Michael,Bakowsky, Udo,Steinmetzer, Torsten

supporting information, p. 340 - 349 (2016/02/16)

Many peptides and peptidomimetic drugs suffer from rapid clearance in vivo; this can be reduced by increasing their size through oligomerization or covalent conjugation with polymers. As proof of principle, an alternative strategy for drug oligomerization

Water soluble multi-biotin-containing compounds

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Page/Page column 24-25, (2010/11/24)

Water-soluble discrete multi-biotin-containing compounds with at least three (3) biotin moieties are disclosed. The water-soluble biotin-containing compounds may additionally comprise one or more moieties that confer resistance to cleavage by biotinidase or that is cleavable in vitro or in vivo. The discrete multi-biotin-containing compounds may include a reactive moiety that provides a site for reaction with yet another moiety, such as a targeting, diagnostic or therapeutic functional moiety. Biotinylation reagents comprising water-soluble linker moieties are also disclosed and may additionally comprise a biotinidase protective group. Methods for amplifying the number of sites for binding biotin-binding proteins at a selected target using multi-biotin compounds also are disclosed.

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