200937-17-3 Boc-D-Leu-OH•H2O

Biochemistry uye Drug Discovery:
Sezvinobuda paamino acid, Boc-D-Leu-OH·H2O inoita basa rakakosha mukugadzira peptides nemapuroteni ane biologically active.Kugadziriswa kwemakemikari emukomboni uyu kunogona kutungamira mukugadzirwa kwemishonga mitsva kana vamiriri vezvinodhaka kurapa zvirwere zvakasiyana.Iyo yakasarudzika zvimiro zveD-leucine inogona kupa chaiyo biological zviitiko kune akagadzirwa peptides kana mapuroteni.
Peptide Synthesis:
In solid-phase peptide synthesis, Boc-D-Leu-OH · H2O inokosha amino acid monomer.Yayo N-terminal Boc yekudzivirira boka inobvumira amino acid ligation uye deprotection pasi pemamiriro akapfava, ichigonesa synthesis ye peptide cheni ine chaiwo kutevedzana uye mabasa.
Tsvagiridzo yemurabhoritari:
Boc-D-Leu-OH · H2O inowanzoshandiswa mu peptide synthesis uye mapuroteni maitiro ezvidzidzo.Nekuisanganisa nemamwe amino acid monomers, akasiyana peptide anoteedzana anogona kugadzirwa kuti aongorore mapuroteni-protein uye mapuroteni-ligand kudyidzana, pamwe nekushanda kweprotein uye nzira dzekutonga.
Peptide Reagents uye Synthetic Auxiliaries:
Boc-D-Leu-OH · H2O inogona kushanda sechinhu chinodzivirira kana condensing agent mu peptide synthesis, kuvandudza kushanda uye kuchena kwepeptide synthesis process.Pamusoro pezvo, inogona kushandiswa se peptide reagent ye peptide kunyora, kugadziridza, uye kuona.
Asymmetric Synthesis:
Nekuda kwechiral chimiro cheD-leucine, Boc-D-Leu-OH · H2O ine zvingangoshandiswa mune asymmetric synthesis.Nekuisanganisa nemamwe mamorekuru echiral, peptides uye mapuroteni ane chaiwo stereoconfigurations anogona kugadzirwa kuti adzidze maitiro echirality pazviitiko zvebiology.