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Tetrahedron

Volumn 70, Issue 42, 2014, Pages 7774-7779

A disulfide bond replacement strategy enables the efficient design of artificial therapeutic peptides

(6) Aoki, Kazuhiro b Maeda, Miki b,c Nakae, Takashi c Okada, Yohei a Ohya, Keiichi b Chiba, Kazuhiro a

a TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY (Japan)

b TOKYO MEDICAL AND DENTAL UNIVERSITY (Japan)

c Research and Development Division Jitsubo Co Ltd (Japan)

Author keywords

Amine cross linkages; Bone resorption blocking activities; Disulfide bonds; Hydrophobic tags; Therapeutic peptides

Indexed keywords

AMINE; CARBOXYPEPTIDASE A; PEPTIDE FRAGMENT; UNCLASSIFIED DRUG; WP9QY PEPTIDE;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; CYTOTOXICITY ASSAY; DISULFIDE BOND; DRUG DESIGN; ENZYME STABILITY; IN VITRO STUDY; IN VIVO STUDY; MITSUNOBU REACTION; MOUSE; NONHUMAN; OSTEOCLAST; OSTEOLYSIS; PROTEIN CROSS LINKING; PROTEIN ENGINEERING; SEQUENCE HOMOLOGY;

EID: 84907939173 PISSN: 00404020 EISSN: 14645416 Source Type: Journal
DOI: 10.1016/j.tet.2014.05.079 Document Type: Article

Times cited : (9)

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