JP2018525353A - Bmp1、tll1および/またはtll2の阻害剤としての使用するための、n−ヒドロキシホルムアミド化合物およびそれらを含んでなる組成物 - Google Patents
Bmp1、tll1および/またはtll2の阻害剤としての使用するための、n−ヒドロキシホルムアミド化合物およびそれらを含んでなる組成物 Download PDFInfo
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- JP2018525353A JP2018525353A JP2018500463A JP2018500463A JP2018525353A JP 2018525353 A JP2018525353 A JP 2018525353A JP 2018500463 A JP2018500463 A JP 2018500463A JP 2018500463 A JP2018500463 A JP 2018500463A JP 2018525353 A JP2018525353 A JP 2018525353A
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- alkyl
- phenyl
- independently selected
- alkoxy
- compound
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- 0 CC(C(C)N(C=O)O)C(NCNC(C12OC(*)C[C@]1C2)=O)=O Chemical compound CC(C(C)N(C=O)O)C(NCNC(C12OC(*)C[C@]1C2)=O)=O 0.000 description 20
- KVCQHIDQQKARLY-UHFFFAOYSA-N CC(C)(C)OP(OCOc1c(C(OCC=C)=O)c(C)ccc1)(OC(C)(C)C)=O Chemical compound CC(C)(C)OP(OCOc1c(C(OCC=C)=O)c(C)ccc1)(OC(C)(C)C)=O KVCQHIDQQKARLY-UHFFFAOYSA-N 0.000 description 1
- SMTDIEBUWFHPON-UHFFFAOYSA-N CC(O1)=C(CI)OC1=O Chemical compound CC(O1)=C(CI)OC1=O SMTDIEBUWFHPON-UHFFFAOYSA-N 0.000 description 1
- LLQCZPWLWFVGRO-UHFFFAOYSA-N CC(c(cc(cc1)OC)c1C(OC)=O)=C Chemical compound CC(c(cc(cc1)OC)c1C(OC)=O)=C LLQCZPWLWFVGRO-UHFFFAOYSA-N 0.000 description 1
- OCLONVIOMSZSPY-UZLVNVLGSA-N CCCCCC([C@@H](CC)N(C=O)OC(c(c(OC)c1)ccc1OC)=O)C(NCNC(c1ccc(-c(cc2)cc(OCC)c2C(N[C@@H](CC(OCc2ccccc2)=O)C(OCc2ccccc2)=O)=O)[o]1)=O)=O Chemical compound CCCCCC([C@@H](CC)N(C=O)OC(c(c(OC)c1)ccc1OC)=O)C(NCNC(c1ccc(-c(cc2)cc(OCC)c2C(N[C@@H](CC(OCc2ccccc2)=O)C(OCc2ccccc2)=O)=O)[o]1)=O)=O OCLONVIOMSZSPY-UZLVNVLGSA-N 0.000 description 1
- NGBFQLRGBXJYIE-UHFFFAOYSA-N CCCCCCC(N(CCO1)C1=O)=O Chemical compound CCCCCCC(N(CCO1)C1=O)=O NGBFQLRGBXJYIE-UHFFFAOYSA-N 0.000 description 1
- WQBDKRBJUVEIAU-UFLAQGTRSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OC(Cc1ccccc1)=O)C(NCNC(c1ccc(-c(cc2)cc(OCC)c2C(N[C@@H](CCC(OCc2ccccc2)=O)C(OCc2ccccc2)=O)=O)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OC(Cc1ccccc1)=O)C(NCNC(c1ccc(-c(cc2)cc(OCC)c2C(N[C@@H](CCC(OCc2ccccc2)=O)C(OCc2ccccc2)=O)=O)[o]1)=O)=O WQBDKRBJUVEIAU-UFLAQGTRSA-N 0.000 description 1
- JLRPINMKGWRNBO-PNIVXLCQSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OC(Nc1ccccc1)=O)C(NCNC(c1ccc(-c2ccc(C(N[C@@H](CC(OC(C)(C)C)=O)C(OC(C)(C)C)=O)=O)c(OCC)c2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OC(Nc1ccccc1)=O)C(NCNC(c1ccc(-c2ccc(C(N[C@@H](CC(OC(C)(C)C)=O)C(OC(C)(C)C)=O)=O)c(OCC)c2)[o]1)=O)=O JLRPINMKGWRNBO-PNIVXLCQSA-N 0.000 description 1
- KIDAZHLDCGRIDA-FCFDBNDOSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OC(c1cccc(C(O)=O)c1)=O)C(NCNC(c1ccc(-c2ccc(C(N[C@@H](CC(OCc3ccccc3)=O)C(OCc3ccccc3)=O)=O)c(OCC(OCc3ccccc3)=O)c2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OC(c1cccc(C(O)=O)c1)=O)C(NCNC(c1ccc(-c2ccc(C(N[C@@H](CC(OCc3ccccc3)=O)C(OCc3ccccc3)=O)=O)c(OCC(OCc3ccccc3)=O)c2)[o]1)=O)=O KIDAZHLDCGRIDA-FCFDBNDOSA-N 0.000 description 1
- GQXNZLSAGWMAKV-WOJBJXKFSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OCOP(O)(O)=O)C(NCNC(c1ccc(-c2ccccc2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OCOP(O)(O)=O)C(NCNC(c1ccc(-c2ccccc2)[o]1)=O)=O GQXNZLSAGWMAKV-WOJBJXKFSA-N 0.000 description 1
- NNKPHRIYXJMAHW-VSGBNLITSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c(cc2)ccc2C(OCC)=O)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c(cc2)ccc2C(OCC)=O)[o]1)=O)=O NNKPHRIYXJMAHW-VSGBNLITSA-N 0.000 description 1
- VYWFCQWIOPUFPV-LQFQNGICSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2cc(P(OCOC(OC(C)C)=O)(OCOC(OC(C)C)=O)=O)cc(OCC)c2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2cc(P(OCOC(OC(C)C)=O)(OCOC(OC(C)C)=O)=O)cc(OCC)c2)[o]1)=O)=O VYWFCQWIOPUFPV-LQFQNGICSA-N 0.000 description 1
- QNBKORBXOTYIIH-OUVVECCDSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2ccc(C(NC(CC(OCc3ccccc3)=O)C(OCOC(C(C)C)=O)=O)=O)c(OCC)c2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2ccc(C(NC(CC(OCc3ccccc3)=O)C(OCOC(C(C)C)=O)=O)=O)c(OCC)c2)[o]1)=O)=O QNBKORBXOTYIIH-OUVVECCDSA-N 0.000 description 1
- HCRDUWHRWBXEDL-FURHFXAJSA-N CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2ccc(C(NC[C@@H](CCOC(C)(C)C)C(OC(C)(C)C)=O)=O)c(OCC)c2)[o]1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)OCc1ccccc1)C(NCNC(c1ccc(-c2ccc(C(NC[C@@H](CCOC(C)(C)C)C(OC(C)(C)C)=O)=O)c(OCC)c2)[o]1)=O)=O HCRDUWHRWBXEDL-FURHFXAJSA-N 0.000 description 1
- JCUFLGMULAMOKC-UHFFFAOYSA-N CCOC(c1ccc(CBr)cc1C)=O Chemical compound CCOC(c1ccc(CBr)cc1C)=O JCUFLGMULAMOKC-UHFFFAOYSA-N 0.000 description 1
- NJNYCVBYUKEPLG-IBGZPJMESA-N CCOc(cc(B1OC(C)(C)C(C)(C)O1)cc1)c1C(N[C@@H](CC(OC(C)(C)C)=O)C(OC(C)(C)C)=O)=O Chemical compound CCOc(cc(B1OC(C)(C)C(C)(C)O1)cc1)c1C(N[C@@H](CC(OC(C)(C)C)=O)C(OC(C)(C)C)=O)=O NJNYCVBYUKEPLG-IBGZPJMESA-N 0.000 description 1
- MGHUCEMUAWKKCL-UHFFFAOYSA-N CN(C)C(Oc(cccc1)c1C(OC)=O)=O Chemical compound CN(C)C(Oc(cccc1)c1C(OC)=O)=O MGHUCEMUAWKKCL-UHFFFAOYSA-N 0.000 description 1
- YQKNOSLUARLTEY-UHFFFAOYSA-N NC(c(c(OCC(OCc1ccccc1)=O)c1)ccc1Br)=O Chemical compound NC(c(c(OCC(OCc1ccccc1)=O)c1)ccc1Br)=O YQKNOSLUARLTEY-UHFFFAOYSA-N 0.000 description 1
- LNGZNDCFMMPFSW-UHFFFAOYSA-N NCNC(OCC1c(cccc2)c2-c2ccccc12)=O Chemical compound NCNC(OCC1c(cccc2)c2-c2ccccc12)=O LNGZNDCFMMPFSW-UHFFFAOYSA-N 0.000 description 1
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- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562190345P | 2015-07-09 | 2015-07-09 | |
| US62/190,345 | 2015-07-09 | ||
| PCT/IB2016/054123 WO2017006296A1 (en) | 2015-07-09 | 2016-07-08 | N-hydroxyformamide compounds and compositions comprising them for use as bmp1, tll1 and/or tll2 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018525353A true JP2018525353A (ja) | 2018-09-06 |
| JP2018525353A5 JP2018525353A5 (enExample) | 2019-08-22 |
Family
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Family Applications (1)
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| JP2018500463A Pending JP2018525353A (ja) | 2015-07-09 | 2016-07-08 | Bmp1、tll1および/またはtll2の阻害剤としての使用するための、n−ヒドロキシホルムアミド化合物およびそれらを含んでなる組成物 |
Country Status (5)
| Country | Link |
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| US (1) | US20180362485A1 (enExample) |
| EP (1) | EP3319961A1 (enExample) |
| JP (1) | JP2018525353A (enExample) |
| TW (1) | TW201716390A (enExample) |
| WO (1) | WO2017006296A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017507915A (ja) | 2014-01-10 | 2017-03-23 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | ヒドロキシホルムアミド誘導体およびそれらの使用 |
| EP4484444A1 (en) | 2023-06-28 | 2025-01-01 | Centre National de la Recherche Scientifique | Protein and fragments thereof, and their use |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002531576A (ja) * | 1998-12-10 | 2002-09-24 | エフ.ホフマン−ラ ロシュ アーゲー | プロコラーゲンc−プロテイナーゼ阻害剤 |
| JP2006516120A (ja) * | 2002-12-11 | 2006-06-22 | スミスクライン・ビーチャム・コーポレイション | ペプチドデホルミラーゼ阻害剤 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2518496A3 (en) | 2006-07-21 | 2013-02-27 | GENERA ISTRAZIVANJA d.o.o. | BMP-1 procollagen C-proteinase for diagnosis and treatment of bone and soft tissue defects and disorders |
| EP2841100A4 (en) | 2012-04-25 | 2016-03-23 | Genera Istrazivanja D O O | METHODS AND COMPOSITIONS FOR TREATMENT AND DIAGNOSIS OF MYOCARDIAL ACUTE INFARCTION |
| JP2017507915A (ja) | 2014-01-10 | 2017-03-23 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | ヒドロキシホルムアミド誘導体およびそれらの使用 |
-
2016
- 2016-07-08 JP JP2018500463A patent/JP2018525353A/ja active Pending
- 2016-07-08 WO PCT/IB2016/054123 patent/WO2017006296A1/en not_active Ceased
- 2016-07-08 US US15/736,911 patent/US20180362485A1/en not_active Abandoned
- 2016-07-08 EP EP16756795.7A patent/EP3319961A1/en not_active Withdrawn
- 2016-07-11 TW TW105121791A patent/TW201716390A/zh unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002531576A (ja) * | 1998-12-10 | 2002-09-24 | エフ.ホフマン−ラ ロシュ アーゲー | プロコラーゲンc−プロテイナーゼ阻害剤 |
| JP2006516120A (ja) * | 2002-12-11 | 2006-06-22 | スミスクライン・ビーチャム・コーポレイション | ペプチドデホルミラーゼ阻害剤 |
Non-Patent Citations (1)
| Title |
|---|
| ERIC D TURTLE ET AL.: "Inhibition of procollagen C-proteinase: Fibrosis and beyond", EXPERT OPINION ON THERAPEUTIC PATENTS, vol. 14(8), JPN6020022876, 2004, pages 1185 - 1197, ISSN: 0004295894 * |
Also Published As
| Publication number | Publication date |
|---|---|
| TW201716390A (zh) | 2017-05-16 |
| US20180362485A1 (en) | 2018-12-20 |
| EP3319961A1 (en) | 2018-05-16 |
| WO2017006296A1 (en) | 2017-01-12 |
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