DK2531518T3 - Oligopeptidforbindelser og anvendelser deraf - Google Patents
Oligopeptidforbindelser og anvendelser deraf Download PDFInfo
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- DK2531518T3 DK2531518T3 DK11701678.2T DK11701678T DK2531518T3 DK 2531518 T3 DK2531518 T3 DK 2531518T3 DK 11701678 T DK11701678 T DK 11701678T DK 2531518 T3 DK2531518 T3 DK 2531518T3
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- C—CHEMISTRY; METALLURGY
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
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- C—CHEMISTRY; METALLURGY
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- 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
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- C—CHEMISTRY; METALLURGY
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Claims (15)
1. Oligopeptidforbindelse omfattende: (i) aminosyresekvensen af YGRKKRRQRRRGKTLRVAKAIYKRYIE (SEQ ID NO: 40); eller (ii) en aminosyresekvens med mindst 85% sekvensidentitet til sekvensen af SEQ ID NO: 40; hvor forbindelsen af (i) eller (ii) har aktivitet i inhibering af væksten og/eller levedygtigheden af mikrobielle og cancerceller, hvor fortrinsvis oligopeptidforbindelsen har sekvensen af SEQ ID NO: 40.
2. Oligopeptidforbindelse ifølge krav 1, hvor forbindelsen omfatter en eller flere D-aminosyrer, hvor fortrinsvis forbindelsen er en inverso-forbindelse som indeholder alle D-aminosyrer.
3. Oligopeptidforbindelse ifølge et hvilket som helst af kravene 1 eller 2, hvor forbindelsen har en eller flere af de følgende egenskaber: a) en netto-ladning ved pH 7,0 på 10-13, b) en pi på 12 til 13; c) en gennemsnitlig hydrofilicitet på 0,7 til 1,0 og/eller d) et forhold mellem hydrofile rester og total antal af rester på 45-60%.
4. Oligopeptidforbindelse ifølge et hvilket som helst af kravene 1 til 3, hvor forbindelsen er antibakteriel og cytotoksisk.
5. Oligopeptidforbindelse ifølge et hvilket som helst af kravene 1 til 4, som er selektivt cytotoksisk mod cancerceller, og/eller hvor forbindelsen kan mindske tumorstørrelse.
6. Nukleinsyremolekyle som koder for en aminosyresekvens som defineret i et hvilket som helst af kravene 1 eller 2, eller komplementet af nukleinsyremolekylet.
7. Vektor omfattende et nukleinsyremolekyle ifølge krav 6.
8. Isoleret celle som er blevet modificeret ved introduktionen af et nukleinsyremolekyle eller en vektor ifølge krav 6 eller 7.
9. Farmaceutisk sammensætning omfattende en oligopeptidforbindelse eller et nukleinsyremolekyle ifølge et hvilket som helst af kravene 1 til 7 sammen med en farmaceutisk acceptabel excipiens.
10. Oligopeptidforbindelse, nukleinsyremolekyle eller sammensætning ifølge et hvilket som helst af kravene 1 til 9 til anvendelse i terapi, fortrinsvis til anvendelse i bekæmpelse af mikrobiel infektion eller til anvendelse i behandlingen af cancer; hvor når anvendt i behandlingen af cancer, da er canceren fortrinsvis valgt fra hjerne-, lunge-, bryst- eller tyktarmscancer eller melanom og/eller hvor oligopeptidforbindelsen, nukleinsyremolekylet, sammensætningen eller medikamentet er til lokal levering til canceren; eller hvor når anvendt til at bekæmpe mikrobiel infektion, da er den mikrobielle infektion fortrinsvis en bakterieinfektion.
11. Anvendelse af oligopeptidforbindelsen eller nukleinsyremolekylet ifølge et hvilket som helst af kravene 1 til 9 i fremstillingen af et medikament til at bekæmpe mikrobiel infektion og/eller at behandle cancer.
12. Produkt omfattende en oligopeptidforbindelse, et nukleinsyremolekyle eller en sammensætning ifølge et hvilket som helst af kravene 1 til 9 og et andet terapeutisk aktivt stof som et kombineret præparat til separat, samtidig eller sekventiel anvendelse i inhibering af levedygtigheden og/eller væksten afen cancer eller mikrobecelle.
13. Kit omfattende en oligopeptidforbindelse, et nukleinsyremolekyle eller en sammensætning ifølge et hvilket som helst af kravene 1 til 9 og et andet terapeutisk aktivt stof.
14. Kit eller produkt ifølge krav 12 eller 13 hvor det andet terapeutisk aktive stof er aktivt mod cancer eller mikrobiel infektion eller cancer, og/eller hvor det andet terapeutisk aktive stof er et kemoterapeutisk stof, et anti-neoplastisk stof, et antibiotika, eller et antiviralt eller svampedræbende stof.
15. In vitro eller ex vivo fremgangsmåde til inhibering af levedygtigheden og/eller væksten afen mikroorganisme eller cancercelle, hvor fremgangsmåden omfatter at bringe mikroorganismen i kontakt med en oligopeptidforbindelse, eller at bringe cancercellen i kontakt med en oligopeptidforbindelse eller et nukleinsyremolekyle, ifølge et hvilket som helst af kravene 1 til 6.
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GBGB1001602.0A GB201001602D0 (en) | 2010-02-01 | 2010-02-01 | Oligopeptidic compounds and uses therof |
PCT/EP2011/051422 WO2011092347A1 (en) | 2010-02-01 | 2011-02-01 | Oligopeptidic compounds and uses thereof |
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SI (1) | SI2531518T1 (da) |
SM (1) | SMT201600261B (da) |
WO (1) | WO2011092347A1 (da) |
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GB201001602D0 (en) | 2010-02-01 | 2010-03-17 | Cytovation As | Oligopeptidic compounds and uses therof |
CN103012562B (zh) * | 2011-09-24 | 2015-01-28 | 复旦大学 | 一种双重靶向的d构型多肽及其递药系统 |
US10039777B2 (en) | 2012-03-20 | 2018-08-07 | Neuro-Lm Sas | Methods and pharmaceutical compositions of the treatment of autistic syndrome disorders |
CN103720655B (zh) * | 2012-10-11 | 2016-05-25 | 上海纳米技术及应用国家工程研究中心有限公司 | 一种d型多肽介导的靶向脂质体及其制备方法和应用 |
KR101782634B1 (ko) * | 2015-06-29 | 2017-10-25 | 주식회사 큐라클 | Amigo2와 3-포스포이노시티드-의존 키나아제 1의 결합 억제용 데코이 펩타이드 |
BR112019019255A2 (pt) * | 2017-03-16 | 2020-04-14 | Microsintesis Inc | composições e métodos envolvendo moléculas probióticas |
CN108314741B (zh) * | 2018-03-22 | 2021-08-03 | 中国人民解放军第四军医大学 | 一种肿瘤血管靶向抗癌肽nkl-dota及其制备方法 |
CN112543595B (zh) * | 2018-05-30 | 2022-11-01 | 莫尔豪斯医学院 | 抗微生物组合物,其制备方法和用途 |
GB201810058D0 (en) * | 2018-06-19 | 2018-08-08 | Cytovation As | Combination therapy using a peptide |
KR102073144B1 (ko) * | 2018-12-13 | 2020-02-04 | 주식회사 엘베이스 | 올리고펩티드를 유효성분으로 포함하는 암의 예방 또는 치료용 약학적 조성물 |
KR102211985B1 (ko) * | 2019-05-02 | 2021-02-05 | 주식회사 엘베이스 | 신규한 올리고펩티드 및 이를 유효성분으로 포함하는 암의 예방 또는 치료용 약학적 조성물 |
CN110408699A (zh) * | 2019-07-11 | 2019-11-05 | 福建卫生职业技术学院 | 肠癌肠道菌群标志物及其应用 |
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CN115044520B (zh) * | 2022-08-12 | 2022-11-15 | 北京百奥茵诺生物科技有限公司 | 一株交替单胞菌及使用其生产单葡萄糖醛酸甘草次酸的方法 |
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DE3925542A1 (de) | 1989-08-02 | 1990-02-15 | Kallos Verlag Und Versand Gmbh | Glueckwunschkarte |
US5534110A (en) | 1993-07-30 | 1996-07-09 | Lam Research Corporation | Shadow clamp |
US5595756A (en) | 1993-12-22 | 1997-01-21 | Inex Pharmaceuticals Corporation | Liposomal compositions for enhanced retention of bioactive agents |
FR2739621B1 (fr) | 1995-10-05 | 1997-12-05 | Centre Nat Rech Scient | Peptides utilisables comme vecteurs pour l'adressage intracellulaire de molecules actives |
DE19840875A1 (de) * | 1997-09-02 | 1999-05-12 | Max Delbrueck Centrum | Mittel zur Diagnose und zur Therapie von Tumorerkrankungen |
AU1818299A (en) | 1997-12-10 | 1999-06-28 | Washington University | Anti-pathogen system and methods of use thereof |
GB9814527D0 (en) | 1998-07-03 | 1998-09-02 | Cyclacel Ltd | Delivery system |
EP1958961A3 (en) | 1998-11-13 | 2008-09-03 | Cyclacel Limited | Transport Vectors |
FR2849603B1 (fr) | 2003-01-07 | 2006-09-08 | Centre Nat Rech Scient | Composition pour le transport intracellulaire de macromolecules ou particules biologiques |
US7442681B2 (en) * | 2004-02-10 | 2008-10-28 | University Of Virginia Patent Foundation | Method of inhibiting vascular permeability |
CA2666057C (en) * | 2006-10-26 | 2016-10-11 | Genentech, Inc. | Genetic variations associated with tumors |
WO2008051048A2 (en) * | 2006-10-27 | 2008-05-02 | Jeong Moon Kim | Method and materials for inhibiting a nuclear export of gsk3 |
GB0803352D0 (en) * | 2008-02-22 | 2008-04-02 | Ntnu Technology Transfer As | Oligopeptidic compounds and uses thereof |
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- 2011-02-01 ES ES11701678.2T patent/ES2585595T3/es active Active
- 2011-02-01 RS RS20160608A patent/RS54992B1/sr unknown
- 2011-02-01 WO PCT/EP2011/051422 patent/WO2011092347A1/en active Application Filing
- 2011-02-01 SI SI201130904A patent/SI2531518T1/sl unknown
- 2011-02-01 EP EP11701678.2A patent/EP2531518B1/en active Active
- 2011-02-01 CN CN201180008036.9A patent/CN102781953B/zh active Active
- 2011-02-01 JP JP2012550478A patent/JP5934654B2/ja active Active
- 2011-02-01 PT PT117016782T patent/PT2531518T/pt unknown
- 2011-02-01 DK DK11701678.2T patent/DK2531518T3/da active
- 2011-02-01 US US13/574,124 patent/US8754042B2/en active Active
- 2011-02-01 HU HUE11701678A patent/HUE028094T2/en unknown
- 2011-02-01 LT LTEP11701678.2T patent/LT2531518T/lt unknown
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2014
- 2014-06-16 US US14/305,743 patent/US9353156B2/en active Active
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2016
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Also Published As
Publication number | Publication date |
---|---|
KR101848518B1 (ko) | 2018-04-12 |
JP2013517787A (ja) | 2013-05-20 |
CA2788726A1 (en) | 2011-08-04 |
GB201001602D0 (en) | 2010-03-17 |
EP2531518A1 (en) | 2012-12-12 |
CA2788726C (en) | 2019-04-02 |
EP2531518B1 (en) | 2016-05-04 |
CN102781953A (zh) | 2012-11-14 |
CY1117872T1 (el) | 2017-05-17 |
KR20120128135A (ko) | 2012-11-26 |
PL2531518T3 (pl) | 2017-01-31 |
JP5934654B2 (ja) | 2016-06-15 |
WO2011092347A1 (en) | 2011-08-04 |
CN102781953B (zh) | 2015-02-04 |
SI2531518T1 (sl) | 2016-09-30 |
HUE028094T2 (en) | 2016-11-28 |
US8754042B2 (en) | 2014-06-17 |
RS54992B1 (sr) | 2016-11-30 |
LT2531518T (lt) | 2016-09-26 |
US20130023461A1 (en) | 2013-01-24 |
US9353156B2 (en) | 2016-05-31 |
US20150038407A1 (en) | 2015-02-05 |
HRP20160922T1 (hr) | 2016-10-07 |
ES2585595T3 (es) | 2016-10-06 |
PT2531518T (pt) | 2016-08-12 |
SMT201600261B (it) | 2016-11-10 |
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