JP2013507446A5 - - Google Patents
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- JP2013507446A5 JP2013507446A5 JP2012534288A JP2012534288A JP2013507446A5 JP 2013507446 A5 JP2013507446 A5 JP 2013507446A5 JP 2012534288 A JP2012534288 A JP 2012534288A JP 2012534288 A JP2012534288 A JP 2012534288A JP 2013507446 A5 JP2013507446 A5 JP 2013507446A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- group
- alkyl
- heteroaryl
- aryl
- 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.)
- Granted
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- 125000001072 heteroaryl group Chemical group 0.000 claims 135
- 125000003118 aryl group Chemical group 0.000 claims 130
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 90
- 229910052739 hydrogen Inorganic materials 0.000 claims 73
- 239000001257 hydrogen Substances 0.000 claims 73
- 125000000217 alkyl group Chemical group 0.000 claims 69
- 125000000753 cycloalkyl group Chemical group 0.000 claims 69
- 125000000623 heterocyclic group Chemical group 0.000 claims 51
- 150000002431 hydrogen Chemical group 0.000 claims 50
- 229910052736 halogen Inorganic materials 0.000 claims 47
- 150000002367 halogens Chemical class 0.000 claims 41
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 37
- 125000004093 cyano group Chemical group *C#N 0.000 claims 37
- 125000003545 alkoxy group Chemical group 0.000 claims 36
- 125000001424 substituent group Chemical group 0.000 claims 34
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 30
- 125000005843 halogen group Chemical group 0.000 claims 30
- 125000001153 fluoro group Chemical group F* 0.000 claims 29
- 229910052757 nitrogen Inorganic materials 0.000 claims 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 26
- -1 C 1 -C 6 alkyl Chemical group 0.000 claims 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 23
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 22
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 19
- 229910052799 carbon Inorganic materials 0.000 claims 18
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 18
- 125000003107 substituted aryl group Chemical group 0.000 claims 16
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 14
- 150000003839 salts Chemical class 0.000 claims 13
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 8
- 102100039364 Metalloproteinase inhibitor 1 Human genes 0.000 claims 8
- 101710150104 Sensory rhodopsin-1 Proteins 0.000 claims 8
- 125000004429 atom Chemical group 0.000 claims 8
- 229910052698 phosphorus Inorganic materials 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 6
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 230000000694 effects Effects 0.000 claims 3
- 102000004626 Colony-Stimulating Factor Receptors Human genes 0.000 claims 2
- 108010003384 Colony-Stimulating Factor Receptors Proteins 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 230000005494 condensation Effects 0.000 claims 2
- 238000009833 condensation Methods 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000003367 polycyclic group Chemical group 0.000 claims 2
- 229940044551 receptor antagonist Drugs 0.000 claims 2
- 239000002464 receptor antagonist Substances 0.000 claims 2
- 108020003175 receptors Proteins 0.000 claims 2
- 102000005962 receptors Human genes 0.000 claims 2
- 206010043554 thrombocytopenia Diseases 0.000 claims 2
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- 229940124108 Growth factor receptor agonist Drugs 0.000 claims 1
- 229940123011 Growth factor receptor antagonist Drugs 0.000 claims 1
- 102000027430 HGF receptors Human genes 0.000 claims 1
- 108091008603 HGF receptors Proteins 0.000 claims 1
- 102100021866 Hepatocyte growth factor Human genes 0.000 claims 1
- 229940122474 Hepatocyte growth factor receptor agonist Drugs 0.000 claims 1
- 102100039064 Interleukin-3 Human genes 0.000 claims 1
- 108010002386 Interleukin-3 Proteins 0.000 claims 1
- 208000012902 Nervous system disease Diseases 0.000 claims 1
- 208000025966 Neurological disease Diseases 0.000 claims 1
- 208000007502 anemia Diseases 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 230000001413 cellular effect Effects 0.000 claims 1
- 238000002512 chemotherapy Methods 0.000 claims 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 125000004404 heteroalkyl group Chemical group 0.000 claims 1
- 208000026278 immune system disease Diseases 0.000 claims 1
- 230000003278 mimic effect Effects 0.000 claims 1
- 208000004235 neutropenia Diseases 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 239000004031 partial agonist Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000005855 radiation Effects 0.000 claims 1
- 238000001959 radiotherapy Methods 0.000 claims 1
- 229940044601 receptor agonist Drugs 0.000 claims 1
- 239000000018 receptor agonist Substances 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 0 C*(C)(C(N)=O)c1nnc(Nc2nnc(*(O)P=C)nn2)nn1 Chemical compound C*(C)(C(N)=O)c1nnc(Nc2nnc(*(O)P=C)nn2)nn1 0.000 description 5
- WHTKAPAWZRHEFP-UHFFFAOYSA-N C=[I]c(cc1)ccc1C(Nc(cc1)ccc1C(C(C=C1)=CCC1NC(c(cc1)ccc1F)=O)=O)=[U] Chemical compound C=[I]c(cc1)ccc1C(Nc(cc1)ccc1C(C(C=C1)=CCC1NC(c(cc1)ccc1F)=O)=O)=[U] WHTKAPAWZRHEFP-UHFFFAOYSA-N 0.000 description 1
- ZPCSMPJFGZYICP-UHFFFAOYSA-N CC(c1cc(C(Nc(cc2)ccc2C(c(cc2)ccc2[N](C)(C)C)=O)=O)ccc1)=[U] Chemical compound CC(c1cc(C(Nc(cc2)ccc2C(c(cc2)ccc2[N](C)(C)C)=O)=O)ccc1)=[U] ZPCSMPJFGZYICP-UHFFFAOYSA-N 0.000 description 1
- HBEAGIZSVJJESK-UHFFFAOYSA-M Cc(cc1)cc(C)c1C([N-]c(cc1)ccc1C(c(cc1)ccc1NC(c1c(C)cc(C)cc1)=O)=N)=O Chemical compound Cc(cc1)cc(C)c1C([N-]c(cc1)ccc1C(c(cc1)ccc1NC(c1c(C)cc(C)cc1)=O)=N)=O HBEAGIZSVJJESK-UHFFFAOYSA-M 0.000 description 1
- UWHGYVXFFUGPIL-UHFFFAOYSA-N Cc1cc(C(Nc(cc2)ccc2-c2nnc(-c(cc3)ccc3NC(c3cc(C)ccc3)=[U])[o]2)=O)ccc1 Chemical compound Cc1cc(C(Nc(cc2)ccc2-c2nnc(-c(cc3)ccc3NC(c3cc(C)ccc3)=[U])[o]2)=O)ccc1 UWHGYVXFFUGPIL-UHFFFAOYSA-N 0.000 description 1
- YHNAKSMBIBBBRQ-UHFFFAOYSA-N N=C(c(ccc(C(O)=O)c1)c1C(Nc(cc1)ccc1C(c(cc1)ccc1NC(c1cc(C(O)=O)ccc1C(O)=O)=O)=O)=O)O Chemical compound N=C(c(ccc(C(O)=O)c1)c1C(Nc(cc1)ccc1C(c(cc1)ccc1NC(c1cc(C(O)=O)ccc1C(O)=O)=O)=O)=O)O YHNAKSMBIBBBRQ-UHFFFAOYSA-N 0.000 description 1
- BYENYMZIPQBBOG-UHFFFAOYSA-N OC(CC1)CCN1c(cc1)ccc1C(Nc(cc1)ccc1Nc(cc1)ccc1NC(c1ccc2[nH]ccc2c1)=O)=O Chemical compound OC(CC1)CCN1c(cc1)ccc1C(Nc(cc1)ccc1Nc(cc1)ccc1NC(c1ccc2[nH]ccc2c1)=O)=O BYENYMZIPQBBOG-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25125909P | 2009-10-13 | 2009-10-13 | |
| US61/251,259 | 2009-10-13 | ||
| PCT/US2010/052359 WO2011046954A1 (en) | 2009-10-13 | 2010-10-12 | Hematopoietic growth factor mimetic small molecule compounds and their uses |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015194455A Division JP6238942B2 (ja) | 2009-10-13 | 2015-09-30 | 造血成長因子模倣小分子化合物およびそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013507446A JP2013507446A (ja) | 2013-03-04 |
| JP2013507446A5 true JP2013507446A5 (enExample) | 2013-11-28 |
| JP5819305B2 JP5819305B2 (ja) | 2015-11-24 |
Family
ID=43876487
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012534288A Active JP5819305B2 (ja) | 2009-10-13 | 2010-10-12 | 造血成長因子模倣小分子化合物およびそれらの使用 |
| JP2015194455A Active JP6238942B2 (ja) | 2009-10-13 | 2015-09-30 | 造血成長因子模倣小分子化合物およびそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015194455A Active JP6238942B2 (ja) | 2009-10-13 | 2015-09-30 | 造血成長因子模倣小分子化合物およびそれらの使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US9144557B2 (enExample) |
| EP (1) | EP2488486B1 (enExample) |
| JP (2) | JP5819305B2 (enExample) |
| KR (1) | KR101804588B1 (enExample) |
| CN (1) | CN102656141B (enExample) |
| AU (1) | AU2010307006B2 (enExample) |
| CA (1) | CA2777565C (enExample) |
| DK (1) | DK2488486T3 (enExample) |
| ES (1) | ES2749504T3 (enExample) |
| PL (1) | PL2488486T3 (enExample) |
| PT (1) | PT2488486T (enExample) |
| WO (1) | WO2011046954A1 (enExample) |
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| GB0821913D0 (en) | 2008-12-02 | 2009-01-07 | Price & Co | Antibacterial compounds |
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| CA2801274C (en) | 2010-06-01 | 2021-06-15 | Summit Corporation Plc | Compounds for the treatment of clostridium difficile-associated disease |
| WO2012068406A2 (en) * | 2010-11-18 | 2012-05-24 | Ligand Pharmaceuticals Incorporated | Use of hematopoietic growth factor mimetics |
| WO2012167133A2 (en) * | 2011-06-01 | 2012-12-06 | The Regents Of The University Of California | Inhibitors of anandamide transport and their therapeutic uses |
| JP6092870B2 (ja) | 2011-08-19 | 2017-03-08 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | メタ置換ビフェニル末梢に限局されたｆａａｈ阻害剤 |
| BR112014029718A2 (pt) * | 2012-05-31 | 2017-06-27 | Pharmascience Inc | inibidores da proteína quinase |
| KR20150046259A (ko) | 2012-08-23 | 2015-04-29 | 앨리오스 바이오파마 인크. | 파라믹소바이러스 바이러스성 감염의 치료용 화합물 |
| ES2968371T3 (es) | 2013-10-10 | 2024-05-09 | Eastern Virginia Medical School | Derivados de 4-((2-hidroxi-3-metoxibencil)amino) bencenosulfonamida como inhibidores de la 12-lipoxigenasa |
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2010
- 2010-10-12 ES ES10823959T patent/ES2749504T3/es active Active
- 2010-10-12 JP JP2012534288A patent/JP5819305B2/ja active Active
- 2010-10-12 US US13/501,622 patent/US9144557B2/en not_active Expired - Fee Related
- 2010-10-12 KR KR1020127012390A patent/KR101804588B1/ko active Active
- 2010-10-12 PT PT108239591T patent/PT2488486T/pt unknown
- 2010-10-12 DK DK10823959T patent/DK2488486T3/da active
- 2010-10-12 EP EP10823959.1A patent/EP2488486B1/en active Active
- 2010-10-12 CN CN201080055349.5A patent/CN102656141B/zh active Active
- 2010-10-12 WO PCT/US2010/052359 patent/WO2011046954A1/en not_active Ceased
- 2010-10-12 CA CA2777565A patent/CA2777565C/en active Active
- 2010-10-12 AU AU2010307006A patent/AU2010307006B2/en active Active
- 2010-10-12 PL PL10823959T patent/PL2488486T3/pl unknown
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2015
- 2015-05-15 US US14/713,930 patent/US9622991B2/en active Active
- 2015-09-30 JP JP2015194455A patent/JP6238942B2/ja active Active
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