P2X3 and/or P2X2/3 receptor antagonist, pharmaceutical composition comprising same, and use thereof
A P2X3 and/or P2X2/3 receptor antagonist of formula (I), a pharmaceutical composition comprising the same, and a use thereof in preparing a drug for preventing or treating a disease mediated by the P2X3 and/or P2X2/3 receptor antagonist.
1 . A compound or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein the compound has the structure of Formula (II′):
wherein:
R 1 is selected from the group consisting of halogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, saturated or partially unsaturated C 3-10 cyclic hydrocarbyl, saturated or partially unsaturated 3- to 10-membered heterocyclyl, C 6-10 aryl, 5- to 14-membered heteroaryl, C 6-12 aralkyl, C 1-6 haloalkyl, —OR a , and —NR a R b ;
R 3 is selected from the group consisting of C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, saturated or partially unsaturated C 3-10 cyclic hydrocarbyl, saturated or partially unsaturated 3- to 10-membered heterocyclyl, C 6-10 aryl, and 5- to 14-membered heteroaryl;
R 2 , R 4 , R 5 and R 6 are H;
the above alkyl, alkenyl, alkynyl, cyclic hydrocarbyl, heterocyclyl, aryl, heteroaryl and aralkyl, at each occurrence, are each optionally substituted with one or more substituents independently selected from the group consisting of halogen, C 1-6 alkyl, saturated or partially unsaturated C 3-6 cyclic hydrocarbyl, saturated or partially unsaturated 3- to 10-membered heterocyclyl, C 6-10 aryl, 5- to 14-membered heteroaryl, and C 6-12 aralkyl; and
R a and R b , at each occurrence, are each independently selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, saturated or partially unsaturated C 3-10 cyclic hydrocarbyl, saturated or partially unsaturated 3- to 10-membered heterocyclyl, C 6-10 aryl, 5- to 14-membered heteroaryl and C 6-12 aralkyl.
2 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein R a and R b , at each occurrence, are each independently selected from the group consisting of H, methyl, ethyl, and cyclopropyl.
3 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein R 1 is selected from the group consisting of Cl, Br, —NH 2 , methyl, ethyl, cyclopropyl, vinyl, ethynyl, trifluoromethyl, —NHCH 3 , —N(CH 3 ) 2 , —N(CH 3 )(C 2 H 5 ), methoxy,
and
4 . The compound according to claim 3 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein R 1 is ethynyl.
5 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein R 3 is C 1-6 alkyl.
6 . The compound according to claim 5 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein R 3 is isopropyl.
7 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein the compound has the following structure:
8 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein the compound has the following structure:
9 . The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, wherein the compound has the following structure:
10 . A pharmaceutical composition comprising a prophylactically or therapeutically effective amount of the compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, and a pharmaceutically acceptable carrier.
11 . The pharmaceutical composition according to claim 10 , wherein the pharmaceutical composition is in the form of a solid, semi-solid, liquid, or gas preparation.
12 . A pharmaceutical composition comprising a prophylactically or therapeutically effective amount of the compound according to claim 7 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, and a pharmaceutically acceptable carrier.
13 . The pharmaceutical composition according to claim 12 , wherein the pharmaceutical composition is in the form of a solid, semi-solid, liquid, or gas preparation.
14 . A pharmaceutical composition comprising a prophylactically or therapeutically effective amount of the compound according to claim 8 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, and a pharmaceutically acceptable carrier.
15 . The pharmaceutical composition according to claim 14 , wherein the pharmaceutical composition is in the form of a solid, semi-solid, liquid, or gas preparation.
16 . A pharmaceutical composition comprising a prophylactically or therapeutically effective amount of the compound according to claim 9 , or a pharmaceutically acceptable salt, stereoisomer, polymorph, solvate, N-oxide, isotopically labeled compound or prodrug thereof, and a pharmaceutically acceptable carrier.
17 . The pharmaceutical composition according to claim 16 , wherein the pharmaceutical composition is in the form of a solid, semi-solid, liquid, or gas preparation.