RU98110565A - NEW COMPOUNDS AND THEIR COMPOSITIONS Possessing ANTI-INFLAMMATORY AND ANTI-THROMBOTIC ACTIVITY - Google Patents
NEW COMPOUNDS AND THEIR COMPOSITIONS Possessing ANTI-INFLAMMATORY AND ANTI-THROMBOTIC ACTIVITYInfo
- Publication number
- RU98110565A RU98110565A RU98110565/04A RU98110565A RU98110565A RU 98110565 A RU98110565 A RU 98110565A RU 98110565/04 A RU98110565/04 A RU 98110565/04A RU 98110565 A RU98110565 A RU 98110565A RU 98110565 A RU98110565 A RU 98110565A
- Authority
- RU
- Russia
- Prior art keywords
- linear
- branched
- ono
- carbon atoms
- permissible
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 6
- 239000000203 mixture Substances 0.000 title claims 3
- 230000003110 anti-inflammatory Effects 0.000 title claims 2
- 230000002785 anti-thrombosis Effects 0.000 title claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- CHNUOJQWGUIOLD-NFZZJPOKSA-N epalrestat Chemical compound C=1C=CC=CC=1\C=C(/C)\C=C1/SC(=S)N(CC(O)=O)C1=O CHNUOJQWGUIOLD-NFZZJPOKSA-N 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 3
- 229940079593 drugs Drugs 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- -1 nitro, amino Chemical group 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 1
- 206010040070 Septic shock Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 239000003146 anticoagulant agent Substances 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atoms Chemical group 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- 125000005265 dialkylamine group Chemical group 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- 239000000546 pharmaceutic aid Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 230000036303 septic shock Effects 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
Claims (5)
A - X1 - NO2,
или их соли, использованные как лекарственные средства, где A = R(COX)t, t = 0 или 1; Х = 0, NH, NR1C, где R1C означает линейный или разветвленный, когда возможно, алкил 1 - 10 углеродных атомов, предпочтительно 1 - 4 или
где m и n означают целые числа от 1 до 6; R2a означает Н, СН3, связывание с X1 может быть в любом положении кольца,
Хo = Х;
R выбран из
где R1 означает OCOR3 группу, где R3 означает метил, этил или линейным или разветвленный С3-C5 алкил, или остаток гетероцикла только с одним кольцом, имеющим 5 или 6 атомов, которое может быть ароматическим, частично или полностью гидрогенированным, содержащим один или больше гетероатомов, независимо выбранных из О, N и S;
R2 означает водород, гидрокси-группу, галоген, линейный или, когда допустимо, разветвленный алкил, имеющий 1 - 4 атомов углерода, линейный или, когда допустимо, разветвленный алкоксил, имеющий 1 - 4 атомов углерода, линейный или, когда допустимо, разветвленный перфторалкил, имеющий 1 - 4 атомов углерода, нитро, амино, моно- или диалкиламин с C1-C4 алкилом, R1 и R2 вместе являются диоксиметиленовой группой, с условием, что, когда X = NH, тогда Y означает этилен и R2 = H, R1 не может быть OCOR3 в положении 2, когда R3 означает метил, nI означает целое число 0 или 1, X1 в формуле A - X1 - NO2 означает бивалентный соединительный мостик, выбранный из следующих
-YO-
где Y выбран из линейный или, когда допустимо, разветвленный C1-C20 алкилен, циклоалкилен, имеющий 5 - 7 атомов углерода, необязательно замещенных,
,
где n означает целое число 1 - 6, R2a как указано выше, r = 0 или 1.1. Compounds of the general formula
A - X 1 - NO 2 ,
or their salts used as medicines, where A = R (COX) t , t = 0 or 1; X = 0, NH, NR 1C , where R 1C means linear or branched, when possible, alkyl of 1 to 10 carbon atoms, preferably 1 to 4 or
where m and n are integers from 1 to 6; R 2a means H, CH 3 , binding to X 1 may be in any position of the ring,
X o = X;
R is selected from
where R 1 means OCOR 3 group, where R 3 means methyl, ethyl or linear or branched C 3 -C 5 alkyl, or a heterocycle residue with only one ring having 5 or 6 atoms, which may be aromatic, partially or completely hydrogenated, containing one or more heteroatoms independently selected from O, N and S;
R 2 means hydrogen, hydroxy group, halogen, linear or, when permissible, branched alkyl having 1 to 4 carbon atoms, linear or, when permissible, branched alkoxyl having 1 to 4 carbon atoms, linear or, when permissible, branched perfluoroalkyl having 1 to 4 carbon atoms, nitro, amino, mono- or dialkylamine with C 1 -C 4 alkyl, R 1 and R 2 together are a dimethylene group, with the proviso that when X = NH then Y is ethylene and R 2 = H, R 1 cannot be OCOR 3 at position 2 when R 3 is methyl, nI is an integer of 0 or 1, X 1 is in f the formula A - X 1 - NO 2 means a bivalent connecting bridge selected from the following
-Y-
where Y is selected from linear or, when permissible, branched C 1 -C 20 alkylene, cycloalkylene having 5 to 7 carbon atoms, optionally substituted,
,
where n is an integer of 1 to 6, R 2a as described above, r = 0 or 1.
где означает -CH2 - ONO2, -CH2CH2CH2CH2ONO2, -CH2CH2ONO2, -CH2CH2OCH2CH2ONO2, -CH2CH2OCH2ONO2.2. The compound of claim 1, wherein R is
Where means -CH 2 - ONO 2 , -CH 2 CH 2 CH 2 CH 2 ONO 2 , -CH 2 CH 2 ONO 2 , -CH 2 CH 2 OCH 2 CH 2 ONO 2 , -CH 2 CH 2 OCH 2 ONO 2 .
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITM195A002263 | 1995-10-31 | ||
IT95MI002263A IT1276071B1 (en) | 1995-10-31 | 1995-10-31 | ANTI-INFLAMMATORY ACTIVITY COMPOSITES |
Publications (2)
Publication Number | Publication Date |
---|---|
RU98110565A true RU98110565A (en) | 2000-04-27 |
RU2165921C2 RU2165921C2 (en) | 2001-04-27 |
Family
ID=11372460
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU98110565/04A RU2165921C2 (en) | 1995-10-31 | 1996-10-29 | Nitrocompounds and pharmaceutical composition showing anti-inflammatory and antithrombotic activity |
Country Status (18)
Country | Link |
---|---|
US (1) | US6040341A (en) |
EP (1) | EP0871606B1 (en) |
JP (1) | JP3880067B2 (en) |
KR (1) | KR100546038B1 (en) |
AT (1) | ATE193883T1 (en) |
AU (1) | AU709338B2 (en) |
BR (1) | BR9611175B1 (en) |
CA (1) | CA2235996C (en) |
DE (1) | DE69608916T2 (en) |
DK (1) | DK0871606T3 (en) |
ES (1) | ES2148808T3 (en) |
GR (1) | GR3033827T3 (en) |
HU (1) | HUP9802986A3 (en) |
IT (1) | IT1276071B1 (en) |
PT (1) | PT871606E (en) |
RU (1) | RU2165921C2 (en) |
SI (1) | SI0871606T1 (en) |
WO (1) | WO1997016405A1 (en) |
Families Citing this family (64)
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US6136804A (en) | 1998-03-13 | 2000-10-24 | Merck & Co., Inc. | Combination therapy for treating, preventing, or reducing the risks associated with acute coronary ischemic syndrome and related conditions |
ES2136581B1 (en) | 1998-05-27 | 2000-09-16 | Uriach & Cia Sa J | USE OF DERIVATIVES OF ACID-2-HIDROXI-4-TRIFLUOROMETILBENZOICO FOR THE PREPARATION OF USEFUL MEDICINES TO INHIBIT THE NUCLEAR TRANSCRIPTION FACTOR NF-KB. |
JP2002517423A (en) | 1998-06-08 | 2002-06-18 | アドバンスド メディスン インコーポレーテッド | Multiple binding inhibitors of cyclooxygenase-2 |
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US6509377B1 (en) * | 1999-05-26 | 2003-01-21 | J. Uriach & Cia, S.A. | Use of a 2-hydroxy-4-trifluoromethylbenzoic acid derivatives as inhibitors of the activation of the nuclear transcription factor NF-κB |
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ITMI991517A1 (en) * | 1999-07-09 | 2001-01-09 | Nicox Sa | PROCEDURE FOR OBTAINING EXTERNAL NITROXYMETHYL FENYL OF SALICYLIC ACID DERIVATIVES |
IT1313596B1 (en) | 1999-08-04 | 2002-09-09 | Nicox Sa | PROCESS FOR THE PREPARATION OF NITROXIALKYL ESTERS OF NAPROXENE |
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IT1319202B1 (en) * | 2000-10-12 | 2003-09-26 | Nicox Sa | DRUGS FOR INFLAMMATORY-BASED DISEASES. |
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ITMI20011240A1 (en) * | 2001-06-13 | 2002-12-13 | Nicox Sa | DRUGS FOR VASCULOPATHIES |
ITMI20011308A1 (en) | 2001-06-21 | 2002-12-21 | Nicox Sa | DRUGS FOR CHRONIC PAIN |
ITMI20011307A1 (en) * | 2001-06-21 | 2002-12-21 | Nicox Sa | DRUGS FOR EPILEPSY |
AU2003208525B9 (en) * | 2002-02-04 | 2009-08-27 | Alfama-Investigacao e Desenvolvimento de Produtos Farmaceuticos Lda | Amend the invention title to read Method for treating a mammal by administration of a compound having the ability to release CO, compounds having the ability to release CO and pharmaceutical compositions thereof |
US7968605B2 (en) * | 2002-02-04 | 2011-06-28 | ALFAMA—Investigação e Desenvolvimento de Produtos Farmacêuticos, Lda. | Methods for treating inflammatory disease by administering aldehydes and derivatives thereof |
US20080026984A1 (en) * | 2002-02-04 | 2008-01-31 | Alfama - Investigacao E Desenvolvimento De Productos Farmaceuticos Lda | Methods for treating inflammatory disease by administering aldehydes and derivatives thereof |
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ITMI20021861A1 (en) * | 2002-08-29 | 2004-02-29 | Nicox Sa | NITROXIALKYL ESTER SYNTHESIS PROCESS OF CARBOXYLIC ACIDS, INTERMEDIATES THAT CAN BE USED IN THAT PROCEDURE AND THEIR PREPARATION. |
WO2004037843A2 (en) * | 2002-10-25 | 2004-05-06 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Steroid compounds comprising superoxide dismutase mimic groups and nitric oxide donor groups, and their use in the preparation of medicaments |
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US7521435B2 (en) * | 2005-02-18 | 2009-04-21 | Pharma Diagnostics, N.V. | Silicon containing compounds having selective COX-2 inhibitory activity and methods of making and using the same |
CA2630805A1 (en) | 2005-11-23 | 2007-05-31 | Nicox S.A. | Salicylic acid derivatives |
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JP2007275193A (en) * | 2006-04-04 | 2007-10-25 | Fujifilm Corp | Optical probe and optical tomographic imaging equipment |
EP2180788B1 (en) * | 2007-08-10 | 2016-12-21 | Basil Rigas | Anti-inflammatory compounds and uses thereof |
WO2010118968A1 (en) | 2009-04-16 | 2010-10-21 | Nicox S.A. | No-donor aspirin derivatives |
WO2011160974A2 (en) | 2010-06-21 | 2011-12-29 | Nicox S.A. | Statin derivatives |
EP2699242B1 (en) | 2011-04-19 | 2017-11-01 | Alfama, Inc. | Carbon monoxide releasing molecules and uses thereof |
EP2734235B1 (en) | 2011-07-21 | 2017-03-22 | Alfama, Inc. | Ruthenium carbon monoxide releasing molecules and uses thereof |
CA2897571C (en) | 2013-01-21 | 2018-12-18 | Apparao Satyam | Nitric oxide releasing prodrugs of therapeutic agents containing at least one carboxylic acid group |
US20140271923A1 (en) | 2013-03-14 | 2014-09-18 | Christopher Brian Reid | Compositions & formulations for preventing and treating chronic diseases that cluster in patients such as cardiovascular disease, diabetes, obesity, polycystic ovary syndrome, hyperlipidemia and hypertension, as well as for preventing and treating other diseases and conditions |
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IT1243367B (en) * | 1990-07-26 | 1994-06-10 | Italfarmaco Spa | BENZOIC ACID DERIVATIVES SUBSTITUTED FOR CARDIOVASCULAR ACTIVITY |
IT1256450B (en) * | 1992-11-26 | 1995-12-05 | Soldato Piero Del | NITRIC ESTERS WITH PHARMACOLOGICAL ACTIVITY AND PROCEDURE FOR THEIR PREPARATION |
DE69412109T2 (en) * | 1993-10-06 | 1999-01-21 | Nicox S.A., Paris | SALT ACID ESTER WITH AN ANTI-INFLAMMATORY AND / OR PAIN-RELATING EFFECT AND METHOD FOR THE PRODUCTION THEREOF |
DK0759899T3 (en) * | 1994-05-10 | 1999-12-20 | Nicox Sa | Nitro compounds and their compositions with anti-inflammatory, analgesic and antithrombotic activities |
IT1276071B1 (en) * | 1995-10-31 | 1997-10-24 | Nicox Ltd | ANTI-INFLAMMATORY ACTIVITY COMPOSITES |
-
1995
- 1995-10-31 IT IT95MI002263A patent/IT1276071B1/en active IP Right Grant
-
1996
- 1996-10-29 RU RU98110565/04A patent/RU2165921C2/en not_active IP Right Cessation
- 1996-10-29 US US09/066,344 patent/US6040341A/en not_active Expired - Fee Related
- 1996-10-29 EP EP96937282A patent/EP0871606B1/en not_active Expired - Lifetime
- 1996-10-29 DK DK96937282T patent/DK0871606T3/en active
- 1996-10-29 CA CA002235996A patent/CA2235996C/en not_active Expired - Fee Related
- 1996-10-29 JP JP51706097A patent/JP3880067B2/en not_active Expired - Fee Related
- 1996-10-29 AT AT96937282T patent/ATE193883T1/en not_active IP Right Cessation
- 1996-10-29 HU HU9802986A patent/HUP9802986A3/en unknown
- 1996-10-29 DE DE69608916T patent/DE69608916T2/en not_active Expired - Fee Related
- 1996-10-29 KR KR1019980703206A patent/KR100546038B1/en not_active IP Right Cessation
- 1996-10-29 ES ES96937282T patent/ES2148808T3/en not_active Expired - Lifetime
- 1996-10-29 AU AU74950/96A patent/AU709338B2/en not_active Ceased
- 1996-10-29 BR BRPI9611175-5A patent/BR9611175B1/en not_active IP Right Cessation
- 1996-10-29 WO PCT/EP1996/004696 patent/WO1997016405A1/en active IP Right Grant
- 1996-10-29 SI SI9630170T patent/SI0871606T1/en unknown
- 1996-10-29 PT PT96937282T patent/PT871606E/en unknown
-
2000
- 2000-06-30 GR GR20000401528T patent/GR3033827T3/en not_active IP Right Cessation
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