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4,6-Di-(O-Thiophosphate)-Inositol-1,2,3,5-Tetra-O-Sulfate For C. Difficile Infection - EP3386994

The patent EP3386994 was granted to ETH Zrich on Dec 11, 2019. The application was originally filed on Dec 12, 2016 under application number EP16808705A. The patent is currently recorded with a legal status of "Opposition Rejected".

EP3386994

ETH ZRICH
Application Number
EP16808705A
Filing Date
Dec 12, 2016
Status
Opposition Rejected
Jun 10, 2022
Grant Date
Dec 11, 2019
External Links
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Patent Citations (6) New

Patent citations refer to prior patents cited during different phases such as opposition or international search.

Citation PhasePublication NumberPublication Link
DESCRIPTIONWO2013045107
EXAMINATIONEP0269105
EXAMINATIONUS9200015
INTERNATIONAL-SEARCH-REPORTWO2013045107
OPPOSITIONWO2012138963
OPPOSITIONWO2013045107

Non-Patent Literature (NPL) Citations (13) New

NPL citations refer to non-patent references such as research papers, articles, or other publications cited during examination or opposition phases.

Citation PhaseReference TextLink
DESCRIPTION- JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, (2005), vol. 127, page 5288-
DESCRIPTION- OHNISHI., ANA/. BIOCHEM., (1978), vol. 85, page 165-
DESCRIPTION- PROTEOMICS, (2001), vol. 1, page 1359-
EXAMINATION- Thomas S. Elliott ET AL, "The use of phosphate bioisosteres in medicinal chemistry and chemical biology", MedChemComm, United Kingdom, (20120101), vol. 3, no. 7, doi:10.1039/c2md20079a, ISSN 2040-2503, page 735, XP055569563
EXAMINATION- M R Hamblin ET AL, "myo -Inositol phosphorothioates, phosphatase-resistant analogues of myo -inositol phosphates. Synthesis of dl- myo -inositol 1,4-bisphosphate and dl- myo -inositol 1,4-bisphosphorothioate", BIOCHEMICAL JOURNAL, GB, (19870915), vol. 246, no. 3, doi:10.1042/bj2460771, ISSN 0264-6021, pages 771 - 774, XP055569564
INTERNATIONAL-SEARCH-REPORT- E DURANTIE, "Chemical Synthesis of Biomolecules Analogs: Inositol Phosphate/Sulfate Hybrids And Fluorinated Carbohydrates", DISS. ETH NO. 22532, ETH Zürich, (20150101), pages 1 - 84, XP055333064 [A] 1-5 * Chapter 2 *-
INTERNATIONAL-SEARCH-REPORT- ESTELLE DURANTIE ET AL, "New Paradigms for the Chiral Synthesis of Inositol Phosphates", CHEMBIOCHEM - A EUROPEAN JOURNAL OF CHEMICAL BIOLOGY., DE, (20150312), vol. 16, no. 7, doi:10.1002/cbic.201500071, ISSN 1439-4227, pages 1030 - 1032, XP055289967 [A] 1-5 * page 1031, column 2, line 25 - line 27 *
OPPOSITION- Cooke Allan M, Et Al, "myo-lnositol 1,4,5-Trisphosphorothioate: A Novel Analogue of a Biological Second Messenger", J. CHEM. SOC., CHEM. COMMUN, (19870101), pages 1525 - 1526, J. CHEM. SOC., CHEM. COMMUN, URL: https://pubs.rsc.org/en/content/articlepdf/1987/c3/c39870001525, (20210621), XP055815959-
OPPOSITION- COOKE A. M., "Synthesis and Biology of Inositol Phosphates and Thiophosphates", PhD Thesis, (19910000), pages 1 - 203-
OPPOSITION- E Durantie, "Chemical Synthesis of Biomolecules Analogs: Inositol Phosphate/Sulfate Hybrids And Fluorinated Carbohydrates", DISS. ETH No. 22532, ETH Zürich, ETH Zürich, ETH Zürich, (20150101), pages 1 - 84, XP055333064-
OPPOSITION- Thomas S. Elliott, Aine Slowey, Yulin Ye, Stuart J. Conway, "The use of phosphate bioisosteres in medicinal chemistry and chemical biology", MedChemComm, Royal Society of Chemistry, United Kingdom, United Kingdom, (20120101), vol. 3, no. 7, doi:10.1039/c2md20079a, ISSN 2040-2503, pages 735 - 751, XP055569563
OPPOSITION- M R Hamblin, J S Flora, B V L Potter, "myo -Inositol phosphorothioates, phosphatase-resistant analogues of myo -inositol phosphates. Synthesis of dl- myo -inositol 1,4-bisphosphate and dl- myo -inositol 1,4-bisphosphorothioate", Biochemical Journal, Published by Portland Press on behalf of the Biochemical Society., GB, GB, (19870915), vol. 246, no. 3, doi:10.1042/bj2460771, ISSN 0264-6021, pages 771 - 774, XP055569564
OPPOSITION- SMITH S. W., "Chiral Toxicology: It's the Same Thing...Only Different", Toxicological Sciences, (20090000), vol. 110, no. 1, doi:10.1093/toxsci/kfp097, pages 4 - 30, XP055172718

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