JP2005510468A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005510468A5 JP2005510468A5 JP2003528842A JP2003528842A JP2005510468A5 JP 2005510468 A5 JP2005510468 A5 JP 2005510468A5 JP 2003528842 A JP2003528842 A JP 2003528842A JP 2003528842 A JP2003528842 A JP 2003528842A JP 2005510468 A5 JP2005510468 A5 JP 2005510468A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- represents hydrogen
- group
- halogen
- cycloalkyl
- 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
Links
- 125000000217 alkyl group Chemical group 0.000 claims 61
- 229910052739 hydrogen Inorganic materials 0.000 claims 56
- 239000001257 hydrogen Substances 0.000 claims 56
- 150000002431 hydrogen Chemical class 0.000 claims 31
- 229910052736 halogen Inorganic materials 0.000 claims 28
- 150000002367 halogens Chemical class 0.000 claims 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims 23
- 150000001875 compounds Chemical class 0.000 claims 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 19
- 125000001424 substituent group Chemical group 0.000 claims 19
- 125000003282 alkyl amino group Chemical group 0.000 claims 17
- -1 trifluoromethoxy, nitro, amino Chemical group 0.000 claims 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 16
- 125000004663 dialkyl amino group Chemical group 0.000 claims 16
- 125000003545 alkoxy group Chemical group 0.000 claims 15
- 229910052731 fluorine Inorganic materials 0.000 claims 13
- 239000011737 fluorine Substances 0.000 claims 13
- 125000003342 alkenyl group Chemical group 0.000 claims 12
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 11
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 10
- 229910052799 carbon Inorganic materials 0.000 claims 9
- 125000004432 carbon atom Chemical group C* 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 9
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 8
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 8
- 125000000623 heterocyclic group Chemical group 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000004423 acyloxy group Chemical group 0.000 claims 6
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical group FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 6
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 5
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 4
- 125000005141 aryl amino sulfonyl group Chemical group 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims 4
- 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 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000012453 solvate Substances 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000000539 amino acid group Chemical group 0.000 claims 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims 2
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 150000001540 azides Chemical class 0.000 claims 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- DYMRYCZRMAHYKE-UHFFFAOYSA-N n-diazonitramide Chemical compound [O-][N+](=O)N=[N+]=[N-] DYMRYCZRMAHYKE-UHFFFAOYSA-N 0.000 claims 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 208000035143 Bacterial infection Diseases 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10146104A DE10146104A1 (de) | 2001-09-19 | 2001-09-19 | Antibakterielle Markrozyklen |
| PCT/EP2002/009968 WO2003024996A2 (de) | 2001-09-19 | 2002-09-06 | Antibakterielle makrozyklen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005510468A JP2005510468A (ja) | 2005-04-21 |
| JP2005510468A5 true JP2005510468A5 (enExample) | 2005-12-22 |
| JP4427326B2 JP4427326B2 (ja) | 2010-03-03 |
Family
ID=7699507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003528842A Expired - Fee Related JP4427326B2 (ja) | 2001-09-19 | 2002-09-06 | 抗菌性マクロ環 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7405201B2 (enExample) |
| EP (1) | EP1430075B1 (enExample) |
| JP (1) | JP4427326B2 (enExample) |
| AU (1) | AU2002329267A1 (enExample) |
| CA (1) | CA2460646A1 (enExample) |
| DE (2) | DE10146104A1 (enExample) |
| ES (1) | ES2280566T3 (enExample) |
| WO (1) | WO2003024996A2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4928261B2 (ja) | 2003-06-18 | 2012-05-09 | トランザイム・ファーマ・インコーポレイテッド | モチリン受容体の大環状拮抗薬 |
| US9428845B1 (en) | 2010-12-28 | 2016-08-30 | Warp Drive Bio, Inc. | Identifying new therapeutic agents |
| US9193767B2 (en) * | 2011-03-30 | 2015-11-24 | Brown University | Enopeptins, uses thereof, and methods of synthesis thereto |
| EP3038640B1 (en) | 2013-08-30 | 2019-01-02 | St. Jude Children's Research Hospital | Substituted urea depsipeptide analogs as activators of the clpp endopeptidase |
| WO2016112295A1 (en) | 2015-01-09 | 2016-07-14 | Warp Drive Bio, Inc. | Compounds that participate in cooperative binding and uses thereof |
| EP3265083B1 (en) | 2015-03-04 | 2022-07-06 | St. Jude Children's Research Hospital | Substituted urea depsipeptide analogs as activators of the clpp endopeptidase |
| EP3506922B1 (en) * | 2016-09-02 | 2024-05-08 | St. Jude Children's Research Hospital | Substituted urea depsipeptide analogs as activators of the clpp endopeptidase |
| AU2018248417A1 (en) * | 2017-04-05 | 2019-11-14 | Revolution Medicines, Inc. | Compounds that participate in cooperative binding and uses thereof |
| WO2024242056A1 (ja) * | 2023-05-22 | 2024-11-28 | 学校法人近畿大学 | 環状ペプチド化合物とそれを含む抗菌剤 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4492650A (en) * | 1982-09-27 | 1985-01-08 | Eli Lilly And Company | A54556 Antibiotics and process for production thereof |
| JPH0565297A (ja) | 1991-01-17 | 1993-03-19 | Rikagaku Kenkyusho | エノペプチンａ、その製造方法、並びに抗ウイルス剤 |
| JP3036923B2 (ja) | 1991-10-28 | 2000-04-24 | 理化学研究所 | デプシペプチドａ、ｂその製造方法、並びに抗ウイルス剤及び抗菌剤 |
| US5858971A (en) * | 1994-10-25 | 1999-01-12 | Sekisui Chemical Co., Ltd. | Cyclic peptide and method of making same by culturing a strain of actinomyces S. nobilis |
| JP2004512256A (ja) * | 1999-07-27 | 2004-04-22 | アベンテイス・フアルマ・ソシエテ・アノニム | ストレプトグラミン誘導体、それらの製造及びそれらを含有する組成物 |
-
2001
- 2001-09-19 DE DE10146104A patent/DE10146104A1/de not_active Withdrawn
-
2002
- 2002-09-06 AU AU2002329267A patent/AU2002329267A1/en not_active Abandoned
- 2002-09-06 CA CA002460646A patent/CA2460646A1/en not_active Abandoned
- 2002-09-06 EP EP02764872A patent/EP1430075B1/de not_active Expired - Lifetime
- 2002-09-06 DE DE50209187T patent/DE50209187D1/de not_active Expired - Lifetime
- 2002-09-06 ES ES02764872T patent/ES2280566T3/es not_active Expired - Lifetime
- 2002-09-06 WO PCT/EP2002/009968 patent/WO2003024996A2/de not_active Ceased
- 2002-09-06 US US10/490,192 patent/US7405201B2/en not_active Expired - Fee Related
- 2002-09-06 JP JP2003528842A patent/JP4427326B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2436780C2 (ru) | Производные 5-фенилтиазола и их применение в качестве ингибиторов рi3 киназы | |
| RU2483061C2 (ru) | Тетрагидропиранохроменовые ингибиторы гамма-секретазы | |
| RU2007134380A (ru) | Антибактериальные производные пиперидина | |
| JP2005501120A5 (enExample) | ||
| JP2005536553A5 (enExample) | ||
| ATE286501T1 (de) | Pyrimidinderivate | |
| IL165264A (en) | Protein kinase inhibitors, pharmaceutical compositions comprising them and use thereof in the preparation of medicaments for treating protein kinase-associated diseases | |
| JP2002534508A5 (enExample) | ||
| MXPA04002338A (es) | Derivados de carbazol y su uso como antagonistas receptores del npy5. | |
| IL205501A (en) | Preparation of preparations for the treatment of arthritis | |
| JP2002030084A5 (enExample) | ||
| JP2006501201A5 (enExample) | ||
| SE0300908D0 (sv) | Azaindole derivatives, preparations thereof, uses thereof and compositions containing them | |
| JP2005526696A5 (enExample) | ||
| RU99101081A (ru) | Режим введения ингибиторов н+, к+-атфазы | |
| RU2007108863A (ru) | Производные пиразола для лечения состояний, опосредованных активацией рецептора аденозина а2в или а3 | |
| SE0302573D0 (sv) | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof | |
| JP2006510606A5 (enExample) | ||
| JP2005527542A5 (enExample) | ||
| JP2009541387A5 (enExample) | ||
| JP2005510468A5 (enExample) | ||
| JP2004315496A5 (enExample) | ||
| CA2382247A1 (en) | Azaindoles having serotonin receptor affinity | |
| JPWO2023095860A5 (enExample) | ||
| JP2003513075A5 (enExample) |