RU2013122696A - SUBSTANCES HAVING ANGIOGENIC ACTIVITY - Google Patents

SUBSTANCES HAVING ANGIOGENIC ACTIVITY Download PDF

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Publication number
RU2013122696A
RU2013122696A RU2013122696/15A RU2013122696A RU2013122696A RU 2013122696 A RU2013122696 A RU 2013122696A RU 2013122696/15 A RU2013122696/15 A RU 2013122696/15A RU 2013122696 A RU2013122696 A RU 2013122696A RU 2013122696 A RU2013122696 A RU 2013122696A
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RU
Russia
Prior art keywords
angiogenic activity
agent
bis
lysine
substances
Prior art date
Application number
RU2013122696/15A
Other languages
Russian (ru)
Other versions
RU2613184C2 (en
Inventor
Сергей Борисович Середенин
Сергей Александрович Крыжановский
Татьяна Александровна Гудашева
Татьяна Алексеевна Антипова
Евгения Сергеевна Пекельдина
Александра Валериановна Сорокина
Андрей Дмитриевич Дурнев
Иосиф Борисович Цорин
Марина Борисовна Вититнова
Валерий Николаевич Столярук
Original Assignee
Федеральное государственное бюджетное учреждение "Научно-исследовательский институт фармакологии имени В.В. Закусова" Российской академии медицинских наук
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Application filed by Федеральное государственное бюджетное учреждение "Научно-исследовательский институт фармакологии имени В.В. Закусова" Российской академии медицинских наук filed Critical Федеральное государственное бюджетное учреждение "Научно-исследовательский институт фармакологии имени В.В. Закусова" Российской академии медицинских наук
Priority to RU2013122696A priority Critical patent/RU2613184C2/en
Publication of RU2013122696A publication Critical patent/RU2013122696A/en
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Publication of RU2613184C2 publication Critical patent/RU2613184C2/en

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/05—Dipeptides
    • 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
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids

Abstract

1. Применение гексаметилендиамида бис-(N-моносукцинил-глутамил-лизина) в качестве средства, обладающего ангиогенной активностью.2. Применение гексаметилендиамида бис-(N-ацетил-лизил-глутаминовой кислоты) в качестве средства, обладающего ангиогенной активностью.3. Применение амида N-аминокапроил-глицил-лизина в качестве средства, обладающего ангиогенной активностью.4. Применение гексаметилендиамида бис-(N-аминокапроил-глицил-лизина) в качестве средства, обладающего ангиогенной активностью.1. The use of bis- (N-monosuccinyl-glutamyl-lysine) hexamethylene diamide as an agent with angiogenic activity. 2. The use of bis- (N-acetyl-lysyl-glutamic acid) hexamethylenediamide as an agent with angiogenic activity. 3. The use of N-aminocaproyl-glycyl-lysine amide as an agent with angiogenic activity. 4. The use of bis- (N-aminocaproyl-glycyl-lysine) hexamethylenediamide as an agent with angiogenic activity.

Claims (4)

1. Применение гексаметилендиамида бис-(N-моносукцинил-глутамил-лизина) в качестве средства, обладающего ангиогенной активностью.1. The use of hexamethylene diamide bis- (N-monosuccinyl-glutamyl-lysine) as an agent with angiogenic activity. 2. Применение гексаметилендиамида бис-(N-ацетил-лизил-глутаминовой кислоты) в качестве средства, обладающего ангиогенной активностью.2. The use of bis- (N-acetyl-lysyl-glutamic acid) hexamethylene diamide as an agent with angiogenic activity. 3. Применение амида N-аминокапроил-глицил-лизина в качестве средства, обладающего ангиогенной активностью.3. The use of the amide N-aminocaproyl-glycyl-lysine as an agent with angiogenic activity. 4. Применение гексаметилендиамида бис-(N-аминокапроил-глицил-лизина) в качестве средства, обладающего ангиогенной активностью. 4. The use of bis- (N-aminocaproyl-glycyl-lysine) hexamethylene diamide as an agent with angiogenic activity.
RU2013122696A 2013-05-17 2013-05-17 Substance with angiogenic activity RU2613184C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU2013122696A RU2613184C2 (en) 2013-05-17 2013-05-17 Substance with angiogenic activity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU2013122696A RU2613184C2 (en) 2013-05-17 2013-05-17 Substance with angiogenic activity

Publications (2)

Publication Number Publication Date
RU2013122696A true RU2013122696A (en) 2014-11-27
RU2613184C2 RU2613184C2 (en) 2017-03-15

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Family Applications (1)

Application Number Title Priority Date Filing Date
RU2013122696A RU2613184C2 (en) 2013-05-17 2013-05-17 Substance with angiogenic activity

Country Status (1)

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RU (1) RU2613184C2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2745062C2 (en) * 2016-02-03 2021-03-18 Тайхо Фармасьютикал Ко., Лтд. Producing method of long-chain alcohol of high purity cyclohexenone

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7906477B2 (en) * 2002-11-18 2011-03-15 Genspera, Inc. Activation of peptide prodrugs by hK2
RU2363488C1 (en) * 2007-11-26 2009-08-10 Закрытое акционерное общество "Эксесс Байосаинс" Pharmaceutical composition based on peptide regulating disturbances of angiogenesis, and way of its application
RU2410392C2 (en) * 2009-02-16 2011-01-27 Учреждение Российской академии медицинских наук Научно-исследовательский институт фармакологии имени В.В. Закусова РАМН Dipeptide mimetics of ngf and bdnf neurotrophins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2745062C2 (en) * 2016-02-03 2021-03-18 Тайхо Фармасьютикал Ко., Лтд. Producing method of long-chain alcohol of high purity cyclohexenone

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Publication number Publication date
RU2613184C2 (en) 2017-03-15

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