HRP20100344T2 - Derivati purina kao agonisti adenozin a1 receptora i postupci za njihovu uporabu - Google Patents
Derivati purina kao agonisti adenozin a1 receptora i postupci za njihovu uporabu Download PDFInfo
- Publication number
- HRP20100344T2 HRP20100344T2 HR20100344T HRP20100344T HRP20100344T2 HR P20100344 T2 HRP20100344 T2 HR P20100344T2 HR 20100344 T HR20100344 T HR 20100344T HR P20100344 T HRP20100344 T HR P20100344T HR P20100344 T2 HRP20100344 T2 HR P20100344T2
- Authority
- HR
- Croatia
- Prior art keywords
- monocyclic
- compound
- bicyclic
- cycloalkyl
- aryl
- Prior art date
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- 229940083251 peripheral vasodilators purine derivative Drugs 0.000 title abstract 2
- 239000002582 adenosine A1 receptor agonist Substances 0.000 title 1
- 150000003212 purines Chemical class 0.000 title 1
- 241001465754 Metazoa Species 0.000 claims abstract 29
- 239000000203 mixture Substances 0.000 claims abstract 8
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract 3
- 208000012902 Nervous system disease Diseases 0.000 claims abstract 3
- 208000008589 Obesity Diseases 0.000 claims abstract 3
- 206010063837 Reperfusion injury Diseases 0.000 claims abstract 3
- 208000010399 Wasting Syndrome Diseases 0.000 claims abstract 3
- 206010012601 diabetes mellitus Diseases 0.000 claims abstract 3
- 230000000302 ischemic effect Effects 0.000 claims abstract 3
- 230000004060 metabolic process Effects 0.000 claims abstract 3
- 230000003680 myocardial damage Effects 0.000 claims abstract 3
- 235000020824 obesity Nutrition 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims 61
- 150000003839 salts Chemical class 0.000 claims 36
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 24
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 24
- 101100294115 Caenorhabditis elegans nhr-4 gene Proteins 0.000 claims 12
- 239000003814 drug Substances 0.000 claims 11
- 239000003795 chemical substances by application Substances 0.000 claims 9
- 125000001475 halogen functional group Chemical group 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 7
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical group [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims 6
- 229940079593 drug Drugs 0.000 claims 6
- 230000001939 inductive effect Effects 0.000 claims 6
- -1 neoheptyl Chemical group 0.000 claims 6
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 5
- 230000002265 prevention Effects 0.000 claims 4
- RGPUSZZTRKTMNA-UHFFFAOYSA-N 1-benzofuran-7-carbaldehyde Chemical compound O=CC1=CC=CC2=C1OC=C2 RGPUSZZTRKTMNA-UHFFFAOYSA-N 0.000 claims 3
- LEBVLXFERQHONN-UHFFFAOYSA-N 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide Chemical compound CCCCN1CCCCC1C(=O)NC1=C(C)C=CC=C1C LEBVLXFERQHONN-UHFFFAOYSA-N 0.000 claims 3
- IVVNZDGDKPTYHK-JTQLQIEISA-N 1-cyano-2-[(2s)-3,3-dimethylbutan-2-yl]-3-pyridin-4-ylguanidine Chemical compound CC(C)(C)[C@H](C)N=C(NC#N)NC1=CC=NC=C1 IVVNZDGDKPTYHK-JTQLQIEISA-N 0.000 claims 3
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 claims 3
- 208000001871 Tachycardia Diseases 0.000 claims 3
- 229960003150 bupivacaine Drugs 0.000 claims 3
- 230000001101 cardioplegic effect Effects 0.000 claims 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 3
- AQNDDEOPVVGCPG-UHFFFAOYSA-N esmolol Chemical compound COC(=O)CCC1=CC=C(OCC(O)CNC(C)C)C=C1 AQNDDEOPVVGCPG-UHFFFAOYSA-N 0.000 claims 3
- 229960003745 esmolol Drugs 0.000 claims 3
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 claims 3
- 229960003132 halothane Drugs 0.000 claims 3
- 229960004194 lidocaine Drugs 0.000 claims 3
- LBHIOVVIQHSOQN-UHFFFAOYSA-N nicorandil Chemical compound [O-][N+](=O)OCCNC(=O)C1=CC=CN=C1 LBHIOVVIQHSOQN-UHFFFAOYSA-N 0.000 claims 3
- 229960002497 nicorandil Drugs 0.000 claims 3
- 229940053973 novocaine Drugs 0.000 claims 3
- 229960002310 pinacidil Drugs 0.000 claims 3
- 235000011164 potassium chloride Nutrition 0.000 claims 3
- 239000001103 potassium chloride Substances 0.000 claims 3
- 229960002816 potassium chloride Drugs 0.000 claims 3
- 229960004919 procaine Drugs 0.000 claims 3
- 230000006794 tachycardia Effects 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 230000008557 oxygen metabolism Effects 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 206010003658 Atrial Fibrillation Diseases 0.000 claims 1
- 208000003734 Supraventricular Tachycardia Diseases 0.000 claims 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 125000000561 purinyl group Chemical class N1=C(N=C2N=CNC2=C1)* 0.000 abstract 3
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/167—Purine radicals with ribosyl as the saccharide radical
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/12—Triazine radicals
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- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Communicable Diseases (AREA)
- Psychology (AREA)
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57480504P | 2004-05-26 | 2004-05-26 | |
US58826304P | 2004-07-15 | 2004-07-15 | |
PCT/US2005/018381 WO2005117910A2 (en) | 2004-05-26 | 2005-05-25 | Purine derivatives as adenosine a1 receptor agonists and methods of use thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
HRP20100344T1 HRP20100344T1 (en) | 2010-08-31 |
HRP20100344T2 true HRP20100344T2 (hr) | 2011-01-31 |
Family
ID=35463332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20100344T HRP20100344T2 (hr) | 2004-05-26 | 2010-06-18 | Derivati purina kao agonisti adenozin a1 receptora i postupci za njihovu uporabu |
Country Status (25)
Country | Link |
---|---|
US (3) | US7423144B2 (pl) |
EP (2) | EP2221307A1 (pl) |
JP (3) | JP4484928B2 (pl) |
KR (2) | KR101167342B1 (pl) |
CN (1) | CN103087133B (pl) |
AT (1) | ATE462704T1 (pl) |
AU (1) | AU2005249430B2 (pl) |
BR (1) | BRPI0510406A (pl) |
CA (1) | CA2567289C (pl) |
CY (1) | CY1110159T1 (pl) |
DE (1) | DE602005020286D1 (pl) |
DK (1) | DK1758596T3 (pl) |
EA (1) | EA011826B1 (pl) |
ES (1) | ES2343421T3 (pl) |
HK (1) | HK1104457A1 (pl) |
HR (1) | HRP20100344T2 (pl) |
IL (1) | IL179400A (pl) |
ME (1) | ME01072B (pl) |
MX (1) | MXPA06013560A (pl) |
NO (1) | NO339450B1 (pl) |
NZ (1) | NZ551951A (pl) |
PL (1) | PL1758596T3 (pl) |
PT (1) | PT1758596E (pl) |
RS (1) | RS51261B (pl) |
WO (1) | WO2005117910A2 (pl) |
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MXPA06013560A (es) * | 2004-05-26 | 2007-03-15 | Inotek Pharmaceuticals Corp | Derivados de purina como agonistas del receptor de adenosina a1 y metodos de uso de los mismos. |
AU2005286946B2 (en) * | 2004-09-20 | 2012-03-15 | Inotek Pharmaceuticals Corporation | Purine derivatives and methods of use thereof |
JP5203214B2 (ja) * | 2005-11-30 | 2013-06-05 | イノテック ファーマシューティカルズ コーポレイション | プリン化合物およびその使用方法 |
BRPI0709124A2 (pt) * | 2006-03-23 | 2011-06-28 | Inotek Pharmaceuticals Corp | composto purina e métodos de uso dos mesmos |
JP5128578B2 (ja) * | 2006-04-04 | 2013-01-23 | エモディス ゲーエムベーハー | 解離性障害の治療のためのκ−オピオイド受容体アンタゴニスト含有組成物の利用 |
PL2424546T3 (pl) * | 2009-05-01 | 2016-04-29 | Inotek Pharmaceuticals Corp | Sposób obniżania ciśnienia wewnątrzgałkowego u ludzi |
EA201270102A1 (ru) | 2009-06-30 | 2012-08-30 | Форест Лэборетериз Холдингз Лимитед | Соединения алкокси-карбонил-амино-алкинил-аденозина и их производные в качестве агонистов ar |
BR112012009841A2 (pt) * | 2009-10-26 | 2016-11-29 | Inotek Pharmaceuticals Corp | formulação oftálmica e processo para a sua preparação |
EP2523669B1 (en) * | 2010-01-11 | 2016-12-07 | Inotek Pharmaceuticals Corporation | Combination, kit and method of reducing intraocular pressure |
ES2613254T3 (es) | 2010-03-19 | 2017-05-23 | Inotek Pharmaceuticals Corporation | Composiciones de combinación de agonistas de adenosina A1 e inhibidores de anhidrasa carbónica para reducir la presión intraocular |
RS55616B1 (sr) * | 2010-03-19 | 2017-06-30 | Inotek Pharmaceuticals Corp | Kombinovane kompozicije adenozinskih a1 agonista i ne-selektivnih beta-adrenergičnih receptor blokera za snižavanje intraokularnog pritiska |
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