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公开(公告)号:AU498925B2
公开(公告)日:1979-03-29
申请号:AU1655776
申请日:1976-08-04
Applicant: ABBOTT LAB
Inventor: WINN M , KYNCL J , DUNNIGAN D A , JONES P H
IPC: C07D405/12 , A61K31/505 , A61P9/12 , A61P25/04 , C07D309/08 , C07D405/14 , A61K31/495 , C07D5/06
Abstract: Described are antihypertensive agents selected from the class consisting of 2[4(tetrahydro-2-furoyl)-piperazino]-4-amino-6,7-dimethoxyquinazoline and 2-[4(tetrahydropyran-2-carbonyl)-piperazinyl]-4-amino-6,7-dimethoxyqui nazoline, and pharmaceutically acceptable acid addition salts thereof. The compounds are highly water soluble and can be administered in time release form as well as parenterally, including intravenously.
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公开(公告)号:SE7412163L
公开(公告)日:1975-03-27
申请号:SE7412163
申请日:1974-09-26
Applicant: ABBOTT LAB
Inventor: DUNNIGAN D A , GEISZLER A O , HOLLAND J B
IPC: C07C217/74 , A61K31/13 , A61K31/135 , C07C67/00 , C07C213/00 , C07C93/24
Abstract: Covers a compound selected from the group consisting of a member of the formula: wherein R1 is a radial selected from the group consisting of higher branched or straight chain alkyl and cycloalkyl radicals wherein said R1 radical contains at least six carbon atoms, R2 is a radical selected from the group consisting of hydrogen, loweralkyl and loweralkanol radicals, wherein said R2 radical contains 1 - 3 carbon atoms, and R3 is methoxy; and nontoxic pharmaceutically acceptable acid addition salts thereof. Also covers the use of said compound as a local anesthetic and pharmaceutical compositions comprising said above compounds as the active ingredient.
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公开(公告)号:SE422685B
公开(公告)日:1982-03-22
申请号:SE7611379
申请日:1976-10-13
Applicant: ABBOTT LAB
Inventor: WINN M , KYNCL J , DUNNIGAN D A , JONES P H
IPC: C07D405/12 , A61K31/505 , A61P9/12 , A61P25/04 , C07D309/08 , C07D405/14
Abstract: Described are antihypertensive agents selected from the class consisting of 2[4(tetrahydro-2-furoyl)-piperazino]-4-amino-6,7-dimethoxyquinazoline and 2-[4(tetrahydropyran-2-carbonyl)-piperazinyl]-4-amino-6,7-dimethoxyqui nazoline, and pharmaceutically acceptable acid addition salts thereof. The compounds are highly water soluble and can be administered in time release form as well as parenterally, including intravenously.
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公开(公告)号:AU502420B2
公开(公告)日:1979-07-26
申请号:AU1759176
申请日:1976-09-09
Applicant: ABBOTT LAB
Inventor: WINN M , KYNCL J , DUNNIGAN D A , JONES P H
IPC: C07D405/14 , A61K31/495 , A61K31/505 , A61K31/55 , A61P9/12 , C07D239/84 , C07D239/95 , C07D243/00 , C07D243/08 , C07D307/14 , C07D405/06 , C07D407/14
Abstract: Described are the compounds 2[4(tetrahydro-2-furoyl)-hexahydro-1,4-diazepinyl-1]-4-amino-6,7-dimet hoxy quinazoline and pharmaceutically acceptable acid addition salts thereof. The compounds are useful as antihypertensive agents.
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公开(公告)号:SE7812825L
公开(公告)日:1979-06-22
申请号:SE7812825
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: DUNNIGAN D A , MARTIN J R , TADANIER J S , FREIBERG L A
IPC: C07H15/224 , C07H15/22
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公开(公告)号:SE431208B
公开(公告)日:1984-01-23
申请号:SE8008533
申请日:1980-12-04
Applicant: ABBOTT LAB
Inventor: WINN M , KYNCL J , DUNNIGAN D A , JONES P H
IPC: C07D405/12 , A61K31/505 , A61P9/12 , A61P25/04 , C07D309/08 , C07D405/14
Abstract: Described are antihypertensive agents selected from the class consisting of 2[4(tetrahydro-2-furoyl)-piperazino]-4-amino-6,7-dimethoxyquinazoline and 2-[4(tetrahydropyran-2-carbonyl)-piperazinyl]-4-amino-6,7-dimethoxyqui nazoline, and pharmaceutically acceptable acid addition salts thereof. The compounds are highly water soluble and can be administered in time release form as well as parenterally, including intravenously.
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公开(公告)号:SE7812825A
公开(公告)日:1979-06-22
申请号:SE7812825
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: DUNNIGAN D A , MARTIN J R , TADANIER J S , FREIBERG L A
IPC: C07H15/224 , C07H15/22
CPC classification number: C07H15/224
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公开(公告)号:SE7611379L
公开(公告)日:1977-04-15
申请号:SE7611379
申请日:1976-10-13
Applicant: ABBOTT LAB
Inventor: WINN M , KYNCL J , DUNNIGAN D A , JONES P H
IPC: C07D405/12 , A61K31/505 , A61P9/12 , A61P25/04 , C07D309/08 , C07D405/14
Abstract: Described are antihypertensive agents selected from the class consisting of 2[4(tetrahydro-2-furoyl)-piperazino]-4-amino-6,7-dimethoxyquinazoline and 2-[4(tetrahydropyran-2-carbonyl)-piperazinyl]-4-amino-6,7-dimethoxyqui nazoline, and pharmaceutically acceptable acid addition salts thereof. The compounds are highly water soluble and can be administered in time release form as well as parenterally, including intravenously.
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