BR112014029368A2 - inibidor de beta-lactamase e processo para preparar o mesmo - Google Patents
inibidor de beta-lactamase e processo para preparar o mesmoInfo
- Publication number
- BR112014029368A2 BR112014029368A2 BR112014029368A BR112014029368A BR112014029368A2 BR 112014029368 A2 BR112014029368 A2 BR 112014029368A2 BR 112014029368 A BR112014029368 A BR 112014029368A BR 112014029368 A BR112014029368 A BR 112014029368A BR 112014029368 A2 BR112014029368 A2 BR 112014029368A2
- Authority
- BR
- Brazil
- Prior art keywords
- lactamase
- same
- beta
- preparing
- lactamase inhibitor
- Prior art date
Links
- 239000003781 beta lactamase inhibitor Substances 0.000 title abstract 5
- 229940126813 beta-lactamase inhibitor Drugs 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- 229940126085 β‑Lactamase Inhibitor Drugs 0.000 title abstract 3
- 102000006635 beta-lactamase Human genes 0.000 abstract 3
- 208000035143 Bacterial infection Diseases 0.000 abstract 2
- 108020004256 Beta-lactamase Proteins 0.000 abstract 2
- 208000022362 bacterial infectious disease Diseases 0.000 abstract 2
- 241000894006 Bacteria Species 0.000 abstract 1
- 101100026178 Caenorhabditis elegans egl-3 gene Proteins 0.000 abstract 1
- 108090000204 Dipeptidase 1 Proteins 0.000 abstract 1
- 239000003782 beta lactam antibiotic agent Substances 0.000 abstract 1
- YZBQHRLRFGPBSL-RXMQYKEDSA-N carbapenem Chemical compound C1C=CN2C(=O)C[C@H]21 YZBQHRLRFGPBSL-RXMQYKEDSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000002132 β-lactam antibiotic Substances 0.000 abstract 1
- 229940124586 β-lactam antibiotics Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
- A61K31/43—Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
- A61K31/546—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
resumo patente de invenção: "inibidor de beta-lactamase e processo para preparar o mesmo". a presente invenção refere-se a inibidores de ß-lactamase atualmente disponíveis que têm um efeito inadequado em comparação à ß-lactamase, que continuam a aumentar constatemente. há uma necessidade quanto a novos inibidores de ß-lactamase que podem ser usados no tratamento de infecções bacterianas causadas por bactérias resistentes que são atualmente difíceis de tratar e que produzem: ß-lactamase de classe c, ß-lactamase de espectro ampliado (esbl) que pertence às classes a e d; kpc-2, que decompõe até carbapenem, o último bastion de antibióticos de ß-lactam, que pertence à classe a; e similares. um composto mostrado por fórmula (i), um método para produzir o mesmo, um inibidor de ?-lactamase e um método para tratar infecções bacterianas são fornecidos.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012122603 | 2012-05-30 | ||
JP2012-122603 | 2012-05-30 | ||
PCT/JP2013/064971 WO2013180197A1 (ja) | 2012-05-30 | 2013-05-30 | 新規β-ラクタマーゼ阻害剤とその製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
BR112014029368A2 true BR112014029368A2 (pt) | 2017-06-27 |
BR112014029368B1 BR112014029368B1 (pt) | 2020-10-27 |
Family
ID=49673384
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112014029368-6A BR112014029368B1 (pt) | 2012-05-30 | 2013-05-30 | inibidor de beta-lactamase e processo para preparar o mesmo |
Country Status (29)
Country | Link |
---|---|
US (7) | US9181250B2 (pt) |
EP (1) | EP2857401B8 (pt) |
JP (1) | JP6265892B2 (pt) |
KR (1) | KR102108590B1 (pt) |
CN (3) | CN106967066B (pt) |
AR (2) | AR091222A1 (pt) |
AU (1) | AU2013268415B2 (pt) |
BR (1) | BR112014029368B1 (pt) |
CA (1) | CA2874279C (pt) |
CL (1) | CL2014003035A1 (pt) |
CO (1) | CO7151513A2 (pt) |
DK (1) | DK2857401T5 (pt) |
ES (1) | ES2758507T3 (pt) |
HK (3) | HK1222651A1 (pt) |
HU (1) | HUE046893T2 (pt) |
IL (1) | IL235944B (pt) |
MX (1) | MX366948B (pt) |
MY (1) | MY174523A (pt) |
NZ (1) | NZ701959A (pt) |
PH (1) | PH12014502683A1 (pt) |
PL (1) | PL2857401T3 (pt) |
PT (1) | PT2857401T (pt) |
RU (1) | RU2693898C2 (pt) |
SG (1) | SG10201605368UA (pt) |
SI (1) | SI2857401T1 (pt) |
TW (1) | TWI565707B (pt) |
UA (1) | UA117734C2 (pt) |
WO (1) | WO2013180197A1 (pt) |
ZA (1) | ZA201408455B (pt) |
Families Citing this family (57)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8772490B2 (en) | 2010-12-22 | 2014-07-08 | Meiji Seika Pharma Co., Ltd. | Optically active diazabicyclooctane derivatives and process for preparing the same |
US8796257B2 (en) | 2011-12-02 | 2014-08-05 | Naeja Pharmaceutical Inc. | Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors |
US9505761B2 (en) | 2011-12-02 | 2016-11-29 | Fedora Pharmaceuticals Inc. | Bicyclic compounds and their use as antibacterial agents and beta-lactamase inhibitors |
EP2831075B1 (en) | 2012-03-30 | 2017-11-08 | Merck Sharp & Dohme Corp. | 1,3,4-oxadiazole and 1,3,4-thiadiazole beta-lactamase inhibitors |
AR090539A1 (es) | 2012-04-02 | 2014-11-19 | Astrazeneca Ab | COMPUESTOS INHIBIDORES DE b LACTAMASA |
CA2874279C (en) | 2012-05-30 | 2021-03-16 | Meiji Seika Pharma Co., Ltd. | Diazabicyclooctane derivatives useful as .beta.-lactamase inhibitor and process for preparing the same |
ES2672100T3 (es) * | 2012-08-25 | 2018-06-12 | Wockhardt Limited | Derivados de 1,6-diazabiciclo[3,2,1]octano-7-ona y su uso en el tratamiento de infecciones bacterianas |
UA111925C2 (uk) * | 2012-12-11 | 2016-06-24 | Федора Фармасьютікалз Інк. | БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ |
WO2014152996A1 (en) | 2013-03-14 | 2014-09-25 | Cubist Pharmaceuticals, Inc. | Crystalline form of a beta-lactamase inhibitor |
NZ718009A (en) | 2013-09-24 | 2018-03-23 | Meiji Seika Pharma Co Ltd | Process for producing diazabicyclooctane derivative and intermediate thereof |
WO2015051101A1 (en) | 2013-10-02 | 2015-04-09 | Cubist Pharmaceuticals, Inc. | B-lactamase inhibitor picoline salt |
CN105612159A (zh) | 2013-10-08 | 2016-05-25 | 明治制果药业株式会社 | 二氮杂二环辛烷衍生物的结晶及其制备方法 |
ES2902456T3 (es) * | 2013-10-22 | 2022-03-28 | Wockhardt Ltd | Composiciones farmacéuticas que comprenden agentes antibacterianos |
US20160296502A1 (en) * | 2013-11-26 | 2016-10-13 | Wockhardt Limited | Antibacterial compositions |
EP3217979B8 (en) | 2014-01-21 | 2020-06-03 | Wockhardt Bio AG | Pharmaceutical compositions comprising antibacterial agents |
EP3097105B1 (en) * | 2014-01-21 | 2018-12-19 | Wockhardt Limited | 2-(1,3,4-oxadiazol-2-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane derivatives and their use as antibacterial agents |
IN2014MU01192A (pt) * | 2014-03-29 | 2015-10-02 | Wockhardt Ltd | |
WO2015159265A1 (en) * | 2014-04-18 | 2015-10-22 | Wockhardt Limited | Pharmaceutical compositions comprising antibacterial agents |
TWI690317B (zh) | 2014-11-17 | 2020-04-11 | 英商安特西醫療有限公司 | 用於治療抗藥性細菌感染之組合療法 |
EP3227306B1 (en) * | 2014-12-02 | 2020-07-15 | Merck Sharp & Dohme Corp. | Process for the preparation of tert-butyl 4-((2s,5r)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)piperidine-1-carboxylate and analogs thereof |
SG11201704576SA (en) | 2014-12-05 | 2017-07-28 | Meiji Seika Pharma Co Ltd | Method for producing crystals of diazabicyclooctane derivative and stable lyophilized preparation |
US20180243286A1 (en) * | 2015-01-24 | 2018-08-30 | Wockhardt Limited | Antibacterial compositions of a beta-lactamase inhibitor with a cephalosporin |
WO2016120752A1 (en) * | 2015-01-28 | 2016-08-04 | Wockhardt Limited | A process for preparation of (2s, 5r)-n-(2-amino ethoxy)-6-(sulfooxy)-7-oxo-1,6- diazabicyclo [3.2.1] octane-2-carboxamide |
JP2018510190A (ja) | 2015-03-31 | 2018-04-12 | ミュタビリスMutabilis | 複素環式化合物及びそれらの細菌感染症の予防または治療のための使用 |
WO2017002083A1 (en) * | 2015-07-02 | 2017-01-05 | Wockhardt Limited | Nitrogen containing bicyclic compounds and their use in treatment of bacterial infections |
MX2017013792A (es) * | 2015-09-16 | 2018-07-06 | Xuanzhu Pharma Co Ltd | INHIBIDORES DE íŸ-LACTAMASA Y USOS DE LOS MISMOS. |
US9951072B2 (en) | 2015-10-02 | 2018-04-24 | Legochem Biosciences, Inc. | Compositions and methods for inhibiting beta-lactamase |
WO2017081615A1 (en) * | 2015-11-09 | 2017-05-18 | Wockhardt Limited | 7-oxo -6-(sulfooxy)- 1,6-diazabicyclo [3.2.1] octane containing compounds and their use in treatment of bacterial infections |
JP6643484B2 (ja) * | 2015-12-11 | 2020-02-12 | ウォックハート リミテッド | 7−オキソ−6−(スルホオキシ)−1,6−ジアザビシクロ[3.2.1]オクタン−2−カルボキサミド含有化合物および細菌感染症の治療におけるそれらの使用 |
EP3411359B1 (en) | 2016-02-04 | 2021-10-13 | Merck Sharp & Dohme Corp. | Methods of preparing hydroxylamine derivatives useful in the preparation of anti-infective agents |
SG11201810725WA (en) | 2016-06-03 | 2018-12-28 | Medshine Discovery Inc | Novel β-lactamase inhibitors |
WO2017216763A1 (en) * | 2016-06-17 | 2017-12-21 | Wockhardt Limited | N-phenylalkoxy-7-oxo-6-sulfooxy-1,6-diazabicyclo[3.2.1]octane-2-carboxamide derivatives and their use as antibacterial agents |
WO2017216764A1 (en) * | 2016-06-17 | 2017-12-21 | Wockhardt Limited | N-(alkanoyl)-7-oxo-6-sulfooxy-1,6-diazabicyclo[3.2.1]octane-2-carbonylhydrazide derivatives and their use as antibacterial agents |
CN106397302B (zh) * | 2016-07-04 | 2019-02-26 | 中国药科大学 | 一种o-取代羟胺荧光衍生化试剂的制备与纯化方法 |
MA46242A (fr) | 2016-09-16 | 2019-07-24 | Entasis Therapeutics Ltd | Composés inhibiteurs de bêta-lactamase |
US10464937B2 (en) | 2016-09-19 | 2019-11-05 | Merck Sharp & Dohme Corp. | Process for preparing beta-lactamase inhibitor hydroxylurea intermediates |
US10208041B2 (en) * | 2016-10-07 | 2019-02-19 | Hoffman-La Roche Inc. | Diazabicyclooctane compounds |
CN106699756B (zh) * | 2016-12-30 | 2019-10-29 | 淄博鑫泉医药技术服务有限公司 | β内酰胺酶抑制剂阿维巴坦的合成方法 |
PE20200333A1 (es) | 2017-05-08 | 2020-02-14 | Entasis Therapeutics Inc | Compuestos y metodos para tratar infecciones bacterianas |
US10085999B1 (en) * | 2017-05-10 | 2018-10-02 | Arixa Pharmaceuticals, Inc. | Beta-lactamase inhibitors and uses thereof |
JP7179058B2 (ja) * | 2017-09-27 | 2022-11-28 | Meiji Seikaファルマ株式会社 | ジアザビシクロオクタン誘導体の剤形およびその生産プロセス |
US10759800B2 (en) | 2017-09-27 | 2020-09-01 | Fedora Pharmaceuticals Inc. | Crystalline forms of diazabicyclooctane derivatives and production process thereof |
EP3687993A1 (en) * | 2017-09-27 | 2020-08-05 | Meiji Seika Pharma Co., Ltd. | Pharmaceutical forms of diazabicyclooctane derivatives and manufacturing method thereof |
CN107941969B (zh) * | 2017-11-07 | 2021-03-02 | 中山奕安泰医药科技有限公司 | (2s,5r)-苯氧胺基哌啶-2-甲酰胺的检测方法 |
CN107907604B (zh) * | 2017-11-07 | 2021-01-22 | 中山奕安泰医药科技有限公司 | (2s,5r)-苯氧胺基哌啶-2-甲酸乙酯草酸盐的检测方法 |
CN107941944B (zh) * | 2017-11-23 | 2020-09-15 | 中山奕安泰医药科技有限公司 | 一种(2s,5r)-苄氧胺基哌啶-2-甲酸乙酯草酸盐的检测方法 |
JP6974614B2 (ja) | 2017-12-01 | 2021-12-01 | チールー ファーマシューティカル カンパニー、リミテッド | β−ラクタマーゼ阻害剤の結晶形およびその製造方法 |
CN109956941B (zh) * | 2017-12-25 | 2020-08-04 | 新发药业有限公司 | 一种阿维巴坦的简便制备方法 |
CN109970625B (zh) * | 2017-12-28 | 2021-02-26 | 新发药业有限公司 | 一种5r-苄氧氨基哌啶-2s-甲酸或其衍生物的制备方法 |
CN108362789B (zh) * | 2018-01-19 | 2020-09-01 | 珠海优润医药科技有限公司 | 一种阿维巴坦钠光学异构体的高效液相色谱检测方法 |
US11497731B2 (en) | 2018-05-14 | 2022-11-15 | National University Corporation Tokai National Higher Education And Research System | β-lactamase inhibitor |
US11905286B2 (en) | 2018-08-09 | 2024-02-20 | Antabio Sas | Diazabicyclooctanones as inhibitors of serine beta-lactamases |
JP7523354B2 (ja) | 2018-09-21 | 2024-07-26 | 株式会社エーピーアイ コーポレーション | アミノ酸誘導体の製造方法 |
CN111198266A (zh) * | 2020-01-09 | 2020-05-26 | 深圳市博奥通科生物制品有限公司 | 舒巴坦快速检测试剂盒 |
WO2023060369A1 (en) * | 2021-10-11 | 2023-04-20 | Ningxia Academy Of Agriculture And Forestry Sciences | Novel carbimidate substituted bicyclic compounds and their use as beta-lactamase inhibitors |
CN116023323A (zh) * | 2022-12-31 | 2023-04-28 | 浙江工业大学 | 一种阿维巴坦中间体的制备方法 |
CN116375706A (zh) * | 2023-02-22 | 2023-07-04 | 时森海(杭州)医药科技有限公司 | 阿维巴坦钠关键中间体及其制备方法 |
Family Cites Families (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6019759B2 (ja) | 1977-11-24 | 1985-05-17 | イ−ライ・リリ−・アンド・カンパニ− | 非経口投予用11115152139199東京都中央区京橋2丁目3番13号 |
GB1589317A (en) | 1977-11-24 | 1981-05-13 | Lilly Co Eli | Freeze drying cephalothin sodium |
JPS60255723A (ja) | 1984-05-31 | 1985-12-17 | Ono Pharmaceut Co Ltd | メシル酸ガベキサートの結晶性凍結乾燥製剤及びその製造方法 |
JPH07117533B2 (ja) | 1985-08-28 | 1995-12-18 | 株式会社生体科学研究所 | トランスフエリンおよびその用途 |
US20030220521A1 (en) | 1989-07-27 | 2003-11-27 | G.D. Searle & Co. | Renal-selective prodrugs for control of renal sympathetic nerve activity in the treatment of hypertension |
TW264475B (pt) | 1991-09-20 | 1995-12-01 | Takeda Pharm Industry Co Ltd | |
DE69416869T2 (de) * | 1993-12-29 | 1999-07-01 | Pfizer Inc., New York, N.Y. | Diazabicyclische neurokinin antagonisten |
JP2843444B2 (ja) | 1994-05-02 | 1999-01-06 | 塩野義製薬株式会社 | ピロリジルチオカルバペネム誘導体の結晶,該結晶を含む凍結乾燥製剤,およびその製造方法 |
US6111098A (en) | 1994-05-02 | 2000-08-29 | Shionogi & Co., Ltd. | Crystal of pyrrolidylthiocarbapenem derivative, lyophilized preparation containing said crystal, and process for producing the same |
DE19531874C1 (de) | 1995-08-30 | 1996-10-02 | Daimler Benz Ag | Seitenwandbaugruppe für eine Kraftfahrzeugkarosserie |
FR2812635B1 (fr) | 2000-08-01 | 2002-10-11 | Aventis Pharma Sa | Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens |
FR2825705B1 (fr) | 2001-06-08 | 2005-05-20 | Aventis Pharma Sa | Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens |
FR2835186B1 (fr) | 2002-01-28 | 2006-10-20 | Aventis Pharma Sa | Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases |
US7439253B2 (en) * | 2002-12-06 | 2008-10-21 | Novexel | Heterocyclic compounds, their preparation and their use as medicaments, in particular as antibacterials and beta-lactamase inhibitors |
FR2921060B1 (fr) | 2007-09-14 | 2012-06-15 | Novexel | Nouveau procede de preparation d'une piperidine disubsituee et nouveaux intermediaires |
KR100931039B1 (ko) * | 2007-10-05 | 2009-12-10 | 현대자동차주식회사 | 가변 밸브 장치 |
EP2666774B1 (en) * | 2008-01-18 | 2015-01-07 | Merck Sharp & Dohme Corp. | Beta-lactamase Inhibitors |
FR2930553B1 (fr) | 2008-04-29 | 2010-05-21 | Novexel | Composes azabicycliques, leur preparation et leur utilisation comme medicaments, notamment inhibiteurs de beta-lactamases |
FR2936798B1 (fr) | 2008-10-03 | 2012-09-28 | Novexel | Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens. |
US20120053350A1 (en) | 2009-04-30 | 2012-03-01 | Ian Mangion | Preparation of alkyl esters of n-protected oxo-azacycloalkylcarboxylic acids |
FR2951171A1 (fr) | 2009-10-09 | 2011-04-15 | Novexel | Nouveau sel de sodium d'un compose azabicyclique sous forme enantiomere cristallisee et nouvelles formes polymorphes et pseudopolymorphes ainsi que leur preparation |
US8496548B2 (en) | 2010-11-10 | 2013-07-30 | Martin T. Connolly | Wide-body arrow having tapered tail |
WO2012086241A1 (ja) | 2010-12-22 | 2012-06-28 | Meiji Seikaファルマ株式会社 | 光学活性なジアザビシクロオクタン誘導体およびその製造法 |
US8772490B2 (en) | 2010-12-22 | 2014-07-08 | Meiji Seika Pharma Co., Ltd. | Optically active diazabicyclooctane derivatives and process for preparing the same |
EP2678861B1 (en) * | 2011-02-22 | 2018-07-11 | Speak With Me, Inc. | Hybridized client-server speech recognition |
TWI565706B (zh) | 2011-06-17 | 2017-01-11 | 阿斯特捷利康公司 | 用於製備包括反-7-酮基-6-(磺酸氧基)-1,6-二氮雜雙環[3,2,1]辛烷-2-甲醯胺之雜環化合物及其鹽類之方法 |
DE102011111964A1 (de) * | 2011-08-31 | 2013-02-28 | Ixetic Bad Homburg Gmbh | Verdampfer-Wärmetauscher-Einheit |
US10158850B2 (en) * | 2011-08-25 | 2018-12-18 | Telefonaktiebolaget Lm Ericsson (Publ) | Depth map encoding and decoding |
CA2833241C (en) * | 2011-08-27 | 2015-05-12 | Wockhardt Limited | 1,6-diazabicyclo [3,2,1] octan-7-one derivatives and their use in the treatment of bacterial infections |
US9006230B2 (en) * | 2011-08-30 | 2015-04-14 | Wockhardt Ltd. | 1,6-diazabicyclo [3,2,1] octan-7-one derivatives and their use in the treatment of bacterial infections |
RU2569307C1 (ru) * | 2011-09-13 | 2015-11-20 | Вокхардт Лимитед | Азотсодержащие соединения и их применение |
US8796257B2 (en) | 2011-12-02 | 2014-08-05 | Naeja Pharmaceutical Inc. | Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors |
US9505761B2 (en) | 2011-12-02 | 2016-11-29 | Fedora Pharmaceuticals Inc. | Bicyclic compounds and their use as antibacterial agents and beta-lactamase inhibitors |
EP2831075B1 (en) * | 2012-03-30 | 2017-11-08 | Merck Sharp & Dohme Corp. | 1,3,4-oxadiazole and 1,3,4-thiadiazole beta-lactamase inhibitors |
CA2874279C (en) | 2012-05-30 | 2021-03-16 | Meiji Seika Pharma Co., Ltd. | Diazabicyclooctane derivatives useful as .beta.-lactamase inhibitor and process for preparing the same |
ES2672100T3 (es) * | 2012-08-25 | 2018-06-12 | Wockhardt Limited | Derivados de 1,6-diazabiciclo[3,2,1]octano-7-ona y su uso en el tratamiento de infecciones bacterianas |
UA111925C2 (uk) * | 2012-12-11 | 2016-06-24 | Федора Фармасьютікалз Інк. | БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ |
WO2014135931A1 (en) * | 2013-03-08 | 2014-09-12 | Wockhardt Limited | A process for preparation of (2s, 5r)-7-oxo-6-sulphooxy-2-[((3r)-piperidine-3-carbonyl)-hydrazino carbonyl]-1,6-diaza-bicyclo [3.2.1]- octane |
KR101774133B1 (ko) * | 2013-03-08 | 2017-09-01 | 욱크하르트 리미티드 | (2s, 5r)-7-옥소-6-술포옥시-2-[((3r)-피롤리딘-3-카보닐)-히드라지노 카보닐]-1,6-디아자-비사이클로[3.2.1]옥탄의 제조 방법 |
NZ718009A (en) * | 2013-09-24 | 2018-03-23 | Meiji Seika Pharma Co Ltd | Process for producing diazabicyclooctane derivative and intermediate thereof |
CN105612159A (zh) * | 2013-10-08 | 2016-05-25 | 明治制果药业株式会社 | 二氮杂二环辛烷衍生物的结晶及其制备方法 |
IN2014MU01192A (pt) * | 2014-03-29 | 2015-10-02 | Wockhardt Ltd | |
SG11201704576SA (en) | 2014-12-05 | 2017-07-28 | Meiji Seika Pharma Co Ltd | Method for producing crystals of diazabicyclooctane derivative and stable lyophilized preparation |
-
2013
- 2013-05-30 CA CA2874279A patent/CA2874279C/en active Active
- 2013-05-30 UA UAA201413987A patent/UA117734C2/uk unknown
- 2013-05-30 NZ NZ701959A patent/NZ701959A/en unknown
- 2013-05-30 JP JP2014518712A patent/JP6265892B2/ja active Active
- 2013-05-30 KR KR1020147036284A patent/KR102108590B1/ko active IP Right Grant
- 2013-05-30 US US14/404,288 patent/US9181250B2/en active Active
- 2013-05-30 PT PT137963575T patent/PT2857401T/pt unknown
- 2013-05-30 SG SG10201605368UA patent/SG10201605368UA/en unknown
- 2013-05-30 CN CN201710135016.7A patent/CN106967066B/zh active Active
- 2013-05-30 SI SI201331628T patent/SI2857401T1/sl unknown
- 2013-05-30 RU RU2014153856A patent/RU2693898C2/ru active
- 2013-05-30 MY MYPI2014703455A patent/MY174523A/en unknown
- 2013-05-30 CN CN201610210823.6A patent/CN105859609B/zh active Active
- 2013-05-30 EP EP13796357.5A patent/EP2857401B8/en active Active
- 2013-05-30 MX MX2014014653A patent/MX366948B/es active IP Right Grant
- 2013-05-30 HU HUE13796357A patent/HUE046893T2/hu unknown
- 2013-05-30 WO PCT/JP2013/064971 patent/WO2013180197A1/ja active Application Filing
- 2013-05-30 CN CN201380028457.7A patent/CN104334559B/zh active Active
- 2013-05-30 AR ARP130101913 patent/AR091222A1/es active IP Right Grant
- 2013-05-30 PL PL13796357T patent/PL2857401T3/pl unknown
- 2013-05-30 ES ES13796357T patent/ES2758507T3/es active Active
- 2013-05-30 AU AU2013268415A patent/AU2013268415B2/en active Active
- 2013-05-30 TW TW102119069A patent/TWI565707B/zh active
- 2013-05-30 DK DK13796357.5T patent/DK2857401T5/da active
- 2013-05-30 BR BR112014029368-6A patent/BR112014029368B1/pt active IP Right Grant
-
2014
- 2014-11-07 CL CL2014003035A patent/CL2014003035A1/es unknown
- 2014-11-18 ZA ZA2014/08455A patent/ZA201408455B/en unknown
- 2014-11-27 IL IL235944A patent/IL235944B/en active IP Right Grant
- 2014-12-01 PH PH12014502683A patent/PH12014502683A1/en unknown
- 2014-12-10 CO CO14271322A patent/CO7151513A2/es unknown
-
2015
- 2015-08-04 HK HK16110777.0A patent/HK1222651A1/zh unknown
- 2015-08-04 HK HK15107465.4A patent/HK1206746A1/xx unknown
- 2015-09-25 HK HK15109486.5A patent/HK1208862A1/xx unknown
- 2015-10-01 US US14/872,988 patent/US9708320B2/en active Active
-
2017
- 2017-05-01 US US15/583,238 patent/US10023573B2/en active Active
-
2018
- 2018-05-08 US US15/973,861 patent/US10556905B2/en active Active
-
2019
- 2019-10-22 US US16/660,682 patent/US11117896B2/en active Active
-
2021
- 2021-08-11 US US17/399,618 patent/US11731971B2/en active Active
- 2021-12-02 AR ARP210103352A patent/AR124237A2/es unknown
-
2023
- 2023-05-18 US US18/199,019 patent/US12103928B2/en active Active
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR112014029368A2 (pt) | inibidor de beta-lactamase e processo para preparar o mesmo | |
BR112013032711A2 (pt) | composições farmacêuticas compreendendo sulbactam e inibidor de beta-lactamase | |
CO2021015264A2 (es) | Inhibidores de dihidroorotato deshidrogenasa | |
WO2013122888A3 (en) | Methods of treating bacterial infections | |
CO6640320A2 (es) | Composición de control de fitoenfermedades y metodo de control de fitoenfermedades | |
DOP2010000218A (es) | Inhibidores de beta-lactamasa | |
EA201391390A1 (ru) | Циклопропиламины в качестве ингибиторов lsd | |
BR112017010132A2 (pt) | terapia combinada para tratamento de infecções bacterianas resistentes | |
BR112014003590A2 (pt) | processo para preparação de ternesite | |
MX2016016115A (es) | Metodo para tratar cancer usando una combinacion de inhibidores de chk1 y relacionado con atm y rad3 (atr). | |
AU2012321815A8 (en) | 1 - arylcarbonyl - 4 - oxy - piperidine compounds useful for the treatment of neurodegenerative diseases | |
BR112014004219A2 (pt) | pirano[3,2-d][1,3]tiazol como inibidores de glicosidase | |
PE20140966A1 (es) | Quinazolincarboxamida azetidinas | |
EA201491970A1 (ru) | Циклические мостиковые простые эфиры в качестве ингибиторов dgat1 | |
BR112014018756A8 (pt) | Processo para preparo de etil éster de ácido n-(4-ciclo-hexil-3-trifluorometil-benziloxi)-acetimídico | |
EA202091676A1 (ru) | Способ лечения потери костной массы альвеолярного отростка посредством применения антител к склеростину | |
BR112019003710A2 (pt) | inibidor de pde7, composto, composição farmacêutica, uso de um inibidor de pde7 ou de um composto, e, método para tratar ou prevenir uma doença que é melhorada pela inibição de pde7. | |
BR112012019561A2 (pt) | hetarilamino naftiridinas | |
BR112017023164A2 (pt) | composto, e, método de prevenir e/ou tratar a esteato-hepatite não alcoólica em um indivíduo em necessidade do mesmo | |
BR112013003121A2 (pt) | moduladores de trpv3 | |
BR112013023880A2 (pt) | vidro plano e processo para produzir o mesmo | |
MX348148B (es) | Metodo para promover el crecimiento de plantas. | |
WO2018125983A8 (en) | Oxopyridine derivatives useful as aminocarboxymuconate semialdehyde decarboxylase (acmsd) inhibitors | |
AU2016248387A8 (en) | Preparation and use of kinase inhibitor | |
BR112018002763A2 (pt) | método para cicatrização de ferimentos |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B07D | Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette] | ||
B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
B06I | Publication of requirement cancelled [chapter 6.9 patent gazette] |
Free format text: ANULADA A PUBLICACAO CODIGO 6.6.1 NA RPI NO 2462 DE 13/03/2018 POR TER SIDO INDEVIDA. |
|
B07E | Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette] |
Free format text: NOTIFICACAO DE ANUENCIA RELACIONADA COM O ART 229 DA LPI |
|
B06T | Formal requirements before examination [chapter 6.20 patent gazette] | ||
B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 30/05/2013, OBSERVADAS AS CONDICOES LEGAIS. |