US2019290636A1PendingUtilityA1
Certain chemical entities, compositions and methods
Est. expiryJul 15, 2029(~3 yrs left)· nominal 20-yr term from priority
A61P 35/02A61P 9/00A61P 7/02A61P 3/10A61P 43/00A61P 37/00A61P 37/06A61P 37/02A61P 5/00A61P 7/00A61P 35/00A61P 37/08A61P 29/00A61P 27/00A61P 25/00A61P 3/00A61P 19/00A61P 19/02A61P 19/08A61P 17/06A61P 11/06A61P 13/00A61P 11/00A61P 17/00A61P 1/00A61K 31/52C07D 473/34A61K 31/506C07D 487/04Y02P20/55A61N 5/10A61K 45/06A61K 39/39558A61K 31/131A61K 31/5377A61K 31/196A61N 5/1007A61K 31/4725A61N 2005/109A61K 39/3955Y02A50/401Y02A50/414Y02A50/465C07D 473/38C07D 473/04C07D 401/06A61K 31/4985Y02A50/30
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Claims
Abstract
Chemical entities that modulate PI3 kinase activity, pharmaceutical compositions containing the chemical 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 - 22 . (canceled)
23 . A compound of Formula I-1:
or a pharmaceutically acceptable salt thereof, wherein
B is alkyl or a moiety of Formula II:
wherein W c is aryl, heteroaryl, heterocycloalkyl, or cycloalkyl, and
q is an integer of 0, 1, or 2;
X is absent or —(CH(R 9 )) z —, and z is an integer of 1, 2, 3, or 4;
Y is absent, —N(R 9 )—, or —N(R 9 )CH(R 9 )—;
wherein at least one of X and Y is present;
W d is
R a′ is hydrogen, halo, or amino;
R 1 is hydrogen, —F, —Cl, —CN, —CH 3 , isopropyl, —CF 3 , —OCH 3 , nitro, or phosphate;
R 2 is halo, hydroxy, cyano, nitro, or phosphate;
R 3 is aryl, heteroaryl, H, —CH 3 , —CF 3 , —Cl, or —F;
each R 9 is independently hydrogen, methyl, or ethyl; and
R 12 is hydrogen, alkyl, alkynyl, alkenyl, halo, aryl, heteroaryl, heterocycloalkyl, cycloalkyl, cyano, amino, carboxylic acid, alkoxycarbonyl, or amido.
24 . The compound of claim 23 , wherein X is —CH 2 —, —CH(CH 2 CH 3 ), or —CH(CH 3 )—.
25 . The compound of claim 23 , wherein Y is —NH—, —N(CH 3 )—, or —N(CH 2 CH 3 )—.
26 . The compound of claim 23 , wherein X—Y is —CH(CH 2 CH 3 )—NH— or —CH(CH 3 )—NH—.
27 . The compound of claim 23 , wherein R 3 is chloro.
28 . The compound of claim 23 , wherein R 3 is methyl.
29 . The compound of claim 23 , wherein R a is hydrogen.
30 . The compound of claim 23 , wherein R 12 is hydrogen, halo, cyano, or amido.
31 . The compound of claim 23 , wherein W d is
32 . The compound of claim 23 , wherein the compound is a compound of Formula IX-A2:
or a pharmaceutically acceptable salt thereof.
33 . The compound of claim 23 , wherein the compound is:
or a pharmaceutically acceptable salt thereof.
34 . The compound of claim 23 , wherein W d
35 . The compound of claim 23 , wherein the compound is a compound of Formula XI-A2:
or a pharmaceutically acceptable salt thereof.
36 . The compound of claim 23 , wherein the compound is:
or a pharmaceutically acceptable salt thereof.
37 . A compound, which is:
or a pharmaceutically acceptable salt thereof.
38 . A compound, which is:
or a pharmaceutically acceptable salt thereof.
39 . A pharmaceutical composition comprising a compound of claim 23 , or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipient.
40 . A method of inhibiting a phosphatidyl inositol-3 kinase (PI3 kinase), comprising contacting the PI3 kinase with an effective amount of a compound of claim 23 , or a pharmaceutically acceptable salt thereof.
41 . A method of inhibiting a phosphatidyl inositol-3 kinase (PI3 kinase), comprising contacting the PI3 kinase with an effective amount of a compound of claim 37 , or a pharmaceutically acceptable salt thereof.
42 . A method of inhibiting a phosphatidyl inositol-3 kinase (PI3 kinase), comprising contacting the PI3 kinase with an effective amount of a compound of claim 38 , or a pharmaceutically acceptable salt thereof.Cited by (0)
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