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EP3797115
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EP About this file: EP3797115
| EP3797115 - NEW SYNTHETIC METHODS USING NATIVE CHEMICAL LIGATION IN FLOW [Right-click to bookmark this link] | Status | Request for examination was made Status updated on 26.02.2021 Database last updated on 19.07.2024 | |
| Former | The international publication has been made Status updated on 30.11.2019 | Most recent event Tooltip | 28.05.2024 | New entry: Renewal fee paid | Applicant(s) | For all designated states The University Of Sydney Parramatta Road The University of Sydney New South Wales 2006 / AU | [2021/13] | Inventor(s) | 01 /
PAYNE, Richard J c/- Parramatta Road The University of Sydney, New South Wales 2006 / AU | 02 /
CHISHOLM, Tim c/- Parramatta Road The University of Sydney New South Wales 2006 / AU | [2021/15] |
| Former [2021/13] | 01 /
PAYNE, Richard J c/- Parramatta Road The University of Sydney, New South Wales 2006 / AU | ||
| 02 /
CHISHOLM, Tim c/- Parramatta Road The University of Sydney, New South Wales 2006 / AU | Representative(s) | McNamara, Kathryn Novagraaf UK Centrum Norwich Research Park Colney Lane Norwich, Norfolk NR4 7UG / GB | [2021/13] | Application number, filing date | 19807175.5 | 22.05.2019 | [2021/13] | WO2019AU50502 | Priority number, date | AU20180901799 | 22.05.2018 Original published format: AU 2018901799 | [2021/13] | Filing language | EN | Procedural language | EN | Publication | Type: | A1 Application with search report | No.: | WO2019222805 | Date: | 28.11.2019 | Language: | EN | [2019/48] | Type: | A1 Application with search report | No.: | EP3797115 | Date: | 31.03.2021 | Language: | EN | The application published by WIPO in one of the EPO official languages on 28.11.2019 takes the place of the publication of the European patent application. | [2021/13] | Search report(s) | International search report - published on: | AU | 28.11.2019 | (Supplementary) European search report - dispatched on: | EP | 09.06.2022 | Classification | IPC: | C07K1/02, C07K1/107, C07C327/22, C07C391/02, C07C323/36, C07C323/25 | [2022/11] | CPC: |
C07C323/25 (EP,AU,KR);
C07K14/001 (AU,KR);
C07K1/026 (EP,KR);
C07K1/1075 (US);
C07C323/36 (EP,AU);
C07C327/22 (EP,AU,KR);
C07C391/02 (EP,AU,KR);
C07K1/08 (AU);
C07K1/107 (EP);
C07K7/06 (KR,US)
(-)
|
| Former IPC [2021/13] | C07K14/00, C07K1/08, C07C327/22, C07C391/02, C07C323/25, C07C323/36 | Designated contracting states | AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR [2021/13] | Title | German: | NEUE SYNTHETISCHE VERFAHREN MIT NATIVER CHEMISCHER LIGATION IM STROM | [2021/13] | English: | NEW SYNTHETIC METHODS USING NATIVE CHEMICAL LIGATION IN FLOW | [2021/13] | French: | NOUVEAUX PROCÉDÉS SYNTHÉTIQUES UTILISANT UNE LIGATURE CHIMIQUE NATIVE EN FLUX | [2021/13] | Entry into regional phase | 21.12.2020 | National basic fee paid | 21.12.2020 | Search fee paid | 21.12.2020 | Designation fee(s) paid | 21.12.2020 | Examination fee paid | Examination procedure | 21.12.2020 | Examination requested [2021/13] | 19.12.2022 | Amendment by applicant (claims and/or description) | Fees paid | Renewal fee | 18.05.2021 | Renewal fee patent year 03 | 25.05.2022 | Renewal fee patent year 04 | 26.05.2023 | Renewal fee patent year 05 | 27.05.2024 | Renewal fee patent year 06 |
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| Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court. | Documents cited: | Search | [XYI]WO2013177221 (MASSACHUSETTS INST TECHNOLOGY [US]) [X] 1,2,4-6 * claim 1 * [Y] 7,10,13-15 [I] 3; | [XY] - LARA R. MALINS ET AL, "PEPTIDE LIGATION CHEMISTRY AT SELENOL AMINO ACIDS", JOURNAL OF PEPTIDE SIENCE, (20140101), vol. 20, no. 2, doi:10.1002/psc.2581, ISSN 1075-2617, pages 64 - 77, XP055480703 [X] 11-15 * page 70, column r, paragraph l * [Y] 7-10 DOI: http://dx.doi.org/10.1002/psc.2581 | [Y] - KULKARNI SAMEER S ET AL, "Rapid and efficient protein synthesis through expansion of the native chemical ligation concept", NATURE REVIEWS CHEMISTRY, NATURE PUBLISHING GROUP UK, LONDON, (20180329), vol. 2, no. 4, doi:10.1038/S41570-018-0122, XP037083894 [Y] 7-10,13-15 * page 3, column l * DOI: http://dx.doi.org/10.1038/s41570-018-0122 | [Y] - NORMAN METANIS ET AL, "Traceless Ligation of Cysteine Peptides Using Selective Deselenization", ANGEWANDTE CHEMIE, WILEY - V C H VERLAG GMBH & CO. KGAA, DE, (20100816), vol. 122, no. 39, doi:10.1002/ANGE.201001900, ISSN 0044-8249, pages 7203 - 7207, XP071346591 [Y] 8-10,13-15 * e.g. scheme 1 * DOI: http://dx.doi.org/10.1002/ange.201001900 | [Y] - ROBERT E. THOMPSON ET AL, "Chemoselective Peptide Ligation-Desulfurization at Aspartate", ANGEWANDTE CHEMIE INTERNATIONAL EDITION, (20130724), vol. 52, no. 37, doi:10.1002/anie.201304793, ISSN 1433-7851, pages 9723 - 9727, XP055297184 [Y] 8-10,13-15 * e.g. scheme 1 * DOI: http://dx.doi.org/10.1002/anie.201304793 | [IY] - BAUMANN MARCUS ET AL, "A Continuous-Flow Method for the Desulfurization of Substituted Thioimidazoles Applied to the Synthesis of Etomidate Derivatives", EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, DE, vol. 2017, no. 44, doi:10.1002/ejoc.201700833, ISSN 1434-193X, (20171201), pages 6518 - 6524, URL: https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fejoc.201700833, XP055925475 [I] 8 * e.g. scheme 3 * [Y] 9,10,13-15 DOI: http://dx.doi.org/10.1002/ejoc.201700833 | [XI] - CUESTA J ET AL, "Photochemical desulfurization of thiols and disulfides", TETRAHEDRON ASYMMETRY, PERGAMON PRESS LTD, OXFORD, GB, (19990716), vol. 10, no. 14, doi:10.1016/S0957-4166(99)00265-7, ISSN 0957-4166, pages 2643 - 2646, XP004177224 [X] 11,13-15 * the whole document * [I] 12 DOI: http://dx.doi.org/10.1016/S0957-4166(99)00265-7 | International search | [X]WO2014194361 (UNIV SYDNEY [AU]) [X] 1-19, 22, 25-28 * see paragraphs [000174]-[000176], pages 64-66; paragraph [00066], page 22 *; | [X] - WATSON, E. E. et al., "Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics", ACS Central Science, (20180000), vol. 4, no. 4, pages 468 - 476, XP055655563 [X] 1-19, 22, 25-28 * . Scheme 2, & column 2, page 472; columns 1-2, page 473; and column 1, page 474 * DOI: http://dx.doi.org/10.1021/acscentsci.7b00612 | [X] - MALINS, L. R. et al., "Synthetic Amino Acids for Applications in Peptide Ligation- Desulfurization Chemistry", Australian Journal of Chemistry, (20150000), vol. 68, no. 4, pages 521 - 537, XP055655567 [X] 1-19, 22, 25-28 * . Schemes 1-2, pages 522-523; columns 1-2, page 534; and Scheme 20(a), page 536; column 1, page 530 * DOI: http://dx.doi.org/10.1071/CH14568 | [X] - DANG, B. et al., "Native Chemical Ligation at Asx-Cys, Glx-Cys: Chemical Synthesis and High-Resolution X-ray Structure of ShK Toxin by Racemic Protein Crystallography", Journal of the American Chemical Society, vol. 135, no. 32, pages 11911 - 11919, XP055655571 [X] 1-19, 22, 25-28 * . Abstract; and "Introduction", page 11911; column 2, page 11913; and column 1, page 11914 * DOI: http://dx.doi.org/10.1021/ja4046795 | [X] - MONBALIU, J-C. et al., "Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs", Chemical Communications, (20120000), vol. 48, no. 95, doi:10.1039/c2cc34434c, pages 11601 - 11622, XP055571155 [X] 1-19, 22, 25-28 * . see Section 2, pages 11602-11612; Section 2.4, pages 11610; and Fig. 5, page 11611; Figs. 4 and 6, page 11605; see Section 5 "Outlook", page 11619 * DOI: http://dx.doi.org/10.1039/c2cc34434c |