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公开(公告)号:SE7812828A
公开(公告)日:1979-06-22
申请号:SE7812828
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: MARTIN J R , TADANIER J S
IPC: C07H15/224 , C07H15/22
CPC classification number: C07H15/224
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公开(公告)号:AU520644B2
公开(公告)日:1982-02-18
申请号:AU4119778
申请日:1978-10-31
Applicant: ABBOTT LAB
Inventor: TADANIER J S , MARTIN J R , COLLUM P
IPC: A01N43/14 , C07H15/224 , C07H15/22 , A61K31/71
Abstract: 3-De-O-methyl-2'-N-acyl and alkyl fortimicin B derivatives represented by the formula wherein R is acyl, aminoacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, hydroxyacyl, an amino acid residue, loweralkyl, aminoloweralkyl, hydroxyloweralkyl, N-loweralkylaminoloweralkyl, N,N-diloweralkylaminoloweralkyl, aminohydroxyloweralkyl, N-loweralkylaminohydroxyloweralkyl N,N-diloweralkylaminohydroxyloweralkyl; and R1 is acyl, aminoacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, an amino acid residue, hydroxyacyl, loweralkyl, aminoloweralkyl, hydroxyloweralkyl, N-loweralkylaminoloweralkyl, N,N-diloweralkylaminoloweralkyl, aminohydroxyloweralkyl, N-loweralkylaminohydroxyloweralkyl, N,N-diloweralkylaminohydroxyloweralkyl, hydrogen; the pharmaceutically acceptable salts thereof; pharmaceutical compositions containing the compounds; and methods of making and using the compounds. The compounds are antibiotics.
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公开(公告)号:AU519064B2
公开(公告)日:1981-11-05
申请号:AU2902577
申请日:1977-09-22
Applicant: ABBOTT LAB
Inventor: TADANIER J S , MARTIN J R , KURATH P
IPC: C07D309/14 , A61K31/35 , A61K31/351 , A61K31/415 , A61P31/04 , C07D405/12 , C07H15/224 , C07H15/22 , C07H15/26
Abstract: This invention provides 4-N-acylfortimicin B derivatives of the structure wherein R is acyl, aminoacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, or substituted aminoacyl of the formula where R1 is an acyl radical derived from an amino acid or a short peptide, and the pharmaceutically acceptable salts thereof.
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公开(公告)号:AU6207080A
公开(公告)日:1981-04-02
申请号:AU6207080
申请日:1980-09-05
Applicant: ABBOTT LAB
Inventor: MARTIN J R , TADANIER J S , JOHNSON P
IPC: A61K31/70 , A61K31/7028 , A61K31/7034 , A61K31/7036 , A61P31/04 , C07H15/224 , C07H15/22
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公开(公告)号:SE7812832A
公开(公告)日:1979-06-22
申请号:SE7812832
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: TADANIER J S , MARTIN J R
IPC: A01N43/14 , C07H15/224 , C07H15/22
CPC classification number: C07H15/224
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公开(公告)号:SE7812829A
公开(公告)日:1979-06-22
申请号:SE7812829
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: MARTIN J R , TADANIER J S , COLLUM P
IPC: A01N43/14 , C07H15/224 , C07H15/22
CPC classification number: C07H15/224
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公开(公告)号:SE7812828L
公开(公告)日:1979-06-22
申请号:SE7812828
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: MARTIN J R , TADANIER J S
IPC: C07H15/224 , C07H15/22
Abstract: 2-Deoxy-2'-N-acyl and alkyl fortimicin B and derivatives, 4,2'-N,N'-diacyl and dialkyl fortimicin B derivatives, 4-N-acyl-2'-N-alkyl- and 4-N-alkyl-2'-N-acyl fortimicin B derivatives represented by the formula wherein R is acyl, aminoacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, hydroxyacyl, an amino acid residue, loweralkyl, aminoloweralkyl, hydroxyloweralkyl, N-loweralkylaminoloweralkyl, N,N-diloweralkylaminoloweralkyl, aminohydroxyloweralkyl, N-loweralkylaminohydroxyloweralkyl or N,N-diloweralkylaminohydroxyloweralkyl; and R1 is acyl, aminoacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, hydroxyacyl, an amino acid residue, loweralkylaminoloweralkyl, hydroxyloweralkyl, N-loweralkylaminoloweralkyl, N,N-diloweralkylaminoloweralkyl, aminohydroxyloweralkyl, N-loweralkylaminohydroxyloweralkyl, N,N-diloweralkylaminohydroxyloweralkyl, hydrogen; and the pharmaceutically acceptable salts therefor, pharmaceutical compositions containing the compounds and methods of making and using the compounds. The compounds of this invention are useful as antibiotics.
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公开(公告)号:SE7812826L
公开(公告)日:1979-06-22
申请号:SE7812826
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: TADANIER J S , MARTIN J R
IPC: C07H15/224 , C07H15/22
Abstract: 6'-Epi-fortimicin A and B derivatives represented by the formula wherein R1 is hydrogen or loweralkyl, R2 is hydrogen or loweralkyl and R3 is selected from the group consisting of hydrogen, loweralkyl, aminoloweralkyl, N-loweralkylaminoloweralkyl, N,N-diloweralkylaminoloweralkyl, aminohydroxyloweralkyl, N-loweralkylaminohydroxyloweralkyl, hydroxyloweralkyl, acyl, aminoacyl, hydroxyacyl, N-monoloweralkylaminoacyl, N,N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl or an amino acid residue; the pharmaceutically acceptable salts thereof; intermediates useful in their preparation, compositions employing the compounds; and methods of using the compounds. The compounds are useful as antibiotics.
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公开(公告)号:SE7812826A
公开(公告)日:1979-06-22
申请号:SE7812826
申请日:1978-12-13
Applicant: ABBOTT LAB
Inventor: TADANIER J S , MARTIN J R
IPC: C07H15/224 , C07H15/22
CPC classification number: C07H15/224
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公开(公告)号:AU517514B2
公开(公告)日:1981-08-06
申请号:AU3129277
申请日:1977-12-07
Applicant: ABBOTT LAB
Inventor: MARTIN J R , TADANIER J S
IPC: A61K31/70 , A61K31/7028 , A61K31/7034 , A61K31/7036 , A61P31/04 , C07H15/224 , C07H15/22 , A61K31/71
Abstract: Described are 3-de-O-methylfortimicins A and B and 4-N-acyl and 4-N-alkyl-3-de-O-methylfortimicin B derivatives, and their preparation, which compounds are useful as antibiotics or as intermediates for preparing other useful derivatives having antibacterial activity. The compounds have the following structural formula wherein R is hydrogen, acyl, aminoacyl, N-monoloweralkylaminoacyl, N.N-diloweralkylaminoacyl, hydroxy-substituted aminoacyl, alkyl, aminoalkyl, N-monoloweralkylaminoalkyl, N.N-diloweralkylaminoalkyl or hydroxy-substituted aminoalkyl and the pharmaceutically acceptable salts thereof, for example, salts formed from hydrochloric, sulfuric, and phosphoric acids.
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