ZA200308379B - N-formyl hydroxylamine compounds as inhibitors of PDF. - Google Patents
N-formyl hydroxylamine compounds as inhibitors of PDF. Download PDFInfo
- Publication number
- ZA200308379B ZA200308379B ZA200308379A ZA200308379A ZA200308379B ZA 200308379 B ZA200308379 B ZA 200308379B ZA 200308379 A ZA200308379 A ZA 200308379A ZA 200308379 A ZA200308379 A ZA 200308379A ZA 200308379 B ZA200308379 B ZA 200308379B
- Authority
- ZA
- South Africa
- Prior art keywords
- pyrrolidine
- methyl
- carboxylic acid
- amide
- pyridin
- Prior art date
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- 239000003112 inhibitor Substances 0.000 title description 20
- KDGKTJGPFXIBEB-UHFFFAOYSA-N n-hydroxyformamide Chemical class ONC=O KDGKTJGPFXIBEB-UHFFFAOYSA-N 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 216
- -1 heteroalkylaryl Chemical group 0.000 claims description 154
- 238000000034 method Methods 0.000 claims description 69
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- 239000001257 hydrogen Substances 0.000 claims description 49
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 49
- 150000003839 salts Chemical class 0.000 claims description 38
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 31
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- 229940002612 prodrug Drugs 0.000 claims description 27
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- 125000004076 pyridyl group Chemical group 0.000 description 18
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- 229940081192 rifamycins Drugs 0.000 description 1
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007974 sodium acetate buffer Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US29841901P | 2001-06-15 | 2001-06-15 | |
US36031302P | 2002-02-27 | 2002-02-27 | |
PCT/EP2002/006604 WO2002102790A1 (en) | 2001-06-15 | 2002-06-14 | N-formyl hydroxylamine compounds as inhibitors of pdf |
Publications (1)
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ZA200308379B true ZA200308379B (en) | 2004-05-21 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ZA200308379A ZA200308379B (en) | 2001-06-15 | 2003-10-28 | N-formyl hydroxylamine compounds as inhibitors of PDF. |
Country Status (31)
Country | Link |
---|---|
US (1) | US7148242B2 (de) |
EP (1) | EP1401828B1 (de) |
JP (1) | JP4361365B2 (de) |
KR (2) | KR100589544B1 (de) |
CN (1) | CN1511152A (de) |
AR (1) | AR036053A1 (de) |
AT (1) | ATE323081T1 (de) |
AU (1) | AU2002321062B2 (de) |
BR (1) | BR0210377A (de) |
CA (1) | CA2448526A1 (de) |
CO (1) | CO5640131A2 (de) |
CY (1) | CY1105085T1 (de) |
CZ (1) | CZ20033388A3 (de) |
DE (1) | DE60210612T2 (de) |
DK (1) | DK1401828T3 (de) |
ES (1) | ES2262824T3 (de) |
HK (1) | HK1064370A1 (de) |
HU (1) | HUP0400208A3 (de) |
IL (1) | IL158770A0 (de) |
MX (1) | MXPA03011628A (de) |
MY (1) | MY138619A (de) |
NO (1) | NO327420B1 (de) |
NZ (1) | NZ529489A (de) |
PE (1) | PE20030100A1 (de) |
PL (1) | PL364476A1 (de) |
PT (1) | PT1401828E (de) |
RU (1) | RU2325386C2 (de) |
SI (1) | SI1401828T1 (de) |
SK (1) | SK15242003A3 (de) |
WO (1) | WO2002102790A1 (de) |
ZA (1) | ZA200308379B (de) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1406893B1 (de) * | 2001-06-15 | 2007-04-18 | Vicuron Pharmaceuticals, Inc. | Bicyclische pyrrolidinverbindungen |
GB0208579D0 (en) * | 2002-04-13 | 2002-05-22 | British Biotech Pharm | Antibacterial agents |
NZ538833A (en) * | 2002-09-19 | 2008-05-30 | Novartis Ag | Process for preparing intermediates |
CN101092342A (zh) * | 2003-02-21 | 2007-12-26 | 诺瓦提斯公司 | 制备用以获得n-甲酰基羟胺的中间体的化学方法 |
TW200427458A (en) * | 2003-04-02 | 2004-12-16 | Novartis Ag | Crystalline N-formyl hydroxylamine compounds |
JP2009513485A (ja) * | 2003-06-26 | 2009-04-02 | ノバルティス アクチエンゲゼルシャフト | ある種の抗菌性n−ホルミルヒドロキシルアミン化合物の製造に有用な中間体の製造法 |
KR100527624B1 (ko) * | 2003-08-21 | 2005-11-22 | 한기종 | 질소에 포밀기를 갖는 아민유도체의 새로운 제조방법 |
WO2006002896A1 (en) * | 2004-06-30 | 2006-01-12 | Novartis Ag | Method for increasing the susceptibility of peptide deformylase inhibitors by using efflux pump inhibitors |
US20080161249A1 (en) | 2004-11-17 | 2008-07-03 | Smithkline Beecham Corporation | Use of Novel Antibacterial Compounds |
GT200600196A (es) * | 2005-05-23 | 2007-01-15 | Compuestos n-formil de hidroxilamina | |
MX2007015421A (es) | 2005-06-07 | 2008-02-21 | Novartis Ag | Inhibidores de desformilasa peptidica (pdf) 4. |
DE102005026231A1 (de) * | 2005-06-07 | 2006-12-14 | Origenis Ag | Peptid-Deformylase (PDF) Inhibitoren 3 |
SG133452A1 (en) * | 2005-12-30 | 2007-07-30 | Novartis Ag | Peptide deformylase inhibitors for treatment of mycobacterial and other parasitic diseases |
KR20080095895A (ko) * | 2006-03-03 | 2008-10-29 | 노파르티스 아게 | N―포르밀 히드록실아민 화합물 |
CN101328155B (zh) * | 2007-06-20 | 2010-11-03 | 上海医药工业研究院 | 噁唑烷衍生物及其制备方法和应用 |
CN101434570B (zh) * | 2007-11-16 | 2011-02-02 | 上海医药工业研究院 | 吡咯烷衍生物及其制备方法和应用 |
CN101584694B (zh) * | 2009-06-15 | 2011-01-12 | 华东师范大学 | 含2,5-二氢吡咯的肽脱甲酰基酶抑制剂及合成方法 |
AU2010291212A1 (en) * | 2009-09-04 | 2012-02-23 | Novartis Ag | Heteroaryl compounds as kinase inhibitors |
NZ601924A (en) * | 2010-03-10 | 2014-10-31 | Astrazeneca Ab | 4-phenyl pyridine analogues as protein kinase inhibitors |
JP5825086B2 (ja) | 2011-12-19 | 2015-12-02 | 住友化学株式会社 | α−置換−β−アミノ酸エステル誘導体不斉加水分解酵素 |
US9512084B2 (en) | 2013-11-29 | 2016-12-06 | Novartis Ag | Amino pyrimidine derivatives |
US20180140602A1 (en) | 2015-04-07 | 2018-05-24 | Novartis Ag | Combination of chimeric antigen receptor therapy and amino pyrimidine derivatives |
US10738028B2 (en) * | 2016-05-11 | 2020-08-11 | Rudong Ruien Pharmaceutical Technology Co. Ltd | Spiro three-membered ring, spiro five-membered ring peptide deformylase inhibitor and use thereof in antibacteria and anti-tumor |
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2002
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- 2002-06-14 BR BR0210377-0A patent/BR0210377A/pt not_active IP Right Cessation
- 2002-06-14 PL PL02364476A patent/PL364476A1/xx not_active Application Discontinuation
- 2002-06-14 KR KR1020037016435A patent/KR100589544B1/ko not_active IP Right Cessation
- 2002-06-14 CN CNA028105966A patent/CN1511152A/zh active Pending
- 2002-06-14 US US10/171,706 patent/US7148242B2/en not_active Expired - Fee Related
- 2002-06-14 ES ES02754681T patent/ES2262824T3/es not_active Expired - Lifetime
- 2002-06-14 IL IL15877002A patent/IL158770A0/xx unknown
- 2002-06-14 AT AT02754681T patent/ATE323081T1/de not_active IP Right Cessation
- 2002-06-14 RU RU2003137565/04A patent/RU2325386C2/ru not_active IP Right Cessation
- 2002-06-14 SI SI200230358T patent/SI1401828T1/sl unknown
- 2002-06-14 DK DK02754681T patent/DK1401828T3/da active
- 2002-06-14 HU HU0400208A patent/HUP0400208A3/hu unknown
- 2002-06-14 NZ NZ529489A patent/NZ529489A/en unknown
- 2002-06-14 CA CA002448526A patent/CA2448526A1/en not_active Abandoned
- 2002-06-14 MY MYPI20022243A patent/MY138619A/en unknown
- 2002-06-14 PE PE2002000516A patent/PE20030100A1/es not_active Application Discontinuation
- 2002-06-14 JP JP2003506263A patent/JP4361365B2/ja not_active Expired - Fee Related
- 2002-06-14 EP EP02754681A patent/EP1401828B1/de not_active Expired - Lifetime
- 2002-06-14 WO PCT/EP2002/006604 patent/WO2002102790A1/en active IP Right Grant
- 2002-06-14 MX MXPA03011628A patent/MXPA03011628A/es active IP Right Grant
- 2002-06-14 DE DE60210612T patent/DE60210612T2/de not_active Expired - Lifetime
- 2002-06-14 CZ CZ20033388A patent/CZ20033388A3/cs unknown
- 2002-06-14 AU AU2002321062A patent/AU2002321062B2/en not_active Ceased
- 2002-06-14 SK SK1524-2003A patent/SK15242003A3/sk not_active Application Discontinuation
- 2002-06-14 PT PT02754681T patent/PT1401828E/pt unknown
- 2002-06-14 KR KR1020067002113A patent/KR20060014083A/ko not_active Application Discontinuation
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2003
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2004
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