RU2001102262A - NITROESTERS AND NITRATE SALTS OF SPECIFIC MEDICINES - Google Patents
NITROESTERS AND NITRATE SALTS OF SPECIFIC MEDICINESInfo
- Publication number
- RU2001102262A RU2001102262A RU2001102262/04A RU2001102262A RU2001102262A RU 2001102262 A RU2001102262 A RU 2001102262A RU 2001102262/04 A RU2001102262/04 A RU 2001102262/04A RU 2001102262 A RU2001102262 A RU 2001102262A RU 2001102262 A RU2001102262 A RU 2001102262A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- salts
- integer
- compounds
- nitrate salts
- Prior art date
Links
- 150000002823 nitrates Chemical class 0.000 title claims 7
- 239000003814 drug Substances 0.000 title claims 5
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000004432 carbon atoms Chemical group C* 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 229940079593 drugs Drugs 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- JBDGDEWWOUBZPM-XYPYZODXSA-N Ambroxol Chemical compound NC1=C(Br)C=C(Br)C=C1CN[C@@H]1CC[C@@H](O)CC1 JBDGDEWWOUBZPM-XYPYZODXSA-N 0.000 claims 2
- 229960005174 Ambroxol Drugs 0.000 claims 2
- KBUZBQVCBVDWKX-UHFFFAOYSA-N Emedastine Chemical compound N=1C2=CC=CC=C2N(CCOCC)C=1N1CCCN(C)CC1 KBUZBQVCBVDWKX-UHFFFAOYSA-N 0.000 claims 2
- NDAUXUAQIAJITI-UHFFFAOYSA-N Salbutamol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 229960001803 cetirizine Drugs 0.000 claims 2
- 229960000325 emedastine Drugs 0.000 claims 2
- ZKLPARSLTMPFCP-UHFFFAOYSA-N levocetirizine Chemical compound C1CN(CCOCC(=O)O)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZKLPARSLTMPFCP-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 229960002052 salbutamol Drugs 0.000 claims 2
- 125000005717 substituted cycloalkylene group Chemical group 0.000 claims 2
- 229940023040 Acyclovir Drugs 0.000 claims 1
- MKXZASYAUGDDCJ-SZMVWBNQSA-N Dextromethorphan Chemical compound C1CCC[C@H]2[C@@]3([H])N(C)CC[C@]21C1=CC(OC)=CC=C1C3 MKXZASYAUGDDCJ-SZMVWBNQSA-N 0.000 claims 1
- 229960001985 Dextromethorphan Drugs 0.000 claims 1
- JAQUASYNZVUNQP-PVAVHDDUSA-N Dextrorphan Chemical compound C1C2=CC=C(O)C=C2[C@@]23CCN(C)[C@@H]1[C@H]2CCCC3 JAQUASYNZVUNQP-PVAVHDDUSA-N 0.000 claims 1
- 229950006878 Dextrorphan Drugs 0.000 claims 1
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 claims 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N Isoniazid Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 claims 1
- ZCVMWBYGMWKGHF-UHFFFAOYSA-N Ketotifene Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2CC(=O)C2=C1C=CS2 ZCVMWBYGMWKGHF-UHFFFAOYSA-N 0.000 claims 1
- 229960003088 Loratadine Drugs 0.000 claims 1
- JCCNYMKQOSZNPW-UHFFFAOYSA-N Loratadine Chemical compound C1CN(C(=O)OCC)CCC1=C1C2=NC=CC=C2CCC2=CC(Cl)=CC=C21 JCCNYMKQOSZNPW-UHFFFAOYSA-N 0.000 claims 1
- 229960000282 Metronidazole Drugs 0.000 claims 1
- RQTOOFIXOKYGAN-UHFFFAOYSA-N Nedocromil Chemical compound CCN1C(C(O)=O)=CC(=O)C2=C1C(CCC)=C1OC(C(O)=O)=CC(=O)C1=C2 RQTOOFIXOKYGAN-UHFFFAOYSA-N 0.000 claims 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N Pyrazinamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 claims 1
- 229960005206 Pyrazinamide Drugs 0.000 claims 1
- 229960000351 Terfenadine Drugs 0.000 claims 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 claims 1
- 229960004150 aciclovir Drugs 0.000 claims 1
- MKUXAQIIEYXACX-UHFFFAOYSA-N acyclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 claims 1
- 239000000043 antiallergic agent Substances 0.000 claims 1
- 229960003276 erythromycin Drugs 0.000 claims 1
- 229960003350 isoniazid Drugs 0.000 claims 1
- 229960004958 ketotifen Drugs 0.000 claims 1
- VAOCPAMSLUNLGC-UHFFFAOYSA-N metronidazole Chemical compound CC1=NC=C([N+]([O-])=O)N1CCO VAOCPAMSLUNLGC-UHFFFAOYSA-N 0.000 claims 1
- 229960004398 nedocromil Drugs 0.000 claims 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 1
- -1 nitrate ions Chemical class 0.000 claims 1
- 210000002345 respiratory system Anatomy 0.000 claims 1
- 239000003675 tocolytic agent Substances 0.000 claims 1
- 0 CC(C1)C(C2)C(CCCC3)C13c1c2ccc(*)c1 Chemical compound CC(C1)C(C2)C(CCCC3)C13c1c2ccc(*)c1 0.000 description 1
Claims (1)
сальбутамол, имеющий формулу (I)
цетиризин, имеющий формулу (II)
лоратадин, имеющий формулу (III)
терфенадин, имеющий формулу (IV)
эмедастин, имеющий формулу (V)
кетотифен, имеющий формулу (VI)
недокромил, имеющий формулу (VII)
амброксол, имеющий формулу (VIII)
декстрометорфан, имеющий формулу (X)
декстрорфан, имеющий формулу (XI)
изониазид, имеющий формулу (XIII)
эритромицин, имеющий формулу (XIV)
пиразинамид, имеющий формулу (XVI)
2. Нитратные соли по п. 1, где соединениями являются сальбутамол, цетиризин, эмедастин, амброксол.1. Nitrate salts of compounds selected from the following:
salbutamol having the formula (I)
cetirizine having the formula (II)
loratadine having the formula (III)
terfenadine having the formula (IV)
emedastine having the formula (V)
ketotifen having the formula (VI)
nedocromil having the formula (VII)
ambroxol having the formula (VIII)
dextromethorphan having the formula (X)
dextrorphan having the formula (XI)
isoniazid having the formula (XIII)
erythromycin having the formula (XIV)
pyrazinamide having the formula (XVI)
2. The nitrate salts of claim 1, wherein the compounds are salbutamol, cetirizine, emedastine, ambroxol.
YO, где Y означает C1-C20 алкилен, линейный или разветвленный, когда это возможно, предпочтительно состоящий из 2-5 атомов углерода, или необязательно замещенный циклоалкилен из 5-7 атомов углерода;
Y1, выбранный из
где n3 означает целое число от 0 до 3;
где nf' означает целое число от 1 до 6, предпочтительно от 2 до 4;
где R1f= H, СН3 и nf означает целое число от 1 до 6, предпочтительно от 2 до 4.3. Nitrate salts according to paragraphs. 1 and 2, where the compounds contain one or more —ONO 2 groups covalently linked to the molecule via one of the following bivalent linking bridges:
YO, where Y is C 1 -C 20 alkylene, linear or branched when possible, preferably consisting of 2-5 carbon atoms, or optionally substituted cycloalkylene of 5-7 carbon atoms;
Y 1 selected from
where n 3 means an integer from 0 to 3;
where nf 'is an integer from 1 to 6, preferably from 2 to 4;
where R 1f = H, CH 3 and nf is an integer from 1 to 6, preferably from 2 to 4.
метронидазол, имеющий формулу (XII)
ацикловир, имеющий формулу (XV)
для получения лекарственных средств для лечения патологий респираторной системы.8. The use of salts and compositions according to claim 7 and the following compounds:
metronidazole having the formula (XII)
acyclovir having the formula (XV)
to obtain drugs for the treatment of pathologies of the respiratory system.
YO, где Y означает C1-C20 алкилен, линейный или разветвленный, когда это возможно, предпочтительно состоящий из 2-5 атомов углерода, или необязательно замещенный циклоалкилен из 5-7 атомов углерода;
Y1, выбранный из:
где n3 означает целое число от 0 до 3;
где nf' означает целое число от 0 до 6, предпочтительно от 2 до 4;
где R1f= H, СН3 и nf означает целое число от 1 до 6, предпочтительно от 2 до 4.11. The compounds of claim 1, having formulas (I), (II), (III), (VII), (VIII), (XI), containing one or more —ONO 2 groups covalently linked to the molecule by one of the following bivalent linking bridges:
YO, where Y is C 1 -C 20 alkylene, linear or branched when possible, preferably consisting of 2-5 carbon atoms, or optionally substituted cycloalkylene of 5-7 carbon atoms;
Y 1 selected from:
where n 3 means an integer from 0 to 3;
where nf 'is an integer from 0 to 6, preferably from 2 to 4;
where R 1f = H, CH 3 and nf is an integer from 1 to 6, preferably from 2 to 4.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1998MI001743A IT1303671B1 (en) | 1998-07-28 | 1998-07-28 | SALTS OF NITRIC ACID WITH ACTIVE DRUGS IN THE TREATMENT OF DISEASES OF THE RESPIRATORY SYSTEM |
ITMI98A001743 | 1998-07-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2001102262A true RU2001102262A (en) | 2003-01-20 |
RU2254330C2 RU2254330C2 (en) | 2005-06-20 |
Family
ID=11380535
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2001102262/04A RU2254330C2 (en) | 1998-07-28 | 1999-07-20 | Acid-additive nitrate salts of compounds and pharmaceutical composition |
Country Status (18)
Country | Link |
---|---|
US (3) | US6410791B1 (en) |
EP (1) | EP1098870B1 (en) |
JP (1) | JP4455760B2 (en) |
KR (1) | KR100687806B1 (en) |
CN (1) | CN1264828C (en) |
AT (1) | ATE307796T1 (en) |
AU (2) | AU770313C (en) |
BR (1) | BR9912375A (en) |
CA (1) | CA2338854C (en) |
DE (1) | DE69927977T2 (en) |
DK (1) | DK1098870T3 (en) |
ES (1) | ES2252958T3 (en) |
HU (1) | HUP0102706A3 (en) |
IL (1) | IL140685A0 (en) |
IT (1) | IT1303671B1 (en) |
RU (1) | RU2254330C2 (en) |
WO (1) | WO2000006531A2 (en) |
ZA (1) | ZA200100457B (en) |
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US5824669A (en) * | 1996-03-22 | 1998-10-20 | Nitromed, Inc. | Nitrosated and nitrosylated compounds and compositions and their use for treating respiratory disorders |
IT1303671B1 (en) * | 1998-07-28 | 2001-02-23 | Nicox Sa | SALTS OF NITRIC ACID WITH ACTIVE DRUGS IN THE TREATMENT OF DISEASES OF THE RESPIRATORY SYSTEM |
IT1317735B1 (en) * | 2000-01-26 | 2003-07-15 | Nicox Sa | SALTS OF ANTIMICROBIAL AGENTS. |
US6642276B2 (en) * | 2001-10-01 | 2003-11-04 | M/S Ind-Swift Limited | Controlled release macrolide pharmaceutical formulations |
US7220749B2 (en) | 2002-06-11 | 2007-05-22 | Nitromed, Inc. | Nitrosated and/or nitrosylated cyclooxygenase-2 selective inhibitors, compositions and methods of use |
EP1539679A4 (en) * | 2002-06-28 | 2007-07-04 | Nitromed Inc | Oxime and/or hydrazone containing nitrosated and/or nitrosylated cyclooxigenase-2 selective inhibitors, compositions and methods of use |
GB0406069D0 (en) * | 2004-03-17 | 2004-04-21 | Thompson James | Process |
RU2008100237A (en) * | 2005-06-14 | 2009-07-20 | Джилид Сайэнс, Инк. (US) | GENERAL MEDICINAL FORMS OF STEROIDS AND β-AGONISTS (OPTIONS), INCLUDING THEIR AEROSOL COMPOSITION (OPTIONS) AND METHOD FOR PREVENTING AND / OR TREATING PULMONARY INFLAMMATION AND / OR IMPLEMENTING |
TW200804241A (en) * | 2006-02-24 | 2008-01-16 | Novartis Ag | New salt |
JP2007275193A (en) * | 2006-04-04 | 2007-10-25 | Fujifilm Corp | Optical probe and optical tomographic imaging equipment |
WO2009142772A2 (en) | 2008-05-23 | 2009-11-26 | Mastcell Pharmaceuticals, Inc. | Methods and treatment for allergies and inflammation associated with gastrointestinal diseases |
US8263581B2 (en) | 2009-07-03 | 2012-09-11 | Jdp Therapeutics, Inc. | Non-sedating antihistamine injection formulations and methods of use thereof |
US8513259B2 (en) | 2009-07-03 | 2013-08-20 | Jdp Therapeutics, Inc. | Non-sedating antihistamine injection formulations and methods of use thereof |
JP6042197B2 (en) * | 2012-12-11 | 2016-12-14 | エア・ウォーター株式会社 | Lung disorder treatment |
CN104211604B (en) * | 2014-08-18 | 2016-05-11 | 江苏正大清江制药有限公司 | Eutectic of a kind of ambroxol and P-hydroxybenzoic acid and preparation method thereof |
CN104211605B (en) * | 2014-08-18 | 2016-04-27 | 江苏正大清江制药有限公司 | A kind of Transbroncho and m-Salicylic acid eutectic and preparation method thereof |
WO2018089797A1 (en) | 2016-11-14 | 2018-05-17 | Mingwu Wang | Formulations for the treatment of ocular surface diseases and related methods |
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DK1041990T3 (en) | 1997-12-23 | 2006-10-02 | Schering Corp | Composition for the treatment of respiratory and skin diseases with at least one leukotriene antagonist and at least one antihistamine |
IT1303671B1 (en) * | 1998-07-28 | 2001-02-23 | Nicox Sa | SALTS OF NITRIC ACID WITH ACTIVE DRUGS IN THE TREATMENT OF DISEASES OF THE RESPIRATORY SYSTEM |
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IT1317735B1 (en) * | 2000-01-26 | 2003-07-15 | Nicox Sa | SALTS OF ANTIMICROBIAL AGENTS. |
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-
1998
- 1998-07-28 IT IT1998MI001743A patent/IT1303671B1/en active
-
1999
- 1999-07-20 AU AU52857/99A patent/AU770313C/en not_active Ceased
- 1999-07-20 EP EP99938300A patent/EP1098870B1/en not_active Expired - Lifetime
- 1999-07-20 DE DE69927977T patent/DE69927977T2/en not_active Expired - Lifetime
- 1999-07-20 RU RU2001102262/04A patent/RU2254330C2/en not_active IP Right Cessation
- 1999-07-20 CA CA2338854A patent/CA2338854C/en not_active Expired - Fee Related
- 1999-07-20 JP JP2000562338A patent/JP4455760B2/en not_active Expired - Fee Related
- 1999-07-20 US US09/743,808 patent/US6410791B1/en not_active Expired - Fee Related
- 1999-07-20 CN CNB998090425A patent/CN1264828C/en not_active Expired - Fee Related
- 1999-07-20 AT AT99938300T patent/ATE307796T1/en active
- 1999-07-20 ES ES99938300T patent/ES2252958T3/en not_active Expired - Lifetime
- 1999-07-20 DK DK99938300T patent/DK1098870T3/en active
- 1999-07-20 KR KR1020017000803A patent/KR100687806B1/en not_active IP Right Cessation
- 1999-07-20 IL IL14068599A patent/IL140685A0/en not_active IP Right Cessation
- 1999-07-20 HU HU0102706A patent/HUP0102706A3/en unknown
- 1999-07-20 WO PCT/EP1999/005171 patent/WO2000006531A2/en not_active Application Discontinuation
- 1999-07-20 BR BR9912375-4A patent/BR9912375A/en not_active Application Discontinuation
-
2001
- 2001-01-16 ZA ZA200100457A patent/ZA200100457B/en unknown
-
2002
- 2002-05-22 US US10/151,955 patent/US6828342B2/en not_active Expired - Fee Related
-
2003
- 2003-12-17 US US10/736,688 patent/US7122539B2/en not_active Expired - Fee Related
-
2004
- 2004-04-07 AU AU2004201457A patent/AU2004201457A1/en not_active Abandoned
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