WO2007051081A8 - Methods and compounds for preparing cc-1065 analogs - Google Patents
Methods and compounds for preparing cc-1065 analogs Download PDFInfo
- Publication number
- WO2007051081A8 WO2007051081A8 PCT/US2006/060050 US2006060050W WO2007051081A8 WO 2007051081 A8 WO2007051081 A8 WO 2007051081A8 US 2006060050 W US2006060050 W US 2006060050W WO 2007051081 A8 WO2007051081 A8 WO 2007051081A8
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- analogs
- preparing
- compounds
- methods
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/58—[b]- or [c]-condensed
- C07D209/60—Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Abstract
Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008538132A JP5116686B2 (en) | 2005-10-26 | 2006-10-18 | Methods for preparing CC-1065 analogs and compounds for preparation |
CN2006800491755A CN101365679B (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
AU2006305842A AU2006305842B2 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing CC-1065 analogs |
ES06839458T ES2375843T3 (en) | 2005-10-26 | 2006-10-18 | PROCEDURES AND COMPOUNDS FOR THE PREPARATION OF ANC? LOGOS OF CC-1065. |
CA2627046A CA2627046C (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
BRPI0619331-5A BRPI0619331A2 (en) | 2005-10-26 | 2006-10-18 | method for making a compound to prepare a cbi cc-1065 analog, method for making a cbi cc-1065 analog and compound |
PL06839458T PL1940789T3 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
US12/090,445 US7847105B2 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing CC-1065 analogs |
DK06839458.4T DK1940789T3 (en) | 2005-10-26 | 2006-10-18 | Methods and Compounds for the Preparation of CC-1065 Analogs |
AT06839458T ATE534629T1 (en) | 2005-10-26 | 2006-10-18 | METHOD AND COMPOUNDS FOR PRODUCING CC-1065 ANALOGUE |
EP06839458A EP1940789B1 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
EA200801176A EA015324B1 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
IL190971A IL190971A (en) | 2005-10-26 | 2008-04-17 | Method of making a tricyclic compound and a method of making a cbi cc-1065 analog |
NO20082243A NO20082243L (en) | 2005-10-26 | 2008-05-15 | Methods and Compounds for Preparation of CC-1065 Analogs |
HK08110088.4A HK1118549A1 (en) | 2005-10-26 | 2008-09-11 | Methods and compounds for preparing cc-1065 analogs |
HR20120058T HRP20120058T1 (en) | 2005-10-26 | 2012-01-19 | Methods and compounds for preparing cc-1065 analogs |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73080405P | 2005-10-26 | 2005-10-26 | |
US60/730,804 | 2005-10-26 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2007051081A1 WO2007051081A1 (en) | 2007-05-03 |
WO2007051081B1 WO2007051081B1 (en) | 2007-07-19 |
WO2007051081A8 true WO2007051081A8 (en) | 2010-12-16 |
Family
ID=37766648
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/060050 WO2007051081A1 (en) | 2005-10-26 | 2006-10-18 | Methods and compounds for preparing cc-1065 analogs |
Country Status (23)
Country | Link |
---|---|
US (1) | US7847105B2 (en) |
EP (1) | EP1940789B1 (en) |
JP (1) | JP5116686B2 (en) |
KR (1) | KR20080068084A (en) |
CN (1) | CN101365679B (en) |
AT (1) | ATE534629T1 (en) |
AU (1) | AU2006305842B2 (en) |
BR (1) | BRPI0619331A2 (en) |
CA (1) | CA2627046C (en) |
CY (1) | CY1112533T1 (en) |
DK (1) | DK1940789T3 (en) |
EA (1) | EA015324B1 (en) |
ES (1) | ES2375843T3 (en) |
HK (1) | HK1118549A1 (en) |
HR (1) | HRP20120058T1 (en) |
IL (1) | IL190971A (en) |
NO (1) | NO20082243L (en) |
PL (1) | PL1940789T3 (en) |
PT (1) | PT1940789E (en) |
RS (1) | RS52100B (en) |
SI (1) | SI1940789T1 (en) |
WO (1) | WO2007051081A1 (en) |
ZA (1) | ZA200804521B (en) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100056762A1 (en) | 2001-05-11 | 2010-03-04 | Old Lloyd J | Specific binding proteins and uses thereof |
US7589180B2 (en) | 2001-05-11 | 2009-09-15 | Abbott Laboratories Inc. | Specific binding proteins and uses thereof |
US8124738B2 (en) | 2005-09-26 | 2012-02-28 | Medarex, Inc. | Human monoclonal antibodies to CD70 |
WO2008091701A2 (en) | 2007-01-25 | 2008-07-31 | Dana-Farber Cancer Institute | Use of anti-egfr antibodies in treatment of egfr mutant mediated disease |
WO2008115404A1 (en) | 2007-03-15 | 2008-09-25 | Ludwing Institute For Cancer Research | Treatment method using egfr antibodies and src inhibitors and related formulations |
US9901567B2 (en) | 2007-08-01 | 2018-02-27 | Syntarga B.V. | Substituted CC-1065 analogs and their conjugates |
CA2696360C (en) | 2007-08-14 | 2018-11-20 | Ludwig Institute For Cancer Research | Monoclonal antibody targeting the egfr receptor and uses thereof |
WO2009026274A1 (en) | 2007-08-22 | 2009-02-26 | Medarex, Inc. | Site-specific attachment of drugs or other agents to engineered antibodies with c-terminal extensions |
PL2195017T3 (en) | 2007-10-01 | 2015-03-31 | Bristol Myers Squibb Co | Human antibodies that bind mesothelin, and uses thereof |
AR072999A1 (en) | 2008-08-11 | 2010-10-06 | Medarex Inc | HUMAN ANTIBODIES THAT JOIN GEN 3 OF LYMPHOCYTARY ACTIVATION (LAG-3) AND THE USES OF THESE |
HUE035798T2 (en) | 2008-11-03 | 2018-05-28 | Syntarga Bv | Cc-1065 analogs and their conjugates |
WO2010096394A2 (en) | 2009-02-17 | 2010-08-26 | Redwood Biosciences, Inc. | Aldehyde-tagged protein-based drug carriers and methods of use |
CN102341412B (en) | 2009-03-05 | 2018-01-05 | 梅达雷克斯有限责任公司 | It is specific to CADM1 human antibody |
US8394922B2 (en) | 2009-08-03 | 2013-03-12 | Medarex, Inc. | Antiproliferative compounds, conjugates thereof, methods therefor, and uses thereof |
ES2815678T3 (en) | 2010-04-21 | 2021-03-30 | Syntarga Bv | Conjugates of CC-1065 Analogs and Bifunctional Linkers |
US8956859B1 (en) | 2010-08-13 | 2015-02-17 | Aviex Technologies Llc | Compositions and methods for determining successful immunization by one or more vaccines |
JOP20210044A1 (en) | 2010-12-30 | 2017-06-16 | Takeda Pharmaceuticals Co | Anti-cd38 antibodies |
AU2012205301B2 (en) | 2011-01-14 | 2017-01-05 | Redwood Bioscience, Inc. | Aldehyde-tagged immunoglobulin polypeptides and method of use thereof |
DK2814829T3 (en) | 2012-02-13 | 2017-03-20 | Bristol Myers Squibb Co | RELATIONSHIPS, CONJUGATES THEREOF AND USES AND RELATED PROCEDURES |
UY34887A (en) | 2012-07-02 | 2013-12-31 | Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware | OPTIMIZATION OF ANTIBODIES THAT FIX THE LYMPHOCYTE ACTIVATION GEN 3 (LAG-3) AND ITS USES |
CN105073139B (en) | 2013-02-14 | 2019-01-11 | 百时美施贵宝公司 | Appropriate Bu Laisen compound, preparation and application |
KR102323301B1 (en) | 2014-01-10 | 2021-11-09 | 비온디스 비.브이. | Method for purifying cys-linked antibody-drug conjugates |
HUE029672T2 (en) | 2014-01-10 | 2017-03-28 | Synthon Biopharmaceuticals Bv | Duocarmycin adcs for use in treatment of endometrial cancer |
KR102344354B1 (en) | 2014-01-10 | 2021-12-28 | 비온디스 비.브이. | Duocarmycin adcs showing improved in vivo antitumor activity |
EP3119803B1 (en) | 2014-03-20 | 2019-09-11 | Bristol-Myers Squibb Company | Stabilized fibronectin based scaffold molecules |
EP3151921B1 (en) | 2014-06-06 | 2019-08-28 | Bristol-Myers Squibb Company | Antibodies against glucocorticoid-induced tumor necrosis factor receptor (gitr) and uses thereof |
US10077287B2 (en) | 2014-11-10 | 2018-09-18 | Bristol-Myers Squibb Company | Tubulysin analogs and methods of making and use |
TWI758928B (en) | 2014-11-21 | 2022-03-21 | 美商必治妥美雅史谷比公司 | Antibodies against cd73 and uses thereof |
HUE052526T2 (en) | 2014-11-21 | 2021-05-28 | Bristol Myers Squibb Co | Antibodies comprising modified heavy constant regions |
JP6701217B2 (en) | 2014-11-25 | 2020-05-27 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 18F-radiolabeling methods and compositions for biologics |
KR102632418B1 (en) | 2014-11-25 | 2024-01-31 | 브리스톨-마이어스 스큅 컴퍼니 | Novel pd-l1 binding polypeptides for imaging |
PL3233912T3 (en) | 2014-12-19 | 2021-12-27 | Regenesance B.V. | Antibodies that bind human c6 and uses thereof |
AU2016206808A1 (en) | 2015-01-14 | 2017-08-31 | Bristol-Myers Squibb Company | Heteroarylene-bridged benzodiazepine dimers, conjugates thereof, and methods of making and using |
CN108884147B (en) | 2015-09-23 | 2024-02-27 | 百时美施贵宝公司 | Fibronectin-based scaffold molecules that bind glypican 3 |
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US20190284293A1 (en) | 2016-03-04 | 2019-09-19 | Bristol-Myers Squibb Company | Combination therapy with anti-cd73 antibodies |
WO2017189432A1 (en) | 2016-04-26 | 2017-11-02 | R.P. Scherer Technologies, Llc | Antibody conjugates and methods of making and using the same |
WO2017210335A1 (en) | 2016-06-01 | 2017-12-07 | Bristol-Myers Squibb Company | Imaging methods using 18f-radiolabeled biologics |
CN109562195A (en) | 2016-06-01 | 2019-04-02 | 百时美施贵宝公司 | PET imaging is carried out with PD-L1 combination polypeptide |
CN117683135A (en) | 2016-07-14 | 2024-03-12 | 百时美施贵宝公司 | Antibodies against TIM3 and uses thereof |
CN109641911B (en) | 2016-08-19 | 2023-02-21 | 百时美施贵宝公司 | seco-cyclopropylpyrroloindole compounds and antibody-drug conjugates thereof and methods of making and using |
WO2018075842A1 (en) | 2016-10-20 | 2018-04-26 | Bristol-Myers Squibb Company | Condensed benzodiazepine derivatives and conjugates made therefrom |
SG11201906947SA (en) | 2017-02-17 | 2019-08-27 | Bristol Myers Squibb Co | Antibodies to alpha-synuclein and uses thereof |
WO2018208868A1 (en) | 2017-05-10 | 2018-11-15 | Smet Pharmaceutical Inc | Human monoclonal antibodies against lag3 and uses thereof |
KR20200013241A (en) | 2017-05-25 | 2020-02-06 | 브리스톨-마이어스 스큅 컴퍼니 | Antibodies Containing Modified Heavy Chain Constant Regions |
US10472361B2 (en) | 2017-08-16 | 2019-11-12 | Bristol-Myers Squibb Company | Toll-like receptor 7 (TLR7) agonists having a benzotriazole moiety, conjugates thereof, and methods and uses therefor |
US10487084B2 (en) | 2017-08-16 | 2019-11-26 | Bristol-Myers Squibb Company | Toll-like receptor 7 (TLR7) agonists having a heterobiaryl moiety, conjugates thereof, and methods and uses therefor |
US10457681B2 (en) | 2017-08-16 | 2019-10-29 | Bristol_Myers Squibb Company | Toll-like receptor 7 (TLR7) agonists having a tricyclic moiety, conjugates thereof, and methods and uses therefor |
US10494370B2 (en) | 2017-08-16 | 2019-12-03 | Bristol-Myers Squibb Company | Toll-like receptor 7 (TLR7) agonists having a pyridine or pyrazine moiety, conjugates thereof, and methods and uses therefor |
US10508115B2 (en) | 2017-08-16 | 2019-12-17 | Bristol-Myers Squibb Company | Toll-like receptor 7 (TLR7) agonists having heteroatom-linked aromatic moieties, conjugates thereof, and methods and uses therefor |
WO2019075090A1 (en) | 2017-10-10 | 2019-04-18 | Tilos Therapeutics, Inc. | Anti-lap antibodies and uses thereof |
KR20200108870A (en) | 2018-01-12 | 2020-09-21 | 브리스톨-마이어스 스큅 컴퍼니 | Antibodies to TIM3 and uses thereof |
CN111886256A (en) | 2018-03-23 | 2020-11-03 | 百时美施贵宝公司 | anti-MICA and/or MICB antibodies and uses thereof |
TWI790370B (en) | 2018-04-02 | 2023-01-21 | 美商必治妥美雅史谷比公司 | Anti-trem-1 antibodies and uses thereof |
US11485741B2 (en) | 2018-04-24 | 2022-11-01 | Bristol-Myers Squibb Company | Macrocyclic toll-like receptor 7 (TLR7) agonists |
US11884729B2 (en) | 2018-06-29 | 2024-01-30 | ApitBio, Inc | Anti-L1CAM antibodies and uses thereof |
US11554120B2 (en) | 2018-08-03 | 2023-01-17 | Bristol-Myers Squibb Company | 1H-pyrazolo[4,3-d]pyrimidine compounds as toll-like receptor 7 (TLR7) agonists and methods and uses therefor |
US11130802B2 (en) | 2018-10-10 | 2021-09-28 | Tilos Therapeutics, Inc. | Anti-lap antibody variants |
EP3887397A1 (en) | 2018-11-28 | 2021-10-06 | Bristol-Myers Squibb Company | Antibodies comprising modified heavy constant regions |
US20210403602A1 (en) | 2018-12-03 | 2021-12-30 | Bristol-Myers Squibb Company | Anti-ido antibody and uses thereof |
CN109762067B (en) | 2019-01-17 | 2020-02-28 | 北京天广实生物技术股份有限公司 | Antibodies that bind human Claudin18.2 and uses thereof |
PE20212305A1 (en) | 2019-01-22 | 2021-12-10 | Bristol Myers Squibb Co | ANTIBODIES AGAINST IL-7R ALPHA SUBUNIT AND USES OF THESE |
WO2021011681A1 (en) | 2019-07-15 | 2021-01-21 | Bristol-Myers Squibb Company | Antibodies against human trem-1 and uses thereof |
WO2021011678A1 (en) | 2019-07-15 | 2021-01-21 | Bristol-Myers Squibb Company | Anti-trem-1 antibodies and uses thereof |
CN114945409A (en) | 2020-01-13 | 2022-08-26 | 新免疫技术有限公司 | Methods of treating tumors with combinations of IL-7 proteins and bispecific antibodies |
CN115087673A (en) | 2020-02-27 | 2022-09-20 | 正大天晴药业集团股份有限公司 | Antibodies that bind IL4R and uses thereof |
EP4132971A1 (en) | 2020-04-09 | 2023-02-15 | Merck Sharp & Dohme LLC | Affinity matured anti-lap antibodies and uses thereof |
CN114685669A (en) | 2020-12-30 | 2022-07-01 | 和铂医药(苏州)有限公司 | Antibodies that bind TROP2 and uses thereof |
JP2024514530A (en) | 2021-04-02 | 2024-04-02 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Antibodies against truncated CDCP1 and uses thereof |
Family Cites Families (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4169888A (en) | 1977-10-17 | 1979-10-02 | The Upjohn Company | Composition of matter and process |
US4391904A (en) | 1979-12-26 | 1983-07-05 | Syva Company | Test strip kits in immunoassays and compositions therein |
US4671958A (en) | 1982-03-09 | 1987-06-09 | Cytogen Corporation | Antibody conjugates for the delivery of compounds to target sites |
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
US4912227A (en) | 1984-02-21 | 1990-03-27 | The Upjohn Company | 1,2,8,8A-tetrahydrocyclopropa(c)pyrrolo(3,2-e)-indol-4-(5H)-ones and related compounds |
US4978757A (en) | 1984-02-21 | 1990-12-18 | The Upjohn Company | 1,2,8,8a-tetrahydrocyclopropa (C) pyrrolo [3,2-e)]-indol-4(5H)-ones and related compounds |
US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
JPH0684377B1 (en) | 1986-04-17 | 1994-10-26 | Kyowa Hakko Kogyo Kk | |
US5332837A (en) | 1986-12-19 | 1994-07-26 | The Upjohn Company | CC-1065 analogs |
US5773435A (en) | 1987-08-04 | 1998-06-30 | Bristol-Myers Squibb Company | Prodrugs for β-lactamase and uses thereof |
US4975278A (en) | 1988-02-26 | 1990-12-04 | Bristol-Myers Company | Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells |
US4952394A (en) | 1987-11-23 | 1990-08-28 | Bristol-Myers Company | Drug-monoclonal antibody conjugates |
US4994578A (en) | 1987-11-27 | 1991-02-19 | Meiji Seika Kaisha, Ltd. | Certain anti-tumor duocarmycin antibiotics from streptomyces |
US5147786A (en) | 1988-04-22 | 1992-09-15 | Monsanto Company | Immunoassay for the detection of α-haloacetamides |
JP2642165B2 (en) | 1988-07-22 | 1997-08-20 | 協和醗酵工業株式会社 | Novel DC-89 compound and method for producing the same |
US5084468A (en) | 1988-08-11 | 1992-01-28 | Kyowa Hakko Kogyo Co., Ltd. | Dc-88a derivatives |
US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
US5176996A (en) | 1988-12-20 | 1993-01-05 | Baylor College Of Medicine | Method for making synthetic oligonucleotides which bind specifically to target sites on duplex DNA molecules, by forming a colinear triplex, the synthetic oligonucleotides and methods of use |
JP2598116B2 (en) | 1988-12-28 | 1997-04-09 | 協和醗酵工業株式会社 | New substance DC113 |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
US5187186A (en) | 1989-07-03 | 1993-02-16 | Kyowa Hakko Kogyo Co., Ltd. | Pyrroloindole derivatives |
JP2510335B2 (en) | 1989-07-03 | 1996-06-26 | 協和醗酵工業株式会社 | DC-88A derivative |
US5495009A (en) | 1989-10-24 | 1996-02-27 | Gilead Sciences, Inc. | Oligonucleotide analogs containing thioformacetal linkages |
US5334528A (en) | 1989-10-30 | 1994-08-02 | The Regents Of The University Of California | Monoclonal antibodies to cyclodiene insecticides and method for detecting the same |
US6075181A (en) | 1990-01-12 | 2000-06-13 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
US6673986B1 (en) | 1990-01-12 | 2004-01-06 | Abgenix, Inc. | Generation of xenogeneic antibodies |
EP1690935A3 (en) | 1990-01-12 | 2008-07-30 | Abgenix, Inc. | Generation of xenogeneic antibodies |
US6150584A (en) | 1990-01-12 | 2000-11-21 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
KR100208957B1 (en) | 1990-04-25 | 1999-07-15 | 로렌스 티. 마이젠헬더 | Novel cc-1065 analogues |
US5427908A (en) | 1990-05-01 | 1995-06-27 | Affymax Technologies N.V. | Recombinant library screening methods |
US5137877B1 (en) | 1990-05-14 | 1996-01-30 | Bristol Myers Squibb Co | Bifunctional linking compounds conjugates and methods for their production |
GB9015198D0 (en) | 1990-07-10 | 1990-08-29 | Brien Caroline J O | Binding substance |
US6172197B1 (en) | 1991-07-10 | 2001-01-09 | Medical Research Council | Methods for producing members of specific binding pairs |
DE69121334T2 (en) | 1990-07-26 | 1997-03-20 | Kyowa Hakko Kogyo Kk | DC-89 derivatives as anti-tumor agents |
GB9017024D0 (en) | 1990-08-03 | 1990-09-19 | Erba Carlo Spa | New linker for bioactive agents |
US5877397A (en) | 1990-08-29 | 1999-03-02 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
US5874299A (en) | 1990-08-29 | 1999-02-23 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
US5814318A (en) | 1990-08-29 | 1998-09-29 | Genpharm International Inc. | Transgenic non-human animals for producing heterologous antibodies |
US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
US5770429A (en) | 1990-08-29 | 1998-06-23 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
US5789650A (en) | 1990-08-29 | 1998-08-04 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
ES2246502T3 (en) | 1990-08-29 | 2006-02-16 | Genpharm International, Inc. | TRANSGENIC NON-HUMAN ANIMALS ABLE TO PRODUCE HETEROLOGICAL ANTIBODIES. |
JPH0597853A (en) | 1991-10-07 | 1993-04-20 | Kyowa Hakko Kogyo Co Ltd | Hydrobromic acid salt of dc-89 derivative |
ATE275198T1 (en) | 1991-12-02 | 2004-09-15 | Medical Res Council | PRODUCTION OF ANTIBODIES ON PHAGE SURFACES BASED ON ANTIBODIES SEGMENT LIBRARIES. |
US5622929A (en) | 1992-01-23 | 1997-04-22 | Bristol-Myers Squibb Company | Thioether conjugates |
ES2149768T3 (en) | 1992-03-25 | 2000-11-16 | Immunogen Inc | CONJUGATES OF BINDING AGENTS OF CELLS DERIVED FROM CC-1065. |
GB9314960D0 (en) | 1992-07-23 | 1993-09-01 | Zeneca Ltd | Chemical compounds |
JP3514490B2 (en) | 1992-08-21 | 2004-03-31 | 杏林製薬株式会社 | Trifluoromethylpyrroloindole carboxylate derivative and method for producing the same |
US5288514A (en) | 1992-09-14 | 1994-02-22 | The Regents Of The University Of California | Solid phase and combinatorial synthesis of benzodiazepine compounds on a solid support |
US5324483B1 (en) | 1992-10-08 | 1996-09-24 | Warner Lambert Co | Apparatus for multiple simultaneous synthesis |
DE4314091A1 (en) | 1993-04-29 | 1994-11-03 | Boehringer Mannheim Gmbh | Immunological detection method for triazines |
US6214345B1 (en) | 1993-05-14 | 2001-04-10 | Bristol-Myers Squibb Co. | Lysosomal enzyme-cleavable antitumor drug conjugates |
US5786377A (en) | 1993-11-19 | 1998-07-28 | Universidad De Santiago De Compostela | Pyrrolo 3,2-E!indol derivatives, process for the preparation thereof and applications |
AU685939B2 (en) | 1994-04-22 | 1998-01-29 | Kyowa Hakko Kogyo Co. Ltd. | DC-89 derivative |
JPH07309761A (en) | 1994-05-20 | 1995-11-28 | Kyowa Hakko Kogyo Co Ltd | Method for stabilizing duocamycin derivative |
US5773001A (en) | 1994-06-03 | 1998-06-30 | American Cyanamid Company | Conjugates of methyltrithio antitumor agents and intermediates for their synthesis |
ES2297832T3 (en) | 1994-08-19 | 2008-05-01 | La Region Wallonne | CONJUGATES UNDERSTANDING AN ANTITUMORAL AGENT AND ITS USE. |
EP0786252A4 (en) | 1994-09-30 | 1998-01-07 | Kyowa Hakko Kogyo Kk | Antitumor agent |
AU693283B2 (en) | 1994-11-29 | 1998-06-25 | Kyorin Pharmaceutical Co. Ltd. | Acrylamide derivatives and process for producing the same |
JP3871713B2 (en) | 1995-05-10 | 2007-01-24 | 協和醗酵工業株式会社 | Novel toxin complex |
US5686237A (en) | 1995-06-05 | 1997-11-11 | Al-Bayati; Mohammed A. S. | Use of biomarkers in saliva to evaluate the toxicity of agents and the function of tissues in both biomedical and environmental applications |
US5646298A (en) * | 1995-06-07 | 1997-07-08 | Procoron, Inc. | Cyclopropylindole prodrugs |
US5712374A (en) | 1995-06-07 | 1998-01-27 | American Cyanamid Company | Method for the preparation of substantiallly monomeric calicheamicin derivative/carrier conjugates |
US5714586A (en) | 1995-06-07 | 1998-02-03 | American Cyanamid Company | Methods for the preparation of monomeric calicheamicin derivative/carrier conjugates |
AU727608B2 (en) * | 1995-10-03 | 2000-12-14 | Scripps Research Institute, The | CBI analogs of CC-1065 and the duocarmycins |
CA2187969C (en) | 1995-10-17 | 2006-05-30 | Dale L. Boger | A template for solution phase synthesis of combinatorial libraries |
DE69626849T2 (en) | 1995-12-22 | 2003-12-24 | Bristol Myers Squibb Co | BRANCHED HYDRAZONE GROUPS OF COUPLERS |
US6143901A (en) | 1996-07-31 | 2000-11-07 | Genesoft, Inc. | Complex formation between dsDNA and pyrrole imidazole polyamides |
US5985908A (en) * | 1996-03-08 | 1999-11-16 | The Scripps Research Institute | MCBI analogs of CC-1065 and the duocarmycins |
AU3217897A (en) * | 1996-05-31 | 1998-01-05 | Scripps Research Institute, The | Analogs of cc-1065 and the duocarmycins |
US6130237A (en) | 1996-09-12 | 2000-10-10 | Cancer Research Campaign Technology Limited | Condensed N-aclyindoles as antitumor agents |
JPH1087666A (en) | 1996-09-18 | 1998-04-07 | Kyorin Pharmaceut Co Ltd | Intermediate for producing duocarmycin sa and its derivative and production thereof |
US6759509B1 (en) | 1996-11-05 | 2004-07-06 | Bristol-Myers Squibb Company | Branched peptide linkers |
CA2285259A1 (en) | 1997-03-28 | 1998-10-08 | The Scripps Research Institute | Sandramycin analogs |
JP2002510968A (en) | 1997-05-07 | 2002-04-09 | ブリストル−マイヤーズ スクイブ カンパニー | Recombinant antibody-enzyme fusion protein |
EP0983248B1 (en) | 1997-05-22 | 2004-07-14 | The Scripps Research Institute | Analogs of duocarmycin and cc-1065 |
IL135616A0 (en) | 1997-10-14 | 2001-05-20 | Scripps Research Inst | Iso-cbi and iso-ci analogs of cc-1065 and the duocarmycins |
CA2313231A1 (en) * | 1997-12-08 | 1999-06-17 | The Scripps Research Institute | Synthesis of cc-1065/duocarmycin analogs |
JP3045706B1 (en) | 1998-09-14 | 2000-05-29 | 科学技術振興事業団 | Compound for alkylating a specific base sequence of DNA and method for synthesizing the same |
US7425541B2 (en) | 1998-12-11 | 2008-09-16 | Medarex, Inc. | Enzyme-cleavable prodrug compounds |
US6909006B1 (en) * | 1999-08-27 | 2005-06-21 | Spirogen Limited | Cyclopropylindole derivatives |
ATE344801T1 (en) | 1999-12-29 | 2006-11-15 | Immunogen Inc | CYTOTOXIC AGENTS CONTAINING DOXORUBICIN AND DAUNORUBICIN AND THEIR THERAPEUTIC USE |
US6559125B1 (en) * | 2000-01-28 | 2003-05-06 | California Institute Of Technology | Polyamide-alkylator conjugates and related products and method |
CN1427839A (en) | 2000-03-16 | 2003-07-02 | 根索福特股份有限公司 | Charged compounds comprising nucleic acid binding moiety and uses therefor |
JP4061819B2 (en) | 2000-05-12 | 2008-03-19 | 独立行政法人科学技術振興機構 | Method for synthesizing interstrand crosslinker |
AU2001275525B2 (en) | 2000-06-14 | 2007-04-26 | Medarex, Inc. | Tripeptide prodrug compounds |
US7115573B2 (en) | 2000-06-14 | 2006-10-03 | Medarex, Inc. | Prodrug compounds with an isoleucine |
EP1243276A1 (en) | 2001-03-23 | 2002-09-25 | Franciscus Marinus Hendrikus De Groot | Elongated and multiple spacers containing activatible prodrugs |
US20030083263A1 (en) | 2001-04-30 | 2003-05-01 | Svetlana Doronina | Pentapeptide compounds and uses related thereto |
US6884869B2 (en) | 2001-04-30 | 2005-04-26 | Seattle Genetics, Inc. | Pentapeptide compounds and uses related thereto |
US7256257B2 (en) | 2001-04-30 | 2007-08-14 | Seattle Genetics, Inc. | Pentapeptide compounds and uses related thereto |
MXPA03010961A (en) | 2001-05-31 | 2004-02-27 | Vertex Pharma | Thiazole compounds useful as inhibitors of protein kinases. |
EP1434778A4 (en) | 2001-05-31 | 2005-07-13 | Medarex Inc | Cytotoxins, prodrugs, linkers and stabilizers useful therefor |
WO2002100353A2 (en) | 2001-06-11 | 2002-12-19 | Medarex, Inc. | Cd10-activated prodrug compounds |
US20050014700A1 (en) | 2001-09-07 | 2005-01-20 | Boger Dale L. | Cbi analogues of cc-1065 and the duocarmycins |
US7091186B2 (en) | 2001-09-24 | 2006-08-15 | Seattle Genetics, Inc. | p-Amidobenzylethers in drug delivery agents |
US6756397B2 (en) * | 2002-04-05 | 2004-06-29 | Immunogen, Inc. | Prodrugs of CC-1065 analogs |
US6534660B1 (en) * | 2002-04-05 | 2003-03-18 | Immunogen, Inc. | CC-1065 analog synthesis |
US7816377B2 (en) | 2002-07-09 | 2010-10-19 | R&D-Biopharmaceuticals Gmbh | Tubulysin analogues |
AU2003253048A1 (en) | 2002-07-09 | 2004-01-23 | Morphochem Aktiengellschaft Fur Kombinatorische Chemie | Tubulysin conjugates |
WO2004101767A2 (en) | 2003-05-13 | 2004-11-25 | The Scripps Research Institute | Cbi analogues of the duocarmycins and cc-1065 |
BRPI0510909A2 (en) * | 2004-05-19 | 2008-12-16 | Medarex Inc | cytotoxic drug-binder binding compound, pharmaceutical formulation, method for killing a cell and method for retarding or stopping tumor growth |
US7714016B2 (en) * | 2005-04-08 | 2010-05-11 | Medarex, Inc. | Cytotoxic compounds and conjugates with cleavable substrates |
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IL190971A0 (en) | 2008-12-29 |
HRP20120058T1 (en) | 2012-02-29 |
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AU2006305842A1 (en) | 2007-05-03 |
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EA015324B1 (en) | 2011-06-30 |
PL1940789T3 (en) | 2012-04-30 |
PT1940789E (en) | 2012-02-01 |
EP1940789B1 (en) | 2011-11-23 |
WO2007051081A1 (en) | 2007-05-03 |
ATE534629T1 (en) | 2011-12-15 |
CY1112533T1 (en) | 2015-12-09 |
CA2627046C (en) | 2015-09-15 |
ZA200804521B (en) | 2009-04-29 |
AU2006305842B2 (en) | 2011-11-03 |
US7847105B2 (en) | 2010-12-07 |
EA200801176A1 (en) | 2009-02-27 |
DK1940789T3 (en) | 2012-03-19 |
JP5116686B2 (en) | 2013-01-09 |
IL190971A (en) | 2013-02-28 |
CN101365679B (en) | 2012-11-14 |
NO20082243L (en) | 2008-07-21 |
WO2007051081B1 (en) | 2007-07-19 |
ES2375843T3 (en) | 2012-03-06 |
RS52100B (en) | 2012-06-30 |
CN101365679A (en) | 2009-02-11 |
SI1940789T1 (en) | 2012-03-30 |
EP1940789A1 (en) | 2008-07-09 |
BRPI0619331A2 (en) | 2011-09-27 |
KR20080068084A (en) | 2008-07-22 |
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