JPH10513463A - うっ血性心不全の治療へのカルバゾール化合物の利用 - Google Patents
うっ血性心不全の治療へのカルバゾール化合物の利用Info
- Publication number
- JPH10513463A JPH10513463A JP8523982A JP52398296A JPH10513463A JP H10513463 A JPH10513463 A JP H10513463A JP 8523982 A JP8523982 A JP 8523982A JP 52398296 A JP52398296 A JP 52398296A JP H10513463 A JPH10513463 A JP H10513463A
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- carvedilol
- compound
- hydrogen
- administered
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 206010019280 Heart failures Diseases 0.000 title claims abstract description 41
- 206010007559 Cardiac failure congestive Diseases 0.000 title claims abstract description 36
- 238000011282 treatment Methods 0.000 title claims description 24
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 59
- 229960004195 carvedilol Drugs 0.000 claims abstract description 58
- 239000003814 drug Substances 0.000 claims abstract description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 35
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 239000001257 hydrogen Substances 0.000 claims abstract description 20
- 239000002934 diuretic Substances 0.000 claims abstract description 19
- 239000005541 ACE inhibitor Substances 0.000 claims abstract description 17
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 16
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- 239000002368 cardiac glycoside Substances 0.000 claims abstract description 15
- 229930002534 steroid glycoside Natural products 0.000 claims abstract description 15
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- 150000008143 steroidal glycosides Chemical class 0.000 claims abstract description 11
- 229940124597 therapeutic agent Drugs 0.000 claims abstract description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 241000124008 Mammalia Species 0.000 claims abstract description 8
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 8
- -1 methylenedioxy Chemical group 0.000 claims abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
- 125000001589 carboacyl group Chemical group 0.000 claims abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
- 239000011737 fluorine Substances 0.000 claims abstract description 4
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims abstract description 4
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 claims abstract description 4
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 4
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 4
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- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims abstract description 4
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- NPAKNKYSJIDKMW-UHFFFAOYSA-N carvedilol Chemical compound COC1=CC=CC=C1OCCNCC(O)COC1=CC=CC2=NC3=CC=C[CH]C3=C12 NPAKNKYSJIDKMW-UHFFFAOYSA-N 0.000 claims abstract 13
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- JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 claims description 5
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- 229960005156 digoxin Drugs 0.000 claims description 5
- LTMHDMANZUZIPE-PUGKRICDSA-N digoxin Chemical compound C1[C@H](O)[C@H](O)[C@@H](C)O[C@H]1O[C@@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@@H]3C[C@@H]4[C@]([C@@H]5[C@H]([C@]6(CC[C@@H]([C@@]6(C)[C@H](O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)C[C@@H]2O)C)C[C@@H]1O LTMHDMANZUZIPE-PUGKRICDSA-N 0.000 claims description 5
- LTMHDMANZUZIPE-UHFFFAOYSA-N digoxine Natural products C1C(O)C(O)C(C)OC1OC1C(C)OC(OC2C(OC(OC3CC4C(C5C(C6(CCC(C6(C)C(O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)CC2O)C)CC1O LTMHDMANZUZIPE-UHFFFAOYSA-N 0.000 claims description 5
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- FAKRSMQSSFJEIM-RQJHMYQMSA-N captopril Chemical group SC[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O FAKRSMQSSFJEIM-RQJHMYQMSA-N 0.000 claims description 4
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- GBXSMTUPTTWBMN-XIRDDKMYSA-N enalapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 GBXSMTUPTTWBMN-XIRDDKMYSA-N 0.000 claims description 4
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- RLAWWYSOJDYHDC-BZSNNMDCSA-N lisinopril Chemical compound C([C@H](N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(O)=O)C(O)=O)CC1=CC=CC=C1 RLAWWYSOJDYHDC-BZSNNMDCSA-N 0.000 claims description 4
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- 229960003746 metildigoxin Drugs 0.000 claims description 4
- IYJMSDVSVHDVGT-PEQKVOOWSA-N metildigoxin Chemical compound O1[C@H](C)[C@@H](OC)[C@@H](O)C[C@@H]1O[C@@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@@H]3C[C@@H]4[C@]([C@@H]5[C@H]([C@]6(CC[C@@H]([C@@]6(C)[C@H](O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)C[C@@H]2O)C)C[C@@H]1O IYJMSDVSVHDVGT-PEQKVOOWSA-N 0.000 claims description 4
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.哺乳類におけるうっ血性心不全に起因する死亡率を減少させる薬剤の製造 のための、単独でのまたは1もしくは複数の別の治療薬と組み合わせたβ−アド レナリン受容体アンタゴニストとα1−アドレナリン受容体アンタゴニストの両 方である化合物の使用であって、前記治療薬がアンギオテンシン変換酵素阻害剤 、利尿薬および強心配糖体から成る群より選択される、化合物の使用。 2.前記化合物が式I: (上式中、 R1は水素、炭素原子数6までの低級アルカノイル、またはベンゾイルおよび ナフトイルより選ばれたアロイルであり; R2は水素、炭素原子数6までの低級アルキル、またはベンジル、フェニルエ チルおよびフェニルプロピルより選ばれたアリールアルキルであり; R3は水素または炭素原子数6までの低級アルキルであり; R4は水素もしくは炭素原子数6までの低級アルキルであるか、またはXが酸 素である時、R4はR5と一緒になって−CH2−O−を表すことができ; Xは一価結合、−CH2−、酸素または硫黄であり; Arはフェニル、ナフチル、インダニルおよびテトラヒドロナフチルより選ば れ; R5およびR6は個々に水素、フッ素、塩素、臭素、ヒドロキシル、炭素原子数 6までの低級アルキル、−CONH2基、炭素原子数6までの低級アルコキシ、 ベンジルオキシ、炭素原子数6までの低級アルキルチオ、炭素原子数6までの低 級アルキルスルホニル、および炭素原子数6までの低級アルキルスルホニルより 選ばれ;または R5とR6は一緒になってメチレンジオキシを表す) により表される化合物および医薬上許容されるその塩である、請求項1に記載の 化合物の使用。 3.前記化合物がカルベジロールである、請求項1または2に記載の化合物の 使用。 4.1単位中に3.125 または6.25mgのカルベジロールを含有する医薬製剤を初 回量として1日1回または2回7〜28日間の期間に渡り投与する、請求項3に記 載の化合物の使用。 5.1単位中に12.5mgのカルベジロールを含有する医薬製剤を1日1回または 2回7〜28日間の期間に渡り投与する、請求項3に記載の化合物の使用。 6.1単位中に25.0または50.0mgのカルベジロールを含有する医薬製剤を維持 量として1回または2回投与する、請求項3に記載の化合物の使用。 7.前記ACE阻害剤がカプトプリル、リシノプリル、フォシノプリルおよび エナラプリル並びにそれらの任意の医薬上許容される塩から成る群より選ばれる 、請求項1に記載の化合物の使用。 8.前記利尿薬がヒドロクロロチアジド、トラセミドおよびフロセミド並びに それらの任意の医薬上許容される塩から成る群より選 ばれる、請求項1に記載の化合物の使用。 9.前記強心配糖体がジゴキシン、β−メチルジゴキシンおよびジギトキシン から成る群より選ばれる、請求項1に記載の化合物の使用。 10.次の摂生: (a) 3.125 または6.25mgカルベジロール/1単位を含有する医薬製剤を1日1回 または2回、7〜28日間の期間に渡り投与し、 (b) その後、12.5mgカルベジロール/1単位を含有する医薬製剤を1日1回また は2回、追加の7〜28日間の期間に渡り投与し、そして (c) 最後に、25.0または50.0mgカルベジロール/1単位を含有する医薬製剤を1 日1回または2回、維持量として投与する に従った、哺乳類においてうっ血性心不全に起因する死亡率を減少させる薬剤の 製造のためのカルベジロールの使用。 11.カルベジロールを1または複数の別の治療薬と組み合わせて投与し、前記 治療薬がアンギオテンシン変換酵素阻害剤、利尿薬および強心配糖体から成る群 より選ばれる、請求項10に記載のカルベジロールの使用。 12.10〜100 mgの1日維持量において投与されるCHFの治療用薬剤の調製の ための化合物の使用であって、前記薬剤が3段階の投薬摂生を含んで成る増分投 薬スキームにおいて投与され、第一摂生が7〜28日間の期間に渡り化合物の1日 維持量の10〜30%の量を投与することを含んで成り、第二摂生が7〜28日間の期 間に渡り前記1日維持量の20〜70%の量を投与することを含んで成り、そして第 三摂生が第二摂生の終了後に始まる前記1日維持量の100 %を投与することを含 んで成る、請求項1に記載の化合物の使用。 13.1投与単位形態あたり1.0 〜10.0mgのカルベジロールの有効 量を含んで成る経口医薬製剤。 14.2.5 〜7.5 mgのカルベジロールを含有する、請求項13に記載の製剤。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1995103995 DE19503995C2 (de) | 1995-02-08 | 1995-02-08 | Verwendung von Carvedilol zur Verminderung der Mortalität bei Patienten mit eingeschränkter myocardialer Funktion |
US08/483,635 | 1995-06-07 | ||
US08/483,635 US5760069A (en) | 1995-02-08 | 1995-06-07 | Method of treatment for decreasing mortality resulting from congestive heart failure |
US19503995.5 | 1995-06-07 | ||
PCT/EP1996/000498 WO1996024348A2 (en) | 1995-02-08 | 1996-02-07 | Use of carbazole compounds for the treatment of congestive heart failure |
Publications (2)
Publication Number | Publication Date |
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JPH10513463A true JPH10513463A (ja) | 1998-12-22 |
JP3546058B2 JP3546058B2 (ja) | 2004-07-21 |
Family
ID=26012210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP52398296A Expired - Lifetime JP3546058B2 (ja) | 1995-02-08 | 1996-02-07 | うっ血性心不全の治療へのカルバゾール化合物の利用 |
Country Status (27)
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US (6) | US5760069A (ja) |
EP (1) | EP0808162B1 (ja) |
JP (1) | JP3546058B2 (ja) |
KR (1) | KR100295940B1 (ja) |
CN (1) | CN1093760C (ja) |
AT (1) | ATE179891T1 (ja) |
AU (1) | AU702106C (ja) |
BR (1) | BR9607111A (ja) |
CA (1) | CA2212548C (ja) |
CZ (1) | CZ292002B6 (ja) |
DE (1) | DE69602424T2 (ja) |
DK (1) | DK0808162T3 (ja) |
ES (1) | ES2134588T3 (ja) |
FI (1) | FI973255A (ja) |
GR (1) | GR3030966T3 (ja) |
HK (1) | HK1014861A1 (ja) |
HU (1) | HUP9900773A3 (ja) |
NO (1) | NO314830B1 (ja) |
NZ (1) | NZ301692A (ja) |
PL (1) | PL321737A1 (ja) |
RO (1) | RO121629B1 (ja) |
RU (1) | RU2197242C2 (ja) |
SI (1) | SI0808162T1 (ja) |
SK (1) | SK106897A3 (ja) |
UA (1) | UA55382C2 (ja) |
WO (1) | WO1996024348A2 (ja) |
ZA (1) | ZA96994B (ja) |
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US20080207726A1 (en) * | 2007-02-26 | 2008-08-28 | Santiago Ini | Process for the purification of carvedilol or its salts thereof |
US20090076116A1 (en) * | 2007-09-13 | 2009-03-19 | Protia, Llc | Deuterium-enriched carvediolo |
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KR20140057604A (ko) | 2011-08-12 | 2014-05-13 | 베링거잉겔하임베트메디카게엠베하 | 고양잇과 동물의 심부전을 치료 및 예방하는 방법에 사용하기 위한 퍼니 전류 억제제 |
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DE2815926A1 (de) | 1978-04-13 | 1979-10-18 | Boehringer Mannheim Gmbh | Neue carbazolyl-(4)-oxy-propanolamin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
DE3319027A1 (de) | 1983-05-26 | 1984-11-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur herstellung von optisch aktiven carbazol-derivaten, neue r- und s-carbazol-derivate, sowie arzneimittel, die diese verbindungen enthalten |
SE460945B (sv) * | 1987-01-15 | 1989-12-11 | Lejus Medical Ab | En multipel-unit-dos komposition av furosemid |
US5312828A (en) * | 1989-06-14 | 1994-05-17 | Finkelstein Joseph A | Substituted imidazoles having angiotensin II receptor blocking activity |
US5308862A (en) * | 1993-03-05 | 1994-05-03 | Boehringer Mannheim Pharmaceuticals Corporation - Smithkline Beecham Corp., Ltd. Partnership No. 1 | Use of, and method of treatment using, carbazolyl-(4)-oxypropanolamine compounds for inhibition of smooth muscle cell proliferation |
US5760069A (en) | 1995-02-08 | 1998-06-02 | Boehringer Mannheim Pharmaceuticals Corporation-Smithkline Beecham Corporation Limited Partnership #1 | Method of treatment for decreasing mortality resulting from congestive heart failure |
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