[go: up one dir, main page]

IN2014MN02175A - - Google Patents

Info

Publication number
IN2014MN02175A
IN2014MN02175A IN2175MUN2014A IN2014MN02175A IN 2014MN02175 A IN2014MN02175 A IN 2014MN02175A IN 2175MUN2014 A IN2175MUN2014 A IN 2175MUN2014A IN 2014MN02175 A IN2014MN02175 A IN 2014MN02175A
Authority
IN
India
Prior art keywords
nme
coh
double bond
independently
single bond
Prior art date
Application number
Inventor
Philip Wilson Howard
David Edwin Thurston
Khondaker Mirazur Rahman
Peter William Taylor
Original Assignee
Ucl Business Plc
Spirogen Sarl
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
Application filed by Ucl Business Plc, Spirogen Sarl filed Critical Ucl Business Plc
Publication of IN2014MN02175A publication Critical patent/IN2014MN02175A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

2 2227231 73 20 5 201011Q Q1 7x11 2 2121m13 20 41 42n3 202n3 20112211 4 A compound of formula (I) or a salt or solvate thereof wherein the dotted double bond indicates the presence of a single or double bond between C2 and C3; Ris selected from H OH =O =CH CN R OR halo dihalo =CHR =CHRR O SO R COR and COR; R is selected from H R OH OR SH SR NH NHR NRR nitro MeSn and halo; where R and R are independently selected from optionally substituted C alkyl Cheterocyclyl and C aryl groups; R and R either together form a double bond or are selected from H and QRrespectively where Q is selected from O S and NH and R is H or C alkyl or H and SOM where x is 2 or 3 and M is a monovalent pharmaceutically acceptable cation; A is selected from (A1) (A2) (A3) (A4) or (A5) where X and Yare selected from: CH and NH; CH and NMe; N and NMe; CH and S; N and S; N and O; and CH and O respectively; Xand Y are selected from: CH and NH; CH and NMe; N and NMe; CH and S; N and S; N and O; and CH and O respectively; Z is selected from O and S; Z is selected from CH and N; F is selected from a single bond and (E F) ; each E is independently selected from a single bond and C(=O) NH ; each F is independently a C heteroarylene group; m is 1 2 or 3; G is selected from hydrogen C1alkyl C(=O) O Calkyl (CH) C heterocycloalkyl and O (CH) C heterocycloalkyl group; each n is 0 4; provided that A2 is not A2 where X and Y of A2 are selected from: CH and NMe; COH and NMe; CH and S; N and NMe; N and S respectively; and provided that A3 is not A3 where X and Y of A3 are selected from: CH and NMe; COH and NMe; CH and S; N and NMe; N and S respectively; B is either a single bond or (B1) where X and Y of B1 are selected from: CH and NMe; COH and NMe; CH and S; N and NMe; N and S respectively; and R is Calkyl.
IN2175MUN2014 2012-04-30 2013-04-30 IN2014MN02175A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261640316P 2012-04-30 2012-04-30
PCT/GB2013/051097 WO2013164592A1 (en) 2012-04-30 2013-04-30 Pyrrolobenzodiazepines

Publications (1)

Publication Number Publication Date
IN2014MN02175A true IN2014MN02175A (en) 2015-08-28

Family

ID=48289484

Family Applications (1)

Application Number Title Priority Date Filing Date
IN2175MUN2014 IN2014MN02175A (en) 2012-04-30 2013-04-30

Country Status (14)

Country Link
US (1) US9321774B2 (en)
EP (1) EP2855481A1 (en)
JP (1) JP6125614B2 (en)
KR (1) KR101960130B1 (en)
CN (1) CN104540827B (en)
AU (1) AU2013255612B2 (en)
BR (1) BR112014027190B1 (en)
CA (1) CA2872205C (en)
HK (1) HK1208217A1 (en)
IN (1) IN2014MN02175A (en)
MX (1) MX2014013144A (en)
NZ (1) NZ701478A (en)
WO (1) WO2013164592A1 (en)
ZA (1) ZA201408043B (en)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0819095D0 (en) 2008-10-17 2008-11-26 Spirogen Ltd Pyrrolobenzodiazepines
NZ602933A (en) 2010-04-15 2014-09-26 Seattle Genetics Inc Pyrrolobenzodiazepines used to treat proliferative diseases
JP5870400B2 (en) 2010-04-15 2016-03-01 シアトル ジェネティクス,インコーポレーテッド Targeted pyrrolobenzodiazepine conjugates
WO2013041606A1 (en) 2011-09-20 2013-03-28 Spirogen Sàrl Pyrrolobenzodiazepines as unsymmetrical dimeric pbd compounds for inclusion in targeted conjugates
EP2751111B1 (en) 2011-10-14 2017-04-26 MedImmune Limited Asymmetrical bis-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one) derivatives for the treatment of proliferative or autoimmune diseases
JP6393617B2 (en) 2011-10-14 2018-09-19 シアトル ジェネティクス,インコーポレーテッド Pyrrolobenzodiazepine and target conjugates
AU2012322613B2 (en) 2011-10-14 2016-04-21 Medimmune Limited Pyrrolobenzodiazepines and targeted conjugates
WO2013053871A1 (en) 2011-10-14 2013-04-18 Spirogen Sàrl Pyrrolobenzodiazepines
JP5993093B2 (en) 2012-10-12 2016-09-14 メドイミューン・リミテッドMedImmune Limited Pyrrolobenzodiazepines and their complexes
DK2906248T3 (en) 2012-10-12 2019-03-04 Medimmune Ltd Pyrrolobenzodiazepines and their conjugates
EP2906249B1 (en) 2012-10-12 2018-06-27 MedImmune Limited Synthesis and intermediates of pyrrolobenzodiazepine derivatives for conjugation
US9931414B2 (en) 2012-10-12 2018-04-03 Medimmune Limited Pyrrolobenzodiazepine-antibody conjugates
HK1216176A1 (en) 2012-12-21 2016-10-21 Medlmmune Limited Unsymmetrical pyrrolobenzodiazepines-dimers for use in the treatment of proliferative and autoimmune diseases
AU2013366493B2 (en) 2012-12-21 2017-08-24 Medimmune Limited Pyrrolobenzodiazepines and conjugates thereof
WO2014159981A2 (en) 2013-03-13 2014-10-02 Spirogen Sarl Pyrrolobenzodiazepines and conjugates thereof
AU2014229529B2 (en) 2013-03-13 2018-02-15 Medimmune Limited Pyrrolobenzodiazepines and conjugates thereof
GB201317982D0 (en) 2013-10-11 2013-11-27 Spirogen Sarl Pyrrolobenzodiazepines and conjugates thereof
GB201317981D0 (en) 2013-10-11 2013-11-27 Spirogen Sarl Pyrrolobenzodiazepines and conjugates thereof
GB201416112D0 (en) 2014-09-12 2014-10-29 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
BR112017011111A2 (en) 2014-11-25 2017-12-26 Adc Therapeutics Sa pyrrolobenzodiazepine-antibody conjugates
GB201506402D0 (en) 2015-04-15 2015-05-27 Berkel Patricius H C Van And Howard Philip W Site-specific antibody-drug conjugates
GB201506411D0 (en) 2015-04-15 2015-05-27 Bergenbio As Humanized anti-axl antibodies
GB201521709D0 (en) * 2015-12-09 2016-01-20 Kings College London And Sec Dep For Health The PBD Antibacterial agents
GB201601431D0 (en) 2016-01-26 2016-03-09 Medimmune Ltd Pyrrolobenzodiazepines
GB201602359D0 (en) 2016-02-10 2016-03-23 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
GB201602356D0 (en) 2016-02-10 2016-03-23 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
GB201607478D0 (en) 2016-04-29 2016-06-15 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
WO2017201132A2 (en) 2016-05-18 2017-11-23 Mersana Therapeutics, Inc. Pyrrolobenzodiazepines and conjugates thereof
WO2017223275A1 (en) * 2016-06-24 2017-12-28 Mersana Therapeutics, Inc. Pyrrolobenzodiazepines and conjugates thereof
GB201617466D0 (en) 2016-10-14 2016-11-30 Medimmune Ltd Pyrrolobenzodiazepine conjugates
HUE054689T2 (en) 2017-02-08 2021-09-28 Adc Therapeutics Sa Pyrrolobenzodiazepine antibody conjugates
GB201702031D0 (en) 2017-02-08 2017-03-22 Medlmmune Ltd Pyrrolobenzodiazepine-antibody conjugates
SI3612537T1 (en) 2017-04-18 2022-10-28 Medimmune Limited Pyrrolobenzodiazepine conjugates
EP3612234B1 (en) 2017-04-20 2024-03-13 ADC Therapeutics SA Combination therapy with an anti-axl antibody-drug conjugate
CA3064804A1 (en) 2017-06-14 2018-12-20 Adc Therapeutics Sa Dosage regimes for the administration of an anti-cd19 adc
SG11202000358YA (en) 2017-08-18 2020-02-27 Medimmune Ltd Pyrrolobenzodiazepine conjugates
TWI885539B (en) 2017-09-29 2025-06-01 日商第一三共股份有限公司 Antibody-pyrrolobenzodiazepine derivative complex
EP3717021A1 (en) 2017-11-27 2020-10-07 Mersana Therapeutics, Inc. Pyrrolobenzodiazepine antibody conjugates
GB201803342D0 (en) 2018-03-01 2018-04-18 Medimmune Ltd Methods
GB201806022D0 (en) 2018-04-12 2018-05-30 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
GB201900929D0 (en) * 2019-01-23 2019-03-13 King S College London Nf-kappa b inhibitors
MX2021010477A (en) 2019-03-15 2021-10-01 Medimmune Ltd Azetidobenzodiazepine dimers and conjugates comprising them for use in the treatment of cancer.
BR112022013008A2 (en) 2019-12-31 2022-09-06 Legochem Biosciences Inc PYRROLOBENZODIAZEPINE DERIVATIVE COMPOUND, PYRROLOBENZODIAZEPINE BINDING DERIVATIVE CONJUGATE, AND, PHARMACEUTICAL COMPOSITION AND METHOD FOR PREVENTION OR TREATMENT OF PROLIFERATIVE DISEASE
GB2597532A (en) 2020-07-28 2022-02-02 Femtogenix Ltd Cytotoxic compounds
US20250367307A1 (en) 2022-06-30 2025-12-04 Toray Industries, Inc. Pharmaceutical composition for cancer treatment and/or prevention
AU2023393382A1 (en) 2022-12-14 2025-06-19 Pheon Therapeutics Ltd Cytotoxic compounds
WO2025262641A1 (en) 2024-06-19 2025-12-26 Pheon Therapeutics Ltd Antibody drug conjugates that bind cdcp1 and uses thereof

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569587A (en) 1978-11-17 1980-05-26 Meiji Seika Kaisha Ltd Novel antibiotic neothramycin derivative and its preparation
JPS5615289A (en) 1979-07-17 1981-02-14 Green Cross Corp:The Novel benzodiazepinnbased compound 3
JPS58180487A (en) 1982-04-16 1983-10-21 Kyowa Hakko Kogyo Co Ltd Antibiotic dc-81 and its preparation
US5229490A (en) 1987-05-06 1993-07-20 The Rockefeller University Multiple antigen peptide system
AU6645998A (en) 1996-12-23 1998-07-17 Du Pont Pharmaceuticals Company Oxygen or sulfur containing heteroaromatics as factor xa inhibitors
US6187797B1 (en) 1996-12-23 2001-02-13 Dupont Pharmaceuticals Company Phenyl-isoxazoles as factor XA Inhibitors
WO1999046244A1 (en) 1998-03-12 1999-09-16 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (ptpases)
GB9818732D0 (en) 1998-08-27 1998-10-21 Univ Portsmouth Collection of compounds
DE69907977T2 (en) 1998-08-27 2004-07-22 Spirogen Ltd., Ryde Pyrrolobenzodiazepine
GB9818730D0 (en) 1998-08-27 1998-10-21 Univ Portsmouth Collections of compounds
GB9818731D0 (en) 1998-08-27 1998-10-21 Univ Portsmouth Compounds
US6909006B1 (en) 1999-08-27 2005-06-21 Spirogen Limited Cyclopropylindole derivatives
DE60032022T2 (en) 1999-12-20 2007-05-16 The University Of North Carolina At Chapel Hill DIAMIDINE COMPOUNDS AS DNA NON-BILATIN BINDER
AU2002251684A1 (en) * 2000-12-27 2002-08-19 Genelab Technologies, Inc. Polyamide analogs as dna minor groove binders
CA2450625A1 (en) * 2001-06-13 2002-12-19 Genesoft Pharmaceuticals, Inc. Isoquinoline compounds having antiinfective activity
JP2005502703A (en) * 2001-09-07 2005-01-27 ザ スクリプス リサーチ インスティテュート CC-1065 and CBI analogs of duocarmycin
US20040138269A1 (en) 2002-10-11 2004-07-15 Sugen, Inc. Substituted pyrroles as kinase inhibitors
GB0226593D0 (en) 2002-11-14 2002-12-24 Consultants Ltd Compounds
GB0321295D0 (en) 2003-09-11 2003-10-15 Spirogen Ltd Synthesis of protected pyrrolobenzodiazepines
WO2005032594A2 (en) * 2003-10-03 2005-04-14 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Alkylators linked to polyamides as dna binding agents
GB0404574D0 (en) 2004-03-01 2004-04-07 Spirogen Ltd Amino acids
GB0404578D0 (en) 2004-03-01 2004-04-07 Spirogen Ltd Pyrrolobenzodiazepines
GB0404577D0 (en) 2004-03-01 2004-04-07 Spirogen Ltd Pyrrolobenzodiazepines
EP1720881B9 (en) 2004-03-01 2013-04-17 Spirogen Sàrl 11-hydroxy-5h-pyrrolo[2,1-c][1,4]benzodiazepin-5-one derivatives as key intermediates for the preparation of c2 substituted pyrrolobenzodiazepins
US7528126B2 (en) 2004-03-09 2009-05-05 Spirogen Limited Pyrrolobenzodiazepines
GB0410725D0 (en) 2004-05-13 2004-06-16 Spirogen Ltd Pyrrolobenzodiazepine therapeutic agents
EP1879901B1 (en) 2005-04-21 2009-12-23 Spirogen Limited Pyrrolobenzodiazepines
WO2007039752A1 (en) * 2005-10-05 2007-04-12 Spirogen Limited Alkyl 4- [4- (5-oxo-2, 3, 5, 11a-tetrahyd0-5h-pyrr0l0 [2, 1-c] [1, 4] benzodiazepine-8-yloxy) -butyrylamino]-1h-pyrrole-2-carboxylate derivatives and related compounds for the treatment of a proliferative disease
US8406170B2 (en) 2006-11-16 2013-03-26 Telefonaktiebolaget Lm Ericsson (Publ) Gateway selection mechanism
GB0722088D0 (en) * 2007-11-09 2007-12-19 Spirogen Ltd Pyrrolobenzodiazepines
GB0813432D0 (en) 2008-07-22 2008-08-27 Spirogen Ltd Pyrrolobenzodiazepines
GB0819095D0 (en) 2008-10-17 2008-11-26 Spirogen Ltd Pyrrolobenzodiazepines

Also Published As

Publication number Publication date
HK1208217A1 (en) 2016-02-26
EP2855481A1 (en) 2015-04-08
KR101960130B1 (en) 2019-03-19
CN104540827B (en) 2018-03-23
JP6125614B2 (en) 2017-05-10
MX2014013144A (en) 2015-05-11
CN104540827A (en) 2015-04-22
BR112014027190A2 (en) 2017-06-27
AU2013255612B2 (en) 2017-06-22
BR112014027190B1 (en) 2020-03-03
ZA201408043B (en) 2017-08-30
US9321774B2 (en) 2016-04-26
KR20150014935A (en) 2015-02-09
AU2013255612A1 (en) 2014-11-20
CA2872205C (en) 2020-07-21
US20150126495A1 (en) 2015-05-07
CA2872205A1 (en) 2013-11-07
NZ701478A (en) 2016-08-26
WO2013164592A1 (en) 2013-11-07
JP2015516987A (en) 2015-06-18

Similar Documents

Publication Publication Date Title
IN2014MN02175A (en)
BR112014027143A2 (en) pyrrolobenzodiazepines
EA201692215A1 (en) Pyrrolbenzodiazepine and conjugates of directed action
MY169495A (en) Pharmaceutical compositions
MX2015012629A (en) Imidazo pyridine compounds.
MX2013011257A (en) Process for preparation of dronedarone by n-butylation.
WO2013152277A3 (en) Moenomycin analogs, methods of synthesis, and uses thereof
MX352607B (en) Process for preparing benzoxaboroles.
MX395406B (en) PIPERIDINOBENZODIAZEPINE COMPOUNDS WITH ANTIPROLIFERATIVE ACTIVITY.
IN2014DN07509A (en)
MX2014004144A (en) Ethynyl derivatives as mglur5 allosteric modulators.
WO2012103071A3 (en) Compounds and compositions
WO2013098836A8 (en) A bis-quinophthalone pigment and a process for preparing the same
MX377644B (en) Steroid 6.7.beta.-epoxides as chemical intermediates
MX2017017022A (en) Method for the synthesis of rapamycin derivatives.
EP4001266A3 (en) Process for preparing methoxy methyl pyridine dicarboxylate
GEAP202215389A (en) Polymorphs
MA39715A (en) Polymorphic forms of 4,5-dihydro-1h-pyrrolo[2,3-f]quinoline-2,7,9-tricarboxylic acid and its disodium salt, process for their preparation and their use
MX2011006095A (en) Dihydroetorphines and their preparation.
MX346980B (en) New hexahydrocyclopentapyrrolone, hexahydropyrrolopyrrolone, octahydropyrrolopyridinone and octahydropyridinone compounds.
PH12015501215A1 (en) Novel selective androgen receptor modulators
MY185971A (en) Pyranodipyridine compound
MX359069B (en) Salt and crystal forms of plk-4 inhibitor.
IN2014MN00411A (en)
MX369470B (en) Means and method for treating solid tumours.