200937-17-3 Boc-D-Leu-OH•H2O

Biochemistry da Gano Drug:
A matsayin tushen amino acid, Boc-D-Leu-OH·H2O yana taka muhimmiyar rawa wajen haɗa peptides da sunadarai masu aiki da ilimin halitta.Canje-canjen sinadarai na wannan fili na iya haifar da haɓakar magunguna ko masu neman magani don magance cututtuka daban-daban.Keɓaɓɓen kaddarorin D-leucine na iya ba da takamaiman ayyukan nazarin halittu zuwa ga hadadden peptides ko sunadarai.
Tsarin Peptide:
A cikin hadakar peptide mai ƙarfi-lokaci, Boc-D-Leu-OH·H2O shine mabuɗin amino acid monomer.Ƙungiya ta N-terminal Boc ta kare tana ba da damar haɗakar amino acid da ƙetare a ƙarƙashin yanayi mara kyau, yana ba da damar haɗin sarƙoƙi na peptide tare da takamaiman jeri da ayyuka.
Binciken Laboratory:
Boc-D-Leu-OH · H2O yawanci ana amfani dashi a cikin haɗin peptide da nazarin tsarin furotin.Ta hanyar haɗa shi tare da sauran amino acid monomers, ana iya haɗa nau'ikan peptide daban-daban don bincika hulɗar furotin-protein da furotin-ligand, da aikin furotin da tsarin tsari.
Peptide Reagents da Abubuwan Taimako na Haɓakawa:
Boc-D-Leu-OH · H2O na iya aiki a matsayin wakili mai kariya ko ma'auni mai mahimmanci a cikin haɗin peptide, inganta ingantaccen aiki da tsabta na tsarin haɗin gwiwar peptide.Bugu da ƙari, ana iya amfani dashi azaman peptide reagent don alamar peptide, gyarawa, da ganowa.
Tsarin asymmetric:
Saboda yanayin chiral na D-leucine, Boc-D-Leu-OH · H2O yana da yuwuwar aikace-aikace a cikin haɗin asymmetric.Ta hanyar haɗa shi tare da sauran ƙwayoyin chiral, peptides da furotin tare da takamaiman stereoconfigurations za a iya haɗa su don nazarin tasirin chirality akan ayyukan nazarin halittu.