[go: up one dir, main page]

AR103194A1 - Formas sólidas de un compuesto antiviral - Google Patents

Formas sólidas de un compuesto antiviral

Info

Publication number
AR103194A1
AR103194A1 ARP150101835A ARP150101835A AR103194A1 AR 103194 A1 AR103194 A1 AR 103194A1 AR P150101835 A ARP150101835 A AR P150101835A AR P150101835 A ARP150101835 A AR P150101835A AR 103194 A1 AR103194 A1 AR 103194A1
Authority
AR
Argentina
Prior art keywords
methyl
imidazol
solid forms
crystalline
compound
Prior art date
Application number
ARP150101835A
Other languages
English (en)
Original Assignee
Gilead Pharmasset Llc
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 Gilead Pharmasset Llc filed Critical Gilead Pharmasset Llc
Publication of AR103194A1 publication Critical patent/AR103194A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Formas sólidas cristalinas de metilo {(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(metoxicarbonilo)amino]-2-fenilacetil}-4-(metoximetilo)pirrolidin-2-il]-1H-imidazol-5-il}-1,11-dihidroisocromeno[4,3:6,7]nafto[1,2-d]imidazol-2-il)-5-metilopirrolidin-1-il]-3-metilo-1-oxobutan-2-il}carbamato (Compuesto I) de fórmula (1) se prepararon y caracterizaron en el estado sólido. Se proporcionan además procesos de fabricación y métodos de uso de estas formas cristalinas, útiles para tratar la hepatitis C. Reivindicación 1: Metilo {(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2 R)-2-[(metoxicarbonilo)amino]-2-fenilacetil}-4-(metoximetilo)pirrolidin-2-il]-1H-imidazol-5-il}-1,11-dihidroisocromeno[4,3:6,7]nafto[1,2-d]imidazol-2-il)-5-metilopirrolidin-1-il]-3-metilo-1-oxobutan-2-il}carbamato cristalino (Compuesto I Forma I) caracterizado por un difractograma de polvo de rayos X que comprende los siguientes picos: 4.8, 5.2, y 6.0º2q ± 0.2º2q, según lo determinado en un difractómetro usando radiación Cu-Ka a una longitud de onda de 1.5406 Å.
ARP150101835A 2014-06-11 2015-06-10 Formas sólidas de un compuesto antiviral AR103194A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201462010919P 2014-06-11 2014-06-11

Publications (1)

Publication Number Publication Date
AR103194A1 true AR103194A1 (es) 2017-04-26

Family

ID=53443009

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP150101835A AR103194A1 (es) 2014-06-11 2015-06-10 Formas sólidas de un compuesto antiviral

Country Status (19)

Country Link
US (4) US9630972B2 (es)
EP (3) EP3822275A1 (es)
JP (3) JP2017517532A (es)
KR (3) KR20200145852A (es)
CN (1) CN106661042A (es)
AR (1) AR103194A1 (es)
AU (2) AU2015274961A1 (es)
BR (1) BR112016028843A2 (es)
CA (1) CA2951188C (es)
EA (1) EA201692220A1 (es)
ES (1) ES2785409T3 (es)
IL (1) IL249041A0 (es)
MX (1) MX2016016299A (es)
PL (1) PL3154983T3 (es)
PT (1) PT3154983T (es)
SG (1) SG11201609810YA (es)
SI (1) SI3154983T1 (es)
TW (1) TWI721947B (es)
WO (1) WO2015191431A1 (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3521297T3 (pl) 2003-05-30 2022-04-04 Gilead Pharmasset Llc Zmodyfikowane fluorowane analogi nukleozydów
TWI548629B (zh) 2010-11-17 2016-09-11 吉李德製藥公司 抗病毒化合物
DK2907816T3 (en) 2011-11-16 2018-09-24 Gilead Pharmasset Llc CONDENSED IMIDAZOLYLIMIDAZOLES AS ANTIVIRAL COMPOUNDS
NZ716840A (en) 2013-08-27 2017-06-30 Gilead Pharmasset Llc Combination formulation of two antiviral compounds
TWI721947B (zh) 2014-06-11 2021-03-21 美商基利法瑪席特有限責任公司 抗病毒化合物的固態形式
TW202014413A (zh) 2014-06-11 2020-04-16 美商基利法瑪席特有限責任公司 製備抗病毒化合物之方法
BR102017011025A2 (pt) 2016-06-02 2017-12-19 Gilead Pharmasset Llc Formulation of combination of three antiviral compounds
CN108368123B (zh) * 2016-07-08 2021-02-19 深圳市塔吉瑞生物医药有限公司 一种取代的咪唑基化合物及其药物组合物
CN106432253B (zh) * 2016-09-21 2019-06-14 上海众强药业有限公司 一种维帕他韦新晶型及其制备方法

Family Cites Families (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5858389A (en) 1996-08-28 1999-01-12 Shaker H. Elsherbini Squalene is an antiviral compound for treating hepatitis C virus carriers
CA2448737C (en) 2001-07-20 2010-06-01 Boehringer Ingelheim (Canada) Ltd. Viral polymerase inhibitors
CN1771245A (zh) 2003-04-02 2006-05-10 安斯泰来制药有限公司 氟苯甲酰胺衍生物的新颖的晶体
ES2456702T3 (es) 2003-05-09 2014-04-23 Boehringer Ingelheim International Gmbh Bolsillo de unión del inhibidor de la polimerasa NS5B del virus de la hepatitis C
AR047541A1 (es) * 2004-02-13 2006-01-25 Sandoz Ag Fosfato de 5-[[4-[2-metil-2-piridinil-amino-etoxi]fenil]metil]-2,4 tiazolidinadiona (rosiglitazona) y sus formas polimorficas
US7157492B2 (en) 2004-02-26 2007-01-02 Wyeth Dibenzo chromene derivatives and their use as ERβ selective ligands
FR2875409B1 (fr) 2004-09-17 2010-05-07 Sanofi Aventis Composition pharmaceutique comprenant une dispersion solide a matrice polymere comprenant une phase continue de polydextrose et une phase continue d'un polymere autre que du polydextrose
RU2355691C2 (ru) * 2004-09-22 2009-05-20 Пфайзер Инк. Полиморфные и аморфная формы фосфатной соли 8-фтор-2-{4-[(метиламино)метил]фенил}-1,3,4,5-тетрагидро-6н-азепино[5.4.3-cd]индол-6-она
EP2016052B1 (en) 2006-05-05 2012-06-06 Merck Patent GmbH Crystalline (3-cyano-1h-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]methanone phosphate
US8891379B2 (en) 2006-06-02 2014-11-18 Riverbed Technology, Inc. Traffic flow inference based on link loads and gravity measures
US8329159B2 (en) 2006-08-11 2012-12-11 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7759495B2 (en) 2006-08-11 2010-07-20 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7659270B2 (en) 2006-08-11 2010-02-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
JP2009286694A (ja) 2006-09-07 2009-12-10 Eisai R & D Management Co Ltd 5−[2−アミノ−4−(2−フリル)ピリミジン−5−イル]−1−メチルピリジン−2(1h)−オンの塩およびそれらの結晶
CA2823981C (en) 2006-12-07 2016-05-17 Daiichi Sankyo Company, Limited Film-coated preparation having improved stability
US7964580B2 (en) 2007-03-30 2011-06-21 Pharmasset, Inc. Nucleoside phosphoramidate prodrugs
US7741347B2 (en) 2007-05-17 2010-06-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2184282B1 (en) 2007-08-10 2014-10-08 Mitsubishi Tanabe Pharma Corporation Novel salt of isoquinoline compound and crystal thereof
EP2250163B1 (en) 2008-02-12 2012-03-28 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
US7704992B2 (en) 2008-02-13 2010-04-27 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8147818B2 (en) 2008-02-13 2012-04-03 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
DK2242752T3 (da) 2008-02-13 2012-11-19 Bristol Myers Squibb Co Imidazolyl-biphenylimidazoler som hepatitis C-virus-inhibitorer
AR072991A1 (es) 2008-08-07 2010-10-06 Schering Corp Formulaciones farmaceuticas de un inhibidor de la enzima proteasa de hcv en una dispersion molecular solida
US20100256184A1 (en) 2008-08-13 2010-10-07 Vertex Pharmaceuticals Incorporated Pharmaceutical composition and administrations thereof
WO2010062821A1 (en) 2008-11-28 2010-06-03 Glaxosmithkline Llc Anti-viral compounds, compositions, and methods of use
WO2010065681A1 (en) 2008-12-03 2010-06-10 Presidio Pharmaceuticals, Inc. Inhibitors of hcv ns5a
EA024853B1 (ru) 2008-12-03 2016-10-31 Пресидио Фармасьютикалс, Инк. Ингибиторы ns5a вгс
WO2010096777A1 (en) 2009-02-23 2010-08-26 Presidio Pharmaceuticals, Inc. Inhibitors of hcv ns5a
SG174146A1 (en) 2009-02-27 2011-10-28 Enanta Pharm Inc Hepatitis c virus inhibitors
AU2010229795A1 (en) 2009-03-27 2011-10-13 Presidio Pharmaceuticals, Inc. Fused ring inhibitors of hepatitis C
HRP20160476T1 (hr) 2009-03-27 2016-06-03 Merck Sharp & Dohme Corp. Inhibitori replikacije virusa hepatitisa c
CA2756255A1 (en) 2009-03-27 2010-09-30 Presidio Pharmaceuticals, Inc. Substituted bicyclic hcv inhibitors
JP2012526834A (ja) 2009-05-12 2012-11-01 シェーリング コーポレイション ウイルス疾患治療に有用な縮合型三環式アリール化合物
SI3309157T1 (sl) 2009-05-13 2020-02-28 Gilead Pharmasset Llc Protivirusne spojine
US8618076B2 (en) 2009-05-20 2013-12-31 Gilead Pharmasset Llc Nucleoside phosphoramidates
TWI576352B (zh) 2009-05-20 2017-04-01 基利法瑪席特有限責任公司 核苷磷醯胺
US8138215B2 (en) 2009-05-29 2012-03-20 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
JP5795316B2 (ja) 2009-09-04 2015-10-14 ヤンセン ファーマシューティカルズ,インコーポレーテッド 化合物
US9156818B2 (en) 2009-09-11 2015-10-13 Enanta Pharmaceuticals, Inc. Hepatitis C virus inhibitors
UA108211C2 (uk) 2009-11-04 2015-04-10 Янссен Рід Айрленд Бензімідазолімідазольні похідні
US20110274648A1 (en) 2009-11-11 2011-11-10 Bristol-Myers Squibb Company Hepatitis C Virus Inhibitors
CA2782024A1 (en) 2009-11-25 2011-06-03 Schering Corporation Fused tricyclic compounds and derivatives thereof useful for the treatment of viral diseases
US8476225B2 (en) 2009-12-04 2013-07-02 Gilead Sciences, Inc. Antiviral compounds
US8377980B2 (en) 2009-12-16 2013-02-19 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
CN104341401B (zh) 2009-12-18 2017-02-15 北京凯因科技股份有限公司 C型肝炎病毒复制的新型抑制剂
EP2516430B1 (en) 2009-12-22 2014-11-05 Merck Sharp & Dohme Corp. Fused tricyclic compounds and methods of use thereof for the treatment of viral diseases
EA201290882A1 (ru) 2010-03-09 2013-04-30 Мерк Шарп Энд Домэ Корп. Конденсированные трициклические силильные соединения и способы их применения для лечения вирусных заболеваний
US9125904B1 (en) 2010-05-11 2015-09-08 Achillion Pharmaceuticals, Inc. Biphenyl imidazoles and related compounds useful for treating HCV infections
WO2011146401A1 (en) 2010-05-17 2011-11-24 Intermune, Inc. Novel inhibitors of hepatitis c virus replication
NZ605440A (en) 2010-06-10 2014-05-30 Abbvie Bahamas Ltd Solid compositions comprising an hcv inhibitor
US8859595B2 (en) 2010-08-26 2014-10-14 Rfs Pharma, Llc Potent and selective inhibitors of hepatitis C virus
KR102163902B1 (ko) 2010-09-21 2020-10-12 이난타 파마슈티칼스, 인코포레이티드 매크로사이클릭 프롤린 유도된 hcv 세린 프로테아제 억제제
WO2012048421A1 (en) 2010-10-14 2012-04-19 Boehringer Ingelheim International Gmbh Hepatitis c inhibitor compounds
TWI548629B (zh) 2010-11-17 2016-09-11 吉李德製藥公司 抗病毒化合物
WO2012087976A2 (en) 2010-12-21 2012-06-28 Intermune, Inc. Novel inhibitors of hepatitis c virus replication
AR088463A1 (es) 2011-10-21 2014-06-11 Abbvie Inc Metodos para el tratamiento de hcv
DK2907816T3 (en) 2011-11-16 2018-09-24 Gilead Pharmasset Llc CONDENSED IMIDAZOLYLIMIDAZOLES AS ANTIVIRAL COMPOUNDS
US9034832B2 (en) 2011-12-29 2015-05-19 Abbvie Inc. Solid compositions
CA2857339C (en) 2011-12-29 2015-11-17 Abbvie Inc. Solid compositions comprising an hcv inhibitor
US9079887B2 (en) 2012-05-16 2015-07-14 Gilead Sciences, Inc. Antiviral compounds
US20130309196A1 (en) 2012-05-16 2013-11-21 Gilead Sciences, Inc. Antiviral compounds
US9233974B2 (en) 2012-12-21 2016-01-12 Gilead Sciences, Inc. Antiviral compounds
TW201434949A (zh) 2013-01-31 2014-09-16 Nitto Denko Corp 環氧組合物及環氧樹脂成形體
WO2015030854A1 (en) 2013-08-27 2015-03-05 Gilead Pharmasset Llc Solid dispersion formulation of an antiviral compound
NZ716840A (en) 2013-08-27 2017-06-30 Gilead Pharmasset Llc Combination formulation of two antiviral compounds
TWI721947B (zh) * 2014-06-11 2021-03-21 美商基利法瑪席特有限責任公司 抗病毒化合物的固態形式
TW202014413A (zh) 2014-06-11 2020-04-16 美商基利法瑪席特有限責任公司 製備抗病毒化合物之方法
JP2016051146A (ja) 2014-09-02 2016-04-11 ウシオ電機株式会社 光検出装置
EP3588013A1 (de) 2018-06-26 2020-01-01 XelectriX Power GmbH Verfahren zur abgabe von elektrischer energie

Also Published As

Publication number Publication date
JP2019172711A (ja) 2019-10-10
CN106661042A (zh) 2017-05-10
US9630972B2 (en) 2017-04-25
US20190270750A1 (en) 2019-09-05
MX2016016299A (es) 2017-04-06
SI3154983T1 (sl) 2020-04-30
CA2951188A1 (en) 2015-12-17
SG11201609810YA (en) 2016-12-29
US11203599B2 (en) 2021-12-21
JP2019070057A (ja) 2019-05-09
TW201609745A (zh) 2016-03-16
KR20170015506A (ko) 2017-02-08
US20200283449A1 (en) 2020-09-10
PL3154983T3 (pl) 2020-06-29
US20170247386A1 (en) 2017-08-31
PT3154983T (pt) 2020-05-06
KR20200145852A (ko) 2020-12-30
AU2018201948A1 (en) 2018-04-12
JP2017517532A (ja) 2017-06-29
EP3154983A1 (en) 2017-04-19
EP3666775A1 (en) 2020-06-17
IL249041A0 (en) 2017-01-31
EA201692220A1 (ru) 2017-05-31
ES2785409T3 (es) 2020-10-06
KR20190007533A (ko) 2019-01-22
US9884873B2 (en) 2018-02-06
CA2951188C (en) 2019-09-24
WO2015191431A1 (en) 2015-12-17
US20150361085A1 (en) 2015-12-17
AU2018201948B2 (en) 2019-10-03
EP3154983B1 (en) 2020-02-12
US10604530B2 (en) 2020-03-31
TWI721947B (zh) 2021-03-21
AU2015274961A1 (en) 2016-12-01
EP3822275A1 (en) 2021-05-19
BR112016028843A2 (pt) 2017-08-22

Similar Documents

Publication Publication Date Title
AR103194A1 (es) Formas sólidas de un compuesto antiviral
AR096582A1 (es) Procesos de fabricación y formas cristalinas de un inhibidor de mdm2
PE20170325A1 (es) Compuestos y composiciones como agonistas del receptor tipo toll
UA110259C2 (uk) Похідні піролопіримідину і пурину
CL2013002821A1 (es) Compuestos derivados de pirrolo[2,3-d]pirimidina; composicion farmaceutica que los comprende; y su uso como antagonista de los receptores tropomiosina (trk) para el tratamiento del dolor.
MX2016006336A (es) Compuestos pirazolopirimidina.
ECSP13012596A (es) Proceso de elaboración para derivados de pirimidina
CY1120325T1 (el) Τρικυκλικες ετεροκυκλικες ενωσεις ως αναστολεις φωσφοϊνοσιτιδιου 3-κινασης
MX388321B (es) Compuestos de aminopurina sustituida, composiciones del mismo, y metodos de tratamiento con los mismos.
EA201791305A1 (ru) Конденсированные пиримидины для лечения вич
UY34261A (es) Compuestos fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-fenil]-2-alcoxi-2-ciclil-etil}-1h-[1,2,4]triazol sustituidos
EA201692219A1 (ru) Способы получения противовирусных соединений
AR102204A1 (es) Compuestos derivados de amino-alquilbenzotiazepinas
BR112014030400A2 (pt) formas sólidas de um composto antiviral
MD20160053A2 (ro) Derivaţi ai purinei 2,6-substituite şi utilizarea acestora în tratamentul tulburărilor proliferative
EA201591512A1 (ru) Борсодержащие молекулы, способы и составы
MX381341B (es) Derivados de 3-alquil-5-fluoro-4-sustituido-imino-3,4-dihidropirimidin-2(1h)-ona como fungicidas.
PE20170148A1 (es) Compuestos de 1,3, 4-tiadiazol y uso de los mismos para el tratamiento del cancer
PE20201495A1 (es) Compuesto de pirimidina como inhibidor de las janocinasas
PE20151535A1 (es) Derivado de dihidropiridazin-3,5-diona
EA201591328A1 (ru) Замещенные гетероциклом тетрациклические соединения и способы их применения для лечения вирусных заболеваний
BR112013024965A2 (pt) composto, composição farmacêutica, método de tratamento de infecções virais, e, processo para preparar um composto
CL2015000056A1 (es) Compuestos derivados de carbamato/urea, inhibidores del receptor de histamina h3; procedimiento de preparación; compuesto intermediario; composicion farmaceutica; combinacion farmaceutica; y uso en el tratamiento de narcolepsia.
AR065714A1 (es) Sal clorhidrato de 5- (3-( 3- hidroxifenoxi ) azetidin- 1 - il ) - 5 - metil - 2, 2 - difenilhexanamida
NI201800071A (es) Compuestos de isoindol

Legal Events

Date Code Title Description
FB Suspension of granting procedure