MA43960B1 - Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1 - Google Patents

Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1

Info

Publication number
MA43960B1
MA43960B1 MA43960A MA43960A MA43960B1 MA 43960 B1 MA43960 B1 MA 43960B1 MA 43960 A MA43960 A MA 43960A MA 43960 A MA43960 A MA 43960A MA 43960 B1 MA43960 B1 MA 43960B1
Authority
MA
Morocco
Prior art keywords
hiv
inhibitors
compounds
modified triterpenoids
relates
Prior art date
Application number
MA43960A
Other languages
English (en)
French (fr)
Other versions
MA43960A (fr
Inventor
Sing-Yuen Sit
Yan Chen
Jie Chen
Jacob Swidorski
Brian Lee Venables
Ny Sin
Alicia Regueiro-Ren
Ira B Dicker
Richard A Hartz
Nicholas A Meanwell
Original Assignee
Viiv Healthcare Uk No 5 Ltd
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 Viiv Healthcare Uk No 5 Ltd filed Critical Viiv Healthcare Uk No 5 Ltd
Publication of MA43960A publication Critical patent/MA43960A/fr
Publication of MA43960B1 publication Critical patent/MA43960B1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/58Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J53/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
    • C07J53/002Carbocyclic rings fused
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/48Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/503Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from viruses
    • C12N9/506Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from viruses derived from RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J63/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
    • C07J63/008Expansion of ring D by one atom, e.g. D homo steroids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/52Ortho- or ortho- and peri-condensed systems containing five condensed rings
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2740/00Reverse transcribing RNA viruses
    • C12N2740/00011Details
    • C12N2740/10011Retroviridae
    • C12N2740/16011Human Immunodeficiency Virus, HIV
    • C12N2740/16211Human Immunodeficiency Virus, HIV concerning HIV gagpol
    • C12N2740/16222New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • AIDS & HIV (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Epidemiology (AREA)
  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
MA43960A 2016-02-04 2017-02-02 Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1 MA43960B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662291298P 2016-02-04 2016-02-04
PCT/IB2017/050568 WO2017134596A1 (en) 2016-02-04 2017-02-02 C-3 and c-17 modified triterpenoids as hiv-1 inhibitors

Publications (2)

Publication Number Publication Date
MA43960A MA43960A (fr) 2018-12-12
MA43960B1 true MA43960B1 (fr) 2021-02-26

Family

ID=57995251

Family Applications (2)

Application Number Title Priority Date Filing Date
MA053358A MA53358A (fr) 2016-02-04 2017-02-02 Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1
MA43960A MA43960B1 (fr) 2016-02-04 2017-02-02 Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MA053358A MA53358A (fr) 2016-02-04 2017-02-02 Triterpénoïdes modifiés en c-3 et c-17 utilisés comme inhibiteurs du vih-1

Country Status (39)

Country Link
US (4) US10421774B2 (enExample)
EP (2) EP3831839B1 (enExample)
JP (1) JP6735837B2 (enExample)
KR (1) KR102795662B1 (enExample)
CN (1) CN109153700B (enExample)
AR (1) AR107512A1 (enExample)
AU (1) AU2017215529B2 (enExample)
BR (1) BR112018015629B1 (enExample)
CA (1) CA3013417C (enExample)
CL (1) CL2018002084A1 (enExample)
CO (1) CO2018008157A2 (enExample)
CR (1) CR20180387A (enExample)
CY (1) CY1124353T1 (enExample)
DK (1) DK3411381T3 (enExample)
DO (1) DOP2018000174A (enExample)
EA (1) EA036211B1 (enExample)
ES (2) ES2957767T3 (enExample)
HR (1) HRP20210502T1 (enExample)
HU (1) HUE054337T2 (enExample)
IL (1) IL260741B (enExample)
JO (1) JOP20170029B1 (enExample)
LT (1) LT3411381T (enExample)
MA (2) MA53358A (enExample)
MD (1) MD3411381T2 (enExample)
MX (1) MX375118B (enExample)
MY (1) MY199668A (enExample)
PE (1) PE20181355A1 (enExample)
PL (1) PL3411381T3 (enExample)
PT (1) PT3411381T (enExample)
RS (1) RS61746B1 (enExample)
RU (1) RU2716502C2 (enExample)
SG (1) SG11201806388XA (enExample)
SI (1) SI3411381T1 (enExample)
SM (1) SMT202100210T1 (enExample)
TW (1) TWI719126B (enExample)
UA (1) UA123867C2 (enExample)
UY (1) UY37109A (enExample)
WO (1) WO2017134596A1 (enExample)
ZA (1) ZA201805044B (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR107512A1 (es) * 2016-02-04 2018-05-09 VIIV HEALTHCARE UK Nº 5 LTD Triterpenoides modificados en c-3 y c-17 como inhibidores del vih-1
JP7436385B2 (ja) * 2018-04-24 2024-02-21 ヴィーブ ヘルスケア ユーケー(ナンバー5)リミテッド Hiv成熟阻害活性を有する化合物
IL293566A (en) 2019-12-09 2022-08-01 Viiv Healthcare Co Pharmaceutical preparations containing Cabotgravir
WO2025068743A1 (en) 2023-09-27 2025-04-03 ViiV Healthcare UK (No.3) Limited Pharmaceutical composition of cabotegravir
WO2024089216A1 (en) 2022-10-27 2024-05-02 Syngenta Crop Protection Ag Novel sulfur-containing heteroaryl carboxamide compounds
WO2025037232A1 (en) 2023-08-11 2025-02-20 ViiV Healthcare UK (No.4) Limited Tosylate salt form of a maturation inhibitor for treatment of hiv
WO2025068912A1 (en) 2023-09-27 2025-04-03 ViiV Healthcare UK (No.3) Limited Pharmaceutical compositions

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5413999A (en) 1991-11-08 1995-05-09 Merck & Co., Inc. HIV protease inhibitors useful for the treatment of AIDS
US5679828A (en) 1995-06-05 1997-10-21 Biotech Research Labs, Inc. Betulinic acid and dihydrobetulinic acid derivatives and uses therefor
US20040110785A1 (en) 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US7365221B2 (en) 2002-09-26 2008-04-29 Panacos Pharmaceuticals, Inc. Monoacylated betulin and dihydrobetulin derivatives, preparation thereof and use thereof
GB0301227D0 (en) 2003-01-20 2003-02-19 Keen Group Ltd Seating apparatus
US7745625B2 (en) 2004-03-15 2010-06-29 Bristol-Myers Squibb Company Prodrugs of piperazine and substituted piperidine antiviral agents
CA2560266A1 (en) 2004-03-17 2005-09-29 Panacos Pharmaceuticals, Inc. Pharmaceutical salts of 3-o-(3',3'-dimethylsuccinyl) betulinic acid
TW200628161A (en) 2004-11-12 2006-08-16 Panacos Pharmaceuticals Inc Novel betulin derivatives, preparation thereof and use thereof
US20110144069A1 (en) 2006-10-16 2011-06-16 Myriad Genetics, Incorporated Compounds for treating viral infections
CA2714049A1 (en) 2008-02-14 2009-08-20 Virochem Pharma Inc. Novel 17.beta. lupane derivatives
US9067966B2 (en) 2009-07-14 2015-06-30 Hetero Research Foundation, Hetero Drugs Ltd. Lupeol-type triterpene derivatives as antivirals
FR2956034B1 (fr) 2010-02-09 2012-02-10 Thales Sa Dispositif d'entrainement pour des joueurs de rugby
HRP20150977T1 (hr) 2010-06-04 2015-10-09 Bristol-Myers Squibb Company C-28 amidi modificiranih derivata c-3 betulinske kiseline kao inhibitori sazrijevanja hiv-a
CN103038245B (zh) 2010-06-04 2015-03-25 百时美施贵宝公司 作为hiv成熟抑制剂的c-3经修饰的桦木酸衍生物
DE102010017786A1 (de) 2010-07-07 2012-01-12 Continental Reifen Deutschland Gmbh Elastomerprodukt, enthaltend ein linienförmiges, textiles Gebilde zur Verstärkung
JP6000283B2 (ja) 2011-01-31 2016-09-28 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Hiv成熟阻害剤としてのc−3修飾ベツリン酸誘導体のc−28アミン
US8846647B2 (en) * 2011-01-31 2014-09-30 Bristol-Myers Squibb Company C-17 and C-3 modified triterpenoids with HIV maturation inhibitory activity
JP6091520B2 (ja) * 2011-12-14 2017-03-08 グラクソスミスクライン エルエルシー ベツリンのプロペン酸誘導体
US8906889B2 (en) * 2012-02-15 2014-12-09 Bristol-Myers Squibb Company C-3 cycloalkenyl triterpenoids with HIV maturation inhibitory activity
US8889854B2 (en) * 2012-05-07 2014-11-18 Bristol-Myers Squibb Company C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity
JP2016505000A (ja) 2012-12-21 2016-02-18 エピザイム,インコーポレイティド Prmt5阻害剤およびその使用
US9378035B2 (en) 2012-12-28 2016-06-28 Commvault Systems, Inc. Systems and methods for repurposing virtual machines
JP6186010B2 (ja) * 2013-02-06 2017-08-23 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Hiv成熟阻害活性を有するc−19修飾トリテルペノイド類
SG11201506445PA (en) 2013-02-25 2015-09-29 Bristol Myers Squibb Co C-3 alkyl and alkenyl modified betulinic acid derivatives useful in the treatment of hiv
CN104877015B (zh) * 2014-02-28 2019-02-01 中国人民解放军军事医学科学院毒物药物研究所 一种三萜-多肽缀合物、其药物组合物及用途
UY36070A (es) 2014-04-11 2015-10-30 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware Triterpenoides con actividad inhibidora de la maduración de hiv
MA40886B1 (fr) 2015-02-09 2020-03-31 Hetero Research Foundation Nouveau triterpénone en c-3 avec des dérivés d'amide inverse en c-28 en tant qu'inhibiteurs du vih
US10508083B2 (en) 2016-02-04 2019-12-17 Takeda Pharmaceutical Company Limited Substituted piperidine compound and use thereof
AR107512A1 (es) * 2016-02-04 2018-05-09 VIIV HEALTHCARE UK Nº 5 LTD Triterpenoides modificados en c-3 y c-17 como inhibidores del vih-1

Also Published As

Publication number Publication date
CO2018008157A2 (es) 2018-08-21
US11084845B2 (en) 2021-08-10
RU2018130181A (ru) 2020-03-05
EA201891649A1 (ru) 2019-02-28
HRP20210502T1 (hr) 2021-05-14
DOP2018000174A (es) 2018-10-31
MA43960A (fr) 2018-12-12
PE20181355A1 (es) 2018-08-22
WO2017134596A1 (en) 2017-08-10
MX2018009514A (es) 2018-09-05
RU2716502C2 (ru) 2020-03-12
MY199668A (en) 2023-11-15
BR112018015629A2 (pt) 2018-12-26
ZA201805044B (en) 2020-08-26
US20190359647A1 (en) 2019-11-28
UY37109A (es) 2017-09-29
AU2017215529A8 (en) 2018-08-30
DK3411381T3 (da) 2021-04-06
MA53358A (fr) 2021-07-21
MD3411381T2 (ro) 2021-07-31
HK1256866A1 (en) 2019-10-04
ES2862325T3 (es) 2021-10-07
CA3013417A1 (en) 2017-08-10
BR112018015629B1 (pt) 2023-10-24
PL3411381T3 (pl) 2021-09-13
TW201739757A (zh) 2017-11-16
AU2017215529A1 (en) 2018-08-23
JP2019504104A (ja) 2019-02-14
CN109153700A (zh) 2019-01-04
LT3411381T (lt) 2021-04-26
NZ744545A (en) 2025-03-28
RU2018130181A3 (enExample) 2020-03-05
HUE054337T2 (hu) 2021-08-30
EP3411381B1 (en) 2021-01-20
UA123867C2 (uk) 2021-06-16
EP3831839B1 (en) 2023-07-26
SI3411381T1 (sl) 2021-04-30
KR20180105229A (ko) 2018-09-27
ES2957767T3 (es) 2024-01-25
KR102795662B1 (ko) 2025-04-14
JOP20170029B1 (ar) 2021-08-17
JP6735837B2 (ja) 2020-08-05
TWI719126B (zh) 2021-02-21
SG11201806388XA (en) 2018-08-30
RS61746B1 (sr) 2021-05-31
CN109153700B (zh) 2021-03-09
EA036211B1 (ru) 2020-10-14
PT3411381T (pt) 2021-03-18
US20210323997A1 (en) 2021-10-21
SMT202100210T1 (it) 2021-05-07
CY1124353T1 (el) 2022-07-22
CL2018002084A1 (es) 2018-09-21
CR20180387A (es) 2018-09-20
US10421774B2 (en) 2019-09-24
EP3411381A1 (en) 2018-12-12
AR107512A1 (es) 2018-05-09
EP3831839A2 (en) 2021-06-09
AU2017215529B2 (en) 2019-01-31
EP3831839A3 (en) 2021-07-21
IL260741B (en) 2020-04-30
US20230295220A1 (en) 2023-09-21
CA3013417C (en) 2024-01-02
MX375118B (es) 2025-03-06
US20190031709A1 (en) 2019-01-31

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