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US 11,952,366 B2Granted
Substituted 1,3,5-triazines as inhibitors for a rho family of GTP-ases
AssigneesFondazione Istituto Italiano Di Tecnologia, The Regents of the University of California
InventorsMarco De Vivo, Anand Ganesan, Jose Antonio Ortega Martinez, Sohail Jahid
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Abstract
The present invention relates to compounds of Formula (I) or pharmaceutically acceptable salts or solvates thereof: It further discloses a pharmaceutical composition comprising the compounds of Formula (I) and their uses, in particular in the treatment of diseases or disorders associated to increased relative to physiological or desired RhoJ/Cdc42 levels of expression or function.
Claims18
A compound of formula (I):
- or a pharmaceutically acceptable salt thereof,
- wherein:
- A is a 6-membered aromatic ring or a 6-membered heteroaromatic ring;
- wherein the 6-membered heteroaromatic ring contains 1 or 2 nitrogen heteroatoms;
- and
- wherein the 6-membered aromatic ring or the 6-membered heteroaromatic ring is optionally substituted with one substituent selected from the group consisting of halogen, C1-6 alkyl, C1-6 haloalkyl, NH2, NHC1-6 alkyl, N(C1-6 alkyl)2, OH, and O(C1-6 alkyl);
- A′ is a 6-membered aromatic ring or a 6-membered heteroaromatic ring;
- wherein the 6-membered heteroaromatic ring contains 1 or 2 nitrogen heteroatoms;
- and
- wherein the 6-membered aromatic ring or the 6-membered heteroaromatic ring is optionally substituted with one substituent selected from the group consisting of halogen, C1-6 alkyl, C1-6 haloalkyl, NH2, NHC1-6 alkyl, N(C1-6 alkyl)2, OH, and O(C1-6 alkyl);
- X1 is —CH2—, —NR2—, or —O—;
- X2 is —CH2—, —NR2—, or —O—;
- R1 is H or C1-6 alkyl;
- R2 is H, C1-6 alkyl, C(O)C1-6 alkyl, C(O)O(C1-6 alkyl), or O(C1-6 alkyl);
- and
- Y is N;
- with the provisos that:
- (1) X1 and X2 are not simultaneously —NR2—;
- (2) X1 and X2 are not simultaneously —NR2— and —O—;
- and
- (3) X1 and X2 are not simultaneously —O—.
18 more elements
Dependencies are inferred from the claim text.