The eosinophil eotaxin receptor has been isolated, cloned and sequenced. This receptor is a human -chemokine receptor and has been designated “CC CKR3”. The eosinophil eotaxin receptor may be used to screen and identify compounds that bind to the eosinophil eotaxin receptor. Such compounds would be useful in the treatment and prevention of atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and particularly bronchial asthma.
The eosinophil eotaxin receptor has been isolated, cloned and sequenced. This receptor is a human β-chemokine receptor and has been designated “CC CKR3”. The eosinophil eotaxin receptor may be used to screen and identify compounds that bind to the eosinophil eotaxin receptor. Such compounds would be useful in the treatment and prevention of atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and particularly bronchial asthma.
Treating Stress Response With Chemokine Receptor Ccr5 Modulators
Richard Pierson III - Ruxton MD, US Agnes Azimzadeh - Timonium MD, US Carsten Schroeder - Baltimore MD, US Julie DeMartino - Westfield NJ, US
International Classification:
A61K039/395 A61K038/00 A61K031/00
US Classification:
424145100, 514001000, 514002000
Abstract:
The use of chemokine receptor CCR5 modulators (e.g., CCR5 antagonists) is disclosed for the treatment or prevention of stress response (e.g., fever) in a subject resulting from surgery, infection or other insult to the subject (e.g., a warm-blooded vertebrate). Methods for treating or preventing disorders involving the activation of pro-inflammatory cytokines by administration of a CCR5 modulator, for inhibiting the endogenous production of pro-inflammatory cytokines by the administration of CCR5 modulators, and for determining the efficacy of CCR5 modulators in correcting abnormal levels of pro-inflammatory cytokines are also disclosed.
Tetrahydropyranyl Cyclopentyl Tetrahydropyridopyridine Modulators Of Chemokine Receptor Activity
Julie DeMartino - Westfield NJ, US Taro Akiyama - Freehold NJ, US Mary Struthers - Edison NJ, US Lihu Yang - Edison NJ, US Joel Berger - Hoboken NJ, US Gregori Morriello - Randolph NJ, US Alexander Pastemak - Princeton NJ, US Changyou Zhou - Plainsboro NJ, US Sander Mills - , US Gabor Butora - Martinsville NJ, US Shankaran Kothandaraman - Kendall Park NJ, US Deodialsingh Guiadeen - Linden NJ, US Cheng Tang - East Brunswick NJ, US Richard Jiao - Havertown PA, US Stephen Goble - West Windsor NJ, US Christopher Moyes - Hertfordshire, GB
International Classification:
A61K 31/4745
US Classification:
514300000
Abstract:
The present invention is directed to methods for treating, preventing, ameliorating, controlling or reducing the risk of a disorder or disease, which method comprises the administration to a patient of an effective amount of the compound of formula I: I (wherein R, R, R, R, R, R, R, R, R, R, X, n and the dashed line are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.
The eosinophil eotaxin receptor has been isolated, cloned and sequenced. This receptor is a human β-chemokine receptor and has been designated “CC CKR3”. The eosinophil eotaxin receptor may be used to screen and identify compounds that bind to the eosinophil eotaxin receptor. Such compounds would be useful in the treatment and prevention of atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and particularly bronchial asthma.
Drug Combination Therapy And Pharmaceutical Compositions For Treating Inflammatory Disorders
Michael J. Forrest - Shrewsbury NJ, US Julie A. DeMartino - Westfield NJ, US Michelle R. Flicker - Bridgewater NJ, US Augustin Melian - Woodcliff Lake NJ, US Samina Kanwar - Hoboken NJ, US Gary J. Romano - Wynnewood PA, US
A combination of a CCR2 antagonist and a statin is useful in the treatment and or prevention of inflammatory and other disorders, and methods of treating inflammatory and other disorders using a combination of a CCR2 antagonist and a statin.
Novel Human Acidic Mammalian Chitinase And Use Thereof
Kalpit A. Vora - Yardley PA, US Julie A. DeMartino - Westfield NJ, US John Stuart Mudgett - Basking Ridge NJ, US Gene Porter - Neptune NJ, US Gloria Wolfe - New York NY, US
Described herein is a variant human acidic mammalian chitinase (AMCase) enzyme having improved stability and an isolated nucleic acid sequence which encodes the variant. The invention also provides to nucleic acid constructs, vectors, and host cells comprising the nucleic acid sequences as well as methods for producing recombinant variant AMCase polypeptide and its use in screening assays to identify modulators.
Bruce L. Daugherty - South Orange NJ Julie A. Demartino - Cranford NJ Salvatore J. Siciliano - East Brunswick NJ Martin S. Springer - Westfield NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C07K 14715 C12N 510 C12N 1512 C12N 1564
US Classification:
530350
Abstract:
The eosinophil eotaxin receptor has been isolated, cloned and sequenced. This receptor is a human. beta. -chemokine receptor and has been designated "CC CKR3". The eosinophil eotaxin receptor may be used to screen and identify compounds that bind to the eosinophil eotaxin receptor. Such compounds would be useful in the treatment and prevention of atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and particularly bronchial asthma.