NZ540870A - Antibiotics containing borinic acid complexes and methods of use - Google Patents
Antibiotics containing borinic acid complexes and methods of useInfo
- Publication number
- NZ540870A NZ540870A NZ540870A NZ54087003A NZ540870A NZ 540870 A NZ540870 A NZ 540870A NZ 540870 A NZ540870 A NZ 540870A NZ 54087003 A NZ54087003 A NZ 54087003A NZ 540870 A NZ540870 A NZ 540870A
- Authority
- NZ
- New Zealand
- Prior art keywords
- alkyl
- species
- aryl
- acid
- bis
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 38
- UYANAUSDHIFLFQ-UHFFFAOYSA-N borinic acid Chemical class OB UYANAUSDHIFLFQ-UHFFFAOYSA-N 0.000 title abstract description 33
- 239000003242 anti bacterial agent Substances 0.000 title abstract description 16
- 229940088710 antibiotic agent Drugs 0.000 title abstract description 16
- 239000002904 solvent Substances 0.000 claims abstract description 38
- 241000894006 Bacteria Species 0.000 claims abstract description 28
- 239000003814 drug Substances 0.000 claims abstract description 15
- 201000010099 disease Diseases 0.000 claims abstract description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 140
- -1 SCF3 Chemical compound 0.000 claims description 107
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 60
- 125000000217 alkyl group Chemical group 0.000 claims description 58
- 239000002253 acid Substances 0.000 claims description 46
- 125000003118 aryl group Chemical group 0.000 claims description 37
- 229910052736 halogen Inorganic materials 0.000 claims description 33
- 150000002367 halogens Chemical class 0.000 claims description 33
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 claims description 31
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 claims description 31
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 27
- 150000003839 salts Chemical class 0.000 claims description 26
- 125000003545 alkoxy group Chemical group 0.000 claims description 25
- 125000003107 substituted aryl group Chemical group 0.000 claims description 25
- 150000002148 esters Chemical class 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 18
- 125000004288 oxazolidin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])OC1([H])* 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- SIRFLBWZSUIYHF-UHFFFAOYSA-N bis(3-chloro-4-methylphenyl)borinic acid Chemical compound C1=C(Cl)C(C)=CC=C1B(O)C1=CC=C(C)C(Cl)=C1 SIRFLBWZSUIYHF-UHFFFAOYSA-N 0.000 claims description 15
- 239000008194 pharmaceutical composition Substances 0.000 claims description 14
- 125000004104 aryloxy group Chemical group 0.000 claims description 13
- HEMGPARMYBRMGB-UHFFFAOYSA-N bis(3-chlorophenyl)borinic acid Chemical compound C=1C=CC(Cl)=CC=1B(O)C1=CC=CC(Cl)=C1 HEMGPARMYBRMGB-UHFFFAOYSA-N 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 10
- 241000894007 species Species 0.000 claims description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 9
- 229910052796 boron Inorganic materials 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims description 9
- 241000186216 Corynebacterium Species 0.000 claims description 8
- BRARRAHGNDUELT-UHFFFAOYSA-N hydroxypicolinic acid Natural products OC(=O)C1=NC=CC=C1O BRARRAHGNDUELT-UHFFFAOYSA-N 0.000 claims description 8
- 241000191940 Staphylococcus Species 0.000 claims description 7
- 241000193403 Clostridium Species 0.000 claims description 6
- 241000588653 Neisseria Species 0.000 claims description 6
- 239000003937 drug carrier Substances 0.000 claims description 6
- 229940081066 picolinic acid Drugs 0.000 claims description 6
- 241000589158 Agrobacterium Species 0.000 claims description 5
- 241000193738 Bacillus anthracis Species 0.000 claims description 5
- 241000588722 Escherichia Species 0.000 claims description 5
- 241000606768 Haemophilus influenzae Species 0.000 claims description 5
- 241000589516 Pseudomonas Species 0.000 claims description 5
- 241000193998 Streptococcus pneumoniae Species 0.000 claims description 5
- 241000607479 Yersinia pestis Species 0.000 claims description 5
- 206010013023 diphtheria Diseases 0.000 claims description 5
- 241000589291 Acinetobacter Species 0.000 claims description 4
- 241000588626 Acinetobacter baumannii Species 0.000 claims description 4
- 241000186046 Actinomyces Species 0.000 claims description 4
- 241000186041 Actinomyces israelii Species 0.000 claims description 4
- 241000193830 Bacillus <bacterium> Species 0.000 claims description 4
- 241000588807 Bordetella Species 0.000 claims description 4
- 241000589562 Brucella Species 0.000 claims description 4
- 241000589567 Brucella abortus Species 0.000 claims description 4
- 241000589876 Campylobacter Species 0.000 claims description 4
- 241000589874 Campylobacter fetus Species 0.000 claims description 4
- 241000589875 Campylobacter jejuni Species 0.000 claims description 4
- 241001647378 Chlamydia psittaci Species 0.000 claims description 4
- 241000606153 Chlamydia trachomatis Species 0.000 claims description 4
- 241000193468 Clostridium perfringens Species 0.000 claims description 4
- 241000588914 Enterobacter Species 0.000 claims description 4
- 241000194033 Enterococcus Species 0.000 claims description 4
- 241000194032 Enterococcus faecalis Species 0.000 claims description 4
- 241000589602 Francisella tularensis Species 0.000 claims description 4
- 241000606790 Haemophilus Species 0.000 claims description 4
- 241000590002 Helicobacter pylori Species 0.000 claims description 4
- 241000588748 Klebsiella Species 0.000 claims description 4
- 241000186359 Mycobacterium Species 0.000 claims description 4
- 241000186367 Mycobacterium avium Species 0.000 claims description 4
- 241000187479 Mycobacterium tuberculosis Species 0.000 claims description 4
- 101150020251 NR13 gene Proteins 0.000 claims description 4
- 241000606860 Pasteurella Species 0.000 claims description 4
- 241000606697 Rickettsia prowazekii Species 0.000 claims description 4
- 241000606695 Rickettsia rickettsii Species 0.000 claims description 4
- 241000607142 Salmonella Species 0.000 claims description 4
- 241000607768 Shigella Species 0.000 claims description 4
- 241000191963 Staphylococcus epidermidis Species 0.000 claims description 4
- 241001478878 Streptobacillus Species 0.000 claims description 4
- 241000194017 Streptococcus Species 0.000 claims description 4
- 241000193985 Streptococcus agalactiae Species 0.000 claims description 4
- 241000193996 Streptococcus pyogenes Species 0.000 claims description 4
- 241000187747 Streptomyces Species 0.000 claims description 4
- 241000607598 Vibrio Species 0.000 claims description 4
- 241000607626 Vibrio cholerae Species 0.000 claims description 4
- 241000607272 Vibrio parahaemolyticus Species 0.000 claims description 4
- 241000607734 Yersinia <bacteria> Species 0.000 claims description 4
- 229940065181 bacillus anthracis Drugs 0.000 claims description 4
- 229940056450 brucella abortus Drugs 0.000 claims description 4
- 229940038705 chlamydia trachomatis Drugs 0.000 claims description 4
- 229940032049 enterococcus faecalis Drugs 0.000 claims description 4
- 229940118764 francisella tularensis Drugs 0.000 claims description 4
- 229940047650 haemophilus influenzae Drugs 0.000 claims description 4
- 229940037467 helicobacter pylori Drugs 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 claims description 4
- 229940046939 rickettsia prowazekii Drugs 0.000 claims description 4
- 229940075118 rickettsia rickettsii Drugs 0.000 claims description 4
- 229940031000 streptococcus pneumoniae Drugs 0.000 claims description 4
- 229940118696 vibrio cholerae Drugs 0.000 claims description 4
- 241000589155 Agrobacterium tumefaciens Species 0.000 claims description 3
- 241000193155 Clostridium botulinum Species 0.000 claims description 3
- 241000193449 Clostridium tetani Species 0.000 claims description 3
- 241000194031 Enterococcus faecium Species 0.000 claims description 3
- 241000588724 Escherichia coli Species 0.000 claims description 3
- 241000589989 Helicobacter Species 0.000 claims description 3
- 241000589242 Legionella pneumophila Species 0.000 claims description 3
- 241000588652 Neisseria gonorrhoeae Species 0.000 claims description 3
- 241000588650 Neisseria meningitidis Species 0.000 claims description 3
- 241000589517 Pseudomonas aeruginosa Species 0.000 claims description 3
- 241000191967 Staphylococcus aureus Species 0.000 claims description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
- 150000002460 imidazoles Chemical class 0.000 claims description 3
- 229940115932 legionella pneumophila Drugs 0.000 claims description 3
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 3
- OFGDSGVGRWPQJQ-UHFFFAOYSA-N 1h-imidazol-1-ium;acetate Chemical compound CC(O)=O.C1=CNC=N1 OFGDSGVGRWPQJQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 241001147691 Staphylococcus saprophyticus Species 0.000 claims description 2
- XLZJZZXLOKXEPC-UHFFFAOYSA-N bis(3-chlorophenyl)borinic acid;2-(2-hydroxypropan-2-yl)pyridin-3-ol Chemical compound CC(C)(O)C1=NC=CC=C1O.C=1C=CC(Cl)=CC=1B(O)C1=CC=CC(Cl)=C1 XLZJZZXLOKXEPC-UHFFFAOYSA-N 0.000 claims description 2
- FCDMYXKIWIKWJQ-UHFFFAOYSA-N bis(3-chlorophenyl)borinic acid;pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1.C=1C=CC(Cl)=CC=1B(O)C1=CC=CC(Cl)=C1 FCDMYXKIWIKWJQ-UHFFFAOYSA-N 0.000 claims description 2
- MELBLDSSBOYXAU-UHFFFAOYSA-N bis(4-chloro-2-methylphenyl)borinic acid Chemical compound CC1=CC(Cl)=CC=C1B(O)C1=CC=C(Cl)C=C1C MELBLDSSBOYXAU-UHFFFAOYSA-N 0.000 claims description 2
- UMGOXYOGGUCEPF-UHFFFAOYSA-N bis(4-chlorophenyl)borinic acid;2-(2-hydroxypropan-2-yl)pyridin-3-ol Chemical compound CC(C)(O)C1=NC=CC=C1O.C=1C=C(Cl)C=CC=1B(O)C1=CC=C(Cl)C=C1 UMGOXYOGGUCEPF-UHFFFAOYSA-N 0.000 claims description 2
- XVLHAJLVMXCATB-UHFFFAOYSA-N bis(4-chlorophenyl)borinic acid;pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1.C=1C=C(Cl)C=CC=1B(O)C1=CC=C(Cl)C=C1 XVLHAJLVMXCATB-UHFFFAOYSA-N 0.000 claims description 2
- KNMXUZFSCITFDI-UHFFFAOYSA-N bis(4-fluorophenyl)borinic acid Chemical compound C=1C=C(F)C=CC=1B(O)C1=CC=C(F)C=C1 KNMXUZFSCITFDI-UHFFFAOYSA-N 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 229910006069 SO3H Inorganic materials 0.000 claims 3
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 3
- BFLFGRWTMMDOJT-UHFFFAOYSA-N bis(3-chloro-4-methylphenyl)borinic acid;1-pyridin-2-ylethanol Chemical compound CC(O)C1=CC=CC=N1.C1=C(Cl)C(C)=CC=C1B(O)C1=CC=C(C)C(Cl)=C1 BFLFGRWTMMDOJT-UHFFFAOYSA-N 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 20
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 27
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 24
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- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 14
- CPRRHERYRRXBRZ-SRVKXCTJSA-N methyl n-[(2s)-1-[[(2s)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]carbamate Chemical compound COC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CO)C[C@@H]1CCNC1=O CPRRHERYRRXBRZ-SRVKXCTJSA-N 0.000 description 14
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
-
- 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
- A61P31/10—Antimycotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
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| US43437502P | 2002-12-18 | 2002-12-18 | |
| US43609502P | 2002-12-23 | 2002-12-23 | |
| US43784903P | 2003-01-03 | 2003-01-03 | |
| PCT/US2003/040982 WO2004056322A2 (en) | 2002-12-18 | 2003-12-18 | Antibiotics containing borinic acid complexes and methods of use |
Publications (1)
| Publication Number | Publication Date |
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| NZ540870A true NZ540870A (en) | 2008-09-26 |
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| NZ540870A NZ540870A (en) | 2002-12-18 | 2003-12-18 | Antibiotics containing borinic acid complexes and methods of use |
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| EP (2) | EP1581500A4 (enExample) |
| JP (2) | JP2006511613A (enExample) |
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| CN (1) | CN101928295A (enExample) |
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| BR (1) | BR0317564A (enExample) |
| CA (1) | CA2509645A1 (enExample) |
| MX (1) | MXPA05006685A (enExample) |
| NZ (1) | NZ540870A (enExample) |
| WO (1) | WO2004056322A2 (enExample) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN1325504C (zh) | 2002-01-10 | 2007-07-11 | 宾夕法尼亚州研究基金会 | 制备二芳基硼酸烷基酯和络合的二芳基硼酸的方法 |
| US7390806B2 (en) * | 2002-12-18 | 2008-06-24 | Anacor Pharmaceuticals, Inc. | Antibiotics containing borinic acid complexes and methods of use |
| MXPA05006685A (es) * | 2002-12-18 | 2005-12-14 | Anacor Pharmaceuticals Inc | Antibioticos que contienen complejos de acido borinico y metodos de uso. |
| AR049916A1 (es) * | 2004-06-14 | 2006-09-13 | Anacor Pharmaceuticals Inc | Usos anti-parasitarios de complejos de acido borinico |
| AR049915A1 (es) * | 2004-06-14 | 2006-09-13 | Anacor Pharmaceuticals Inc | Compuestos con contenido de boro y metodos de uso de los mismos |
| EP1765360B1 (en) | 2004-06-14 | 2009-11-11 | Anacor Pharmaceuticals, Inc. | Anti-viral uses of borinic acid complexes |
| US7767657B2 (en) | 2005-02-16 | 2010-08-03 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| ES2872962T3 (es) | 2005-02-16 | 2021-11-03 | Anacor Pharmaceuticals Inc | Boronoftalidas para uso terapéutico |
| MX2007011486A (es) * | 2005-03-24 | 2007-11-20 | Anacor Pharmaceuticals Inc | Formulaciones topicas de antibioticos de acido borinico y sus metodos de uso. |
| EP1965647A2 (en) * | 2005-12-28 | 2008-09-10 | Anacor Pharmaceuticals, Inc. | Process for manufacturing picolinate borinic esters |
| RU2642628C2 (ru) | 2006-02-16 | 2018-01-25 | Анакор Фармасьютикалз, Инк. | Бор-содержащие малые молекулы в качестве противовоспалительных средств |
| US20070286822A1 (en) * | 2006-06-12 | 2007-12-13 | Anacor Pharmaceuticals Inc. | Compounds for the Treatment of Periodontal Disease |
| BRPI0713010A2 (pt) * | 2006-06-12 | 2012-10-09 | Anacor Pharmaceuticals Inc | compostos para o tratamento de doença periodontal |
| EP2069370A4 (en) * | 2006-11-22 | 2011-05-04 | Anacor Pharmaceuticals Inc | MICRO-ORGANISMS KILLING COMPOUNDS |
| EP3246034A1 (en) | 2008-03-06 | 2017-11-22 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as anti-inflammatory agents |
| US20100256092A1 (en) * | 2008-05-12 | 2010-10-07 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| WO2010027975A1 (en) | 2008-09-04 | 2010-03-11 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| US8461336B2 (en) | 2008-09-04 | 2013-06-11 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| US9493489B2 (en) | 2008-10-15 | 2016-11-15 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as anti-protozoal agents |
| SG172040A1 (en) * | 2008-12-17 | 2011-07-28 | Anacor Pharmaceuticals Inc | Polymorphs of (s)-3-aminomethyl-7-(3-hydroxy-propoxy)-3h-benzo[c][1,2] oxaborol-1-ol |
| EP2458995A1 (en) | 2009-07-28 | 2012-06-06 | Anacor Pharmaceuticals, Inc. | Trisubstituted boron-containing molecules |
| AP4039A (en) | 2009-08-14 | 2017-02-28 | Daitao Chen | Boron-containing small molecules as antiprotozoal agents |
| US20110207701A1 (en) * | 2009-08-19 | 2011-08-25 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
| US20110124597A1 (en) * | 2009-09-25 | 2011-05-26 | Anacor Pharmaceuticals, Inc. | Boron containing small molecules |
| WO2011049971A1 (en) | 2009-10-20 | 2011-04-28 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
| US8461134B2 (en) * | 2009-11-11 | 2013-06-11 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| US8716478B2 (en) | 2010-01-27 | 2014-05-06 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| WO2011116348A1 (en) | 2010-03-19 | 2011-09-22 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as anti-protozoal agent |
| DK2613788T3 (en) | 2010-09-07 | 2017-08-07 | Anacor Pharmaceuticals Inc | BENZOXABOROLD DERIVATIVES FOR TREATMENT OF BACTERIA INFECTIONS |
| US8669207B1 (en) | 2013-01-30 | 2014-03-11 | Dow Agrosciences, Llc. | Compounds and compositions |
| AR094666A1 (es) | 2013-01-30 | 2015-08-19 | Dow Agrosciences Llc | Uso de benzoxaborolas como agentes antimicrobianos volátiles en carnes, plantas o partes de plantas |
| US10070649B2 (en) | 2013-01-30 | 2018-09-11 | Agrofresh Inc. | Volatile applications against pathogens |
| US11039617B2 (en) | 2013-01-30 | 2021-06-22 | Agrofresh Inc. | Large scale methods of uniformly coating packaging surfaces with a volatile antimicrobial to preserve food freshness |
| US9585396B2 (en) | 2013-01-30 | 2017-03-07 | Agrofresh Inc. | Volatile applications against pathogens |
| BR112016003692B1 (pt) * | 2013-08-20 | 2022-02-08 | 3M Innovative Properties Company | Complexo poliéter boro-silano |
| KR101756785B1 (ko) * | 2015-03-10 | 2017-07-12 | 한국화학연구원 | 4배위 유기 붕소 화합물의 제조방법 |
| WO2017155879A1 (en) | 2016-03-07 | 2017-09-14 | Agrofresh Inc. | Synergistic methods of using benzoxaborole compounds and preservative gases as an antimicrobial for crops |
| US11447506B2 (en) | 2016-05-09 | 2022-09-20 | Anacor Pharmaceuticals, Inc. | Crystal forms of crisaborole in free form and preparation method and use thereof |
| IL248150B (en) | 2016-09-29 | 2018-05-31 | Garti Nissim | Method for selective extraction of cannabinoids from a plant source |
| IL248149B (en) | 2016-09-29 | 2020-03-31 | Garti Nissim | Dilutable formulations of cannbinoids and processes for their preparation |
| EP3522892A4 (en) * | 2016-10-05 | 2020-05-13 | The Global Alliance for TB Drug Development, Inc. | HETEROARYL TRIFLUORBORATE COMPOUNDS FOR TREATING MYCOBACTERIAL INFECTIONS |
| US10961261B2 (en) | 2017-03-01 | 2021-03-30 | Anacor Pharmaceuticals, Inc. | Oxaborole analogs and uses thereof |
| CA3054138A1 (en) * | 2017-03-09 | 2018-09-13 | The Penn State Research Foundation | Boron-containing small molecules for inhibiting activity of a receptor-like protein tyrosine phosphatase |
| EP3840637B1 (en) * | 2018-08-20 | 2025-08-06 | Senseonics, Incorporated | Mediated drug release for reducing in vivo analyte indicator degradation |
| WO2022043936A1 (en) | 2020-08-31 | 2022-03-03 | Pfizer Inc. | Methods of protecting rna |
| US12357552B2 (en) | 2021-03-09 | 2025-07-15 | Juris GERMANAS | Hydroxyquinoline compounds and methods of use as pigment modifying agents |
Family Cites Families (12)
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| EP0496757B1 (de) * | 1989-10-18 | 1995-07-12 | Hoechst Schering AgrEvo GmbH | Verfahren zur bekämpfung von schadpflanzen in reis |
| US5348947A (en) * | 1993-05-07 | 1994-09-20 | American Cyanamid Company | Diarylboron ester and thioester fungicidal agents |
| US5348948A (en) * | 1993-05-07 | 1994-09-20 | American Cyanamid Company | 2,2-diaryl-1-(oxa and thia)-2a-azonia-2-borataacenaphthene fungicidal |
| JPH0952893A (ja) * | 1995-08-10 | 1997-02-25 | Yoshitomi Pharmaceut Ind Ltd | キノロンカルボン酸誘導体の工業的な製造法およびその合成中間体 |
| DE19829947A1 (de) * | 1998-07-04 | 2000-01-05 | Bayer Ag | Elektrolumineszierende Anordnungen mit Bor-Chelaten |
| EP1155698A4 (en) * | 1999-01-29 | 2003-01-15 | Nitto Kasei Co Ltd | ORGANOBORAL COMPOUNDS HAVING COCCIDIOSTAT ACTIVITY |
| CN1370170A (zh) * | 1999-05-25 | 2002-09-18 | 宾夕法尼亚州研究基金会 | Dna甲基转移酶抑制剂 |
| DE10110051C2 (de) * | 2001-03-02 | 2003-07-03 | Clariant Gmbh | Verfahren zur Herstellung von Boron- und Borinsäuren |
| JP2002322007A (ja) * | 2001-04-27 | 2002-11-08 | Shionogi & Co Ltd | 有機ホウ素化合物を含有する植物用殺線虫剤 |
| CN1325504C (zh) * | 2002-01-10 | 2007-07-11 | 宾夕法尼亚州研究基金会 | 制备二芳基硼酸烷基酯和络合的二芳基硼酸的方法 |
| MXPA05006685A (es) * | 2002-12-18 | 2005-12-14 | Anacor Pharmaceuticals Inc | Antibioticos que contienen complejos de acido borinico y metodos de uso. |
| US7390806B2 (en) * | 2002-12-18 | 2008-06-24 | Anacor Pharmaceuticals, Inc. | Antibiotics containing borinic acid complexes and methods of use |
-
2003
- 2003-12-18 MX MXPA05006685A patent/MXPA05006685A/es active IP Right Grant
- 2003-12-18 CN CN2010101656749A patent/CN101928295A/zh active Pending
- 2003-12-18 AU AU2003299821A patent/AU2003299821B2/en not_active Ceased
- 2003-12-18 KR KR1020057011194A patent/KR20050084378A/ko not_active Ceased
- 2003-12-18 EP EP03800095A patent/EP1581500A4/en not_active Withdrawn
- 2003-12-18 JP JP2005502662A patent/JP2006511613A/ja not_active Withdrawn
- 2003-12-18 US US10/740,304 patent/US20040224923A1/en not_active Abandoned
- 2003-12-18 WO PCT/US2003/040982 patent/WO2004056322A2/en not_active Ceased
- 2003-12-18 NZ NZ540870A patent/NZ540870A/en not_active IP Right Cessation
- 2003-12-18 CA CA002509645A patent/CA2509645A1/en not_active Abandoned
- 2003-12-18 EP EP08155302A patent/EP1980564A1/en not_active Withdrawn
- 2003-12-18 BR BR0317564-2A patent/BR0317564A/pt not_active IP Right Cessation
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2007
- 2007-09-06 US US11/851,259 patent/US20080146803A1/en not_active Abandoned
-
2009
- 2009-02-02 JP JP2009021716A patent/JP2009161540A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US20040224923A1 (en) | 2004-11-11 |
| EP1980564A1 (en) | 2008-10-15 |
| AU2003299821A1 (en) | 2004-07-14 |
| EP1581500A2 (en) | 2005-10-05 |
| CA2509645A1 (en) | 2004-07-08 |
| EP1581500A4 (en) | 2008-03-05 |
| MXPA05006685A (es) | 2005-12-14 |
| KR20050084378A (ko) | 2005-08-26 |
| WO2004056322A3 (en) | 2004-09-16 |
| WO2004056322A2 (en) | 2004-07-08 |
| CN101928295A (zh) | 2010-12-29 |
| US20080146803A1 (en) | 2008-06-19 |
| AU2003299821B2 (en) | 2010-02-18 |
| JP2009161540A (ja) | 2009-07-23 |
| JP2006511613A (ja) | 2006-04-06 |
| BR0317564A (pt) | 2005-11-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RENW | Renewal (renewal fees accepted) | ||
| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) | ||
| LAPS | Patent lapsed |