Novel thiourea or urea derivative, preparation method thereof, and pharmaceutical composition for preventing or treating aids, containing same as active ingredient
AssigneeAvixgen Inc.
InventorsJi Chang You, Gyoon Hee Han, Chul Ho Lee, Doo Na Song, Koo Hwan Chung
Life of this patent
Estimating the term…
Abstract
Disclosed are novel thiourea or urea derivatives inhibitory of HIV activity. Also provided are a method for preparing the thiourea or urea derivatives, and a pharmaceutical composition for the prophylaxis or therapy of AIDS comprising the derivatives. Having high inhibitory activity against HIV, the thiourea or urea derivatives can be effectively used in the prophylaxis or therapy of AIDS.
Claims10
A thiourea or urea derivative, represented by the following Chemical Formula 1, or a pharmaceutically acceptable salt thereof:
- wherein,
- A represents —CH2 or —C(═O),
- B represents —C(═O) or —C(═S),
- R1 represents H, a halogen atom, linear or branched alkyl of C1˜C4, phenyl, phenyl substituted with linear or branched alkyl of C1˜C4, linear or branched alkoxy of C1˜C4, aryloxy of C6˜C20, or
- R2 and R3, which may be the same or different, independently represent H, linear or branched alkyl of C1˜C4, cycloalkyl of C3˜C8, -(linear or branched alkyl of C2˜C6)-N-(alkyl of C1˜C2)2, -(linear or branched alkyl of C1˜C4)-NH-(linear or branched alkyl of C1˜C4),
- 5,6,7,8-tetrahydronaphthalen-1-yl, (naphthalen-2-yl)-methyl,
- (pyridin-3-yl)-methyl, 2-chloro-pyridin-4-yl, pyrazin-2-yl, quinolin-5-yl, quinolin-8-yl, or 4-hydroxy-biphenyl-3-yl, or R2 and R3 are fused to each other, forming
- n is an integer of 0, or 1 to 4,
- m is an integer of 0, 1 or 2,
- X represents H, linear or branched alkyl of C1˜C4, aryl of C6˜C20, hydroxy, or a halogen atom, and
- Y represents H or hydroxy,
- with the provisos of the following conditions:
- when A, B, and R1 represent —C(═O), —C(═S), and H, respectively, to the exclusion of the options that R2 represents H, and R3 represents —CH2—C(CH3)2—CH2—N—(CH3)2, —(CH2)3—N—(CH3)2, phenyl, 4-methyl-benzyl, 4-chloro-benzyl, or (pyridin-2-yl)-ethyl, or R2 does not represent H, excluding the option that R2 and R3 are fused to each other, forming
- when A, B, and R1 represent —C(═O), —C(═S), and tert-butyl, respectively, to the exclusion of the option that R2 is H, and R3 represents phenyl, naphthalene, 3-chloro-phenyl, 3-toyl, 2-fluoro-phenyl or (pyridin-2-yl)-methyl,
- when A, B, and R1 represent —C(═O), —C(═S), and methyl, respectively, to the exclusion of the option that R2 represents H, and R3 represents phenyl, naphthalene or pyridin-2-yl,
- when A, B, and R1 represent —C(═O), —C(═S), and Cl, respectively, to the exclusion of the option that R2 represents H, and R3 represents cyclohexyl or naphthalene,
- when A, B, and R1 represent —C(═O), —C(═O), and H, respectively, to the exclusion of the option that R2 represents H, and R3 represents benzyl.
(canceled)
(canceled)
(canceled)
(canceled)
(canceled)
A method of preventing or treating AIDS in a subject comprising:
- administering to the subject in need of such prevention or treatment a compound selected from the group consisting of
- 4-tert-butyl-N-(4-methyl-piperazin-1-carbothioyl)-benzamide,
- 1-benzoyl-3-(3-dimethylamino-2,2-dimethyl-propyl)-thiourea,
- 1-benzoyl-3-(4-methyl-benzyl)-thiourea,
- 1-benzoyl-3-(3-dimethylamino-propyl)-thiourea,
- N-(4-ethyl-piperazin-1-carbothioyl)-benzamide,
- 1-benzoyl-3-(4-chloro-benzyl)-thiourea,
- 1-benzoyl-3-phenyl-thiourea,
- 1-benzoyl-3-(2-pyridin-2-yl-ethyl)-thiourea,
- 1-(4-tert-butyl-benzoyl)-3-phenyl-thiourea,
- 1-(4-tert-butyl-benzoyl)-3-(pyridin-2-ylmethyl)-thiourea,
- 1-(4-tert-butyl-benzoyl)-3-(pyridin-4-ylmethyl)-thiourea,
- 1-(4-methyl-benzoyl)-3-(pyridin-2-yl)-thiourea,
- 1-(4-methyl-benzoyl)-3-phenyl-thiourea,
- 1-(4-chloro-benzoyl)-3-thiohexyl-thiourea,
- 1-(4-chloro-benzoyl)-3-(naphthalen-2-ylmethyl)-thiourea, and
- 1-benzoyl-3-benzyl-urea.
Dependencies are inferred from the claim text.