US2018042902A1PendingUtilityA1
Heterocyclic Compounds and Uses Thereof
Est. expiryAug 17, 2029(~3.1 yrs left)· nominal 20-yr term from priority
A61P 7/04A61P 35/04A61P 37/06A61P 7/00A61P 9/00A61P 43/00A61P 3/10A61P 37/02A61P 37/08A61P 9/10A61P 29/00A61P 29/02A61P 31/12A61P 25/14A61P 25/04A61P 25/02A61P 25/28A61P 25/00A61P 27/02A61P 31/04A61P 3/00A61P 35/00A61P 11/08A61P 13/08A61P 1/18A61P 11/00A61P 19/00A61P 21/00A61P 17/06A61P 17/02A61P 17/00A61P 19/02A61P 17/16A61P 11/06A61P 15/00A61P 1/04A61P 1/00A61P 13/12A61P 15/08A61P 1/16A61K 31/497A61K 31/498C12N 9/1205A61K 31/428A61K 31/422A61K 31/4709C07D 471/04C07D 519/06C07D 413/14A61K 31/496C07D 519/00C07D 417/04A61K 31/423A61K 31/517A61K 31/444A61K 31/5025C07D 401/14A61K 31/551C07D 487/04C07D 413/04C07D 417/14A61K 31/5377A61K 31/541A61K 31/437C07B 2200/05Y02A50/30
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Claims
Abstract
Heterocyclic entities that modulate PI3 kinase activity, pharmaceutical compositions containing the heterocyclic entities, and methods of using these chemical entities for treating diseases and conditions associated with PI3 kinase activity are described herein.
Claims
exact text as granted — not AI-modified1 .- 53 . (canceled)
54 . A method of providing therapeutic benefit in a subject having a cancer selected from lung cancer and gastric cancer by inhibiting phosphatidyl inositol-3 kinases comprising administering to the subject a therapeutically effective amount of a compound of the following formula:
or a pharmaceutically acceptable salt thereof, wherein
W 1 is CR 3 ;
W 2 is CR 4 ;
W 3 is N;
W 4 is N;
W 5 is CR 7 ;
W 6 is CR 8 ;
R 1 and R 2 are independently hydrogen, alkyl, heteroalkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, alkoxy, heterocycloalkyloxy, amido, amino, acyl, acyloxy, alkoxycarbonyl, sulfonamido, halo, cyano, hydroxy, nitro, phosphate, urea, or carbonate;
R 3 is amido of formula —C(O)N(R) 2 , or —NHC(O)R, wherein R is hydrogen, alkyl, cylcloalkyl, aryl, heteroaryl, or heteroalicyclic; or wherein said (R) 2 groups taken together with the nitrogen to which they are attached form an optionally substituted 4-, 5-, 6-, or 7-membered ring; and
R 4 , R 7 and R 8 are each hydrogen.
55 . The method of claim 54 , wherein R 1 is hydrogen and R 2 is amino.
56 . The method of claim 55 , wherein R 2 is NH 2 .
57 . The method of claim 54 , wherein R 3 is amido of formula —C(O)N(R) 2 wherein said (R) 2 groups taken together with the nitrogen to which they are attached form an optionally substituted 4-, 5-, 6-, or 7-membered ring.
58 . The method claim 57 , wherein R 1 is hydrogen and R 2 is amino.
59 . The method claim 58 , wherein R 2 is NH 2 .
60 . The method of claim 59 , wherein R 3 is amido of formula —C(O)N(R) 2 wherein said (R) 2 groups taken together with the nitrogen to which they are attached form an optionally substituted 6-membered ring.
61 . The method of claim 54 , wherein the compound or pharmaceutically acceptable salt is
62 . The method of claim 54 , wherein the cancer is lung cancer.
63 . The method of claim 62 , wherein the lung cancer is non-small cell lung cancer.
64 . The method of claim 62 , wherein the lung cancer is small cell lung cancer.
65 . The method of claim 54 , wherein the cancer is gastric cancer.Cited by (0)
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