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  • 95
    Millipore farnesyl acetate
    HPLC analysis of starting material and crude reaction mixture from the alkylation of pure 9 to yield a -factor ( 1 ). Panel A: HPLC of purified starting material 9 . Panel B: HPLC of crude alkylation reaction mixture containing 9 and <t>farnesyl</t> bromide in the presence of Zn(OAc) 2 to yield 1 .
    Farnesyl Acetate, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 49 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/farnesyl acetate/product/Millipore
    Average 95 stars, based on 49 article reviews
    Price from $9.99 to $1999.99
    farnesyl acetate - by Bioz Stars, 2020-12
    95/100 stars
      Buy from Supplier

    91
    TCI Tokyo Chemical Industry farnesyl acetate
    HPLC analysis of starting material and crude reaction mixture from the alkylation of pure 9 to yield a -factor ( 1 ). Panel A: HPLC of purified starting material 9 . Panel B: HPLC of crude alkylation reaction mixture containing 9 and <t>farnesyl</t> bromide in the presence of Zn(OAc) 2 to yield 1 .
    Farnesyl Acetate, supplied by TCI Tokyo Chemical Industry, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/farnesyl acetate/product/TCI Tokyo Chemical Industry
    Average 91 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    farnesyl acetate - by Bioz Stars, 2020-12
    91/100 stars
      Buy from Supplier

    Image Search Results


    HPLC analysis of starting material and crude reaction mixture from the alkylation of pure 9 to yield a -factor ( 1 ). Panel A: HPLC of purified starting material 9 . Panel B: HPLC of crude alkylation reaction mixture containing 9 and farnesyl bromide in the presence of Zn(OAc) 2 to yield 1 .

    Journal: Bioorganic & medicinal chemistry

    Article Title: Synthesis of a-factor peptide from Saccharomyces cerevisiae and photoactive analogues via Fmoc solid phase methodology

    doi: 10.1016/j.bmc.2010.11.006

    Figure Lengend Snippet: HPLC analysis of starting material and crude reaction mixture from the alkylation of pure 9 to yield a -factor ( 1 ). Panel A: HPLC of purified starting material 9 . Panel B: HPLC of crude alkylation reaction mixture containing 9 and farnesyl bromide in the presence of Zn(OAc) 2 to yield 1 .

    Article Snippet: Farnesyl bromide ( > 95% E, E ) was obtained from Sigma-Aldrich.

    Techniques: High Performance Liquid Chromatography, Purification

    ESI-MS-MS analysis of a -factor ( 1) produced by Fmoc SPPS. -f: loss of farnesyl (loss of C 15 H 25 ).

    Journal: Bioorganic & medicinal chemistry

    Article Title: Synthesis of a-factor peptide from Saccharomyces cerevisiae and photoactive analogues via Fmoc solid phase methodology

    doi: 10.1016/j.bmc.2010.11.006

    Figure Lengend Snippet: ESI-MS-MS analysis of a -factor ( 1) produced by Fmoc SPPS. -f: loss of farnesyl (loss of C 15 H 25 ).

    Article Snippet: Farnesyl bromide ( > 95% E, E ) was obtained from Sigma-Aldrich.

    Techniques: Mass Spectrometry, Produced