JP2013500270A5 - - Google Patents
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- Publication number
- JP2013500270A5 JP2013500270A5 JP2012521874A JP2012521874A JP2013500270A5 JP 2013500270 A5 JP2013500270 A5 JP 2013500270A5 JP 2012521874 A JP2012521874 A JP 2012521874A JP 2012521874 A JP2012521874 A JP 2012521874A JP 2013500270 A5 JP2013500270 A5 JP 2013500270A5
- Authority
- JP
- Japan
- Prior art keywords
- deoxy
- dihydro
- acetylaminospectinomycin
- substituted
- phenyl
- 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
- 150000001875 compounds Chemical class 0.000 claims 24
- -1 2-substituted phenyl Chemical group 0.000 claims 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims 8
- 208000015181 infectious disease Diseases 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
- 208000035143 Bacterial infection Diseases 0.000 claims 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 208000022362 bacterial infectious disease Diseases 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 230000000844 anti-bacterial effect Effects 0.000 claims 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- AEUTYOVWOVBAKS-UWVGGRQHSA-N ethambutol Chemical compound CC[C@@H](CO)NCCN[C@@H](CC)CO AEUTYOVWOVBAKS-UWVGGRQHSA-N 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000004306 triazinyl group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- 201000008827 tuberculosis Diseases 0.000 claims 2
- VCOPTHOUUNAYKQ-WBTCAYNUSA-N (3s)-3,6-diamino-n-[[(2s,5s,8e,11s,15s)-15-amino-11-[(6r)-2-amino-1,4,5,6-tetrahydropyrimidin-6-yl]-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentazacyclohexadec-5-yl]methyl]hexanamide;(3s)-3,6-diamino-n-[[(2s,5s,8 Chemical compound N1C(=O)\C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)C[C@@H](N)CCCN)NC(=O)[C@H](C)NC(=O)[C@@H](N)CNC(=O)[C@@H]1[C@@H]1NC(N)=NCC1.N1C(=O)\C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)C[C@@H](N)CCCN)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CNC(=O)[C@@H]1[C@@H]1NC(N)=NCC1 VCOPTHOUUNAYKQ-WBTCAYNUSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 241000894006 Bacteria Species 0.000 claims 1
- 108010065839 Capreomycin Proteins 0.000 claims 1
- 208000019359 Enterococcus faecalis infection Diseases 0.000 claims 1
- 206010062207 Mycobacterial infection Diseases 0.000 claims 1
- 241000193998 Streptococcus pneumoniae Species 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 208000022338 anthrax infection Diseases 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 239000004305 biphenyl Substances 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
- 229960004602 capreomycin Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229960000285 ethambutol Drugs 0.000 claims 1
- 229960003350 isoniazid Drugs 0.000 claims 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 claims 1
- 229930027917 kanamycin Natural products 0.000 claims 1
- 229960000318 kanamycin Drugs 0.000 claims 1
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 claims 1
- 229930182823 kanamycin A Natural products 0.000 claims 1
- TYZROVQLWOKYKF-ZDUSSCGKSA-N linezolid Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCOCC1 TYZROVQLWOKYKF-ZDUSSCGKSA-N 0.000 claims 1
- 229960003907 linezolid Drugs 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 208000027531 mycobacterial infectious disease Diseases 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- JQXXHWHPUNPDRT-WLSIYKJHSA-N rifampicin Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C([O-])=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N1CC[NH+](C)CC1 JQXXHWHPUNPDRT-WLSIYKJHSA-N 0.000 claims 1
- 229960001225 rifampicin Drugs 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229940031000 streptococcus pneumoniae Drugs 0.000 claims 1
- 229960005322 streptomycin Drugs 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22826609P | 2009-07-24 | 2009-07-24 | |
| US61/228,266 | 2009-07-24 | ||
| PCT/US2010/043244 WO2011011783A1 (en) | 2009-07-24 | 2010-07-26 | Spectinamides as anti-tuberculosis agents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013500270A JP2013500270A (ja) | 2013-01-07 |
| JP2013500270A5 true JP2013500270A5 (enExample) | 2013-09-12 |
| JP5770181B2 JP5770181B2 (ja) | 2015-08-26 |
Family
ID=43499454
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012521874A Active JP5770181B2 (ja) | 2009-07-24 | 2010-07-26 | 抗結核剤としてのスペクチナミド類 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US8685978B2 (enExample) |
| EP (1) | EP2461805B1 (enExample) |
| JP (1) | JP5770181B2 (enExample) |
| CN (1) | CN102548552B (enExample) |
| AU (1) | AU2010275375B2 (enExample) |
| CA (1) | CA2768582C (enExample) |
| WO (1) | WO2011011783A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103319496B (zh) * | 2012-03-23 | 2015-06-17 | 中国科学院微生物研究所 | 来源于海洋疣孢菌的多环聚酮类化合物及其制备方法与应用 |
| EP3049154B1 (en) * | 2013-09-29 | 2019-11-13 | St. Jude Children's Research Hospital, Inc. | Aryl substituted aminomethyl spectinomycin analogs as antibacterial agents |
| CN104725392B (zh) * | 2013-12-24 | 2017-01-11 | 中国农业大学 | 半抗原spe-ede及其相应的人工抗原与应用 |
| CN104886160A (zh) * | 2015-07-08 | 2015-09-09 | 孟宪胜 | 一种眼科诊断室用杀菌剂 |
| CN108218886B (zh) * | 2018-02-11 | 2020-06-12 | 中国医药集团总公司四川抗菌素工业研究所 | 一种大观霉素衍生物及其制备方法和应用 |
| CN108148072A (zh) * | 2018-02-11 | 2018-06-12 | 中国医药集团总公司四川抗菌素工业研究所 | 一种大观霉素衍生物及其制备方法和应用 |
| US20210388012A1 (en) * | 2018-11-05 | 2021-12-16 | St. Jude Children's Research Hospital, Inc. | Methods and compositions for prodrug forms of spectinomycin and spectinamide analogs |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2756914A1 (de) * | 1977-12-21 | 1979-07-05 | Thomae Gmbh Dr K | 4-spectinomycylamin und seine physiologisch vertraegliche salze, verfahren zur herstellung und diese stoffe enthaltende arzneimittel |
| DE2851953A1 (de) * | 1978-12-01 | 1980-06-19 | Thomae Gmbh Dr K | Neue spectinomycylamine, verfahren zu ihrer herstellung und diese enthaltenden arzneimittel |
| US4465848A (en) * | 1981-10-23 | 1984-08-14 | The Upjohn Company | Spectinomycin compounds |
| EP0079125B1 (en) | 1981-10-23 | 1989-04-05 | The Upjohn Company | 3-substituted spectinomycin analogues and their preparation |
| US4730059A (en) * | 1986-03-10 | 1988-03-08 | The Upjohn Company | 6'-thiomethylsubstituted spectinomycins |
| US5399558A (en) * | 1993-11-24 | 1995-03-21 | Pathogenesis Corporation | Isoflavonoid antibacterial compounds, compositions and use |
| US5556879A (en) * | 1995-03-01 | 1996-09-17 | Rhone Merieux, Inc. | Aqueous spectinomycin borate solutions |
| US5628984A (en) * | 1995-07-31 | 1997-05-13 | University Of North Carolina At Chapel Hill | Method of detecting lung disease |
| ES2482700T3 (es) * | 2005-02-14 | 2014-08-04 | Venus Remedies Limited | Terapia de combinación parenteral para enfermedades infecciosas causadas por una bacteria resistente a los medicamentos |
-
2010
- 2010-07-26 JP JP2012521874A patent/JP5770181B2/ja active Active
- 2010-07-26 CA CA2768582A patent/CA2768582C/en active Active
- 2010-07-26 US US12/843,551 patent/US8685978B2/en active Active
- 2010-07-26 AU AU2010275375A patent/AU2010275375B2/en active Active
- 2010-07-26 WO PCT/US2010/043244 patent/WO2011011783A1/en not_active Ceased
- 2010-07-26 CN CN201080042448.XA patent/CN102548552B/zh active Active
- 2010-07-26 EP EP10803015.6A patent/EP2461805B1/en active Active
-
2014
- 2014-03-23 US US14/222,647 patent/US9284325B2/en active Active
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