JP2016513128A5 - - Google Patents

Download PDF

Info

Publication number
JP2016513128A5
JP2016513128A5 JP2015559275A JP2015559275A JP2016513128A5 JP 2016513128 A5 JP2016513128 A5 JP 2016513128A5 JP 2015559275 A JP2015559275 A JP 2015559275A JP 2015559275 A JP2015559275 A JP 2015559275A JP 2016513128 A5 JP2016513128 A5 JP 2016513128A5
Authority
JP
Japan
Prior art keywords
compound according
group
atoms
ring
compound
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.)
Granted
Application number
JP2015559275A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016513128A (ja
JP6356160B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/018380 external-priority patent/WO2014131023A1/en
Publication of JP2016513128A publication Critical patent/JP2016513128A/ja
Publication of JP2016513128A5 publication Critical patent/JP2016513128A5/ja
Application granted granted Critical
Publication of JP6356160B2 publication Critical patent/JP6356160B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2015559275A 2013-02-25 2014-02-25 ネオセプチン:低分子アジュバント Expired - Fee Related JP6356160B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361768712P 2013-02-25 2013-02-25
US61/768,712 2013-02-25
PCT/US2014/018380 WO2014131023A1 (en) 2013-02-25 2014-02-25 Neoseptins: small molecule adjuvants

Publications (3)

Publication Number Publication Date
JP2016513128A JP2016513128A (ja) 2016-05-12
JP2016513128A5 true JP2016513128A5 (cg-RX-API-DMAC7.html) 2017-04-06
JP6356160B2 JP6356160B2 (ja) 2018-07-11

Family

ID=51391916

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015559275A Expired - Fee Related JP6356160B2 (ja) 2013-02-25 2014-02-25 ネオセプチン:低分子アジュバント

Country Status (7)

Country Link
US (1) US9649373B2 (cg-RX-API-DMAC7.html)
EP (1) EP2958889B1 (cg-RX-API-DMAC7.html)
JP (1) JP6356160B2 (cg-RX-API-DMAC7.html)
CN (1) CN105339346B (cg-RX-API-DMAC7.html)
AU (1) AU2014218598B2 (cg-RX-API-DMAC7.html)
CA (1) CA2902342C (cg-RX-API-DMAC7.html)
WO (1) WO2014131023A1 (cg-RX-API-DMAC7.html)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5922791B2 (ja) 2012-10-29 2016-05-24 京セラ株式会社 弾性表面波センサ
WO2016011195A1 (en) 2014-07-17 2016-01-21 Threshold Pharmaceuticals, Inc. Th-302 solid forms and methods related thereto
EP3747508B1 (en) 2015-03-10 2021-10-13 Ascenta Pharmaceuticals, Ltd. Dna alkylating agents for use in the treatment of cancer
WO2016161342A2 (en) * 2015-04-02 2016-10-06 Threshold Pharmaceuticals, Inc. Nitrobenzyl derivatives of anti-cancer agents
EP3313385B8 (en) 2015-06-24 2021-04-21 ImmunoGenesis, Inc. Aziridine containing dna alkylating agents
US20180327364A1 (en) * 2015-11-13 2018-11-15 Brandeis University Mtor inhibitors and methods of use thereof
AU2017290238B2 (en) * 2016-06-29 2021-02-18 The Board Of Regents Of The University Of Texas System Diprovocims: a new and potent class of TLR agonists
WO2019099578A1 (en) 2017-11-14 2019-05-23 Chidren's Medical Center Corporation Use of imidazopyrimidine for modulating human immune response
JP7304855B2 (ja) 2017-11-14 2023-07-07 ザ チルドレンズ メディカル センター コーポレーション 新規イミダゾピリミジン化合物およびそれらの使用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4031083A (en) 1975-10-24 1977-06-21 Yeda Research And Development Co., Ltd. Cephalosporin antibiotics
US4045438A (en) 1975-10-24 1977-08-30 Yeda Research And Development Co. Ltd. Cephalosporin antibiotics
WO2005016235A2 (en) * 2003-04-14 2005-02-24 The Regents Of The University Of California Combined use of impdh inhibitors with toll-like receptor agonists
CN103012304B (zh) * 2005-06-30 2014-07-23 卫材R&D管理有限公司 用于制备免疫佐剂的化合物
ES2577514T3 (es) 2005-08-22 2016-07-15 The Regents Of The University Of California Antagonistas de TLR
EP2043672A4 (en) * 2006-07-07 2009-10-21 Univ Leland Stanford Junior SELECTIVE INHIBITORS OF CASPASES
SI2510946T1 (sl) * 2007-02-07 2015-12-31 The Regents Of The University Of California Konjugati sintetičnih agonistov TLR in njihove uporabe
JP5380465B2 (ja) * 2008-03-03 2014-01-08 アイアールエム・リミテッド・ライアビリティ・カンパニー Tlr活性モジュレーターとしての化合物および組成物
WO2010037402A1 (en) * 2008-10-02 2010-04-08 Dako Denmark A/S Molecular vaccines for infectious disease
WO2010088395A2 (en) * 2009-01-30 2010-08-05 Idera Pharmaceuticals, Inc. Novel synthetic agonists of tlr9

Similar Documents

Publication Publication Date Title
JP2016513128A5 (cg-RX-API-DMAC7.html)
CY1120342T1 (el) Ανταγωνιστης πολυκυκλικου lpa1 και χρησεις εξ' αυτου
JP2018511647A5 (cg-RX-API-DMAC7.html)
MX384752B (es) ANTAGONISTAS SOLUBLES DE RECEPTOR DE C5a (C5aR).
RU2018138828A (ru) Уменьшение массы опухоли путем введения ccr1 антагонистов в комбинации с pd-1 ингибиторами или pd-l1 ингибиторами
PE20181269A1 (es) Agonistas del receptor de apelina y metodos de uso
JP2013510124A5 (cg-RX-API-DMAC7.html)
JP2008525417A5 (cg-RX-API-DMAC7.html)
EA201590873A1 (ru) Соединения, обладающие активностью антагонистов мускариновых рецепторов и агонистов бета2 адренергических рецепторов
RU2013142448A (ru) Новые сульфонаминохинолиновые антагонисты гепсидина
JP2014523881A5 (cg-RX-API-DMAC7.html)
CL2016000816A1 (es) Forma de dosificación que comprende al compuesto (s)-3-(4-((4-morfolinometil)bencil)oxi)-1-oxoisoindolin-2-il)piperidin-2,6-diona, una cantidad de 90 hasta 99,9 por ciento en peso del peso total de una mezcla de almidón y lactosa como portador o excipiente, y acido esteárico como lubricante; su uso en el tratamiento de cáncer y enfermedades autoinmunes, entre otras.
PE20121474A1 (es) Nuevos compuestos de espiropiperidina
JP2013510123A5 (cg-RX-API-DMAC7.html)
RU2018120318A (ru) ИМИДАЗО[4,5-c]ХИНОЛИН-2-ОНОВЫЕ СОЕДИНЕНИЯ И ИХ ПРИМЕНЕНИЕ В ЛЕЧЕНИИ РАКА
JP2015516427A5 (cg-RX-API-DMAC7.html)
EA201391662A1 (ru) Соединения с активностью антагонистов мускариновых рецепторов и агонистов адренергического рецептора бета2
AR080467A1 (es) Derivados tetrazolicos moduladores selectivos de receptores cb2, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del dolor y otras enfermedades
JP2013508417A5 (cg-RX-API-DMAC7.html)
PE20190806A1 (es) Agonistas heterociclicos del receptor de apelina (apj) y usos de los mismos
RU2015118581A (ru) Лиофилизированные препараты мелфалана флуфенамида
JP2013523814A5 (cg-RX-API-DMAC7.html)
CR20170371A (es) Compuestos de benzoxaboral 4-sustituidos y uso de los mismos
CL2008003383A1 (es) Compuestos derivados de (espiro piperidin)-benzamida, inhibidores del transportador equilibrativo de nucleosidos ent1; composicion farmaceutica que comprende uno de los compuestos; proceso para preparar la composicion; y proceso para preparar los compuestos, utiles para tratamientos del dolor agudo y cronico.
AR057770A1 (es) Inhibidores de la p38-map-quinasa y composicion farmaceutica