JP2013505261A5 - - Google Patents

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Publication number
JP2013505261A5
JP2013505261A5 JP2012529937A JP2012529937A JP2013505261A5 JP 2013505261 A5 JP2013505261 A5 JP 2013505261A5 JP 2012529937 A JP2012529937 A JP 2012529937A JP 2012529937 A JP2012529937 A JP 2012529937A JP 2013505261 A5 JP2013505261 A5 JP 2013505261A5
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JP
Japan
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formula
compound
iodine
solution
acid
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JP2012529937A
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English (en)
Japanese (ja)
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JP5671040B2 (ja
JP2013505261A (ja
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Priority claimed from PCT/US2010/049341 external-priority patent/WO2011035161A1/en
Publication of JP2013505261A publication Critical patent/JP2013505261A/ja
Publication of JP2013505261A5 publication Critical patent/JP2013505261A5/ja
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JP2012529937A 2009-09-18 2010-09-17 4,5,6,7−テトラクロロ−3’,6’−ジヒドロキシ−2’,4’,5’,7’−テトラヨード−3h−スピロ[イソベンゾフラン−1,9’−キサンテン]−3−オン(ローズベンガル)及び関連するキサンテンを合成するプロセス Active JP5671040B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US24370109P 2009-09-18 2009-09-18
US61/243,701 2009-09-18
PCT/US2010/049341 WO2011035161A1 (en) 2009-09-18 2010-09-17 Process for the synthesis of 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5'7'-tetraiodo-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one (rose bengal) and related xanthenes

Publications (3)

Publication Number Publication Date
JP2013505261A JP2013505261A (ja) 2013-02-14
JP2013505261A5 true JP2013505261A5 (cg-RX-API-DMAC10.html) 2013-08-01
JP5671040B2 JP5671040B2 (ja) 2015-02-18

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ID=43757167

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012529937A Active JP5671040B2 (ja) 2009-09-18 2010-09-17 4,5,6,7−テトラクロロ−3’,6’−ジヒドロキシ−2’,4’,5’,7’−テトラヨード−3h−スピロ[イソベンゾフラン−1,9’−キサンテン]−3−オン(ローズベンガル)及び関連するキサンテンを合成するプロセス

Country Status (9)

Country Link
US (2) US8530675B2 (cg-RX-API-DMAC10.html)
EP (1) EP2464225B8 (cg-RX-API-DMAC10.html)
JP (1) JP5671040B2 (cg-RX-API-DMAC10.html)
KR (1) KR101494055B1 (cg-RX-API-DMAC10.html)
CN (1) CN102548406B (cg-RX-API-DMAC10.html)
CA (1) CA2771988C (cg-RX-API-DMAC10.html)
ES (1) ES2548575T3 (cg-RX-API-DMAC10.html)
MX (1) MX2012003063A (cg-RX-API-DMAC10.html)
WO (1) WO2011035161A1 (cg-RX-API-DMAC10.html)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2699965T3 (es) 2011-03-10 2019-02-13 Provectus Pharmatech Inc Una combinación de rosa de bengala y anticuerpo anti-CTLA4 para su uso en el tratamiento del cáncer
US20150111301A1 (en) * 2013-10-22 2015-04-23 The Government Of The United States As Represented By The Secretary Of The Air Force Rose bengal for detection of oxidative decomposition of contaminants
JP7015232B2 (ja) * 2018-11-21 2022-02-02 東レ・ファインケミカル株式会社 高純度のフルオレセイン類化合物の製造方法
EP3931197B1 (en) * 2019-02-26 2024-04-24 F. Hoffmann-La Roche AG Process for the preparation of (6s)-3-[(4s)-4-cyano-2-oxo-pyrrolidin-1-yl]-6-methyl-n-(3,4,5-trifluorophenyl)-6,7-dihydro-4h-pyrazolo[1,5-a]pyrazine-5-carboxamide
WO2021195400A1 (en) 2020-03-26 2021-09-30 Provectus Pharmatech, Inc. Novel uses of halogenated xanthenes in oncology and virology
US11938182B2 (en) 2020-03-26 2024-03-26 Provectus Pharmatech, Inc. Halogenated xanthenes as vaccine adjuvants
AU2022425066A1 (en) 2021-12-28 2024-06-06 Provectus Pharmatech, Inc Photodynamic anti-gram-positive bacterial activity of pharmaceutical-grade rose bengal
CN120957716A (zh) * 2023-03-29 2025-11-14 普罗维克图斯药品技术公司 卤化荧光素对耐粘菌素革兰氏阴性菌的抗细菌作用

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US1965842A (en) * 1931-11-21 1934-07-10 Nat Aniline & Chem Co Inc Production of hydroxybenzenephthaleins
US1931049A (en) * 1931-11-21 1933-10-17 Nat Aniline & Chem Co Inc Process of making dihydroxyfluoranes
US3829440A (en) * 1972-12-21 1974-08-13 Richardson Merrell Inc Xanthene derivatives
SU517222A1 (ru) 1974-10-25 1977-06-25 Институт Биофизики Министерства Здравохранения Ссср Способ получени препарата бенгальска роза, меченного радиоизотопами йода
SU792878A1 (ru) 1978-08-29 1982-02-07 Ленинградский институт ядерной физики им. Б.П.Константинова Способ получени галогенированных производных флуоресцеина,меченных радиоизотопом йода
EP0050684B1 (en) 1980-10-27 1986-01-22 Syva Company Novel ether substituted fluorescein compounds as fluorescers and quenchers
SU992516A1 (ru) 1981-06-11 1983-01-30 Ленинградский Институт Ядерной Физики Им.Б.П.Константинова Способ получени галогенированных производных флуоресцеина,меченных радиоизотопом иода -123
ES8606451A1 (es) 1985-10-28 1986-04-16 Zoster Sa Procedimiento para la obtencion de la eritrosina sodica
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US5945526A (en) * 1996-05-03 1999-08-31 Perkin-Elmer Corporation Energy transfer dyes with enhanced fluorescence
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AU2002256991A1 (en) * 2001-02-05 2002-08-19 The Government Of The United States Of America, As Represented By The Secretary, Department Of Healt Use of 9h-xanthenes in a method of inhibiting viral replication targeting the nucleocapsid protein
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