JP2010525024A5 - - Google Patents
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- Publication number
- JP2010525024A5 JP2010525024A5 JP2010504685A JP2010504685A JP2010525024A5 JP 2010525024 A5 JP2010525024 A5 JP 2010525024A5 JP 2010504685 A JP2010504685 A JP 2010504685A JP 2010504685 A JP2010504685 A JP 2010504685A JP 2010525024 A5 JP2010525024 A5 JP 2010525024A5
- Authority
- JP
- Japan
- Prior art keywords
- hydroxyphenyl
- indoline
- difluoro
- optionally substituted
- methylindoline
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- -1 amino, carbamoyl Chemical group 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 5
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000004104 aryloxy group Chemical group 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 2
- 125000001769 aryl amino group Chemical group 0.000 claims 2
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 2
- 125000005241 heteroarylamino group Chemical group 0.000 claims 2
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims 2
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- JXMYTTYAJFLBIA-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6,7-difluoro-3-(4-hydroxyphenyl)-1h-indol-2-one;3-cyclopentyl-6,7-difluoro-3-(4-hydroxyphenyl)-1h-indol-2-one Chemical compound C1=CC(O)=CC=C1C1(C2CCCC2)C(C=CC(F)=C2F)=C2NC1=O.C1=CC(O)=CC=C1C1(CC2CCCCC2)C(C=CC(F)=C2F)=C2NC1=O JXMYTTYAJFLBIA-UHFFFAOYSA-N 0.000 claims 1
- JAOIUUVKSOYRCR-UHFFFAOYSA-N 3-cycloheptyl-3-(4-hydroxyphenyl)-7-(trifluoromethyl)-1h-indol-2-one Chemical compound C1=CC(O)=CC=C1C1(C2CCCCCC2)C(C=CC=C2C(F)(F)F)=C2NC1=O JAOIUUVKSOYRCR-UHFFFAOYSA-N 0.000 claims 1
- UPODFDYIWFWTDQ-UHFFFAOYSA-N 3-cyclohexyl-3-(4-hydroxyphenyl)-5-methoxy-6,7-dimethyl-1h-indol-2-one Chemical compound CC1=C(C)C(OC)=CC2=C1NC(=O)C2(C=1C=CC(O)=CC=1)C1CCCCC1 UPODFDYIWFWTDQ-UHFFFAOYSA-N 0.000 claims 1
- ZAGUHJJEUIZMEQ-UHFFFAOYSA-N 3-cyclohexyl-3-(4-hydroxyphenyl)-6-methoxy-7-methyl-1H-indol-2-one 3-(4-hydroxyphenyl)-3-imidazol-1-yl-7-(trifluoromethyl)-1H-indol-2-one Chemical compound OC1=CC=C(C=C1)C1(C(NC2=C(C=CC=C12)C(F)(F)F)=O)N1C=NC=C1.C1(CCCCC1)C1(C(NC2=C(C(=CC=C12)OC)C)=O)C1=CC=C(C=C1)O ZAGUHJJEUIZMEQ-UHFFFAOYSA-N 0.000 claims 1
- BGKNARSAMJTTCY-UHFFFAOYSA-N 3-cyclohexyl-6,7-difluoro-3-(4-hydroxyphenyl)-1h-indol-2-one Chemical compound C1=CC(O)=CC=C1C1(C2CCCCC2)C(C=CC(F)=C2F)=C2NC1=O BGKNARSAMJTTCY-UHFFFAOYSA-N 0.000 claims 1
- YZQOTLPLSCZECK-UHFFFAOYSA-N 3-cyclooctyl-6,7-difluoro-3-(4-hydroxyphenyl)-1h-indol-2-one Chemical compound C1=CC(O)=CC=C1C1(C2CCCCCCC2)C(C=CC(F)=C2F)=C2NC1=O YZQOTLPLSCZECK-UHFFFAOYSA-N 0.000 claims 1
- HMPZCDUFMHXMQV-UHFFFAOYSA-N 3-cyclopentyl-3-(4-hydroxyphenyl)-7-methyl-6-(trifluoromethyl)-1h-indol-2-one Chemical compound C12=CC=C(C(F)(F)F)C(C)=C2NC(=O)C1(C=1C=CC(O)=CC=1)C1CCCC1 HMPZCDUFMHXMQV-UHFFFAOYSA-N 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- FCZHRTBNLCOFCA-UHFFFAOYSA-N 6,7-difluoro-3-(4-hydroxyphenyl)-3-pyridin-3-yl-1h-indol-2-one Chemical compound C1=CC(O)=CC=C1C1(C=2C=NC=CC=2)C(C=CC(F)=C2F)=C2NC1=O FCZHRTBNLCOFCA-UHFFFAOYSA-N 0.000 claims 1
- ZDCIKWFLFNGSKC-UHFFFAOYSA-N 7-chloro-3-cycloheptyl-3-(4-hydroxyphenyl)-6-methyl-1h-indol-2-one Chemical compound ClC=1C(C)=CC=C2C=1NC(=O)C2(C=1C=CC(O)=CC=1)C1CCCCCC1 ZDCIKWFLFNGSKC-UHFFFAOYSA-N 0.000 claims 1
- IIPKMWSJYUQQKA-UHFFFAOYSA-N BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCC1)C.BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCC1)C.C1(CCCCC1)C1(C(NC2=C(C(=CC=C12)O)C)=O)C1=CC=C(C=C1)O Chemical compound BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCC1)C.BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCC1)C.C1(CCCCC1)C1(C(NC2=C(C(=CC=C12)O)C)=O)C1=CC=C(C=C1)O IIPKMWSJYUQQKA-UHFFFAOYSA-N 0.000 claims 1
- LGGYBDBMKHYSJC-UHFFFAOYSA-N BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCC1.BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCC1.C1(CCCCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O Chemical compound BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCC1.BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCC1.C1(CCCCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O LGGYBDBMKHYSJC-UHFFFAOYSA-N 0.000 claims 1
- SVVPHCKBGDJPKX-UHFFFAOYSA-N C1(CCCCC1)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O.C1(CCCC1)CC1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O Chemical compound C1(CCCCC1)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O.C1(CCCC1)CC1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O SVVPHCKBGDJPKX-UHFFFAOYSA-N 0.000 claims 1
- GWFHEOQPSFQUJM-UHFFFAOYSA-N C1(CCCCC1)C1(C(NC2=C(C=CC=C12)C(F)(F)F)=O)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C=1C=NN(C1)O Chemical compound C1(CCCCC1)C1(C(NC2=C(C=CC=C12)C(F)(F)F)=O)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C=1C=NN(C1)O GWFHEOQPSFQUJM-UHFFFAOYSA-N 0.000 claims 1
- NQTSKEWDAHFHCX-UHFFFAOYSA-N C1(CCCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O.C1(CCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O.BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCC1)C Chemical compound C1(CCCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O.C1(CCCC1)C1(C(NC2=C(C=CC=C12)C)=O)C1=CC=C(C=C1)O.BrC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCC1)C NQTSKEWDAHFHCX-UHFFFAOYSA-N 0.000 claims 1
- CNAWHSRBEGWGIX-UHFFFAOYSA-N C1(CCCCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O.C1(CCCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O.C1(CCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O Chemical compound C1(CCCCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O.C1(CCCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O.C1(CCCC1)C1(C(NC2=C(C=C(C=C12)C)C)=O)C1=CC=C(C=C1)O CNAWHSRBEGWGIX-UHFFFAOYSA-N 0.000 claims 1
- GDAFJFIYDKFFBN-UHFFFAOYSA-N ClC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCCC1)C.C1(CCCCCCC1)C1(C(NC2=C(C=CC=C12)C(F)(F)F)=O)C1=CC=C(C=C1)O.BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCC1 Chemical compound ClC=1C(=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCCC1)C.C1(CCCCCCC1)C1(C(NC2=C(C=CC=C12)C(F)(F)F)=O)C1=CC=C(C=C1)O.BrC=1C=CC=C2C(C(NC12)=O)(C1=CC=C(C=C1)O)C1CCCCCC1 GDAFJFIYDKFFBN-UHFFFAOYSA-N 0.000 claims 1
- ZWWVKWRQANOBRQ-UHFFFAOYSA-N ClC=1C=C2C(C(NC2=C(C1)C)=O)(O)C1CCCCCC1.ClC=1C=C2C(C(NC2=C(C1)C)=O)(C1=CC=C(C=C1)O)C1CCCCC1.ClC=1C=C2C(C(NC2=C(C1)C)=O)(C1=CC=C(C=C1)O)C1CCCC1 Chemical compound ClC=1C=C2C(C(NC2=C(C1)C)=O)(O)C1CCCCCC1.ClC=1C=C2C(C(NC2=C(C1)C)=O)(C1=CC=C(C=C1)O)C1CCCCC1.ClC=1C=C2C(C(NC2=C(C1)C)=O)(C1=CC=C(C=C1)O)C1CCCC1 ZWWVKWRQANOBRQ-UHFFFAOYSA-N 0.000 claims 1
- WDLIBPKZARCSAX-UHFFFAOYSA-N FC1=CC=C2C(C(NC2=C1F)=O)(C)C1=CC=C(C=C1)O.C(C1=CC=CC=C1)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O.C(#C)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O Chemical compound FC1=CC=C2C(C(NC2=C1F)=O)(C)C1=CC=C(C=C1)O.C(C1=CC=CC=C1)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O.C(#C)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O WDLIBPKZARCSAX-UHFFFAOYSA-N 0.000 claims 1
- QMNDAWLNHGDLRM-UHFFFAOYSA-N FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=C(C=C(C=C1)O)C.FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=CC(=C(C=C1)O)C Chemical compound FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=C(C=C(C=C1)O)C.FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=CC(=C(C=C1)O)C QMNDAWLNHGDLRM-UHFFFAOYSA-N 0.000 claims 1
- YLCUIEJSYQQSMZ-UHFFFAOYSA-N FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=CC(=C(C=C1)C)F.FC=1C=C(C=CC1F)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O Chemical compound FC1=CC=C2C(C(NC2=C1F)=O)(C1=CC=C(C=C1)O)C1=CC(=C(C=C1)C)F.FC=1C=C(C=CC1F)C1(C(NC2=C(C(=CC=C12)F)F)=O)C1=CC=C(C=C1)O YLCUIEJSYQQSMZ-UHFFFAOYSA-N 0.000 claims 1
- CLAUIYYAMJWENL-UHFFFAOYSA-N FC1=CC=C2C(C(NC2=C1F)=O)(CCCCC)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(CCCCC)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(CCC)C1=CC=C(C=C1)O Chemical compound FC1=CC=C2C(C(NC2=C1F)=O)(CCCCC)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(CCCCC)C1=CC=C(C=C1)O.FC1=CC=C2C(C(NC2=C1F)=O)(CCC)C1=CC=C(C=C1)O CLAUIYYAMJWENL-UHFFFAOYSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 235000013877 carbamide Nutrition 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 229940127089 cytotoxic agent Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000000651 prodrug Substances 0.000 claims 1
- 229940002612 prodrug Drugs 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91362507P | 2007-04-24 | 2007-04-24 | |
| PCT/EP2008/054990 WO2008129075A1 (en) | 2007-04-24 | 2008-04-24 | Substituted 3-(4-hydroxyphenyl)-indolin-2-one-compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010525024A JP2010525024A (ja) | 2010-07-22 |
| JP2010525024A5 true JP2010525024A5 (OSRAM) | 2011-06-16 |
Family
ID=39643405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010504685A Withdrawn JP2010525024A (ja) | 2007-04-24 | 2008-04-24 | 置換３−（４−ヒドロキシフェニル）−インドリン−２−オン化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100227863A1 (OSRAM) |
| EP (1) | EP2139856A1 (OSRAM) |
| JP (1) | JP2010525024A (OSRAM) |
| AU (1) | AU2008240599A1 (OSRAM) |
| CA (1) | CA2684552A1 (OSRAM) |
| WO (1) | WO2008129075A1 (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1718611A4 (en) | 2004-02-13 | 2009-09-23 | Harvard College | 3-3-DI-SUBSTITUTED OXINDOLES AS INHIBITORS OF INITIATION OF TRANSLATION |
| WO2010109008A1 (en) | 2009-03-26 | 2010-09-30 | Topotarget A/S | Prodrugs of substituted 3-(4-hydroxyphenyl)-indolin-2-ones |
| US20160106711A1 (en) * | 2012-09-20 | 2016-04-21 | President And Fellows Of Harvard College | 3-3-Di-Substituted-Oxindoles as Inhibitors of Translation Initiation |
| CN105017129B (zh) * | 2015-07-02 | 2017-12-26 | 广东药科大学 | 一种吲哚生物碱及其应用 |
| CN110526853B (zh) * | 2018-05-23 | 2021-02-26 | 浙江大学 | 3,3-二取代-2-吲哚酮衍生物及其制备方法 |
| CA3103958A1 (en) * | 2018-07-03 | 2020-01-09 | The Board Of Trustees Of The University Of Illinois | Activators of the unfolded protein response |
| EP3912625A1 (en) * | 2020-05-20 | 2021-11-24 | Kaerus Bioscience Limited | Novel maxi-k potassium channel openers for the treatment of fragile x associated disorders |
| CA3196210A1 (en) * | 2020-10-23 | 2022-04-28 | The Board Of Trustees Of The University Of Illinois | Anticancer compounds selective for er-positive cancers |
| CN113149888B (zh) * | 2021-05-06 | 2023-03-03 | 中山大学 | 一种羟基吲哚酮类衍生物及其制备方法和应用 |
| CN115490673B (zh) * | 2022-01-11 | 2024-10-15 | 苏州浦合医药科技有限公司 | 3,3-二取代吲哚酮类化合物及其用途 |
| CN120677152A (zh) * | 2023-02-23 | 2025-09-19 | 上海济煜医药科技有限公司 | 双环类化合物及其制备方法和用途 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1718611A4 (en) * | 2004-02-13 | 2009-09-23 | Harvard College | 3-3-DI-SUBSTITUTED OXINDOLES AS INHIBITORS OF INITIATION OF TRANSLATION |
| US20070299102A1 (en) * | 2004-04-08 | 2007-12-27 | Topo Target A/S | Diphenyl Ox-Indol-2-One Compounds and Their Use in the Treatment of Cancer |
-
2008
- 2008-04-24 JP JP2010504685A patent/JP2010525024A/ja not_active Withdrawn
- 2008-04-24 AU AU2008240599A patent/AU2008240599A1/en not_active Abandoned
- 2008-04-24 WO PCT/EP2008/054990 patent/WO2008129075A1/en not_active Ceased
- 2008-04-24 EP EP08749700A patent/EP2139856A1/en not_active Withdrawn
- 2008-04-24 CA CA002684552A patent/CA2684552A1/en not_active Abandoned
- 2008-04-28 US US12/597,208 patent/US20100227863A1/en not_active Abandoned
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