Celgene International Ii Sarl

Receptos, Inc.

Kalvista Pharmaceuticals Limited

Step Pharma S.a.s.

Andrew Richard Novak

Premji Meghani

Esther Martinborough

Marcus F Boehm

Liming Huang

Junko Tamiya

Manisha Moorjani

Thomas Fowler

Adam Richard Yeager

Enugurthi Brahmachary

Michael Knaggs

David Michael Evans

Hannah Joy Edwards

Joseph William Wrigglesworth

Lorna Duffy

Geraint Jones

Louise Birch

Mark T Griffith

Daniel Glynn

Mark Mills

Pascal George

Rebecca Louise Davie

David Cousin

Simon Teanby Hodgson

Alun John Smith

Saleh Ahmed

Abdul Quddus

Michael John Stocks

Emma Blackham

Jennifer Thomas

Iain Miller

Elli Chatzopoulou

Gianna Toschi

Joseph Wrigglesworth

Compounds of formula (I) and related aspects.

Compounds

Compounds of formula (I): (I) and related aspects. 

Aminothiazole compounds as inhibitors of CTPS1

Compounds of formula (I) and related aspects. 

The present invention provides compounds of formula (I), compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease or condition in which plasma kallikrein activity is implicated); and methods of treating patients with such compounds; wherein R5, R6, R7, R12, R13, A, L, B, n, W, X, Y and Z are as defined herein.

Inhibitors of plasma kallikrein

Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where '' represents either or both the R and S form of the compound): where A, B, C, Y, Y, Z, R, R, R, R, R, W, n, p and q are as defined herein.

GLP-1 receptor modulators

The present invention provides compounds of formula (I), compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease or condition in which plasma kallikrein activity is implicated); and methods of treating patients with such compounds; wherein R5, R6, R7, R12, R13, A, L, B, n, W, X, Y and Z are as defined herein. 

Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36), GLP-1(9-36), and oxyntomodulin, or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where '' represents either or both the R and S form of the compound): where A, B, C, R, R, R, R, R, n, p and q are as defined herein.

Compounds that bind the glucagon-like peptide 1 (GLP-1) receptor, methods of their synthesis, methods of their therapeutic and/or prophylactic use, and methods of their use in stabilizing GLP-1 receptor in vitro for crystallization of the GLP-1 receptor are provided. Certain compounds may have activity as modulators or potentiators with respect to glucagon receptor, GIP receptor, GLP-1 and GLP-2 receptors, and PTH receptor on their own or in the presence of receptor ligands such as GIP(1-42), PTH(1-34), Glucagon(1-29), GLP-2(1-33), GLP-1(7-36), GLP-1(9-36), oxyntomodulin and exendin variants.

GLP-1 receptor stabilizers and modulators

The present invention provides compounds of formula (I): compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease or condition in which plasma kallikrein activity is implicated); and methods of treating patients with such compounds; wherein R5, R6, R7, A, B, W, X, Y and Z are as defined herein. 

Heterocyclic derivates

Compounds that bind the glucagon-like peptide 1 (GLP-1) receptor, methods of their synthesis, methods of their therapeutic and/or prophylactic use, and methods of their use in stabilizing GLP-1 receptor in vitro for crystallization of the GLP-1 receptor are provided. Certain compounds may have activity as modulators or potentiators with respect to glucagon receptor, GIP receptor, GLP-1 and GLP-2 receptors, and PTH receptor on their own or in the presence of receptor ligands such as GIP(1-42), PTH(1-34), Glucagon(1-29), GLP-2(1-33), GLP-1 (7-36), GLP-1 (9-36), oxyntomodulin and exendin variants.

Growing community of inventors

Nottingham, United Kingdom

Andrew Richard Novak