Peptides and compounds that bind to the IL-5 receptor
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61K-038/00
C07K-005/00
출원번호
US-0485302
(1995-06-07)
발명자
/ 주소
Barrett Ronald W. (Saratoga CA) England Bruce P. (Fremont CA) Schatz Peter J. (Mountain View CA) Sloan Derek (Los Gatos CA) Chen Min-Jia (San Francisco CA)
출원인 / 주소
Affymax Technologies N.V. (Greenford GB2 03)
인용정보
피인용 횟수 :
59인용 특허 :
4
초록▼
Described are peptides and peptide mimetics that bind to and the IL-5 receptor. Such peptides and peptide mimetics are useful in methods for treating disorders that involve improper production of or response to IL-5 and or the production and accumulation of eosinophils, such as asthma, as well as in
Described are peptides and peptide mimetics that bind to and the IL-5 receptor. Such peptides and peptide mimetics are useful in methods for treating disorders that involve improper production of or response to IL-5 and or the production and accumulation of eosinophils, such as asthma, as well as in diagnostic methods employing labeled peptides and peptide mimetics.
대표청구항▼
A method for treating a patient suffering from a disorder that is mediated by IL-5, comprising administering to the patient, a therapeutically effective dose of a compound comprising: (1) a core sequence of amino acids: CX1RX2X7X8X3X4X5WX6C where X1 is D, E, I, S, T, W, or Y; X2 is D, F, G, I, L, S,
A method for treating a patient suffering from a disorder that is mediated by IL-5, comprising administering to the patient, a therapeutically effective dose of a compound comprising: (1) a core sequence of amino acids: CX1RX2X7X8X3X4X5WX6C where X1 is D, E, I, S, T, W, or Y; X2 is D, F, G, I, L, S, V, W, or Y; X3 is D, E, G, L, N, S, T, or W; X4 is H or R; X5 is A, K, R, S, T, V, or W; X6 is D, E, F, L, M, P, Q, or V; X7 is I or V; (SEQ ID NO:1), and dimers and oligomers thereof, having (a) a molecular weight of less than about 5000 daltons, and (b) a binding affinity to IL5-R as expressed by an IC50 of no more than about 100 m2OC(O)NR-linkage; a phosphonate linkage; a -CH2S(O)2NR-linkage; a -CH2NR-linkage; and a -C(O)NR6-linkage; and a -NHC(O)NH-linkage where R is Hydrogen or lower alkyl and R6 is lower alkyl, further wherein the N-terminus of said peptide or peptide mimetic is selected from the group consisting of a -NRR1 group; a -NRC(O)R group; a -NRC(O)OR group; a -NRS(O)2R group; a -NHC(O)NHR group; a succinimide group; a benzyloxycarbonyl-NH-group; and a benzyloxycarbonyl-NH-group having from 1 to 3 substituents on the phenyl ring selected from the group consisting of lower alkyl, lower alkoxy, chloro, and bromo, where R and R1 are independently selected from the group consisting of hydrogen and lower alkyl, and still further wherein the C-terminus of said peptide or peptide mimetic has the formula -C(O)R2 where R2 is selected from the group consisting of hydroxy, lower alkoxy, and -NR3R4 where R3 and R4 are independently selected from the group consisting of hydrogen and lower alkyl and where the nitrogen atom of the -NR3R4 group can optionally be amine group of the N-terminus of the peptide so as to form a cyclic peptide, or a physiologically acceptable salt thereof.
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