JP2017503016A5 - - Google Patents

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Publication number
JP2017503016A5
JP2017503016A5 JP2016560857A JP2016560857A JP2017503016A5 JP 2017503016 A5 JP2017503016 A5 JP 2017503016A5 JP 2016560857 A JP2016560857 A JP 2016560857A JP 2016560857 A JP2016560857 A JP 2016560857A JP 2017503016 A5 JP2017503016 A5 JP 2017503016A5
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JP
Japan
Prior art keywords
compound
diffractometer
determined
powder
item
Prior art date
Legal status (The legal status 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 status listed.)
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Application number
JP2016560857A
Other languages
English (en)
Japanese (ja)
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JP2017503016A (ja
JP6568541B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/071310 external-priority patent/WO2015100144A1/en
Publication of JP2017503016A publication Critical patent/JP2017503016A/ja
Publication of JP2017503016A5 publication Critical patent/JP2017503016A5/ja
Application granted granted Critical
Publication of JP6568541B2 publication Critical patent/JP6568541B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016560857A 2013-12-23 2014-12-18 大環状hcv ns3阻害トリペプチドの結晶形態 Expired - Fee Related JP6568541B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361920427P 2013-12-23 2013-12-23
US61/920,427 2013-12-23
PCT/US2014/071310 WO2015100144A1 (en) 2013-12-23 2014-12-18 Crystalline forms of a macrocyclic hcv ns3 inhibiting tripeptide

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2019020540A Division JP2019089819A (ja) 2013-12-23 2019-02-07 大環状hcv ns3阻害トリペプチドの結晶形態

Publications (3)

Publication Number Publication Date
JP2017503016A JP2017503016A (ja) 2017-01-26
JP2017503016A5 true JP2017503016A5 (enExample) 2018-01-18
JP6568541B2 JP6568541B2 (ja) 2019-08-28

Family

ID=52282995

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2016560857A Expired - Fee Related JP6568541B2 (ja) 2013-12-23 2014-12-18 大環状hcv ns3阻害トリペプチドの結晶形態
JP2019020540A Pending JP2019089819A (ja) 2013-12-23 2019-02-07 大環状hcv ns3阻害トリペプチドの結晶形態

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2019020540A Pending JP2019089819A (ja) 2013-12-23 2019-02-07 大環状hcv ns3阻害トリペプチドの結晶形態

Country Status (12)

Country Link
US (2) US9562058B2 (enExample)
EP (1) EP3087086B1 (enExample)
JP (2) JP6568541B2 (enExample)
AR (1) AR098958A1 (enExample)
AU (1) AU2014370124A1 (enExample)
CA (1) CA2934049A1 (enExample)
ES (1) ES2708993T3 (enExample)
NZ (1) NZ720887A (enExample)
PT (1) PT3087086T (enExample)
TW (1) TW201609752A (enExample)
UY (1) UY35918A (enExample)
WO (1) WO2015100144A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9440991B2 (en) 2013-12-23 2016-09-13 Gilead Sciences, Inc. Synthesis of an antiviral compound
CN118286245A (zh) 2014-12-26 2024-07-05 埃莫里大学 N4-羟基胞苷和衍生物及与其相关的抗病毒用途
BR102017011025A2 (pt) 2016-06-02 2017-12-19 Gilead Pharmasset Llc Formulation of combination of three antiviral compounds
RS66222B1 (sr) 2017-12-07 2024-12-31 Univ Emory N4-hidroksicitidin i derivati i antivirusne upotrebe povezane sa njim
CN115417803B (zh) * 2022-08-30 2023-10-03 四川同晟生物医药有限公司 乌帕替尼中间体(3r,4s)-1-苄氧羰基-4-乙基吡咯烷-3-羧酸的合成方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
CL2008003384A1 (es) * 2007-11-14 2009-12-11 Enanta Pharm Inc Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c.
SI2310095T1 (sl) * 2008-07-22 2013-01-31 Merck Sharp & Dohme Corp. Makrocikliäśne kuinoksalinske spojine kot hcv ns3 proteazni inhibitorji
DK2618831T3 (en) * 2010-09-21 2016-04-04 Enanta Pharm Inc Macrocyclic prolinafledte HCV serine protease inhibitors
US20130178413A1 (en) * 2010-09-21 2013-07-11 John A. McCauley Hcv ns3 protease inhibitors
UA110354C2 (uk) 2011-11-16 2015-12-25 Гайлід Фармассет Елелсі Противірусні сполуки
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с

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