US2010291533A1PendingUtilityA1
Indole and indazole derivatives having a cell-, tissue- and organ-preserving effect
Est. expiryJan 4, 2028(~1.5 yrs left)· nominal 20-yr term from priority
C07D 417/04A61P 39/06C07D 401/14C07D 401/04C07D 405/14C07D 413/14C07D 209/08C07D 405/12C07D 231/54C07D 417/14C07D 403/04A61P 43/00A61K 31/404
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Claims
Abstract
The present invention relates to a composition for preserving cells, tissues and organs, comprising as an active ingredient indole and indazole compounds of formula (1), or a pharmaceutically acceptable salt or isomer thereof, which are effective for preventing injury of organs, isolated cell systems or tissues caused by cold storage, transplant operation or post-transplantation reperfusion; a preservation method; and a preparation method of the composition.
Claims
exact text as granted — not AI-modified1 . A composition for preserving cells and organs comprising as an effective ingredient, a compound of the following formula (1) or a pharmaceutically acceptable salt or isomer thereof:
wherein
X represents C or N,
n is 0 or 1, and n is 1 when X is C and n is 0 when X is N,
A represents a direct bond, C 3 -C 8 -cycloalkyl, phenyl, or 5˜6-membered heteroaryl or heterocycle, each of which includes 1˜3 heteroatoms selected from N, O and S atoms,
R1 represents hydrogen, —C(O)—B—X′—R7 or —(CR5R6) m -B—X′—R7,
m is an integer of 0 to 4,
each of R5 and R6 independently represents hydrogen or C 1 -C 5 -alkyl,
B represents a direct bond, C 3 -C 8 -cycloalkyl optionally containing oxo, or 3˜10-membered heterocycle or heteroaryl, each of which includes 1˜3 heteroatoms selected from O, S and N atoms,
X′ represents a direct bond, —C(O)—, —SO 2 —, —CO 2 — or —C(O)NR5-,
R7 represents hydrogen, C 1 -C 6 -alkyl, halogeno-C 1 -C 6 -alkyl, halogen, (CR5R6) m -phenyl, (CR5R6) m -hydroxy or (CR5R6) m -heterocycle where the heterocycle optionally contains oxo and is a 3˜10-membered ring including 1˜3 heteroatoms selected from N, O and S atoms,
R2 represents —(CR5R6) m -D-X″—R8,
D represents a direct bond or a 3˜10-membered heterocycle or heteroaryl, each of which optionally contains oxo and is optionally fused, and includes 1˜4 heteroatoms selected from N, O and S atoms,
X″ represents a direct bond, —C(O)—, —C(O)O—, —NR5C(O)—, —C(O)NR5- or —O—,
R8 represents hydrogen, halogen, C 1 -C 6 -alkyl, halogeno-C 1 -C 6 -alkyl, tri(C 1 -C 6 -alkyl)silane or hydroxy-C 1 -C 6 -alkyl,
R3 represents hydrogen, halogen, cyano, nitro, aryl-R9 or (CR5R6) m -D-R9,
R9 represents hydrogen, halogen, C 1 -C 6 -alkyl, cyano, nitro or C 1 -C 6 -alkoxy,
R4 represents —(CR5R6) m —Y-D-R10,
Y represents a direct bond, —C(O)O— or —O—, and
R10 represents hydrogen, nitro, halogen, C 1 -C 6 -alkyl, carboxy-C 1 -C 6 -alkyl, aryl or —C(O)O—R5,
wherein each of said alkyl, alkoxy, aryl, cycloalkyl, heterocycle and heteroaryl is optionally substituted with one or more substituents selected from the group consisting of hydroxy, halogen, nitrile, amino, C 1 -C 6 -alkylamino, di(C 1 -C 6 -alkyl)amino, C 1 -C 6 -alkyl, halogeno-C 1 -C 6 -alkyl, C 1 -C 6 -alkylsulfonyl, aryl-C 1 -C 6 -alkoxy and oxo.
2 . The composition according to claim 1 , wherein
X represents C or N, n is 0 or 1, and n is 1 when X is C and n is 0 when X is N, A represents a direct bond, phenyl, or 5˜6-membered heteroaryl or heterocycle, each of which includes 1˜3 heteroatoms selected from N, O and S atoms, R1 represents hydrogen, —C(O)—B—X′—R7 or —(CR5R6) m -B—X′—R7, m is an integer of 0 to 2, each of R5 and R6 independently represents hydrogen or C 1 -C 5 -alkyl, B represents a direct bond, C 4 -C 7 -cycloalkyl optionally containing oxo, or 4˜8-membered heterocycle or heteroaryl, each of which includes 1˜3 heteroatoms selected from O, S and N atoms, X′ represents a direct bond, —C(O)—, —SO 2 —, —CO 2 — or —C(O)NH—, R7 represents hydrogen, C 1 -C 6 -alkyl, halogeno-C 1 -C 6 -alkyl, halogen, (CR5R6) m -phenyl, (CR5R6) m -hydroxy or (CR5R6) m -heterocycle where the heterocycle optionally contains oxo and is a 4˜8-membered ring including 1˜3 heteroatoms selected from N, O and S atoms, R2 represents —(CR5R6) m -D-X″—R8, D represents a direct bond or a 4˜8-membered heterocycle or heteroaryl, each of which optionally contains oxo and is optionally fused, and includes 1˜4 heteroatoms selected from N, O and S atoms, X″ represents —C(O)—, —C(O)O—, —NR5C(O)—, —C(O)NR5- or —O—, R8 represents hydrogen, halogen, C 1 -C 6 -alkyl, halogeno-C 1 -C 6 -alkyl, tri(C 1 -C 6 -alkyl)silane or hydroxy-C 1 -C 6 -alkyl, R3 represents hydrogen, halogen, cyano, nitro, aryl-R9 or (CR5R6) m -D-R9, R9 represents hydrogen, halogen, C 1 -C 6 -alkyl, cyano, nitro or C 1 -C 6 -alkoxy, R4 represents —(CR5R6) m —Y-D-R10, Y represents a direct bond, —C(O)O— or —O—, and R10 represents hydrogen, nitro, halogen, C 1 -C 6 -alkyl, carboxy-C 1 -C 6 -alkyl, aryl or —C(O)O—R5.
3 . The composition according to claim 2 , wherein the compound of the formula (1) has an indole structure of the following formula (1a) or an indazole structure of the following formula (1b):
4 . The composition according to claim 2 , wherein A is selected from the group consisting of phenyl, pyridine, 1,4-pyrazine, 4,5-dihydro-thiazole, thiazole, 4,5-dihydrooxazole, [1,2,4]oxadiazole and [1,3,4]oxadiazole.
5 . The composition according to claim 2 , wherein R1 represents —C(O)—B—X′—R7 or —(CHR5) m —B—X′—R7 where m is an integer of 0 to 2; R5 represents C 1 -C 3 -alkyl; B represents a direct bond, C 5 -C 6 -cycloalkyl optionally containing oxo, or 5˜6-membered heterocycle or heteroaryl, each of which includes 1˜3 heteroatoms selected from O, S and N atoms; X′ represents a direct bond, —C(O)—, —SO 2 —, —CO 2 — or —C(O)NH—; and R7 represents hydrogen, C 1 -C 3 -alkyl, halogeno-C 1 -C 3 -alkyl, halogen, (CH 2 ) m -phenyl, (CH 2 ) m -hydroxy or (CH 2 ) m -heterocycle where the heterocycle optionally contains oxo and is a 5˜6-membered ring including 1˜3 heteroatoms selected from N, O and S atoms.
6 . The composition according to claim 5 , wherein B is selected from the group consisting of cyclopentyl, cyclohexyl, piperidine, tetrahydropyran, oxocyclohexyl, pyrrolidine, difluorocyclohexyl and tetrahydrofuran.
7 . The composition according to claim 5 , wherein R7 is selected from the group consisting of hydrogen, methyl, ethyl, isopropyl, benzyl, hydroxymethyl, (morpholine-4-yl)-ethyl, tetrahydrofuran, 2,2,2-trifluoroethyl, hydroxyethyl, 1,1-dioxothiomorpholine, tetrahydropyran, (tetrahydropyran-4-yl)-methyl and trifluoromethyl.
8 . The composition according to claim 2 , wherein D represents a direct bond, or is selected from the group consisting of piperazine, pyrrolidine, morpholine, 1,1-dioxothiomorpholine and oxopiperazine.
9 . The composition according to claim 2 , wherein R8 is selected from the group consisting of hydrogen, ethyl, hydroxymethyl, methyl and fluorine.
10 . The composition according to claim 2 , wherein R3 represents hydrogen; halogen; phenyl optionally substituted with alkoxy; or 6-membered heterocyclylmethyl including 1˜3 heteroatoms selected from N, S and O atoms as ring members and optionally containing oxo.
11 . The composition according to claim 10 , wherein R3 is selected from the group consisting of hydrogen, bromine, phenyl, methoxy-phenyl, morpholine-4-yl-methyl, oxopiperazine-4-yl-methyl and 1,1-dioxo-thiomorpholine-4-yl-methyl.
12 . The composition according to claim 2 , wherein R4 represents —(CH 2 ) m —Y-D-R10 where m is an integer of 0 to 2; Y represents a direct bond, —C(O)O— or —O—; D represents pyridine or 5˜6-membered heterocycle including 1˜3 heteroatoms selected from N, S and O atoms and optionally containing oxo; and R10 represents hydrogen, halogen, C 1 -C 3 -alkyl, —(CH 2 )—CO 2 H, aryl or —C(O)O—R5.
13 . The composition according to claim 12 , wherein D is selected from the group consisting of 1,1-dioxo-thio-morpholine, oxopiperazine, pyridine, morpholine and 4,5-dihydro-thiazole.
14 . The composition according to claim 12 , wherein R10 is selected from the group consisting of hydrogen, fluorine, chlorine, bromine, methyl, ethyl and —(CH 2 )—CO 2 H.
15 . The composition according to claim 2 , wherein the compound is selected from the group consisting of:
cyclopentyl-[2-(4,5-dihydro-1,3-thiazole-2-yl)-1H-indole-7-yl]-amine; [2-(4,5-dihydro-thiazole-2-yl)-1H-indole-7-yl]-(4-methyl-cyclohexyl)-amine; [2-(4,5-dihydro-thiazole-2-yl)-1H-indole-7-yl]-piperidine-4-yl-amine; 2-5-[7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-[1,2,4]oxadiazole-3-yl}-ethanol; [(R)-2-(7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-1,3-thiazole-4-yl]-methanol; cyclopentyl-[2-((R)-4-pyrrolidine-1-ylmethyl-4,5-dihydro-thiazole-2-yl)-1H-indole-7-yl]-amine; {(R)-2-[7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-thiazole-4-yl}-met hanol; [(R)-2-(7-cyclopentylamino-5-fluoro-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-methan ol; {(R)-2-[5-fluoro-7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-thiazole-4-yl}-methanol; {(R)-2-[5-(pyridine-3-yloxy)-7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihyd ro-thiazole-4-yl}-methanol; [(R)-2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid; [(R)-2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid ethyl ester; 2-{(R)-2-[5-chloro-7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-thiazol e-4-yl}-ethanol; 1-[4-(2-{(R)-2-[5-chloro-7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-th iazole-4-yl}-ethyl)-piperazine-1-yl]-2-hydroxy-ethanone; 1-(2-{(R)-2-[5-chloro-7-(tetrahydro-pyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-thiaz ole-4-yl}-ethyl)-pyrrolidine-3-ol; [(R)-2-(5-bromo-7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid; [(R)-2-(7-cyclopentylamino-5-ethoxy-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid; [(R)-2-(7-cyclopentylamino-5-ethoxy-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid; [2-(7-cyclopentylamino-5-phenoxy-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-acetic acid; [(R)-2-(7-cyclopentylamino-5-phenoxy-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-aceti c acid; [(S)-2-(7-cyclopentylamino-5-phenoxy-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-aceti c acid; 3-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-propi onic acid ethyl ester; 3-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-4,5-dihydro-thiazole-4-yl]-propi onic acid; cyclopentyl-(2-pyridine-2-yl-1H-indole-7-yl)-amine; cyclopentyl-(2-pyrazine-2-yl-1H-indole-7-yl)amine; (2-pyrazine-2-yl-1H-indole-7-yl)-(tetrahydropyran-4-yl)-amine; cyclopentyl-(2-thiazole-2-yl-1H-indole-7-yl)-amine; 2-(7-cyclopentylamino-5-methyl-1H-indole-2-yl)-thiazole-4-carboxylic acid ethyl ester; 2-(7-cyclopentylamino-5-methyl-1H-indole-2-yl)-thiazole-4-carboxylic acid; [2-(7-cyclopentylamino-5-methyl-1H-indole-2-yl)-thiazole-4-yl]-methanol; [2-(7-cyclopentylamino-5-methyl-1H-indole-2-yl)-thiazole-5-yl]-methanol; cyclopentyl-(5-methyl-2-[1,3,4]oxadiazole-2-yl-1H-indole-7-yl)-amine; cyclopentyl-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-amine; (5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-(tetrahydro-pyran-4-yl)-amine; cyclohexyl-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-amine; 1-[4-(5-methyl-2-pyridine-2-yl-1H-indole-7-ylamino)-piperidine-1-yl]-ethanone; (1-methyl-piperidine-4-yl)-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-amine; 4-(5-methyl-2-pyridine-2-yl-1H-indole-7-ylamino)-cyclohexanone; (1-benzyl-pyrrolidine-3-yl)-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-amine; cyclopentylmethyl-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-amine; N-(5-methyl-2-pyridine-2-yl-1H-indole-7-yl)-benzamide; cyclopentyl-(5-methyl-2-pyrazine-2-yl-1H-indole-7-yl)-amine; cyclopentyl-(5-ethoxy-2-pyridine-2-yl-1H-indole-7-yl)-amine; cyclopentyl-(5-phenoxy-2-pyridine-2-yl-1H-indole-7-yl)-amine; cyclopentyl-(3,5-dimethyl-2-phenyl-1H-indole-7-yl)-amine; cyclopentyl-(5-methyl-2-phenyl-1H-indole-7-yl)-amine; (2-cyclohexyl-5-methyl-1H-indole-7-yl)-cyclopentyl-amine; cyclopentyl-[5-methyl-2-(6-methyl-pyridine-2-yl)-1H-indole-7-yl]-amine; (5-methyl-2-phenyl-1H-indole-7-yl)-(tetrahydro-pyran-4-yl)-amine; (5-methyl-2-phenyl-1H-indole-7-yl)-(1-methyl-piperidine-4-yl)-amine; 1-[4-(5-methyl-2-phenyl-1H-indole-7-ylamino)-piperidine-1-yl]-ethanone; (5-methyl-2-phenyl-1H-indole-7-yl)-piperidine-4-yl-amine hydrochloride; 2-hydroxy-1-[4-(5-methyl-2-phenyl-1H-indole-7-ylamino)-piperidine-1-yl]-ethanone; (1-methanesulfonyl-piperidine-4-yl)-(5-methyl-2-phenyl-1H-indole-7-yl)-amine; 4-(5-methyl-2-phenyl-1H-indole-7-ylamino)-cyclohexanecarboxylic acid; 4-(5-methyl-2-phenyl-1H-indole-7-ylamino)-cyclohexanecarboxylic acid (2-morpholine-4-yl-ethyl)-amide; cyclopentylmethyl-(5-methyl-2-phenyl-1H-indole-7-yl)-amine; (5-methyl-2-phenyl-1H-indole-7-yl)-(tetrahydro-pyran-4-ylmethyl)-amine; (5-chloro-2-phenyl-1H-indole-7-yl)-cyclopentyl-amine; (5-chloro-2-phenyl-1H-indole-7-yl)-(tetrahydro-pyran-4-yl)-amine; (5-chloro-2-phenyl-1H-indole-7-yl)-(1-methyl-piperidine-4-yl)-amine; (5-chloro-2-phenyl-1H-indole-7-yl)-cyclohexyl-amine; (1-benzyl-pyrrolidine-3-yl)-(5-chloro-2-phenyl-1H-indole-7-yl)-amine; 4-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-benzoic acid methyl ester; 4-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-benzoic acid; [4-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-phenyl]-methanol; 4-(7-cyclopentylamino-5-methyl-1H-indole-2-yl)-benzoic acid methyl ester; 2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-benzoic acid methyl ester; 2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-benzoic acid; [2-(5-chloro-7-cyclopentylamino-1H-indole-2-yl)-phenyl]-methanol; 7-cyclopentylamino-2-phenyl-1H-indole-5-carboxylic acid ethylester; 7-cyclopentylamino-2-phenyl-1H-indole-5-carboxylic acid; (7-cyclopentylamino-2-phenyl-1H-indole-5-yl)-methanol; (7-cyclopentylamino-2-phenyl-1H-indole-5-yl)-acetic acid ethyl ester; (7-cyclopentylamino-2-phenyl-1H-indole-5-yl)-acetic acid; 2-[(4S)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazol e-4-yl]acetic acid; 2-[(4S)-2-[5-chloro-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazol e-4-yl]acetic acid; 2-[(4S)-2-[7-[(4,4-difluorocyclohexyl)amino]-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]acetic acid; 2-[(4S)-2-[7-(oxane-4-ylamino)-5-phenoxy-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-y l]acetic acid; 2-[(4R)-2-[7-(oxane-4-ylamino)-5-phenoxy-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-y l]acetic acid; 2-[(4R)-2-[7-(oxane-4-ylmethylamino)-5-phenoxy-1H-indole-2-yl]-4,5-dihydro-1,3-thiaz ole-4-yl]acetic acid; 2-[(4S)-2-[7-(cyclopentylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]acetic acid; 2-[(4S)-2-[7-[(1-acetylpyrrolidine-3-yl)amino]-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]acetic acid; 2-[(4S)-2-[7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ace tic acid; 2-[(4S)-2-[7-(oxane-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]acetic acid; 2-[(4S)-2-[7-(oxane-2-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ace tic acid; 2-[(4S)-2-[5-methyl-7-[[1-(3,3,3-trifluoropropanoyl)piperidine-4-yl]amino]-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]acetic acid; 2-[(4R)-2-[7-(cyclopentylamino)-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl ]acetic acid; 2-[(4R)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazol e-4-yl]acetic acid; 4-[2-[(4S)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thia zole-4-yl]ethyl]piperazine-2-one; 2-[(4S)-4-[2-(1,1-dioxo-1,4-thiazinane-4-yl)ethyl]-4,5-dihydro-1,3-thiazole-2-yl]-5-meth yl-N-(oxane-4-ylmethyl)-1H-indole-7-yl-amine; N-(4,4-difluorocyclohexyl)-5-methyl-2-[(4S)-4-(2-morpholine-4-ylethyl)-4,5-dihydro-1,3-thiazole-2-yl]-1H-indole-7-yl-amine; 4-[2-[(4S)-2-[7-[(4,4-difluorocyclohexyl)amino]-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ethyl]piperazine-2-one; 4-[2-[(4S)-2-[7-(oxane-4-ylmethylamino)-5-phenoxy-1H-indole-2-yl]-4,5-dihydro-1,3-thi azole-4-yl]ethyl]piperazine-2-one; 2-[(4S)-4-(2-morpholine-4-ylethyl)-4,5-dihydro-1,3-thiazole-2-yl]-N-(oxane-4-ylmethyl)-5-phenoxy-1H-indole-7-amine; 5-methyl-2-[(4S)-4-(2-morpholine-4-ylethyl)-4,5-dihydro-1,3-thiazole-2-yl]-N-(oxane-4-ylmethyl)-1H-indole-7-amine; 1-[2-[(4S)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thia zole-4-yl]ethyl]piperidine-4-carboxyamide; [(2R)-1-[2-[(4S)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ethyl]pyrrolidine-2-yl]methanol; (2S)-1-[2-[(4S)-2-[5-methyl-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ethyl]pyrrolidine-2-carboxyamide; 4-[2-[(4R)-2-[7-(cyclopentylamino)-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-thiazole-4-yl]ethyl]piperazine-2-one; 2-[(4S)-2-[7-(cyclopentylamino)-5-methyl-1H-indole-2-yl]-4,5-dihydro-1,3-oxazole-4-yl ]acetic acid; {(S)-2-[5-methyl-7-(tetrahydropyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-oxazole-4-yl}-acetic acid; 2-[(4S)-2-[5-methyl-7-(tetrahydropyran-4-ylamino)-1H-indole-2-yl]-4,5-dihydro-1,3-oxa zole-4-yl]ethanol; {5-methyl-2-[(S)-4-(2-morpholine-4-yl-ethyl)-4,5-dihydro-1,3-oxazole-2-yl]-1H-indole-7-yl}-(tetrahydro-pyran-4-yl)amine 4-[(5-chloro-2-phenyl-1H-indole-7-yl)amino]-N-ethylpiperidine-1-carboxyamide; [4-[(5-chloro-2-phenyl-1H-indole-7-yl)amino]piperidine-1-yl]-(oxolan-3-yl)methanone; 2-[7-(oxane-4-ylamino)-2-phenyl-1H-indole-5-yl]acetic acid; 2-[7-(cyclopentylmethylamino)-2-phenyl-1H-indole-5-yl]acetic acid; 5-fluoro-N-(1-methylpiperidine-4-yl)-2-phenyl-1H-indole-7-amine; 2-[4-[(5-fluoro-2-phenyl-1H-indole-7-yl)amino]piperidine-1-yl]ethanone; 5-fluoro-N-[1-(oxane-4-yl)piperidine-4-yl]-2-phenyl-1H-indole-7-amine; N-[1-(1,1-dioxan-4-yl)piperidine-4-yl]-5-fluoro-2-phenyl-1H-indole-7-amine; N-(oxane-4-yl)-5-phenoxy-2-phenyl-1H-indole-7-amine; methyl 2-[(5-fluoro-2-phenyl-1H-indole-7-yl)amino]acetate; 2-[(5-fluoro-2-phenyl-1H-indole-7-yl)amino]acetic acid; methyl 2-[(5-chloro-2-phenyl-1H-indole-7-yl)amino]propanoate; 2-[(5-chloro-2-phenyl-1H-indole-7-yl)amino]propanoic acid; 2-[(5-phenoxy-2-phenyl-1H-indole-7-yl)amino]acetic acid; 2-[(5-phenoxy-2-phenyl-1H-indole-7-yl)amino]propanoic acid; 2-[(4S)-2-[7-(oxane-4-ylmethylamino)-2-phenyl-1H-indole-5-yl]-4,5-dihydro-1,3-thiazol e-4-yl]acetic acid; 2-[(4S)-2-[7-(cyclopentylamino)-2-phenyl-1H-indole-5-yl]-4,5-dihydro-1,3-thiazole-4-yl ]acetic acid; methyl 2-[4-[5-chloro-7-(oxane-4-ylamino)-1H-indole-2-yl]phenyl]acetate; methyl 2-[4-[5-chloro-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]phenyl]acetate; 2-[4-[5-chloro-7-(oxane-4-ylamino)-1H-indole-2-yl]phenyl]acetic acid; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(oxane-4-yl)-2-phenyl-1H-indole-7-amine; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(oxane-4-ylmethyl)-2-phenyl-1H-indole-7-a mine; 4-[[7-(oxane-4-ylamino)-2-phenyl-1H-indole-5-yl]methyl]piperazine-2-one; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-phenyl-N-piperidine-4-yl-1H-indole-7-amin e; [4-[[5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-phenyl-1H-indole-7-yl]amino]piperidin e-1-yl]-(oxolan-3-yl)methanone; N-[4-[5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-7-(oxane-4-ylamino)-1H-indole-2-yl]ph enyl]acetamide; N-[4-[7-(dicyclopentylamino)-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-1H-indole-2-yl] phenyl]acetamide; N-[4-[5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-7-(oxane-4-ylmethylamino)-1H-indole-2-yl]phenyl]acetamide; N-cyclopentyl-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-(4-methoxyphenyl)-1H-indol e-7-amine; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-(4-methoxyphenyl)-N-(oxane-4-yl)-1H-indo le-7-amine; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(3-methoxybutyl)-2-phenyl-1H-indole-7-am ine; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-(3-fluorophenyl)-N-(oxane-4-yl)-1H-indole-7-amine; N-cyclopentyl-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-(3-fluorophenyl)-1H-indole-7-amine; 3-bromo-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(oxane-4-yl)-2-phenyl-1H-indole-7-amine; 3-bromo-5-(morpholine-4-ylmethyl)-N-(oxane-4-yl)-2-phenyl-1H-indole-7-amine; 3-bromo-N-cyclopentyl-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-2-phenyl-1H-indole-7-amine; 3-bromo-5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(oxane-4-yl)-2-phenyl-1H-indole-7-amine; 5-chloro-N-(oxane-4-yl)-3-phenyl-1H-indole-7-amine; 5-chloro-N-cyclopentyl-3-phenyl-1H-indole-7-amine; 5-chloro-N-(oxane-4-ylmethyl)-3-phenyl-1H-indole-7-amine; 5-[(1,1-dioxo-1,4-thiazinane-4-yl)methyl]-N-(oxane-4-yl)-3-phenyl-2-trimethylsilyl-1H-i ndole-7-amine; 4-[[5-chloro-7-(cyclopentylamino)-2-phenyl-1H-indole-3-yl]methyl]piperazine-2-one; 4-[[5-chloro-7-(oxane-4-ylamino)-2-phenyl-1H-indole-3-yl]methyl]piperazine-2-one; 4-[[5-chloro-7-(oxane-4-ylmethylamino)-2-phenyl-1H-indole-3-yl]methyl]piperazine-2-o ne; N-cyclopentyl-3-(4-methoxyphenyl)-1H-indazol-7-amine; 3-(4-methoxyphenyl)-N-(oxane-4-yl)-1H-indazol-7-amine; 3-(4-methoxyphenyl)-N-(oxane-4-ylmethyl)-1H-indazol-7-amine; and 2-(7-cyclopentylamino-2-phenyl-1H-indole-5-yl)-ethanol.
16 . The composition according to claim 1 for preserving cells, tissues and organs, which comprises as an effective ingredient, a pharmaceutically acceptable salt or isomer of the compound of formula (1).
17 . The composition according to claim 1 , wherein the cell is animal cell isolated from tissues or organs of human or non-human animals and selected from the group consisting of liver cell, skin cell, mucous membrane cell, Langerhans islet cell, nerve cell, cartilage cell, endothelium cell, epithelial cell, bone cell and muscle cell; or sperm, egg or fertilized egg of livestock or fish.
18 . The composition according to claim 1 , wherein the organ is selected from the group consisting of skin, cornea, kidney, heart, liver, pancreas, intestine, nerve, lung, placenta, umbilical cord and blood vessel.
19 . The composition according to claim 1 , wherein the tissue is selected from the group consisting of skin, cornea, kidney, heart, liver, pancreas, intestine, nerve, lung, placenta, umbilical cord and blood vessel.
20 . The composition according to claim 1 for preventing injury of organs, isolated cell systems or tissues caused by cold storage, transplant operation or post-transplantation reperfusion.
21 . A method of using the composition according to claim 1 for preserving cells, tissues or organs of animals for transplantation.
22 . A preparation method of a composition for preserving cells, tissues or organs of animals, comprising a step of mixing a compound of formula (1) according to claim 1 or a pharmaceutically acceptable salt or isomer thereof as an effective ingredient, together with a pharmaceutically acceptable carrier.
23 . A method of using the composition according to claim 20 for cultivating or preserving cells, tissues or organs, in manufacturing an artificial organ.Cited by (0)
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