IL89770A - Analgesic peptides and pharmaceutical compositions containing them and the process for the preparation of some such compounds - Google Patents

Analgesic peptides and pharmaceutical compositions containing them and the process for the preparation of some such compounds

Info

Publication number: IL89770A
Authority: IL; Israel
Prior art keywords: pro; lys; peptide; arg; val
Prior art date: 1988-03-28

Application number

IL8977089A

Other languages

English (en)

Original Assignee

British Tech Group

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.)

1988-03-28

Filing date

1989-03-28

Publication date

1994-12-29

1988-03-28 Priority claimed from GB888807427A external-priority patent/GB8807427D0/en

1989-03-28 Application filed by British Tech Group filed Critical British Tech Group

1994-12-29 Publication of IL89770A publication Critical patent/IL89770A/en

Links

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AFLBTVGQCQLOFJ-AVGNSLFASA-N Lys-Pro-Arg Chemical compound NCCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(O)=O AFLBTVGQCQLOFJ-AVGNSLFASA-N 0.000 claims abstract description 4
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LOGFVTREOLYCPF-KXNHARMFSA-N (2s,3r)-2-[[(2r)-1-[(2s)-2,6-diaminohexanoyl]pyrrolidine-2-carbonyl]amino]-3-hydroxybutanoic acid Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H]1CCCN1C(=O)[C@@H](N)CCCCN LOGFVTREOLYCPF-KXNHARMFSA-N 0.000 claims description 25
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims description 13
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230000001754 anti-pyretic effect Effects 0.000 description 1
230000000259 anti-tumor effect Effects 0.000 description 1
230000002238 attenuated effect Effects 0.000 description 1
230000008901 benefit Effects 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000000872 buffer Substances 0.000 description 1
244000309466 calf Species 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
230000002860 competitive effect Effects 0.000 description 1
238000000432 density-gradient centrifugation Methods 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
230000003292 diminished effect Effects 0.000 description 1
229940120889 dipyrone Drugs 0.000 description 1
231100000673 dose–response relationship Toxicity 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
239000003102 growth factor Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
208000027866 inflammatory disease Diseases 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000007928 intraperitoneal injection Substances 0.000 description 1
125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 description 1
210000002540 macrophage Anatomy 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
DJGAAPFSPWAYTJ-UHFFFAOYSA-M metamizole sodium Chemical compound [Na+].O=C1C(N(CS([O-])(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 DJGAAPFSPWAYTJ-UHFFFAOYSA-M 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
230000036441 nociceptive stimulation Effects 0.000 description 1
108091008700 nociceptors Proteins 0.000 description 1
ODBDXKPHRXKFCM-UHFFFAOYSA-N octa-1,4,7-triene-3,6-dione Chemical group C=CC(=O)C=CC(=O)C=C ODBDXKPHRXKFCM-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
229940094443 oxytocics prostaglandins Drugs 0.000 description 1
230000007170 pathology Effects 0.000 description 1
125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
150000003815 prostacyclins Chemical class 0.000 description 1
230000002997 prostaglandinlike Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
238000003127 radioimmunoassay Methods 0.000 description 1
108020003175 receptors Proteins 0.000 description 1
230000003252 repetitive effect Effects 0.000 description 1
QEVHRUUCFGRFIF-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C(C5=CC=C(OC)C=C5N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 QEVHRUUCFGRFIF-MDEJGZGSSA-N 0.000 description 1
238000004007 reversed phase HPLC Methods 0.000 description 1
206010039073 rheumatoid arthritis Diseases 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
230000020341 sensory perception of pain Effects 0.000 description 1
125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
210000002966 serum Anatomy 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
230000002123 temporal effect Effects 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
239000003053 toxin Substances 0.000 description 1
231100000765 toxin Toxicity 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0815—Tripeptides with the first amino acid being basic
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Biomedical Technology (AREA)
Public Health (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Neurology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Engineering & Computer Science (AREA)
Pharmacology & Pharmacy (AREA)
Pain & Pain Management (AREA)
Veterinary Medicine (AREA)
Bioinformatics & Cheminformatics (AREA)
Neurosurgery (AREA)
Animal Behavior & Ethology (AREA)
Biochemistry (AREA)
Biophysics (AREA)
Genetics & Genomics (AREA)
Molecular Biology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Peptides Or Proteins (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

IL8977089A 1988-03-28 1989-03-28 Analgesic peptides and pharmaceutical compositions containing them and the process for the preparation of some such compounds IL89770A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB888807427A GB8807427D0 (en)	1988-03-28	1988-03-28	Peptides
GB888828833A GB8828833D0 (en)	1988-03-28	1988-12-09	Peptides

Publications (1)

Publication Number	Publication Date
IL89770A true IL89770A (en)	1994-12-29

Family

ID=26293705

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL8977089A IL89770A (en)	1988-03-28	1989-03-28	Analgesic peptides and pharmaceutical compositions containing them and the process for the preparation of some such compounds

Country Status (12)

Country	Link
EP (1)	EP0335662B1 (de)
JP (2)	JP2633369B2 (de)
AT (1)	ATE125548T1 (de)
CA (1)	CA1340186C (de)
DE (1)	DE68923572T2 (de)
FI (1)	FI95273C (de)
GB (1)	GB2217331C (de)
HK (1)	HK45895A (de)
IE (1)	IE61222B1 (de)
IL (1)	IL89770A (de)
NO (1)	NO300978B1 (de)
WO (1)	WO1989009226A1 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE68923572T2 (de)	1988-03-28	1996-01-18	British Tech Group	Peptide.
IL99527A (en) *	1990-09-28	1997-08-14	Lilly Co Eli	Tripeptide antithrombotic agents
IT1277841B1 (it) *	1995-04-19	1997-11-12	Molteni & C Dei Fratelli Alitt	Ammine dotate di attivita' analgesica, loro preparazione e uso
FR2738746B1 (fr) *	1995-09-19	1997-11-14	Oreal	Utilisation d'au moins un peptide dans une composition cosmetique ou pour la preparation d'un medicament
US7402559B2 (en)	1999-03-24	2008-07-22	Msh Pharma, Incorporated	Composition and method of treatment for urogenital conditions
JP4767418B2 (ja) *	1999-03-24	2011-09-07	エムエスエイチファーマ，インコーポレイテッド	アルファ−メラノサイト−刺激ホルモン由来の抗菌性アミノ酸配列
DE10106852A1 (de)	2001-02-14	2002-09-05	T Luger	Entzündungshemmende Verbindungen
DK3049428T3 (en) *	2013-09-23	2019-03-04	Dr August Wolff Gmbh & Co Kg Arzneimittel	ANTI-INFLAMMATORY TRIPEPTIDES
AU2014345802B2 (en) *	2013-11-07	2018-01-25	Dr. August Wolff Gmbh & Co. Kg Arzneimittel	Storage stable lyophilized tripeptide formulations

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3778426A (en) *	1970-12-16	1973-12-11	Research Corp	Therapeutically useful polypeptides
IT8021120A0 (it) *	1979-04-02	1980-04-01	Inst Organicheskogo Sinteza Ak	Analogo ciclico del peptide naturale stimolante la fagocitosi: treonile-ciclo (n-lisile-prolile-arginile).
US4377515A (en) *	1979-10-01	1983-03-22	Merck & Co., Inc.	Long lasting agonists and antagonists of LH-RH
US4585757A (en) *	1984-07-27	1986-04-29	Texas Tech University Health Sciences Center	Hypotensive active peptides
EP0215805A1 (de) *	1985-01-18	1987-04-01	MERCK PATENT GmbH	Immunoregulatorische peptide
DE68923572T2 (de)	1988-03-28	1996-01-18	British Tech Group	Peptide.

1989
- 1989-03-28 DE DE68923572T patent/DE68923572T2/de not_active Expired - Fee Related
- 1989-03-28 AT AT89303054T patent/ATE125548T1/de not_active IP Right Cessation
- 1989-03-28 JP JP1503798A patent/JP2633369B2/ja not_active Expired - Lifetime
- 1989-03-28 CA CA000594884A patent/CA1340186C/en not_active Expired - Fee Related
- 1989-03-28 IL IL8977089A patent/IL89770A/en not_active IP Right Cessation
- 1989-03-28 EP EP89303054A patent/EP0335662B1/de not_active Expired - Lifetime
- 1989-03-28 GB GB8906972A patent/GB2217331C/en not_active Expired - Fee Related
- 1989-03-28 WO PCT/GB1989/000319 patent/WO1989009226A1/en not_active Ceased
- 1989-03-29 IE IE99889A patent/IE61222B1/en not_active IP Right Cessation
- 1989-11-27 NO NO894720A patent/NO300978B1/no not_active IP Right Cessation
- 1989-11-27 FI FI895675A patent/FI95273C/fi not_active IP Right Cessation
1995
- 1995-03-30 HK HK45895A patent/HK45895A/xx not_active IP Right Cessation
1996
- 1996-07-23 JP JP8193524A patent/JP2781782B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
WO1989009226A1 (en)	1989-10-05
DE68923572D1 (de)	1995-08-31
JPH02504280A (ja)	1990-12-06
GB2217331A (en)	1989-10-25
CA1340186C (en)	1998-12-15
IE890998L (en)	1989-09-28
GB2217331B (en)	1991-12-11
NO894720D0 (no)	1989-11-27
FI95273B (fi)	1995-09-29
HK45895A (en)	1995-04-07
EP0335662A1 (de)	1989-10-04
GB8906972D0 (en)	1989-05-10
AU3363789A (en)	1989-10-16
NO300978B1 (no)	1997-08-25
AU629826B2 (en)	1992-10-15
FI95273C (fi)	1996-01-10
JP2781782B2 (ja)	1998-07-30
GB2217331C (en)	1994-11-16
DE68923572T2 (de)	1996-01-18
EP0335662B1 (de)	1995-07-26
JPH09165400A (ja)	1997-06-24
FI895675A0 (fi)	1989-11-27
NO894720L (no)	1990-01-29
IE61222B1 (en)	1994-10-19
ATE125548T1 (de)	1995-08-15
JP2633369B2 (ja)	1997-07-23

Legal Events

Date	Code	Title
1997-06-10	FF	Patent granted
1998-02-08	KB	Patent renewed
1999-08-17	KB	Patent renewed
2003-12-10	RH1	Patent not in force

Publication	Publication Date	Title
JP4006021B2 (ja)	2007-11-14	ケモカインの生物学的活性の強化法
JP3266311B2 (ja)	2002-03-18	新規ポリペプチドおよびこれを用いる抗ｈｉｖ剤
AU2008260326A1 (en)	2008-12-11	Cyclic peptide CXCR4 antagonists
SK83995A3 (en)	1996-09-04	New peptides
EP0647656B1 (de)	2000-05-31	Dem Motilin ähnliche Peptide mit hemmender Wirkung auf den gastrointestinalem Trakt
JPWO1992004374A1 (ja)	1992-09-03	新規ポリペプチドおよびこれを用いる抗ｈｉｖ剤
JPH07324097A (ja)	1995-12-12	インターロイキン６拮抗剤、及びペプチド類または医薬として許容されるその塩類
CA1340186C (en)	1998-12-15	Peptides
US5811400A (en)	1998-09-22	Peptide derivatives with δ opioid receptor antagonist or mixed μ agδ antagonist effects
US5580855A (en)	1996-12-03	Peptides
HU185229B (en)	1984-12-28	Process for preparing pharmaceutically active peptides and acetates thereof
EP0755942B1 (de)	1999-08-04	N-amidino- dermorphin-derivat
AU629826C (en)	1994-12-22	Peptides
EP0101929A1 (de)	1984-03-07	Diester von Polypeptiden, ihre Herstellung und Verwendung
US5215964A (en)	1993-06-01	Peptides useful in regulating the immune and nervous systems
CA2405724C (en)	2010-09-07	Substance p analogs for the treatment of cancer
HK40100630A (zh)	2024-05-03	抗病毒多肽类似物
Śleszyńska et al.	2009	New bradykinin B2 receptor antagonists-influence of C-terminal segment modifications on their pharmacological properties
Sleszyńska et al.	2009	New bradykinin B (2) receptor antagonists-influence of C-terminal segment modifications on their pharmacological properties.
JPH06509571A (ja)	1994-10-27	タキキニン拮抗薬としての環状ヘキサペプチドの製法およびその薬学的化合物
Śleszyńska et al.	0	receptor antagonists—influence of C-terminal segment modifications on their pharmacological properties
JPH10330399A (ja)	1998-12-15	神経伝達ポリペプチド