JP2006316001A5 - - Google Patents
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- JP2006316001A5 JP2006316001A5 JP2005140550A JP2005140550A JP2006316001A5 JP 2006316001 A5 JP2006316001 A5 JP 2006316001A5 JP 2005140550 A JP2005140550 A JP 2005140550A JP 2005140550 A JP2005140550 A JP 2005140550A JP 2006316001 A5 JP2006316001 A5 JP 2006316001A5
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- hydrogen atom
- acceptable salt
- pharmacologically acceptable
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- -1 naphthoquinone derivative compound Chemical class 0.000 claims 17
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 7
- 239000011780 sodium chloride Substances 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 6
- 125000002252 acyl group Chemical group 0.000 claims 4
- 125000004423 acyloxy group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000003158 alcohol group Chemical group 0.000 claims 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 2
- 125000005082 alkoxyalkenyl group Chemical group 0.000 claims 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000005019 carboxyalkenyl group Chemical group 0.000 claims 2
- 125000004990 dihydroxyalkyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000005020 hydroxyalkenyl group Chemical group 0.000 claims 2
- 125000000466 oxiranyl group Chemical group 0.000 claims 2
- 125000005359 phenoxyalkyl group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000005080 alkoxycarbonylalkenyl group Chemical group 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
Claims (7)
式中、R4がアルキニルオキシアルキル基又はブチルジメチルシリルオキシアルケニル基である場合には、R1は水素原子、アルキル基、ヒドロキシル基、アルコキシル基、又はヒドロキシアルキル基であり、R2はヒドロキシル基、アシルオキシ基、又はアルコキシル基であり、R3は水素原子、ヒドロキシアルキル基、ハロゲン原子、又はアリールアルコール基であり、
式中、R1がアシルオキシ基である場合には、R2はヒドロキシル基、アシルオキシ基、又はアルコキシル基であり、R3は水素原子、ヒドロキシアルキル基、又はハロゲン原子であり、R4はアシル基、ヒドロキシアルキル基、ヒドロキシアルケニル基、カルボキシル基、アルコキシカルボニル基、アルコキシアルキル基、アルコキシアルケニル基、フェノキシアルキル基、フェノキシアルケニル基、カルボキシアルケニル基、アルコキシカルボニルアルケニル基、アシルオキシアルケニル基、ヒドロキシアルキルオキシランアルキル基、アルコキシアルキルオキシランアルキル基、ジヒドロキシアルキル基、ヒドロキシアルコキシアルキル基、オキシラン基、又は2−ジメタン−1,3−ジオキサン−4−アルキル基であり、
式中、R1及びR2がメトキシ基であり、R4がヒドロキシブタ−2−エニル基である場合には、R3はヒドロキシエチル基、ヒドロキシプロピル基、又はヒドロキシヘキシル基であり、
式中、R2がメトキシ基であり、R3が水素原子であり、R4がメトキシメチル基である場合には、R1はヒドロキシル基であり、
式中、R1及びR2がメトキシ基であり、R3が水素原子である場合には、R4はへキシルオキシメチル基であり、
前記R3と前記R4とで環状を構成しない。) A naphthoquinone derivative compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof.
In the formula, when R 4 is an alkynyloxyalkyl group or a butyldimethylsilyloxyalkenyl group, R 1 is a hydrogen atom, an alkyl group, a hydroxyl group, an alkoxyl group, or a hydroxyalkyl group, and R 2 is a hydroxyl group. , An acyloxy group, or an alkoxyl group, and R 3 is a hydrogen atom, a hydroxyalkyl group, a halogen atom, or an aryl alcohol group,
In the formula, when R 1 is an acyloxy group, R 2 is a hydroxyl group, an acyloxy group, or an alkoxyl group, R 3 is a hydrogen atom, a hydroxyalkyl group, or a halogen atom, and R 4 is an acyl group. , Hydroxyalkyl group, hydroxyalkenyl group, carboxyl group, alkoxycarbonyl group, alkoxyalkyl group, alkoxyalkenyl group, phenoxyalkyl group, phenoxyalkenyl group, carboxyalkenyl group, alkoxycarbonylalkenyl group, acyloxyalkenyl group, hydroxyalkyloxirane alkyl group An alkoxyalkyloxirane alkyl group, a dihydroxyalkyl group, a hydroxyalkoxyalkyl group, an oxirane group, or a 2-dimethane-1,3-dioxane-4-alkyl group,
In the formula, when R 1 and R 2 are methoxy groups and R 4 is a hydroxybut-2-enyl group, R 3 is a hydroxyethyl group, a hydroxypropyl group, or a hydroxyhexyl group,
In the formula, when R 2 is a methoxy group, R 3 is a hydrogen atom, and R 4 is a methoxymethyl group, R 1 is a hydroxyl group,
In the formula, when R 1 and R 2 are methoxy groups and R 3 is a hydrogen atom, R 4 is a hexyloxymethyl group,
R 3 and R 4 do not form a ring. )
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005140550A JP4822312B2 (en) | 2005-05-13 | 2005-05-13 | Naphthoquinone derivative compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005140550A JP4822312B2 (en) | 2005-05-13 | 2005-05-13 | Naphthoquinone derivative compounds |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2006316001A JP2006316001A (en) | 2006-11-24 |
JP2006316001A5 true JP2006316001A5 (en) | 2008-06-26 |
JP4822312B2 JP4822312B2 (en) | 2011-11-24 |
Family
ID=37536985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2005140550A Expired - Fee Related JP4822312B2 (en) | 2005-05-13 | 2005-05-13 | Naphthoquinone derivative compounds |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4822312B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5110502B2 (en) * | 2007-02-16 | 2012-12-26 | 学校法人慶應義塾 | Naphthoquinone derivative compounds |
JP5451628B2 (en) * | 2008-10-09 | 2014-03-26 | Lsipファンド運営合同会社 | Protein phosphatase inhibitor |
WO2014103862A1 (en) * | 2012-12-26 | 2014-07-03 | Nakajima Toshihiro | Obesity preventive or therapeutic agent and rheumatism preventive or therapeutic agent |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2159056A (en) * | 1984-04-04 | 1985-11-27 | Alan Alaexander Torrance Sime | Biocidal compositions comprising polyhydroxynaphthoquinones |
JPS63139125A (en) * | 1986-12-01 | 1988-06-10 | Tosoh Corp | Aromatase inhibitor |
LU87403A1 (en) * | 1988-12-06 | 1990-07-10 | Oreal | PROCESS FOR DYEING KERATINIC FIBERS WITH A HYDROXYINDOLE, ASSOCIATED WITH A QUINON DERIVATIVE |
CA2224874A1 (en) * | 1995-06-19 | 1997-03-13 | Ontogen Corporation | Aryl acrylic acid derivatives useful as protein tyrosine phosphatase inhibitors |
JPH11222474A (en) * | 1998-02-04 | 1999-08-17 | Microbial Chem Res Found | Antidiabetic drug |
JP2000256330A (en) * | 1999-03-15 | 2000-09-19 | Microbial Chem Res Found | Tyrosine phosphatase inhibitor |
JP2002121186A (en) * | 2000-05-22 | 2002-04-23 | Takeda Chem Ind Ltd | Tyrosine phosphatase inhibitor |
JP2003055288A (en) * | 2001-06-08 | 2003-02-26 | Hokko Chem Ind Co Ltd | Method for distilling oxystyrene derivative |
GB0117326D0 (en) * | 2001-07-16 | 2001-09-05 | Univ Aberdeen | Napthoquinone-type inhibitors of protein aggregation |
JP4018610B2 (en) * | 2003-09-12 | 2007-12-05 | 株式会社サン・クロレラ | Tyrosine phosphatase inhibitor |
-
2005
- 2005-05-13 JP JP2005140550A patent/JP4822312B2/en not_active Expired - Fee Related
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