AU3847997A

AU3847997A – Inhibitors of the interaction between P53 and MDM2
– Google Patents

AU3847997A – Inhibitors of the interaction between P53 and MDM2
– Google Patents
Inhibitors of the interaction between P53 and MDM2

Info

Publication number
AU3847997A

AU3847997A
AU38479/97A
AU3847997A
AU3847997A
AU 3847997 A
AU3847997 A
AU 3847997A
AU 38479/97 A
AU38479/97 A
AU 38479/97A
AU 3847997 A
AU3847997 A
AU 3847997A
AU 3847997 A
AU3847997 A
AU 3847997A
Authority
AU
Australia
Prior art keywords
compounds
mdm2
interaction
human
inhibitors
Prior art date
1996-07-05
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.)

Abandoned

Application number
AU38479/97A
Inventor
Angelika Bottger
Volker Bottger
Patrick Chene
Pascal Furet
Carlos Garcia-Echeverria
Heinz-Kurt Hochkeppel
David Lane
Stephen Picksley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Cancer Research Campaign Technology Ltd

Original Assignee
Ciba Geigy AG
Novartis AG
Cancer Research Campaign Technology Ltd
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.)
1996-07-05
Filing date
1997-07-04
Publication date
1998-02-02

1996-07-05
Priority claimed from GBGB9614197.3A
external-priority
patent/GB9614197D0/en

1997-04-07
Priority claimed from GBGB9707041.1A
external-priority
patent/GB9707041D0/en

1997-07-04
Application filed by Ciba Geigy AG, Novartis AG, Cancer Research Campaign Technology Ltd
filed
Critical
Ciba Geigy AG

1998-02-02
Publication of AU3847997A
publication
Critical
patent/AU3847997A/en

2001-01-15
Priority to AU14979/01A
priority
Critical
patent/AU777766B2/en

2002-01-31
Assigned to CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED
reassignment
CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED
Alteration of Name(s) of Applicant(s) under S113
Assignors: CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED, NOVARTIS AG

Status
Abandoned
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07K—PEPTIDES

C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof

C07K7/04—Linear peptides containing only normal peptide links

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

A61P35/00—Antineoplastic agents

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES

A61K38/00—Medicinal preparations containing peptides

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07K—PEPTIDES

C07K2319/00—Fusion polypeptide

Abstract

The present invention relates to compounds capable of binding to the oncogene protein MDM2, processes for the preparation of such compounds, pharmaceutical preparations comprising such compounds, and uses of said compounds, e.g. in the therapeutic (including prophylactic) treatment of an animal or especially of the human body. The present further relates to methods of and compounds for inhibiting the growth of tumor cells which comprise the wild type p53 suppressor by interfering with the interaction between human p53 and human MDM2.

AU38479/97A
1996-07-05
1997-07-04
Inhibitors of the interaction between P53 and MDM2

Abandoned

AU3847997A
(en)

Priority Applications (1)

Application Number
Priority Date
Filing Date
Title

AU14979/01A

AU777766B2
(en)

1996-07-05
2001-01-15
Inhibitors of the interaction between p53 and MDM2

Applications Claiming Priority (5)

Application Number
Priority Date
Filing Date
Title

GB9614197

1996-07-05

GBGB9614197.3A

GB9614197D0
(en)

1996-07-05
1996-07-05

GB9707041

1997-04-07

GBGB9707041.1A

GB9707041D0
(en)

1997-04-07
1997-04-07
Inhibitors of the interaction between p53 and mdm2

PCT/EP1997/003549

WO1998001467A2
(en)

1996-07-05
1997-07-04
Inhibitors of the interaction between p53 and mdm2

Related Child Applications (1)

Application Number
Title
Priority Date
Filing Date

AU14979/01A
Division

AU777766B2
(en)

1996-07-05
2001-01-15
Inhibitors of the interaction between p53 and MDM2

Publications (1)

Publication Number
Publication Date

AU3847997A
true

AU3847997A
(en)

1998-02-02

Family
ID=26309649
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

AU38479/97A
Abandoned

AU3847997A
(en)

1996-07-05
1997-07-04
Inhibitors of the interaction between P53 and MDM2

Country Status (8)

Country
Link

EP
(1)

EP0958305B1
(en)

JP
(1)

JP2001500365A
(en)

AT
(1)

ATE397621T1
(en)

AU
(1)

AU3847997A
(en)

CA
(1)

CA2259149A1
(en)

DE
(1)

DE69738754D1
(en)

NZ
(1)

NZ333609A
(en)

WO
(1)

WO1998001467A2
(en)

Families Citing this family (50)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US7083983B2
(en)

1996-07-05
2006-08-01
Cancer Research Campaign Technology Limited
Inhibitors of the interaction between P53 and MDM2

GB9708092D0
(en)

*

1997-04-22
1997-06-11
Univ Dundee
Materials and methods relating to inhibiting the interaction of p53 and mdm2

AU7238098A
(en)

*

1997-05-15
1998-12-08
Kyowa Hakko Kogyo Co. Ltd.
Peptides having cyclic structures and exerting p53 protein activty-restoring effect on p53 protein mutants

US6238921B1
(en)

*

1998-03-26
2001-05-29
Isis Pharmaceuticals, Inc.
Antisense oligonucleotide modulation of human mdm2 expression

EP0947494A1
(en)

*

1998-03-30
1999-10-06
F. Hoffmann-La Roche Ag
Derivatives of phenoxy acetic acid and phenoxymethyltetrazole having antitumor activity

ATE283915T1
(en)

*

1998-05-26
2004-12-15
Inst Of Molecul & Cell Biology

POLYPEPTIDES FROM CREB-BINDING PROTEIN AND RELATED PROTEIN P-300 FOR USE IN TRANSCRIPTIONAL REGULATION

GB9819860D0
(en)

*

1998-09-12
1998-11-04
Zeneca Ltd
Chemical compounds

US7192713B1
(en)

1999-05-18
2007-03-20
President And Fellows Of Harvard College
Stabilized compounds having secondary structure motifs

US20040038902A1
(en)

2000-04-05
2004-02-26
Pincus Matthew R.
Peptides selectively lethal to malignant and transformed mammalian cells

US7498336B2
(en)

2003-02-13
2009-03-03
The United States Of America As Represented By The Secretary, Department Of Health And Human Services
Deazaflavin compounds and methods of use thereof

WO2005044839A2
(en)

2003-11-05
2005-05-19
Dana-Farber Cancer Institute, Inc.
Stabilized alpha helical peptides and uses thereof

US8598127B2
(en)

*

2004-04-06
2013-12-03
Korea Research Institute Of Bioscience & Biotechnology
Peptides for inhibiting MDM2 function

AU2004319946A1
(en)

*

2004-04-22
2005-12-01
3-Dimensional Pharmaceuticals, Inc.
HDM2-inhibitor complexes and uses thereof

ES2558928T3
(en)

2007-01-31
2016-02-09
Dana-Farber Cancer Institute, Inc.

Stabilized p53 peptides and uses thereof

JP5631201B2
(en)

2007-03-28
2014-11-26
プレジデント アンド フェローズ オブ ハーバード カレッジ

Stitched polypeptide

WO2010083347A2
(en)

2009-01-14
2010-07-22
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles

US20120135917A1
(en)

*

2009-06-16
2012-05-31
Eisaku Yoshihara
Anti-Gram Negative Bacteria Agent

WO2011005219A1
(en)

*

2009-07-07
2011-01-13
Agency For Science, Technology And Research
Novel mdm2 binding peptides and uses thereof

CA2771936A1
(en)

2009-08-26
2011-03-03
Novartis Ag
Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators

JP2013505300A
(en)

2009-09-22
2013-02-14
エルロン・セラピューティクス・インコーポレイテッド

Peptidomimetic macrocycle

CU24130B1
(en)

2009-12-22
2015-09-29
Novartis Ag

ISOQUINOLINONES AND REPLACED QUINAZOLINONES

US8440693B2
(en)

2009-12-22
2013-05-14
Novartis Ag
Substituted isoquinolinones and quinazolinones

PL2603600T3
(en)

2010-08-13
2019-06-28
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles

US8859535B2
(en)

2011-06-20
2014-10-14
Novartis Ag
Hydroxy substituted isoquinolinone derivatives

US8859586B2
(en)

2011-06-20
2014-10-14
Novartis Ag
Cyclohexyl isoquinolinone compounds

TWI643868B
(en)

2011-10-18
2018-12-11
艾利倫治療公司
Peptidomimetic macrocycles

KR20150000468A
(en)

*

2011-11-09
2015-01-02
메르츠 파마 게엠베하 운트 코. 카가아
Neurotoxins exhibiting shortened biological activity

US9408885B2
(en)

*

2011-12-01
2016-08-09
Vib Vzw
Combinations of therapeutic agents for treating melanoma

SG11201404648PA
(en)

2012-02-15
2014-09-26
Aileron Therapeutics Inc
Peptidomimetic macrocycles

CA2864120A1
(en)

2012-02-15
2013-08-22
Aileron Therapeutics, Inc.
Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles

US9365576B2
(en)

2012-05-24
2016-06-14
Novartis Ag
Pyrrolopyrrolidinone compounds

SG11201503052RA
(en)

2012-11-01
2015-05-28
Aileron Therapeutics Inc
Disubstituted amino acids and methods of preparation and use thereof

WO2014115077A1
(en)

2013-01-22
2014-07-31
Novartis Ag
Substituted purinone compounds

EP2948453B1
(en)

2013-01-22
2017-08-02
Novartis AG
Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction

MX2015016344A
(en)

2013-05-27
2016-03-01
Novartis Ag
Imidazopyrrolidinone derivatives and their use in the treatment of disease.

PT3004108T
(en)

2013-05-28
2018-01-24
Novartis Ag
Pyrazolo-pyrrolidin-4-one derivatives as bet inhibitors and their use in the treatment of disease

KR20160012197A
(en)

2013-05-28
2016-02-02
노파르티스 아게
Pyrazolo-pyrrolidin-4-one derivatives and their use in the treatment of disease

EA029269B1
(en)

2013-11-21
2018-02-28
Новартис Аг
Pyrrolopyrrolone derivatives and their use for treating diseases

SG11201702175YA
(en)

2014-09-24
2017-04-27
Aileron Therapeutics Inc
Peptidomimetic macrocycles and formulations thereof

CA2961258A1
(en)

2014-09-24
2016-03-31
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles and uses thereof

CA2979847A1
(en)

2015-03-20
2016-09-29
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles and uses thereof

US10059741B2
(en)

2015-07-01
2018-08-28
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles

CN108368161A
(en)

2015-09-10
2018-08-03
艾瑞朗医疗公司
Peptidomimetic macrocyclic compound as MCL-1 conditioning agents

WO2017201449A1
(en)

2016-05-20
2017-11-23
Genentech, Inc.
Protac antibody conjugates and methods of use

CN112119085A
(en)

2017-12-15
2020-12-22
丹娜-法伯癌症研究院有限公司
Stable peptide-mediated targeted protein degradation

US11091522B2
(en)

2018-07-23
2021-08-17
Aileron Therapeutics, Inc.
Peptidomimetic macrocycles and uses thereof

CN109206474A
(en)

*

2018-11-27
2019-01-15
青岛海洋生物医药研究院
A kind of linear peptide symthesis method

US20220153868A1
(en)

*

2019-02-20
2022-05-19
Oncolyze, Inc
Hdm2 antibody for use in treating cancer

CN112266407B
(en)

*

2020-09-28
2023-05-12
宁夏医科大学总医院
Heptapeptide specifically combined with p53 protein, coding gene, preparation method and application

WO2023056069A1
(en)

2021-09-30
2023-04-06
Angiex, Inc.
Degrader-antibody conjugates and methods of using same

1997

1997-07-04
JP
JP10504775A
patent/JP2001500365A/en
not_active
Withdrawn

1997-07-04
CA
CA002259149A
patent/CA2259149A1/en
not_active
Abandoned

1997-07-04
DE
DE69738754T
patent/DE69738754D1/en
not_active
Expired – Fee Related

1997-07-04
EP
EP97935511A
patent/EP0958305B1/en
not_active
Expired – Lifetime

1997-07-04
AU
AU38479/97A
patent/AU3847997A/en
not_active
Abandoned

1997-07-04
WO
PCT/EP1997/003549
patent/WO1998001467A2/en
active
IP Right Grant

1997-07-04
NZ
NZ333609A
patent/NZ333609A/en
unknown

1997-07-04
AT
AT97935511T
patent/ATE397621T1/en
not_active
IP Right Cessation

Also Published As

Publication number
Publication date

EP0958305B1
(en)

2008-06-04

ATE397621T1
(en)

2008-06-15

JP2001500365A
(en)

2001-01-16

CA2259149A1
(en)

1998-01-15

EP0958305A2
(en)

1999-11-24

NZ333609A
(en)

2000-08-25

DE69738754D1
(en)

2008-07-17

WO1998001467A2
(en)

1998-01-15

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Legal Events

Date
Code
Title
Description

2001-02-22
MK5
Application lapsed section 142(2)(e) – patent request and compl. specification not accepted

2002-01-31
PC1
Assignment before grant (sect. 113)

Owner name:
CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED

Free format text:
THE FORMER OWNER WAS: NOVARTIS AG, CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED

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