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Title:
Gタンパク質共役受容体および関連組成物を使用するスクリーニング方法
Document Type and Number:
Japanese Patent JP5711966
Kind Code:
B2
Abstract:
The present invention relates to a polypeptide, or pharmaceutically acceptable salt thereof, comprising the formula PTH(1-X)/PTHrP(Y-36). Further, the present invention refers to a polypeptide which binds the PTH receptor and has a high affinity for the R 0 form of the PTH receptor and to a polypeptide having affinity for PTH RG and a low affinity for PTH R 0 . Moreover, the present invention includes to a pharmaceutical composition comprising such polypeptide. The present invention further relates to a polypeptide or a pharmaceutical composition of the present invention for use in a method for treating a disease or condition. Moreover, the present invention refers to a nucleic acid comprising a sequence encoding a polypeptide of the present invention, a vector comprising said nucleic acid, a cell comprising said vector and a method of making a polypeptide of the present invention. Finally, the present invention further relates to a method for determining whether a candidate compound is a long-acting agonist of a G protein coupled receptor (GPCR).

Inventors:
Gardener Thomas Jay.
Potts John Tea.
Masaru Shimizu
Fumihiko Ichikawa
Jupner Harald Tea.
Makoto Okazaki
Application Number:
JP2010519932A
Publication Date:
May 07, 2015
Filing Date:
August 01, 2008
Export Citation:
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Assignee:
The General Hospital Corporation
Chugai Pharmaceutical Co., Ltd.
International Classes:
C12Q1/02; A61K38/00; A61P5/18; A61P19/08; A61P19/10; A61P43/00; C07K14/635; C12N15/09; C40B30/06; G01N33/15; G01N33/50
Other References:
The Journal of Clinical Endocrinology & Metabolism,2003年,Vol.88,p.569-575
Journal of Bone and Mineral Research,2006年,Vol.21,p.354-365
The Journal of Biological Chemistry,2001年,Vol.276,p.7741-7753
Attorney, Agent or Firm:
Hatsushi Shimizu
Masao Haruna
Hirotaka Yamaguchi
Toshi Gobe
Ryuichi Inoue
Toshimitsu Sato
Koichi Niimi
Tomohiko Kobayashi
Shinichi Watanabe
Masato Ozeki
Kazuya Kawamoto



 
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