Dipeptide mimetics can substitute for the receptor activation domain resulting in highly potent analogues of hPTH(1-36) fragment

Bioorganic and Medicinal Chemistry Letters

Volumn 6, Issue 10, 1996, Pages 1151-1156

  Waelchli, Rudolf ^a   Gamse, Rainer ^a   Bauer, Wilfried ^a   Meigel, Harald ^a   Lier, Edouard ^a   Feyen, Jean H M ^a  

^a Sandoz Pharma Ltd   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADENYLATE CYCLASE; ALKENE; CYCLIC AMP; DIPEPTIDE; PARATHYROID HORMONE DERIVATIVE; PARATHYROID HORMONE[1-36]; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CANCER CELL CULTURE; CELL LINE; CHEMICAL BOND; CHEMICAL MODIFICATION; DRUG ACTIVITY; DRUG POTENCY; DRUG SYNTHESIS; ENZYME ACTIVATION; HUMAN; HUMAN CELL; NONHUMAN; RAT;

EID: 0029972913     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-894X(96)00188-6     Document Type: Article

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