MA43120A - Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih - Google Patents

Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih

Info

Publication number
MA43120A
MA43120A MA043120A MA43120A MA43120A MA 43120 A MA43120 A MA 43120A MA 043120 A MA043120 A MA 043120A MA 43120 A MA43120 A MA 43120A MA 43120 A MA43120 A MA 43120A
Authority
MA
Morocco
Prior art keywords
nitrogen containing
hiv replication
inhibitor activity
replication inhibitor
tricyclic derivative
Prior art date
Application number
MA043120A
Other languages
English (en)
Inventor
Toshiyuki Akiyama
Takashi Kawasuji
Akira Matsumura
Shuichi Sugiyama
Yoshinori Tamura
Yutaka Tomida
Original Assignee
Shionogi & Co
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
Application filed by Shionogi & Co filed Critical Shionogi & Co
Publication of MA43120A publication Critical patent/MA43120A/fr

Links

Classifications

    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4985—Pyrazines or piperazines ortho- or peri-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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
    • 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
    • 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
    • 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
    • C07D487/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/06—Peri-condensed systems
    • 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)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Virology (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
MA043120A 2015-05-29 2016-05-27 Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih MA43120A (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2015109547 2015-05-29
JP2015170222 2015-08-31
JP2015223036 2015-11-13
JP2016054215 2016-03-17

Publications (1)

Publication Number Publication Date
MA43120A true MA43120A (fr) 2018-09-05

Family

ID=57442245

Family Applications (1)

Application Number Title Priority Date Filing Date
MA043120A MA43120A (fr) 2015-05-29 2016-05-27 Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih

Country Status (16)

Country Link
US (2) US10494380B2 (fr)
EP (1) EP3305789A4 (fr)
JP (2) JP6614585B2 (fr)
KR (1) KR20180011267A (fr)
CN (2) CN107922423B (fr)
AU (1) AU2016271762B2 (fr)
BR (1) BR112017025367A2 (fr)
CA (1) CA2987384A1 (fr)
HK (1) HK1253539A1 (fr)
IL (1) IL255580B (fr)
MA (1) MA43120A (fr)
MX (1) MX2017015256A (fr)
RU (1) RU2720145C2 (fr)
SG (1) SG11201709634QA (fr)
TW (1) TWI700284B (fr)
WO (1) WO2016194806A1 (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11201506924YA (en) 2013-03-15 2015-09-29 Incyte Corp Tricyclic heterocycles as bet protein inhibitors
EP3019502B1 (fr) 2013-07-08 2017-05-17 Incyte Holdings Corporation Hétérocycles tricycliques en tant qu'inhibiteurs de protéines bet
US9399640B2 (en) 2013-11-26 2016-07-26 Incyte Corporation Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors
WO2015095492A1 (fr) 2013-12-19 2015-06-25 Incyte Corporation Hétérocycles tricycliques en tant qu'inhibiteurs des protéines bet
PL3134403T3 (pl) 2014-04-23 2020-07-13 Incyte Corporation 1H-pirolo[2,3-c]pirydyn-7(6H)-ony i pirazolo[3,4-c]pirydyn-7(6H)-ony jako inhibitory białek BET
JP6599979B2 (ja) 2014-09-15 2019-10-30 インサイト・コーポレイション Ｂｅｔタンパク質阻害剤として用いるための三環式複素環化合物
WO2017075377A1 (fr) 2015-10-29 2017-05-04 Incyte Corporation Forme solide amorphe d'un inhibiteur de protéine bet
CA3028689A1 (fr) 2016-06-20 2017-12-28 Incyte Corporation Formes cristallines solides d'un inhibiteur bet
JP6689013B2 (ja) * 2016-11-28 2020-04-28 塩野義製薬株式会社 含窒素３環性誘導体を含有する医薬組成物
WO2020151232A1 (fr) * 2019-01-23 2020-07-30 上海和誉生物医药科技有限公司 Dérivé de 1,2,3,4-tétrahydroquinoxaline, son procédé de préparation et son utilisation
EP4066839A4 (fr) * 2019-11-28 2023-12-27 Shionogi & Co., Ltd Agent pharmaceutique prophylactique et thérapeutique pour maladies infectieuses à vih, caractérisé en ce qu'il comprend une combinaison d'un inhibiteur d'intégrase et d'un agent anti-vih
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms
CN112409493B (zh) * 2020-08-12 2022-09-30 浙江工业大学 一种重组融合酶及其在乙醛酸甲酯合成中的应用
CN114075212B (zh) * 2020-08-14 2023-05-12 江苏恒瑞医药股份有限公司 稠合三环类衍生物、其制备方法及其在医药上的应用
LT4122926T (lt) * 2021-04-14 2025-07-25 Shionogi & Co., Ltd. Triazino dariniai, turintys virusų replikaciją slopinantį poveikį, ir juos apimanti farmacinė kompozicija

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5792774A (en) 1996-02-21 1998-08-11 Chiroscience Limited Quinolones and their therapeutic use
CA2241891A1 (fr) 1996-02-21 1997-08-21 Darwin Discovery Limited Quinolones et leur utilisation therapeutique
WO1997030999A1 (fr) * 1996-02-21 1997-08-28 Darwin Discovery Limited Quinolones et leur utilisation therapeutique
DE19946289A1 (de) 1999-09-28 2001-03-29 Basf Ag Benzodiazepin-Derivate, deren Herstellung und Anwendung
EP1309594B1 (fr) * 2000-08-08 2004-12-15 Sanofi-Aventis Derives de benzimidazole, leur preparation et leur application en therapeutique
US7026311B2 (en) 2002-01-10 2006-04-11 Abbott Gmbh & Co., Kg Dibenzodiazepine derivatives, their preparation and use
JP2004256531A (ja) 2003-02-07 2004-09-16 Takeda Chem Ind Ltd 三環性化合物、その製造法および用途
WO2004069834A1 (fr) * 2003-02-07 2004-08-19 Takeda Pharmaceutical Company Limited Compose tricyclique, procede de production et utilisation dudit compose
TW200637862A (en) 2005-01-10 2006-11-01 Tibotec Pharm Ltd 1,5,6-substituted-2-oxo-3-cyano-1,6a-diaza-tetrahydro-fluoranthenes
US20070032469A1 (en) 2005-08-05 2007-02-08 Astrazeneca Ab Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators
US7939545B2 (en) 2006-05-16 2011-05-10 Boehringer Ingelheim International Gmbh Inhibitors of human immunodeficiency virus replication
ES2402322T3 (es) 2007-11-15 2013-04-30 Gilead Sciences, Inc. Inhibidores de la replicación del virus de la inmunodeficiencia humana
ATE541841T1 (de) 2007-11-15 2012-02-15 Boehringer Ingelheim Int Inhibitoren der replikation des human immunodeficiency virus
ES2463720T3 (es) 2007-11-16 2014-05-29 Gilead Sciences, Inc. Inhibidores de la replicación del virus de inmunodeficiencia humana
EA019259B1 (ru) 2007-11-16 2014-02-28 Джилид Сайенсиз, Инк. Ингибиторы репликации вируса иммунодефицита человека
GB0908394D0 (en) 2009-05-15 2009-06-24 Univ Leuven Kath Novel viral replication inhibitors
US8338441B2 (en) * 2009-05-15 2012-12-25 Gilead Sciences, Inc. Inhibitors of human immunodeficiency virus replication
GB0913636D0 (en) 2009-08-05 2009-09-16 Univ Leuven Kath Novel viral replication inhibitors
SG181423A1 (en) 2009-12-23 2012-07-30 Univ Leuven Kath Novel antiviral compounds
MX2012015097A (es) 2010-07-02 2013-05-28 Gilead Sciences Inc Derivados de acido naft-2-ilacetico para tratar sida.
EP2588455B1 (fr) 2010-07-02 2018-04-04 Gilead Sciences, Inc. Dérivés de l'acide 2-quinolinyl-acétique en tant que composés antiviraux hiv
US8633200B2 (en) 2010-09-08 2014-01-21 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
KR20140003438A (ko) 2010-11-15 2014-01-09 카톨리에케 유니버시테이트 루벤 항바이러스성 축합 헤테로사이클릭 화합물
EP2640729B1 (fr) 2010-11-15 2016-12-21 VIIV Healthcare UK Limited Inhibiteurs de la réplication du vih
WO2012102985A1 (fr) 2011-01-24 2012-08-02 Glaxosmithkline Llc Composés d'isoquinoléine et procédés pour traiter le vih
EP2508511A1 (fr) 2011-04-07 2012-10-10 Laboratoire Biodim Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques
EP2511273B8 (fr) * 2011-04-15 2019-06-26 Hivih Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques
UA111841C2 (uk) 2011-04-21 2016-06-24 Гіліад Сайєнсіз, Інк. Сполуки бензотіазолу та їх фармацевтичне застосування
WO2013002357A1 (fr) 2011-06-30 2013-01-03 塩野義製薬株式会社 Inhibiteur de réplication du vih
WO2013012649A1 (fr) 2011-07-15 2013-01-24 Glaxosmithkline Llc Composés d'aza-indole et procédés pour traiter le vih
US8791108B2 (en) 2011-08-18 2014-07-29 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
EP2757887B1 (fr) 2011-09-22 2017-04-26 VIIV Healthcare UK Limited Composés pyrrolopyridinones et méthodes de traitement du vih
WO2013062028A1 (fr) 2011-10-25 2013-05-02 塩野義製薬株式会社 Inhibiteur de la réplication du vih
WO2013073875A1 (fr) 2011-11-15 2013-05-23 한국화학연구원 Dérivé antiviral inédit de pyrrolopyridine et son procédé de production
US9376392B2 (en) 2012-01-04 2016-06-28 Gilead Sciences, Inc. 2-(tert-butoxy)-2-(7-methylquinolin-6-yl) acetic acid derivatives for treating AIDS
US9284323B2 (en) 2012-01-04 2016-03-15 Gilead Sciences, Inc. Naphthalene acetic acid derivatives against HIV infection
US8629276B2 (en) 2012-02-15 2014-01-14 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
US9034882B2 (en) 2012-03-05 2015-05-19 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
US9006235B2 (en) 2012-03-06 2015-04-14 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
WO2013157622A1 (fr) 2012-04-19 2013-10-24 塩野義製薬株式会社 Inhibiteur de la réplication du vih
UY34750A (es) 2012-04-20 2013-11-29 Gilead Sciences Inc ?compuestos para el tratamiento del hiv, composiciones,métodos de preparación, intermediarios y métodos terapéuticos?.
CA2876370A1 (fr) * 2012-07-12 2014-01-16 Viiv Healthcare Uk Limited Composes et procedes de traitement du vih
US8906929B2 (en) 2012-08-16 2014-12-09 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
EP2716639A1 (fr) 2012-10-05 2014-04-09 Laboratoire Biodim Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques
EP2716632A1 (fr) 2012-10-05 2014-04-09 Laboratoire Biodim Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques
EP2719685A1 (fr) 2012-10-11 2014-04-16 Laboratoire Biodim Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques
TW201441197A (zh) 2013-01-31 2014-11-01 Shionogi & Co Ｈｉｖ複製抑制劑
WO2014164467A1 (fr) 2013-03-13 2014-10-09 Bristol-Myers Squibb Company Inhibiteurs de la réplication du virus de l'immunodéficience humaine
WO2014164409A1 (fr) 2013-03-13 2014-10-09 Bristol-Myers Squibb Company Inhibiteurs de la réplication du virus de l'immunodéficience humaine
JP2016512558A (ja) 2013-03-14 2016-04-28 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ ヒト免疫不全ウイルス複製の阻害剤
PT3107913T (pt) 2014-02-19 2018-09-28 Viiv Healthcare Uk No 5 Ltd Inibidores da replicação do vírus da imunodeficiência humana
WO2015147247A1 (fr) 2014-03-28 2015-10-01 塩野義製薬株式会社 Dérivé tricyclique présentant une activité inhibitrice de la réplication du vih
US9975906B2 (en) * 2014-05-16 2018-05-22 Shionogi & Co., Ltd. Tricyclic heterocycle derivatives having HIV replication inhibitory effect
WO2015179448A1 (fr) 2014-05-21 2015-11-26 Gilead Sciences, Inc. Composés thérapeutiques
TR201807217T4 (tr) 2014-07-08 2018-06-21 Viiv Healthcare Uk Ltd Bir viral enfeksiyon sahasının tedavisinde kullanım için izoindolin türevleri.
CA2954733A1 (fr) 2014-07-22 2016-01-28 Viiv Healthcare Uk Limited Derives d'isoindolinone utiles a titre d'agents antiviraux
US10065953B2 (en) 2014-08-27 2018-09-04 VIIV Healthcare UK (No.5) Limited Imidazo[1,2-A]pyridine derivatives for use as inhibitors of human immunodeficiency virus replication
TW201720798A (zh) 2015-09-17 2017-06-16 Ｖｉｉｖ醫療保健英國有限公司 苯并氮呯衍生物
JP2019501143A (ja) 2015-12-04 2019-01-17 ヴィーブ ヘルスケア ユーケー リミテッド テトラヒドロイソキノリン誘導体
JP2018536001A (ja) 2015-12-04 2018-12-06 ヴィーブ ヘルスケア ユーケー リミテッド イソインドリン誘導体
EP3383862A1 (fr) 2015-12-04 2018-10-10 ViiV Healthcare UK Limited Dérivés d'isoindoline
US20180327355A1 (en) 2015-12-04 2018-11-15 Viiv Healthcare Uk Limited Isoindoline derivatives

Also Published As

Publication number Publication date
CN111138458A (zh) 2020-05-12
IL255580A (en) 2018-01-31
JP2020097568A (ja) 2020-06-25
US10870661B2 (en) 2020-12-22
TWI700284B (zh) 2020-08-01
JPWO2016194806A1 (ja) 2018-03-22
EP3305789A4 (fr) 2018-11-21
AU2016271762A1 (en) 2017-11-30
TW201706275A (zh) 2017-02-16
KR20180011267A (ko) 2018-01-31
CN107922423B (zh) 2020-10-27
JP6797464B2 (ja) 2020-12-09
IL255580B (en) 2020-11-30
AU2016271762B2 (en) 2020-01-23
CN107922423A (zh) 2018-04-17
MX2017015256A (es) 2018-02-19
JP6614585B2 (ja) 2019-12-04
US20200055873A1 (en) 2020-02-20
SG11201709634QA (en) 2017-12-28
US20180162876A1 (en) 2018-06-14
EP3305789A1 (fr) 2018-04-11
US10494380B2 (en) 2019-12-03
RU2017145082A (ru) 2019-07-01
WO2016194806A1 (fr) 2016-12-08
CA2987384A1 (fr) 2016-12-08
BR112017025367A2 (pt) 2018-08-07
RU2720145C2 (ru) 2020-04-24
RU2017145082A3 (fr) 2019-10-24
HK1253539A1 (en) 2019-06-21

Similar Documents

Publication Publication Date Title
MA43120A (fr) Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih
EP3694846C0 (fr) Dérivés 1-benzyl-2-imino-4-phényl-5-oxoimidazolidine comme inhibiteurs de protéase de vih
EP3314590A4 (fr) Alerte de proximité d'articles
EA201692105A1 (ru) Новые пиразолопиримидиновые производные и их применение в качестве ингибиторов malt1
IL257379A (en) Diacerein or its analogs for inhibiting expression of asc, nlrp3, and/or formation of nlrp3 inflammasome complex
EP3501009A4 (fr) Tri dynamique d'opérations matricielles
EP3518934A4 (fr) Inhibiteurs de l'adénosine 5'-nucléotidase
ECSP16076566A (es) Compuestos de heteroarilo o arilo biciclicos fusionados y su aplicación a inhibidores de irak4
LT3122752T (lt) 4'-pakeistųjų nukleozidų dariniai kaip živ atvirkštinės transkriptazės inhibitoriai
ECSP17029203A (es) Inhibidor de cinasa aurora a
EP3449940A4 (fr) Préparation contenant un anticorps
EP3507370A4 (fr) Plantes présentant des traits modifiés
MX2016016993A (es) Compuestos de heteroarilo utiles como inhibidores de enzima activadora de sumo.
HRP20181698T1 (hr) 2-amino-6-(difluormetil)-5,5-difluor-6-fenil-3,4,5,6-tetrahidropiridini kao inhibitori bace1
MX373320B (es) Compuestos inhibidores de pde2.
CL2015002897A1 (es) Inhibidores de bace1
EP3449001A4 (fr) Inhibition de l'arnmi mir-22 par apt-110
BR112017028549A2 (pt) derivados de pirimidina como inibidores de btk e usos dos mesmos
EP3730110A4 (fr) Article pouvant être porté de type culotte
EP3459369A4 (fr) Composition pharmaceutique utilisant la souchelactobacillus
MX2016013240A (es) Rutas semi-sinteticas para compuestos organicos.
MX2016014166A (es) Compuestos de triaminopirimidina utiles para evitar o tratar la malaria.
EP3423499A4 (fr) Compositions photodurcissables contenant des oléfines déficientes en électrons
EP3357634A4 (fr) Centre d'usinage
MA41174A (fr) Dérivés d'imidazopyridazine utilisés en tant qu'inhibiteurs de pi3kbeta