HUP0000320A2 - Biológiailag aktív peptidek,és eljárás előállításukra - Google Patents

Biológiailag aktív peptidek,és eljárás előállításukra

Info

Publication number
HUP0000320A2
HUP0000320A2 HU0000320A HUP0000320A HUP0000320A2 HU P0000320 A2 HUP0000320 A2 HU P0000320A2 HU 0000320 A HU0000320 A HU 0000320A HU P0000320 A HUP0000320 A HU P0000320A HU P0000320 A2 HUP0000320 A2 HU P0000320A2
Authority
HU
Hungary
Prior art keywords
peptide
leű
nval
ile
tyr
Prior art date
Application number
HU0000320A
Other languages
English (en)
Inventor
Vladislav Isakovich Dejgin
Andrej Markovich Korotkov
Original Assignee
Immunotech Developments 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
Application filed by Immunotech Developments Inc. filed Critical Immunotech Developments Inc.
Publication of HUP0000320A2 publication Critical patent/HUP0000320A2/hu
Publication of HUP0000320A3 publication Critical patent/HUP0000320A3/hu

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0821Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/0205Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/021Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)n-C(=0)-, n being 5 or 6; for n > 6, classification in C07K5/06 - C07K5/10, according to the moiety having normal peptide bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06104Dipeptides with the first amino acid being acidic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0812Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0815Tripeptides with the first amino acid being basic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0819Tripeptides with the first amino acid being acidic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0821Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
    • C07K5/0823Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp and Pro-amino acid; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1016Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1021Tetrapeptides with the first amino acid being acidic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1024Tetrapeptides with the first amino acid being heterocyclic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Immunology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A találmány tárgya új, biőlógiailag aktív, közelebbről imműnszabályőzóhatású peptid és ennek előállítása. Ez a peptid biőlógiai aktivitásakövetkeztében az ember- és állatgyógyászatban, valamint a kísérletibiőkémiában használható. A peptid szerkezete megfelel az X-Glű-Trp-Yáltalánős képletnek, ahől X jelentése hidrőgénatőm vagy Gly, Ala, Leű, Ile, Val, NVal, Prő, Tyr,Phe, Trp, D-Ala, D-Leű, D-Ile, D-Val, D-NVal, D-Prő, D-Tyr, D-Phe, D-Trp, g-aminő-vajsav vagy z-aminő-kaprőnsav; és Y jelentése Gly, Ala, Leű, Ile, Val, NVal, Prő, Tyr, Phe, Trp, D-Ala,D-Leű, D-Ile, D-Val, D-NVal, D-Prő, D-Tyr, D-Phe, D-Trp, g-aminő-vajsav, z-aminő-kaprőnsav, OH-csőpőrt, vagy 1-3szénatőmős csőpőrttalmőnő- vagy diszűbsztitűált amidcsőpőrt. A peptid szintézisét őldatbanvégzik lánchősszabbítással a mőlekűla C-terminálisától kezdve, afűnkciós csőpőrtők maximális védelmének stratégiájával; az aminősav-alkil-észterből indűlnak ki, az észtereket aktiválják, és a vegyesanhidridek módszerét alkalmazzák. Az így kapőtt terméket hangyasavvalkezelve, átkristályősítás űtán főrdítőtt fázisú krőmatőgráfiávaltisztítják. A találmány szerinti peptid hatását a tengerimalacőklimfőcitáinak hőzamára kifejtett hatásűkkal tesztelték; kiműtatták,hőgy a találmány szerinti peptid hatása ezerszer nagyőbb, mint másismert vegyületeké, és e peptidnek tőxikűs sajátságai nincsenek. ŕ
HU0000320A 1995-03-02 1996-02-28 Peptide and a method of obtaining it HUP0000320A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU95102461A RU2107691C1 (ru) 1995-03-02 1995-03-02 Пептид и способ его получения

Publications (2)

Publication Number Publication Date
HUP0000320A2 true HUP0000320A2 (hu) 2000-08-28
HUP0000320A3 HUP0000320A3 (en) 2000-10-30

Family

ID=20164981

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0000320A HUP0000320A3 (en) 1995-03-02 1996-02-28 Peptide and a method of obtaining it

Country Status (20)

Country Link
US (1) US6051683A (hu)
EP (1) EP0818462B1 (hu)
JP (1) JP3902226B2 (hu)
CN (1) CN1161373C (hu)
AT (1) ATE306495T1 (hu)
AU (1) AU708084B2 (hu)
BR (1) BR9607901A (hu)
CA (1) CA2214410C (hu)
CZ (1) CZ288418B6 (hu)
DE (1) DE69635272T2 (hu)
DK (1) DK0818462T3 (hu)
ES (1) ES2250984T3 (hu)
HK (1) HK1012859A1 (hu)
HU (1) HUP0000320A3 (hu)
LT (1) LT4393B (hu)
LV (1) LV11993B (hu)
RU (1) RU2107691C1 (hu)
SK (1) SK282604B6 (hu)
UA (1) UA51647C2 (hu)
WO (1) WO1996026955A1 (hu)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6159940A (en) * 1996-02-28 2000-12-12 Immunotech Developments Inc. Method for modulating hemopoiesis
DE19712633A1 (de) * 1997-03-26 1998-10-08 Laves Arzneimittel Verwendung von gamma-Aminobuttersäure als Interleukinbildungsstimulans
IL137820A (en) * 2000-08-10 2009-06-15 S I S Shulov Inst For Science Pharmaceutical composition for topical administration comprising an analgesic peptide
US20020098999A1 (en) * 2000-10-06 2002-07-25 Gallop Mark A. Compounds for sustained release of orally delivered drugs
AU2002211863A1 (en) * 2000-10-06 2002-04-15 Xenoport, Inc. Bile-acid derived compounds for providing sustained systemic concentrations of drugs after oral administration
AU2002239257A1 (en) * 2000-11-17 2002-06-03 Xenoport, Inc. Amino acid conjugates providing for sustained systemic concentrations of gaba analogues
EP1412324A4 (en) * 2001-06-11 2004-09-29 Xenoport Inc AMINO ACID CONJUGATES THAT RESULT IN GABA ANALOGA LASTING SYSTEMIC CONCENTRATIONS
US7919468B2 (en) 2005-04-07 2011-04-05 Centre National De La Recherche Scientifique (C.N.R.S.) Compounds useful as modulators of the proteasome activity
CA2571645A1 (en) 2006-12-19 2008-06-19 Apotex Technologies Inc. Pharmaceutically acceptable salts of thymodepressin and processes for their manufacture
MX2010005597A (es) * 2007-11-20 2010-10-25 Immunotech Dev Inc Péptidos inmunoreguladores novedosos, composiciones y usos de los mismos.
EP2464379B1 (en) 2009-08-10 2014-07-30 Immunotech Developments Inc. Vaccine having a peptide adjuvant for eliciting a specific immune response to treat influenza viral infection
RU2458935C1 (ru) * 2011-02-18 2012-08-20 Общество с ограниченной ответственностью "ЦитоНИР" (ООО "ЦитоНИР") Средство для коррекции метаболического синдрома
EP2818477B1 (de) * 2012-05-18 2016-05-04 Obshestvo S Organichennoj Otvetstvennostju "CytoNIR" L-lysyl-l-glutamyl-l-tryptophan zur korrektur des stoffwechselsyndroms
RU2540496C1 (ru) * 2014-01-20 2015-02-10 Общество с ограниченной ответственностью "ПРОМОМЕД" Композиция для назального применения, лекарственное средство на его основе и способ его пременения
EA025690B1 (ru) * 2014-07-15 2017-01-30 Государственное бюджетное образовательное учреждение высшего профессионального образования "Курский государственный медицинский университет" Министерства здравоохранения Российской Федерации Ранозаживляющее средство, обладающее иммуностимулирующим и антиоксидантным эффектами
RU2672888C1 (ru) 2018-04-18 2018-11-20 Пивипи Лабс Пте. Лтд. Противовирусное иммунотропное средство для лечения ОРВИ

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3100974A1 (de) * 1980-01-18 1982-01-21 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V., 3400 Göttingen Thymosin(alpha)(pfeil abwaerts)1(pfeil abwaerts)-fragmente enthaltende arzneimittel mit immunregulierender wirkung, und thymosin(alpha)(pfeil abwaerts)1(pfeil abwaerts)-fragmente
HU185263B (en) * 1981-06-12 1984-12-28 Richter Gedeon Vegyeszet Process for producing peptides effective on the immuncontroll analogous with the tp5
JPS609182Y2 (ja) * 1981-06-18 1985-04-02 アルファレコ−ド株式会社 カセツトテ−プケ−スマガジン
HU184481B (en) * 1981-10-02 1984-08-28 Richter Gedeon Vegyeszet Process for producing tripeptides for diminishing appetite
US4699897A (en) * 1983-06-04 1987-10-13 Amgen Biologically active peptides structurally related to regions within growth hormones
US4603121A (en) * 1983-10-06 1986-07-29 G. D. Searle & Co. Enkephalin analogs
IT1172391B (it) * 1983-12-23 1987-06-18 Polifarma Spa Composti tirpeptidici contenenti acido piroglutaminico e triptofano,procedimentio di produzione ed applicazioni terapeutiche
CH659586A5 (de) 1985-07-02 1987-02-13 Le G Ped I Arzneimittel aus dem thymus und verfahren zu dessen herstellung.
US5070076A (en) * 1985-07-02 1991-12-03 Leningradsky Gosudarstvenny Pedagogichesky Institut Thymus-gland preparation and method for producing same
US4751216A (en) * 1985-12-26 1988-06-14 Imreg, Inc. Methods for treating AIDS and ARC
CA1286989C (en) 1985-12-26 1991-07-30 A. Arthur Gottlieb Immunoamplifiers and related compositions
IT1216908B (it) * 1987-03-19 1990-03-14 Eniricerche Spa Analoghi retro-inversi della timopentina e dei suoi frammenti, il metodo per la loro sintesi ed il loro impiego per la preparazionedi composizioni farmaceutiche.
JP2511159B2 (ja) * 1987-12-30 1996-06-26 オブシェストボ エス オグラニチェンノイ オトベツベンノスチュ “ツィトメド―ペプトス” 免疫欠損状態の治療のための医薬製剤
HU201095B (en) * 1988-06-14 1990-09-28 Richter Gedeon Vegyeszet New peptides inhibiting the activity of the immune system and pharmaceutical compositions comprising same, as well as process for producing these peptides and compositions
GB2231051B (en) * 1989-05-05 1992-12-16 Erba Carlo Spa Bombesin antagonists
AU9140891A (en) * 1990-11-23 1992-06-25 Immunodynamics, Inc. Synthetic immunoactive peptides having immunomodulating and therapeutic activities
ATE188219T1 (de) * 1991-10-28 2000-01-15 Cytran Ltd Pharmazeutische dipeptid zusammensetzungen und verwendungsmethoden.
IT1264129B1 (it) * 1993-04-09 1996-09-16 Codev S A Peptidi ad attivita' immunomodulatoria derivati da frammenti di leucochinina
WO1995003067A1 (en) * 1993-07-21 1995-02-02 Khavinson Vladimir Khatskelevi Pharmaceutical with immunomodulating activity
RU2107692C1 (ru) * 1995-06-07 1998-03-27 Дейгин Владислав Исакович Пептид и способ его получения
RU2067000C1 (ru) * 1994-06-29 1996-09-27 Владислав Исакович Дейгин Пептид и способ его получения

Also Published As

Publication number Publication date
CA2214410C (en) 2001-05-29
JPH11505515A (ja) 1999-05-21
CN1161373C (zh) 2004-08-11
AU708084B2 (en) 1999-07-29
LV11993A (lv) 1998-03-20
UA51647C2 (uk) 2002-12-16
HK1012859A1 (en) 1999-08-13
DE69635272T2 (de) 2006-07-20
EP0818462A1 (en) 1998-01-14
DK0818462T3 (da) 2006-02-27
CA2214410A1 (en) 1996-09-06
BR9607901A (pt) 1999-09-08
WO1996026955A1 (fr) 1996-09-06
EP0818462A4 (en) 2000-05-31
DE69635272D1 (de) 2006-02-23
RU95102461A (ru) 1996-12-20
CN1185160A (zh) 1998-06-17
RU2107691C1 (ru) 1998-03-27
US6051683A (en) 2000-04-18
CZ288418B6 (en) 2001-06-13
LV11993B (lv) 1998-05-20
EP0818462B1 (en) 2005-10-12
HUP0000320A3 (en) 2000-10-30
AU4959496A (en) 1996-09-18
SK118097A3 (en) 1998-04-08
JP3902226B2 (ja) 2007-04-04
LT4393B (lt) 1998-10-26
CZ270397A3 (cs) 1998-05-13
SK282604B6 (sk) 2002-10-08
LT97158A (en) 1998-05-25
ATE306495T1 (de) 2005-10-15
ES2250984T3 (es) 2006-04-16

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