WO2007051081A8 - Methods and compounds for preparing cc-1065 analogs - Google Patents

Methods and compounds for preparing cc-1065 analogs Download PDF

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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
Application number
PCT/US2006/060050
Other languages
French (fr)
Other versions
WO2007051081A1 (en
WO2007051081B1 (en
Inventor
Sanjeev Gangwar
Qian Zhang
Original Assignee
Medarex, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to AT06839458T priority Critical patent/ATE534629T1/en
Priority to DK06839458.4T priority patent/DK1940789T3/en
Priority to CN2006800491755A priority patent/CN101365679B/en
Priority to AU2006305842A priority patent/AU2006305842B2/en
Priority to ES06839458T priority patent/ES2375843T3/en
Priority to CA2627046A priority patent/CA2627046C/en
Priority to BRPI0619331-5A priority patent/BRPI0619331A2/en
Application filed by Medarex, Inc. filed Critical Medarex, Inc.
Priority to US12/090,445 priority patent/US7847105B2/en
Priority to JP2008538132A priority patent/JP5116686B2/en
Priority to PL06839458T priority patent/PL1940789T3/en
Priority to EP06839458A priority patent/EP1940789B1/en
Priority to EA200801176A priority patent/EA015324B1/en
Publication of WO2007051081A1 publication Critical patent/WO2007051081A1/en
Publication of WO2007051081B1 publication Critical patent/WO2007051081B1/en
Priority to IL190971A priority patent/IL190971A/en
Priority to NO20082243A priority patent/NO20082243L/en
Priority to HK08110088.4A priority patent/HK1118549A1/en
Publication of WO2007051081A8 publication Critical patent/WO2007051081A8/en
Priority to HR20120058T priority patent/HRP20120058T1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56Ring systems containing three or more rings
    • C07D209/58[b]- or [c]-condensed
    • C07D209/60Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic 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
    • A61K31/403Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Abstract

A method of forming a CBI CC- 1065 analog utilizes NH2 as a starting material, where R3 is H or alkyl and R6 is H, substituted or unsubstituted lower alkyl, cyano, or alkoxy. Intermediates (I) are used and are claimed.
PCT/US2006/060050 2005-10-26 2006-10-18 Methods and compounds for preparing cc-1065 analogs WO2007051081A1 (en)

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)

* Cited by examiner, † Cited by third party
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
AU2016356780A1 (en) 2015-11-19 2018-06-28 Bristol-Myers Squibb Company Antibodies against glucocorticoid-induced tumor necrosis factor receptor (GITR) and uses thereof
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)

* Cited by examiner, † Cited by third party
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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