CN107529754A - 去乙酰氧基微管溶素h及其类似物 - Google Patents
去乙酰氧基微管溶素h及其类似物 Download PDFInfo
- Publication number
- CN107529754A CN107529754A CN201680023813.XA CN201680023813A CN107529754A CN 107529754 A CN107529754 A CN 107529754A CN 201680023813 A CN201680023813 A CN 201680023813A CN 107529754 A CN107529754 A CN 107529754A
- Authority
- CN
- China
- Prior art keywords
- substituted
- cycloalkyl
- alkylene
- groups
- alkyl
- 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.)
- Pending
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- 0 CC(C)[C@@](C[C@@](*)C(*1)=C*C=C1C(*(C)(C)[C@](C[C@](C)*)Cc1ccccc1)=O)*(C*C[C@@]1*(C)(C)C([C@@]2*(C)CCCC2)=C)C1=O Chemical compound CC(C)[C@@](C[C@@](*)C(*1)=C*C=C1C(*(C)(C)[C@](C[C@](C)*)Cc1ccccc1)=O)*(C*C[C@@]1*(C)(C)C([C@@]2*(C)CCCC2)=C)C1=O 0.000 description 24
- ZDYRSVVNRAEDEC-UHFFFAOYSA-N CC(C)C(CC(C(C1)C1SCC(COC(C)=O)N)O)N(C)C Chemical compound CC(C)C(CC(C(C1)C1SCC(COC(C)=O)N)O)N(C)C ZDYRSVVNRAEDEC-UHFFFAOYSA-N 0.000 description 1
- CNMOKBIDJYGNRL-UHFFFAOYSA-N CC(C)C(CC1)CC1C(N)=O Chemical compound CC(C)C(CC1)CC1C(N)=O CNMOKBIDJYGNRL-UHFFFAOYSA-N 0.000 description 1
- HUIXYLAASYKCMX-UHFFFAOYSA-N CC(C)C(CCO)N(C)C Chemical compound CC(C)C(CCO)N(C)C HUIXYLAASYKCMX-UHFFFAOYSA-N 0.000 description 1
- QEJUSVXBQZTZSA-RMVZNSSTSA-N CC(C)[C@@H](C[C@H](c1nc(C(N[C@H](C[C@H](C)C(O)=O)Cc2ncc[s]2)=O)c[s]1)OC(C)=O)N(C)C(CCC1CC1)=O Chemical compound CC(C)[C@@H](C[C@H](c1nc(C(N[C@H](C[C@H](C)C(O)=O)Cc2ncc[s]2)=O)c[s]1)OC(C)=O)N(C)C(CCC1CC1)=O QEJUSVXBQZTZSA-RMVZNSSTSA-N 0.000 description 1
- BLRHTMWXHCKKGZ-OJKIGWCBSA-N CCN[C@@H](C)C[C@H](Cc1ncc(C)cn1)NC(c1c[s]c(C2(C[C@H](C(C)C)N(C)C([C@H]([C@@H](C)C3CC3)NC3OC3[C@@H]3N(CC4)CCC4C3)=O)CC2)n1)=O Chemical compound CCN[C@@H](C)C[C@H](Cc1ncc(C)cn1)NC(c1c[s]c(C2(C[C@H](C(C)C)N(C)C([C@H]([C@@H](C)C3CC3)NC3OC3[C@@H]3N(CC4)CCC4C3)=O)CC2)n1)=O BLRHTMWXHCKKGZ-OJKIGWCBSA-N 0.000 description 1
- BLRDPTQCUONMPI-PELQVZONSA-N CC[C@H](C)[C@@H](C(N(C)[C@H](C[C@H](c1nc(C(/N=C(/C[C@H](C)C(OC)=O)\Cc2ccccc2)=O)c[s]1)OC(C)=O)C(C)C)=O)NC(c1ncccn1)=O Chemical compound CC[C@H](C)[C@@H](C(N(C)[C@H](C[C@H](c1nc(C(/N=C(/C[C@H](C)C(OC)=O)\Cc2ccccc2)=O)c[s]1)OC(C)=O)C(C)C)=O)NC(c1ncccn1)=O BLRDPTQCUONMPI-PELQVZONSA-N 0.000 description 1
- OZCJTNLELXWUTQ-SSDOTTSWSA-N NC([C@@H]1N(CC2)CCC2C1)=O Chemical compound NC([C@@H]1N(CC2)CCC2C1)=O OZCJTNLELXWUTQ-SSDOTTSWSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
- A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/021—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)n-C(=0)-, n being 5 or 6; for n > 6, classification in C07K5/06 - C07K5/10, according to the moiety having normal peptide bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06165—Dipeptides with the first amino acid being heterocyclic and Pro-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cell Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562120613P | 2015-02-25 | 2015-02-25 | |
| US62/120,613 | 2015-02-25 | ||
| US201662275667P | 2016-01-06 | 2016-01-06 | |
| US62/275,667 | 2016-01-06 | ||
| PCT/US2016/019604 WO2016138288A1 (en) | 2015-02-25 | 2016-02-25 | Desacetoxytubulysin h and analogs thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN107529754A true CN107529754A (zh) | 2018-01-02 |
Family
ID=56789084
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201680023813.XA Pending CN107529754A (zh) | 2015-02-25 | 2016-02-25 | 去乙酰氧基微管溶素h及其类似物 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US10808007B2 (enExample) |
| EP (1) | EP3261443B1 (enExample) |
| JP (1) | JP2018509404A (enExample) |
| KR (1) | KR20170137725A (enExample) |
| CN (1) | CN107529754A (enExample) |
| AU (1) | AU2016222575A1 (enExample) |
| BR (1) | BR112017018305A2 (enExample) |
| CA (1) | CA2977589A1 (enExample) |
| CL (1) | CL2017002170A1 (enExample) |
| CO (1) | CO2017008600A2 (enExample) |
| CR (1) | CR20170438A (enExample) |
| DO (1) | DOP2017000202A (enExample) |
| EA (1) | EA201791896A1 (enExample) |
| EC (1) | ECSP17057131A (enExample) |
| GT (1) | GT201700190A (enExample) |
| HK (1) | HK1248069A1 (enExample) |
| IL (1) | IL254089A0 (enExample) |
| MX (1) | MX2017011024A (enExample) |
| PE (1) | PE20180355A1 (enExample) |
| PH (1) | PH12017501539A1 (enExample) |
| SG (1) | SG11201706820RA (enExample) |
| WO (1) | WO2016138288A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017049140A2 (en) | 2015-09-18 | 2017-03-23 | Wake Forest University Health Sciences | Angiotensin (1-7) analogs and methods relating thereto |
| CA2914601A1 (en) * | 2015-12-11 | 2017-06-11 | Wake Forest University Health Sciences | Angiotensin-(1-7) analogs and methods relating thereto |
| JP2020525513A (ja) * | 2017-07-03 | 2020-08-27 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | 癌および他の疾患を治療するためのatf4阻害剤としてのn−(3−(2−(4−クロロフェノキシ)アセトアミドビシクロ[1.1.1]ペンタン−1−イル)−2−シクロブタン−1−カルボキサミド誘導体および関連化合物 |
| MA49858A (fr) | 2017-08-09 | 2021-04-28 | Denali Therapeutics Inc | Composés, compositions et procédés |
| JP7382308B2 (ja) | 2017-09-01 | 2023-11-16 | デナリ セラピューティクス インコーポレイテッド | 化合物、組成物、及び、方法 |
| BR112020004495A2 (pt) * | 2017-09-08 | 2020-09-08 | Seattle Genetics, Inc. | composto, composição, e, método para preparar uma composição. |
| US11274124B2 (en) | 2017-11-29 | 2022-03-15 | William Marsh Rice University | Tubulysin analogues as anticancer agents and payloads for antibody-drug conjugates and methods of treatment therewith |
| MA53765B2 (fr) | 2018-12-21 | 2025-04-30 | Regeneron Pharmaceuticals, Inc. | Tubulysines et conjugués tubulysines-protéines |
| CA3129609A1 (en) | 2019-02-13 | 2020-08-20 | Denali Therapeutics Inc. | Eukaryotic initiation factor 2b modulators |
| EP3924341A4 (en) | 2019-02-13 | 2022-11-02 | Denali Therapeutics Inc. | Compounds, compositions and methods |
| TWI750728B (zh) * | 2019-07-11 | 2021-12-21 | 大陸商蘇州亞盛藥業有限公司 | 2-吲哚啉螺環酮類化合物的製備方法及其中間體 |
| US11694341B2 (en) | 2019-12-23 | 2023-07-04 | Texas Instmments Incorporated | Cascaded architecture for disparity and motion prediction with block matching and convolutional neural network (CNN) |
| CN112645833A (zh) * | 2021-01-29 | 2021-04-13 | 上海吉奉生物科技有限公司 | 一种(s)-2,6-二氨基-5-氧己酸的合成方法 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004005327A1 (de) * | 2002-07-09 | 2004-01-15 | Morphochem Ag Komb Chemie | Neue tubulysinanaloga |
| US20050249740A1 (en) * | 2002-07-09 | 2005-11-10 | R & D Biopharmaceuticals Gmbh | Tubulysin conjugates |
| WO2010034724A1 (en) * | 2008-09-25 | 2010-04-01 | Universität des Saarlandes | Bioactive pre-tubulysins and use thereof |
| US20100240701A1 (en) * | 2007-10-25 | 2010-09-23 | Endocyte, Inc. | Tubulysins and processes for preparing |
| WO2011069116A1 (en) * | 2009-12-04 | 2011-06-09 | Endocyte, Inc. | Binding ligand linked drug delivery conjugates of tubulysins |
| CN102725001A (zh) * | 2009-08-03 | 2012-10-10 | 米德列斯公司 | 抗增殖化合物、其缀合物、其方法及其用途 |
| US20130137139A1 (en) * | 2010-08-06 | 2013-05-30 | Endocyte, Inc. | Processes for preparing tubulysins |
| WO2013149185A1 (en) * | 2012-03-29 | 2013-10-03 | Endocyte, Inc. | Processes for preparing tubulysin derivatives and conjugates thereof |
| US20140227295A1 (en) * | 2013-02-14 | 2014-08-14 | Bristol-Myers Squibb Company | Tubulysin compounds, methods of making and use |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008106080A2 (en) * | 2007-02-27 | 2008-09-04 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Synthesis of desacetoxytubulysin h and analogs thereof |
| US8980833B2 (en) * | 2007-05-10 | 2015-03-17 | R&D-Biopharmaceuticals Gmbh | Tubulysine derivatives |
| WO2009012958A2 (en) | 2007-07-20 | 2009-01-29 | Helmholtz-Zentrum für Infektionsforschung GmbH | Tubulysin d analogues |
| IT1394860B1 (it) * | 2009-07-22 | 2012-07-20 | Kemotech S R L | Composti farmaceutici |
| EP2322537A1 (en) * | 2009-11-12 | 2011-05-18 | R & D Biopharmaceuticals Gmbh | Tubulin inhibitors |
| EP2409983A1 (en) * | 2010-07-19 | 2012-01-25 | Leibniz-Institut für Pflanzenbiochemie (IPB) | Tubulysin analogues |
| SG11201608203RA (en) * | 2014-04-11 | 2016-10-28 | Medimmune Llc | Tubulysin derivatives |
-
2016
- 2016-02-25 JP JP2017545239A patent/JP2018509404A/ja active Pending
- 2016-02-25 WO PCT/US2016/019604 patent/WO2016138288A1/en not_active Ceased
- 2016-02-25 CR CR20170438A patent/CR20170438A/es unknown
- 2016-02-25 SG SG11201706820RA patent/SG11201706820RA/en unknown
- 2016-02-25 EP EP16756378.2A patent/EP3261443B1/en active Active
- 2016-02-25 CA CA2977589A patent/CA2977589A1/en not_active Abandoned
- 2016-02-25 MX MX2017011024A patent/MX2017011024A/es unknown
- 2016-02-25 BR BR112017018305A patent/BR112017018305A2/pt not_active Application Discontinuation
- 2016-02-25 AU AU2016222575A patent/AU2016222575A1/en not_active Abandoned
- 2016-02-25 CN CN201680023813.XA patent/CN107529754A/zh active Pending
- 2016-02-25 EA EA201791896A patent/EA201791896A1/ru unknown
- 2016-02-25 PE PE2017001465A patent/PE20180355A1/es unknown
- 2016-02-25 HK HK18107653.3A patent/HK1248069A1/zh unknown
- 2016-02-25 US US15/553,674 patent/US10808007B2/en active Active
- 2016-02-25 KR KR1020177027116A patent/KR20170137725A/ko not_active Withdrawn
-
2017
- 2017-08-22 IL IL254089A patent/IL254089A0/en unknown
- 2017-08-25 CL CL2017002170A patent/CL2017002170A1/es unknown
- 2017-08-25 PH PH12017501539A patent/PH12017501539A1/en unknown
- 2017-08-25 CO CONC2017/0008600A patent/CO2017008600A2/es unknown
- 2017-08-25 DO DO2017000202A patent/DOP2017000202A/es unknown
- 2017-08-25 GT GT201700190A patent/GT201700190A/es unknown
- 2017-08-30 EC ECIEPI201757131A patent/ECSP17057131A/es unknown
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004005327A1 (de) * | 2002-07-09 | 2004-01-15 | Morphochem Ag Komb Chemie | Neue tubulysinanaloga |
| US20050249740A1 (en) * | 2002-07-09 | 2005-11-10 | R & D Biopharmaceuticals Gmbh | Tubulysin conjugates |
| US20100240701A1 (en) * | 2007-10-25 | 2010-09-23 | Endocyte, Inc. | Tubulysins and processes for preparing |
| WO2010034724A1 (en) * | 2008-09-25 | 2010-04-01 | Universität des Saarlandes | Bioactive pre-tubulysins and use thereof |
| CN102725001A (zh) * | 2009-08-03 | 2012-10-10 | 米德列斯公司 | 抗增殖化合物、其缀合物、其方法及其用途 |
| WO2011069116A1 (en) * | 2009-12-04 | 2011-06-09 | Endocyte, Inc. | Binding ligand linked drug delivery conjugates of tubulysins |
| US20130137139A1 (en) * | 2010-08-06 | 2013-05-30 | Endocyte, Inc. | Processes for preparing tubulysins |
| CN103140227A (zh) * | 2010-08-06 | 2013-06-05 | 恩多塞特公司 | 制备微管蛋白细胞溶素的方法 |
| WO2013149185A1 (en) * | 2012-03-29 | 2013-10-03 | Endocyte, Inc. | Processes for preparing tubulysin derivatives and conjugates thereof |
| US20140227295A1 (en) * | 2013-02-14 | 2014-08-14 | Bristol-Myers Squibb Company | Tubulysin compounds, methods of making and use |
| CN105073139A (zh) * | 2013-02-14 | 2015-11-18 | 百时美施贵宝公司 | 妥布赖森化合物、制备和使用方法 |
Non-Patent Citations (2)
| Title |
|---|
| ANDREW W. PATTERSON ET AL: ""Expedient Synthesis of N-Methyl Tubulysin Analogues with High"", 《JOURNAL OF ORGANIC CHEMISTRY》 * |
| WANG ZHIYONG ET AL: ""Structure–activity and High-content Imaging"", 《CHEMICAL BIOLOGY & DRUG DESIGN 》 * |
Also Published As
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| IL254089A0 (en) | 2017-10-31 |
| EP3261443A1 (en) | 2018-01-03 |
| EP3261443A4 (en) | 2018-09-26 |
| WO2016138288A1 (en) | 2016-09-01 |
| EA201791896A1 (ru) | 2018-02-28 |
| HK1248069A1 (zh) | 2018-10-12 |
| GT201700190A (es) | 2018-11-26 |
| PH12017501539A1 (en) | 2018-02-05 |
| JP2018509404A (ja) | 2018-04-05 |
| CR20170438A (es) | 2018-01-30 |
| CA2977589A1 (en) | 2016-09-01 |
| ECSP17057131A (es) | 2019-03-29 |
| DOP2017000202A (es) | 2017-09-29 |
| EP3261443B1 (en) | 2021-04-28 |
| AU2016222575A1 (en) | 2017-09-07 |
| BR112017018305A2 (pt) | 2018-04-17 |
| CL2017002170A1 (es) | 2018-06-08 |
| US10808007B2 (en) | 2020-10-20 |
| CO2017008600A2 (es) | 2018-02-09 |
| MX2017011024A (es) | 2017-10-20 |
| US20180127463A1 (en) | 2018-05-10 |
| KR20170137725A (ko) | 2017-12-13 |
| PE20180355A1 (es) | 2018-02-21 |
| SG11201706820RA (en) | 2017-09-28 |
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