PT914340E - Analogos de hgh-rh(1-29)nh2 possuindo actividade antagonista - Google Patents

Analogos de hgh-rh(1-29)nh2 possuindo actividade antagonista

Info

Publication number: PT914340E
Authority: PT; Portugal
Prior art keywords: ala; abu; leu; arg; cit
Prior art date: 1996-05-03

Application number

PT97926399T

Other languages

English (en)

Inventor

Andrew V Schally

Marta Zarandi

Katalin Toth

Original Assignee

Univ Tulane

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.)

1996-05-03

Filing date

1997-05-02

Publication date

2003-11-28

1997-05-02 Application filed by Univ Tulane filed Critical Univ Tulane

2003-11-28 Publication of PT914340E publication Critical patent/PT914340E/pt

Links

239000005557 antagonist Substances 0.000 title 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 6
MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical group OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 abstract 4
KDXKERNSBIXSRK-RXMQYKEDSA-N D-lysine Chemical compound NCCCC[C@@H](N)C(O)=O KDXKERNSBIXSRK-RXMQYKEDSA-N 0.000 abstract 4
-1 R3 is Asp Chemical compound 0.000 abstract 4
AHLPHDHHMVZTML-SCSAIBSYSA-N D-Ornithine Chemical compound NCCC[C@@H](N)C(O)=O AHLPHDHHMVZTML-SCSAIBSYSA-N 0.000 abstract 3
QNAYBMKLOCPYGJ-UWTATZPHSA-N D-alanine Chemical compound C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 abstract 3
ODKSFYDXXFIFQN-SCSAIBSYSA-N D-arginine Chemical group OC(=O)[C@H](N)CCCNC(N)=N ODKSFYDXXFIFQN-SCSAIBSYSA-N 0.000 abstract 3
JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 3
125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 abstract 3
DCXYFEDJOCDNAF-UWTATZPHSA-N D-Asparagine Chemical compound OC(=O)[C@H](N)CC(N)=O DCXYFEDJOCDNAF-UWTATZPHSA-N 0.000 abstract 2
CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 abstract 2
CKLJMWTZIZZHCS-UWTATZPHSA-N D-aspartic acid Chemical compound OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 abstract 2
ZDXPYRJPNDTMRX-GSVOUGTGSA-N D-glutamine Chemical compound OC(=O)[C@H](N)CCC(N)=O ZDXPYRJPNDTMRX-GSVOUGTGSA-N 0.000 abstract 2
ROHFNLRQFUQHCH-RXMQYKEDSA-N D-leucine Chemical compound CC(C)C[C@@H](N)C(O)=O ROHFNLRQFUQHCH-RXMQYKEDSA-N 0.000 abstract 2
AYFVYJQAPQTCCC-STHAYSLISA-N D-threonine Chemical compound C[C@H](O)[C@@H](N)C(O)=O AYFVYJQAPQTCCC-STHAYSLISA-N 0.000 abstract 2
DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 abstract 2
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical group C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 abstract 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
125000002252 acyl group Chemical group 0.000 abstract 2
QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical compound CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 abstract 2
125000003118 aryl group Chemical group 0.000 abstract 2
125000002038 D-arginyl group Chemical group N[C@@H](C(=O)*)CCCNC(=N)N 0.000 abstract 1
WHUUTDBJXJRKMK-GSVOUGTGSA-N D-glutamic acid Chemical compound OC(=O)[C@H](N)CCC(O)=O WHUUTDBJXJRKMK-GSVOUGTGSA-N 0.000 abstract 1
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 1
ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical group OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 abstract 1
ULEBESPCVWBNIF-BYPYZUCNSA-N L-arginine amide Chemical compound NC(=O)[C@@H](N)CCCNC(N)=N ULEBESPCVWBNIF-BYPYZUCNSA-N 0.000 abstract 1
125000002059 L-arginyl group Chemical group O=C([*])[C@](N([H])[H])([H])C([H])([H])C([H])([H])C([H])([H])N([H])C(=N[H])N([H])[H] 0.000 abstract 1
125000000010 L-asparaginyl group Chemical group O=C([*])[C@](N([H])[H])([H])C([H])([H])C(=O)N([H])[H] 0.000 abstract 1
ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical group OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 abstract 1
LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 abstract 1
125000000534 N(2)-L-lysino group Chemical group [H]OC(=O)[C@@]([H])(N([H])[*])C([H])([H])C([H])([H])C(C([H])([H])N([H])[H])([H])[H] 0.000 abstract 1
KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical compound CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 abstract 1
108010047254 alanyl-4-fluorophenylalanyl-arginyl-cyclohexylalanyl-citrulline-tyrosinamide Proteins 0.000 abstract 1
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
FXHCFPUEIDRTMR-UHFFFAOYSA-N hydron;1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid;chloride Chemical compound Cl.C1=CC=C2CNC(C(=O)O)CC2=C1 FXHCFPUEIDRTMR-UHFFFAOYSA-N 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
108090000765 processed proteins & peptides Proteins 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/60—Growth hormone-releasing factor [GH-RF], i.e. somatoliberin
- 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

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Endocrinology (AREA)
Medicinal Chemistry (AREA)
General Health & Medical Sciences (AREA)
Biophysics (AREA)
Molecular Biology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Genetics & Genomics (AREA)
Biochemistry (AREA)
Gastroenterology & Hepatology (AREA)
Zoology (AREA)
Toxicology (AREA)
General Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Chemical Kinetics & Catalysis (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Peptides Or Proteins (AREA)

PT97926399T 1996-05-03 1997-05-02 Analogos de hgh-rh(1-29)nh2 possuindo actividade antagonista PT914340E (pt)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US08/642,472 US5942489A (en)	1996-05-03	1996-05-03	HGH-RH(1-29)NH2 analogues having antagonistic activity

Publications (1)

Publication Number	Publication Date
PT914340E true PT914340E (pt)	2003-11-28

Family

ID=24576702

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PT97926399T PT914340E (pt)	1996-05-03	1997-05-02	Analogos de hgh-rh(1-29)nh2 possuindo actividade antagonista

Country Status (12)

Country	Link
US (1)	US5942489A (pt)
EP (1)	EP0914340B1 (pt)
JP (1)	JP2001501585A (pt)
AT (1)	ATE244731T1 (pt)
AU (1)	AU3117297A (pt)
CA (1)	CA2253663C (pt)
DE (1)	DE69723448T2 (pt)
DK (1)	DK0914340T3 (pt)
ES (1)	ES2200178T3 (pt)
PT (1)	PT914340E (pt)
WO (1)	WO1997042223A1 (pt)
ZA (1)	ZA973793B (pt)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6057422A (en) *	1998-11-25	2000-05-02	The Administrators Of The Tulane Educational Fund	Antagonistic analogs of GH-RH inhibiting IGF-I and -II
US20040121407A1 (en) *	2002-09-06	2004-06-24	Elixir Pharmaceuticals, Inc.	Regulation of the growth hormone/IGF-1 axis
TW200517400A (en) *	2003-08-05	2005-06-01	Univ Tulane	Antagonistic analogs of GH-RH (2003)
WO2005090388A1 (en)	2004-03-19	2005-09-29	The University Of Queensland	Alpha helical mimics, their uses and methods for their production
US8691942B2 (en)	2008-03-28	2014-04-08	University Of Miami	N- and C- terminal substituted antagonistic analogs of GH-RH
JP5588963B2 (ja) *	2008-03-28	2014-09-10	ザユニバーシティーオブマイアミ	Ｇｈ−ｒｈの新規なｎ−およびｃ−末端が置換されたアンタゴニスト類似体
US8796216B2 (en)	2008-06-12	2014-08-05	Syntaxin Limited	Suppression of neuroendocrine diseases
JP5799397B2 (ja)	2008-06-12	2015-10-28	イプセン・バイオイノベーション・リミテッドＩｐｓｅｎＢｉｏｉｎｎｏｖａｔｉｏｎＬｉｍｉｔｅｄ	癌の抑制
CA2727082C (en)	2008-06-12	2019-02-26	Syntaxin Limited	Fusion proteins for use in suppression of acromegaly
GB0820970D0 (en)	2008-11-17	2008-12-24	Syntaxin Ltd	Suppression of cancer
WO2010146059A2 (en)	2009-06-16	2010-12-23	F. Hoffmann-La Roche Ag	Biomarkers for igf-1r inhibitor therapy
US9079974B2 (en) *	2011-12-21	2015-07-14	The University Of Miami	GH-RH analogs with potent agonistic effects
WO2014100809A2 (en)	2012-12-21	2014-06-26	University Of Miami	Ghrh agonists for the treatment of ischemic disorders
WO2014100816A2 (en)	2012-12-21	2014-06-26	University Of Miami	Ghrh agonists for islet cell transplantation and function and the treatment of diabetes
US9119832B2 (en)	2014-02-05	2015-09-01	The Regents Of The University Of California	Methods of treating mild brain injury
EP3218395B1 (en)	2014-11-12	2022-01-05	The United States of America, as represented by The Secretary, Department of Health and Human Services	Treatment of hormonal disorders of growth
WO2017075535A1 (en)	2015-10-28	2017-05-04	Oxeia Biopharmaceuticals, Inc.	Methods of treating neurodegenerative conditions
AU2020218272A1 (en)	2019-02-08	2021-09-02	United States Government As Represented By The Department Of Veterans Affairs	Growth hormone-releasing hormone antagonists and uses thereof
WO2021011874A1 (en)	2019-07-18	2021-01-21	University Of Miami	Ghrh antagonists for use in a method of treating sarcoidosis
USD1085845S1 (en)	2022-10-24	2025-07-29	Gbrs Group Llc	Multi-accessory mount
USD1099256S1 (en)	2024-08-01	2025-10-21	Gbrs Group Llc	Multi-accessory mount
USD1098350S1 (en)	2024-08-01	2025-10-14	Gbrs Group Llc	Multi-accessory mount
USD1098349S1 (en)	2024-08-01	2025-10-14	Gbrs Group Llc	Multi-accessory mount

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4493934A (en) *	1979-10-01	1985-01-15	Merck & Co., Inc.	2(3-Amino-2-oxopyrrolidin-1-yl) acetic acid and n-acylated derivatives thereof
US4377515A (en) *	1979-10-01	1983-03-22	Merck & Co., Inc.	Long lasting agonists and antagonists of LH-RH
US5043322A (en) *	1988-07-22	1991-08-27	The Salk Institute For Biological Studies	Cyclic GRF analogs
US5084442A (en) *	1988-09-06	1992-01-28	Hoffmann-La Roche Inc.	Cyclic growth hormone releasing factor analogs and method for the manufacture thereof
EP0527914A4 (en) *	1990-05-04	1993-08-11	The Administrators Of The Tulane University Educational Fund	Novel synthetic grf analogs
JP3401005B2 (ja) *	1992-12-11	2003-04-28	ユニバーシティオブフロリダ	有害生物の防除のための材料および方法
US5550212A (en) *	1993-12-17	1996-08-27	The Administrators Of The Tulane Educational Fund	Analogues of hGH-RH(1-29)NH2 having antagonistic activity
US5516759A (en) *	1994-12-08	1996-05-14	Tap Holdings Inc.	LHRH antagonists having lactam groups at the N-terminus
DE19514567A1 (de) *	1995-04-20	1996-10-24	Merck Patent Gmbh	Benzofurane

1996
- 1996-05-03 US US08/642,472 patent/US5942489A/en not_active Expired - Fee Related
1997
- 1997-05-02 AU AU31172/97A patent/AU3117297A/en not_active Abandoned
- 1997-05-02 EP EP97926399A patent/EP0914340B1/en not_active Expired - Lifetime
- 1997-05-02 ZA ZA9703793A patent/ZA973793B/xx unknown
- 1997-05-02 WO PCT/US1997/007452 patent/WO1997042223A1/en not_active Ceased
- 1997-05-02 CA CA002253663A patent/CA2253663C/en not_active Expired - Fee Related
- 1997-05-02 DK DK97926399T patent/DK0914340T3/da active
- 1997-05-02 PT PT97926399T patent/PT914340E/pt unknown
- 1997-05-02 JP JP09540054A patent/JP2001501585A/ja not_active Ceased
- 1997-05-02 AT AT97926399T patent/ATE244731T1/de not_active IP Right Cessation
- 1997-05-02 DE DE69723448T patent/DE69723448T2/de not_active Expired - Fee Related
- 1997-05-02 ES ES97926399T patent/ES2200178T3/es not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DE69723448D1 (de)	2003-08-14
DK0914340T3 (da)	2003-10-27
DE69723448T2 (de)	2004-05-19
AU3117297A (en)	1997-11-26
ZA973793B (en)	1997-11-19
EP0914340A1 (en)	1999-05-12
US5942489A (en)	1999-08-24
CA2253663C (en)	2002-07-16
CA2253663A1 (en)	1997-11-13
ATE244731T1 (de)	2003-07-15
ES2200178T3 (es)	2004-03-01
EP0914340B1 (en)	2003-07-09
JP2001501585A (ja)	2001-02-06
WO1997042223A1 (en)	1997-11-13

Publication	Publication Date	Title
PT914340E (pt)	2003-11-28	Analogos de hgh-rh(1-29)nh2 possuindo actividade antagonista
AU693143B2 (en)	1998-06-25	CS-1 peptidomimetics, compositions and methods of using the same
Chorev et al.	1979	Partially modified retro-inverso-enkephalinamides: topochemical long-acting analogs in vitro and in vivo
AU707094B2 (en)	1999-07-01	Analogs of parathyroid hormone
KR850001230A (ko)	1985-03-16	옥타펩티드 바조프레신 길항물질의 제조방법
FI82254B (fi)	1990-10-31	Foerfarande foer framstaellning av nya, terapeutiskt anvaendbara peptider och salter daerav.
AR022392A1 (es)	2002-09-04	PEPTIDO SINTÉTICOS QUE INHIBEN LA LIBERACIoN DE LA HORMONA DE CRECIMIENTO DESDE LA PITUITARIA DE LOS MAMíFEROS Y USOS DE LOS MISMOS PARA LA FABRICACIoN DE UN MEDICAMENTO.
ES2152380T3 (es)	2001-02-01	Analogos de hgh-rh(1-29)nh2 con actividad antagonista.
GR68039B (pt)	1981-10-27
Dutta et al.	2000	Potent cyclic monomeric and dimeric peptide inhibitors of VLA‐4 (α4β1 integrin)‐mediated cell adhesion based on the Ile‐Leu‐Asp‐Val tetrapeptide
AU707245B2 (en)	1999-07-08	Novel MU opioid receptor ligands: agonists and antagonists
IE800743L (en)	1980-10-12	Peptides having thymopoietin-like activity
IL72789A (en)	1988-10-31	Basic hexa and heptapeptide vasopressin antagonists and their preparation
EP0189326A3 (en)	1988-10-26	Derivatives of arginine vasopressin antagonists
EP0138604A3 (en)	1987-04-01	Arginine vasopressin antagonists
ES8707740A1 (es)	1987-08-16	Un procedimiento para preparar octapeptidos ciclicos
EP0737204A1 (en)	1996-10-16	Cs-1 peptidomimetics, compositions and methods of using the same
EP0273645A3 (en)	1990-07-18	Novel derivatives of arginine vasopressin antagonists
HUT61033A (en)	1992-11-30	Process for producing intermediates of lh-rh-antagonist peptides