MA39809A - Derives de nucleoside substitues en 4' en tant qu'inhibiteurs de la transcriptase inverse du vih - Google Patents

Derives de nucleoside substitues en 4' en tant qu'inhibiteurs de la transcriptase inverse du vih

Info

Publication number
MA39809A
MA39809A MA039809A MA39809A MA39809A MA 39809 A MA39809 A MA 39809A MA 039809 A MA039809 A MA 039809A MA 39809 A MA39809 A MA 39809A MA 39809 A MA39809 A MA 39809A
Authority
MA
Morocco
Prior art keywords
reverse transcriptase
transcriptase inhibitors
hiv reverse
substituted nucleoside
nucleoside derivatives
Prior art date
Application number
MA039809A
Other languages
English (en)
Other versions
MA39809B1 (fr
Inventor
Jianmin Fu
Vinay M Girijavallabhan
David B Olsen
Bing-Yu Tang
Zhibo Zhang
Original Assignee
Merck Sharp & Dohme
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=52824598&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA39809(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MA39809A publication Critical patent/MA39809A/fr
Publication of MA39809B1 publication Critical patent/MA39809B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/14—Pyrrolo-pyrimidine radicals
    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • 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
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06—Pyrimidine radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/12—Triazine radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Communicable Diseases (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA39809A 2014-03-28 2015-03-26 Derives de nucleoside substitues en 4' en tant qu'inhibiteurs de la transcriptase inverse du vih MA39809B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/CN2014/074294 WO2015143712A1 (fr) 2014-03-28 2014-03-28 Inhibiteurs nucléosidiques substitués en 4' de la transcriptase inverse
PCT/US2015/022621 WO2015148746A1 (fr) 2014-03-28 2015-03-26 Dérivés nucléosidiques 4'-substitués utilisés comme inhibiteurs de la transcriptase inverse du vih

Publications (2)

Publication Number Publication Date
MA39809A true MA39809A (fr) 2021-04-07
MA39809B1 MA39809B1 (fr) 2021-10-29

Family

ID=52824598

Family Applications (1)

Application Number Title Priority Date Filing Date
MA39809A MA39809B1 (fr) 2014-03-28 2015-03-26 Derives de nucleoside substitues en 4' en tant qu'inhibiteurs de la transcriptase inverse du vih

Country Status (41)

Country Link
US (2) US9777035B2 (fr)
EP (1) EP3122752B1 (fr)
JP (1) JP6182680B2 (fr)
KR (1) KR101961009B1 (fr)
CN (1) CN106795199B (fr)
AP (1) AP2016009482A0 (fr)
AR (1) AR099788A1 (fr)
AU (2) AU2015236018B2 (fr)
CA (1) CA2943792C (fr)
CL (1) CL2016002414A1 (fr)
CR (1) CR20160451A (fr)
CY (1) CY1124829T1 (fr)
DK (1) DK3122752T3 (fr)
DO (1) DOP2016000265A (fr)
EA (1) EA031476B1 (fr)
EC (1) ECSP16085206A (fr)
ES (1) ES2894228T3 (fr)
GE (1) GEP20197009B (fr)
GT (1) GT201600201A (fr)
HR (1) HRP20211622T1 (fr)
HU (1) HUE056913T2 (fr)
IL (1) IL247923B (fr)
JO (1) JO3636B1 (fr)
LT (1) LT3122752T (fr)
MA (1) MA39809B1 (fr)
MD (1) MD4812C1 (fr)
MX (1) MX367058B (fr)
MY (1) MY194635A (fr)
NI (1) NI201600145A (fr)
NZ (1) NZ724343A (fr)
PE (1) PE20170197A1 (fr)
PH (1) PH12016501897A1 (fr)
PL (1) PL3122752T3 (fr)
PT (1) PT3122752T (fr)
RS (1) RS62418B1 (fr)
SG (1) SG11201608031PA (fr)
SI (1) SI3122752T1 (fr)
SV (1) SV2016005290A (fr)
TW (1) TWI660967B (fr)
UA (1) UA120758C2 (fr)
WO (2) WO2015143712A1 (fr)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA41213A (fr) * 2014-12-19 2017-10-24 Alios Biopharma Inc Nucléosides substitués, nucléotides et analogues de ceux-ci
CR20180101A (es) 2015-08-13 2018-04-12 Merck Sharp & Dohme Compuestos di-nucleóticos cíclicos como agonistas de sting
US11453697B1 (en) 2015-08-13 2022-09-27 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
RU2720811C2 (ru) * 2015-09-23 2020-05-13 Мерк Шарп И Доум Лимитед 4'-замещенные нуклеозидные ингибиторы обратной транскриптазы и их получение
JOP20170038B1 (ar) 2016-02-12 2021-08-17 Merck Sharp & Dohme مركبات للاستخدام لعلاج عدوى بفيروس hiv والوقاية منه
TW201803871A (zh) 2016-06-24 2018-02-01 英塞特公司 作為ＰＩ３Ｋ-γ抑制劑之雜環化合物
CN110036001B (zh) 2016-10-04 2022-03-22 默沙东公司 作为STING激动剂的苯并[b]噻吩化合物
JP7125714B2 (ja) * 2016-12-13 2022-08-25 ヤマサ醤油株式会社 抗ウイルス活性を有する２’－デオキシ－７－デアザプリンヌクレオシド誘導体
EP3621624B1 (fr) 2017-05-12 2023-08-30 Merck Sharp & Dohme LLC Composés dinucléotidiques cycliques en tant qu'agonistes sting
US11312772B2 (en) 2017-08-04 2022-04-26 Merck Sharp & Dohme Corp. Combinations of PD-1 antagonists and benzo [b] thiophene STING agonists for cancer treatment
CA3071538A1 (fr) 2017-08-04 2019-02-07 Merck Sharp & Dohme Corp. Agonistes benzo[b]thiophene de sting pour le traitement du cancer
MA50172A (fr) 2017-09-18 2021-04-07 Janssen Biopharma Inc Nucléosides substitués, nucléotides et analogues de ceux-ci
EP3727401A4 (fr) 2017-12-20 2022-04-06 Merck Sharp & Dohme Corp. Composés dinucléotidiques cycliques utilisés comme agonistes sting
CN111971284A (zh) * 2017-12-27 2020-11-20 埃默里大学 核苷和/或nadph氧化酶(nox)抑制剂作为髓样特异性抗病毒剂的联合模式
WO2019171285A1 (fr) * 2018-03-07 2019-09-12 Glaxosmithkline Intellectual Property (No.2) Limited Composés utiles dans la thérapie du vih
WO2019195063A1 (fr) 2018-04-03 2019-10-10 Merck Sharp & Dohme Corp. Composés aza-benzothiophènes utilisés en tant qu'agonistes de sting
BR112020020085A8 (pt) 2018-04-03 2023-04-11 Merck Sharp & Dohme Composto, composição farmacêutica, e, métodos para induzir uma resposta imune, para induzir produção de interferons de tipo i dependentes de sting e para tratar um distúrbio de proliferação celular
WO2020014041A1 (fr) * 2018-07-09 2020-01-16 Merck Sharp & Dohme Corp. Synthèse enzymatique d'analogues de nucléosides de type 4'-éthynyle
MA53280A (fr) * 2018-08-09 2021-11-17 Glaxosmithkline Ip No 2 Ltd Composés utiles dans la thérapie du vih
WO2020154656A1 (fr) 2019-01-25 2020-07-30 Brown University Compositions et procédés pour traiter, prévenir ou inverser une inflammation et des troubles associés à l'âge
EP3934760A1 (fr) * 2019-03-06 2022-01-12 GlaxoSmithKline Intellectual Property (No.2) Limited Composés utiles dans la thérapie du vih
CN110054654B (zh) * 2019-05-27 2022-12-27 武汉百科药物开发有限公司 一种地西他滨中间体α-取代脱氧核糖的合成方法
CN114793421B (zh) * 2019-09-11 2024-09-13 斯克里普斯研究所 抗病毒前体药物及其药物组合物
MX2022006940A (es) * 2019-12-09 2022-07-11 Viiv Healthcare Co Composiciones farmaceuticas.
TW202245800A (zh) 2020-02-18 2022-12-01 美商基利科學股份有限公司 抗病毒化合物
CN118598916A (zh) 2020-02-18 2024-09-06 吉利德科学公司 抗病毒化合物
CN112321589B (zh) * 2020-02-18 2022-05-03 山东科巢生物制药有限公司 一种抗病毒药物瑞德西韦及其中间体的合成方法
TW202322824A (zh) 2020-02-18 2023-06-16 美商基利科學股份有限公司 抗病毒化合物
WO2021188959A1 (fr) 2020-03-20 2021-09-23 Gilead Sciences, Inc. Promédicaments de nucléosides de 4'-c-substitué-2-halo-2'-désoxyadénosine et leurs procédés de fabrication et d'utilisation
CN112778310A (zh) * 2020-04-20 2021-05-11 中国科学院上海药物研究所 核苷类似物或含有核苷类似物的组合制剂在抗病毒中的应用
CN113527303B (zh) * 2020-04-21 2022-06-10 浙江工业大学 一种瑞德西韦母核中间体的制备工艺
CN113637041B (zh) * 2020-05-11 2024-02-27 上海科胜药物研发有限公司 一种核糖核苷的制备方法
WO2022031894A1 (fr) 2020-08-07 2022-02-10 Gilead Sciences, Inc. Promédicaments d'analogues nucléotidiques de phosphonamide et leur utilisation pharmaceutique
WO2022074391A1 (fr) 2020-10-08 2022-04-14 Storm Therapeutics Limited Composés inhibiteurs de mettl3
CN112300236A (zh) * 2020-10-21 2021-02-02 佛山科学技术学院 核苷酸混合氨基磷酸酯化合物、其药物组合物及其应用
WO2022159877A1 (fr) 2021-01-25 2022-07-28 Brii Biosciences, Inc. Polythérapie contre le vih comprenant un dérivé d'adénosine et des inhibiteurs de capside
EP4281081A1 (fr) 2021-01-25 2023-11-29 Brii Biosciences, Inc. Dérivé d'adénosine et composition pharmaceutique le comprenant
WO2022221514A1 (fr) 2021-04-16 2022-10-20 Gilead Sciences, Inc. Procédés de préparation de carbanucléosides à l'aide d'amides
IL310854A (en) 2021-08-20 2024-04-01 Shionogi & Co Nucleoside compounds and their drug derivatives possessing viral growth inhibitory activity
EP4405357A1 (fr) 2021-09-23 2024-07-31 Katholieke Universiteit Leuven KU Leuven Research & Development Analogues de ribonucléosides dirigés contre le sars-cov-2
US20240287124A1 (en) 2023-01-30 2024-08-29 Merck Sharp & Dohme Llc Prodrugs of 4'-substituted nucleoside reverse transcriptase inhibitors

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5681941A (en) 1990-01-11 1997-10-28 Isis Pharmaceuticals, Inc. Substituted purines and oligonucleotide cross-linking
KR927003044A (ko) 1990-01-11 1992-12-17 크리스토퍼 케이. 미라벨리 Rna 활성과 유전자 발현을 검출하고 조절하는 조성물 및 그 방법
ATE271063T1 (de) 1996-10-16 2004-07-15 Icn Pharmaceuticals Purin-l-nukleoside, deren analoga und verwendungen
DE60005501T2 (de) 1999-05-12 2004-06-24 Yamasa Corp., Choshi 4'-c-ethynyl-pyrimidine nukleoside
US6831069B2 (en) 1999-08-27 2004-12-14 Ribapharm Inc. Pyrrolo[2,3-d]pyrimidine nucleoside analogs
WO2003062256A1 (fr) 2002-01-17 2003-07-31 Ribapharm Inc. Analogues d'adenosine 2'-beta-modifiee-6-substituee et leur utilisation en tant qu'agents antiviraux
WO2003099840A1 (fr) 2002-05-24 2003-12-04 Isis Pharmaceuticals, Inc. Oligonucleotides a unites nucleosidiques modifiees
US20040229839A1 (en) 2003-05-14 2004-11-18 Biocryst Pharmaceuticals, Inc. Substituted nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases
WO2004106356A1 (fr) 2003-05-27 2004-12-09 Syddansk Universitet Derives de nucleotides fonctionnalises
WO2005003047A1 (fr) 2003-07-03 2005-01-13 Philips Intellectual Property & Standards Gmbh Vitre pouvant etre chauffee par une lumiere invisible
CA2502109C (fr) 2004-03-24 2010-02-23 Yamasa Corporation Derive de 2-haloadenosine avec substitution sur le carbone en position 4'
WO2007095269A2 (fr) 2006-02-14 2007-08-23 Merck & Co., Inc. phosphoramidates d'aryle nucleosidiques pour le traitement d'infections ribovirales dependantes de l'arn
US7960569B2 (en) 2006-10-17 2011-06-14 Bristol-Myers Squibb Company Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
US20080261913A1 (en) 2006-12-28 2008-10-23 Idenix Pharmaceuticals, Inc. Compounds and pharmaceutical compositions for the treatment of liver disorders
CN101003550B (zh) * 2006-12-30 2010-05-19 河南省分析测试研究中心 8-卤代腺嘌呤类核苷化合物、合成方法和其药物用途
MX2009007333A (es) 2007-01-12 2009-08-31 Biocryst Pharm Inc Analogos de nucleosidos antivirales.
CN100532388C (zh) * 2007-07-16 2009-08-26 郑州大学 2’-氟-4’-取代-核苷类似物、其制备方法及应用
US20090318380A1 (en) 2007-11-20 2009-12-24 Pharmasset, Inc. 2',4'-substituted nucleosides as antiviral agents
MX2010011659A (es) 2008-04-23 2010-11-30 Gilead Sciences Inc Analogos de carba-nucleosido para tratamiento antiviral.
WO2010036407A2 (fr) 2008-05-15 2010-04-01 Biocryst Pharmaceuticals, Inc. Analogues nucléosidiques antiviraux
EP2313102A2 (fr) 2008-07-03 2011-04-27 Biota Scientific Management Nucléosides bicycliques et nucléotides convenant comme agents thérapeutiques
GB0815968D0 (en) 2008-09-03 2008-10-08 Angeletti P Ist Richerche Bio Antiviral agents
CN102216316A (zh) 2008-09-05 2011-10-12 寿制药株式会社 取代胺衍生物及以其为有效成分的药物组合物
EA201100851A1 (ru) 2008-12-23 2012-04-30 Фармассет, Инк. Аналоги нуклеозидов
CL2009002207A1 (es) 2008-12-23 2011-02-18 Gilead Pharmasset Llc Compuestos derivados de 3-hidroxi-5-(9h-purin-9-il)tetrahidrofuran-2-il, inhibidor de la replicacion de arn viral dependiente de arn; composicion farmaceutica; uso para el tratamiento de hepatitis c.
DE102009000180A1 (de) 2009-01-13 2010-07-15 Evonik Degussa Gmbh Verfahren zur Herstellung von mehrschichtig beschichteten Gummipartikeln und mehrschichtig beschichtete Gummipartikel
GB0900914D0 (en) 2009-01-20 2009-03-04 Angeletti P Ist Richerche Bio Antiviral agents
CN102421293A (zh) 2009-03-20 2012-04-18 艾丽奥斯生物制药有限公司 取代的核苷和核苷酸类似物
WO2011005860A2 (fr) 2009-07-07 2011-01-13 Alnylam Pharmaceuticals, Inc. Mimétiques de 5' phosphate
CA2782889C (fr) 2009-12-17 2014-08-05 Merck Canada Inc. Aminopyrimidines en tant qu'inhibiteurs de la syk
MX2012013824A (es) 2010-05-28 2013-03-12 Biocryst Pharm Inc Compuestos heterociclicos como inhibidores de cinasa janus.
ES2524356T3 (es) 2010-07-22 2014-12-05 Gilead Sciences, Inc. Métodos y compuestos para tratar infecciones provocadas por virus Paramyxoviridae
TW201305185A (zh) 2010-09-13 2013-02-01 Gilead Sciences Inc 用於抗病毒治療之２’－氟取代之碳－核苷類似物
JP6242378B2 (ja) * 2012-03-13 2017-12-06 ギリアード サイエンシーズ， インコーポレイテッド 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体
UA119050C2 (uk) * 2013-11-11 2019-04-25 Ґілеад Саєнсиз, Інк. ПІРОЛО[1.2-f][1.2.4]ТРИАЗИНИ, ЯКІ ВИКОРИСТОВУЮТЬСЯ ДЛЯ ЛІКУВАННЯ РЕСПІРАТОРНО-СИНЦИТІАЛЬНИХ ВІРУСНИХ ІНФЕКЦІЙ

Also Published As

Publication number Publication date
ECSP16085206A (es) 2017-08-31
IL247923B (en) 2021-01-31
RS62418B1 (sr) 2021-10-29
UA120758C2 (uk) 2020-02-10
NI201600145A (es) 2016-10-27
EP3122752B1 (fr) 2021-08-25
CN106795199B (zh) 2020-01-10
WO2015148746A1 (fr) 2015-10-01
DOP2016000265A (es) 2017-04-30
MD20160117A2 (ro) 2017-02-28
CA2943792A1 (fr) 2015-10-01
AU2017225090B2 (en) 2018-08-09
PT3122752T (pt) 2021-10-20
AU2017225090A1 (en) 2017-09-28
PH12016501897A1 (en) 2016-12-19
CY1124829T1 (el) 2022-11-25
CR20160451A (es) 2016-12-06
EA031476B1 (ru) 2019-01-31
TW201619180A (zh) 2016-06-01
PL3122752T3 (pl) 2022-01-03
TWI660967B (zh) 2019-06-01
AP2016009482A0 (en) 2016-10-31
EP3122752A1 (fr) 2017-02-01
DK3122752T3 (da) 2021-10-25
NZ724343A (en) 2020-02-28
JP2017512797A (ja) 2017-05-25
HUE056913T2 (hu) 2022-03-28
BR112016022438A2 (pt) 2017-08-15
SG11201608031PA (en) 2016-10-28
SV2016005290A (es) 2018-05-03
ES2894228T3 (es) 2022-02-14
KR101961009B1 (ko) 2019-03-21
AU2015236018A1 (en) 2016-10-06
EA201691931A1 (ru) 2017-02-28
GT201600201A (es) 2018-12-18
AU2015236018B2 (en) 2017-09-28
MX367058B (es) 2019-08-02
US20180002366A1 (en) 2018-01-04
WO2015143712A1 (fr) 2015-10-01
CL2016002414A1 (es) 2017-05-05
MX2016012659A (es) 2016-12-14
IL247923A0 (en) 2016-11-30
US9777035B2 (en) 2017-10-03
CA2943792C (fr) 2020-02-25
GEP20197009B (en) 2019-08-12
MY194635A (en) 2022-12-08
SI3122752T1 (sl) 2021-11-30
MD4812C1 (ro) 2023-01-31
JP6182680B2 (ja) 2017-08-16
MA39809B1 (fr) 2021-10-29
KR20160128437A (ko) 2016-11-07
AR099788A1 (es) 2016-08-17
PE20170197A1 (es) 2017-03-22
US20150274767A1 (en) 2015-10-01
CN106795199A (zh) 2017-05-31
HRP20211622T1 (hr) 2022-03-04
BR112016022438A8 (pt) 2021-06-29
LT3122752T (lt) 2021-11-10
MD4812B1 (ro) 2022-06-30
JO3636B1 (ar) 2020-08-27

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