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公开(公告)号:ES2054115T3
公开(公告)日:1994-08-01
申请号:ES90101946
申请日:1990-02-01
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR , MURRAY WILLIAM V , WACHTER MICHAEL P , BELL STANLEY
IPC: A61K31/15 , A61K8/00 , A61K8/30 , A61K8/40 , A61K8/41 , A61K8/42 , A61K8/46 , A61K8/49 , A61K8/55 , A61K8/58 , A61K31/165 , A61K31/18 , A61K31/19 , A61K31/225 , A61K31/235 , A61K31/275 , A61K31/33 , A61K31/445 , A61K31/495 , A61K31/535 , A61K31/5375 , A61K31/54 , A61K31/66 , A61P17/00 , A61P19/06 , A61P27/02 , A61P29/00 , A61P31/04 , A61P35/00 , A61Q17/04 , A61Q19/00 , C07C243/22 , C07C251/86 , C07C251/88 , C07C255/58 , C07C255/61 , C07C255/66 , C07C259/10 , C07C309/45 , C07C309/46 , C07C311/39 , C07C317/32 , C07C323/48 , C07D211/06 , C07D215/22 , C07D215/227 , C07D241/04 , C07D295/18 , C07D295/192 , C07D295/22 , C07D295/26 , C07D311/58 , C07D317/32 , C07F9/11 , C07F9/40
Abstract: Phenylhydrazones of formula I I in which R1 to R6 and m and n have the meanings stated above, and the manufacture thereof. The substances are suitable for combating disease and for cosmetic use.
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公开(公告)号:DE59001281D1
公开(公告)日:1993-06-03
申请号:DE59001281
申请日:1990-02-01
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR
IPC: A61K31/075 , A61K31/10 , A61K31/11 , A61K31/12 , A61K31/135 , A61K31/165 , A61K31/19 , A61K31/235 , A61K31/255 , A61K31/41 , A61P17/00 , A61P27/02 , A61P29/00 , A61P31/04 , A61P35/00 , C07C39/18 , C07C43/23 , C07C45/46 , C07C49/697 , C07C59/90 , C07C65/21 , C07C65/26 , C07C65/32 , C07C65/40 , C07C69/76 , C07C69/773 , C07C205/45 , C07C211/42 , C07C217/48 , C07C225/18 , C07C229/60 , C07C233/25 , C07C255/53 , C07C255/54 , C07C309/42 , C07C317/22 , C07C317/44 , C07C323/00 , C07C323/16 , C07C323/19 , C07C323/22 , C07C323/41 , C07C323/56 , C07C323/62 , C07D257/04 , C07D317/22 , C07D405/12
Abstract: Oxidised diphenylheteroalkanes of the formula I in which R to R and A have the meanings given in the description, and their preparation are described. The substances are suitable for combating diseases and as cosmetic agents.
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公开(公告)号:DE59000769D1
公开(公告)日:1993-03-04
申请号:DE59000769
申请日:1990-02-01
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR , MURRAY WILLIAM V , WACHTER MICHAEL P , BELL STANLEY
IPC: A61K31/15 , A61K8/00 , A61K8/30 , A61K8/40 , A61K8/41 , A61K8/42 , A61K8/46 , A61K8/49 , A61K8/55 , A61K8/58 , A61K31/165 , A61K31/18 , A61K31/19 , A61K31/225 , A61K31/235 , A61K31/275 , A61K31/33 , A61K31/445 , A61K31/495 , A61K31/535 , A61K31/5375 , A61K31/54 , A61K31/66 , A61P17/00 , A61P19/06 , A61P27/02 , A61P29/00 , A61P31/04 , A61P35/00 , A61Q17/04 , A61Q19/00 , C07C243/22 , C07C251/86 , C07C251/88 , C07C255/58 , C07C255/61 , C07C255/66 , C07C259/10 , C07C309/45 , C07C309/46 , C07C311/39 , C07C317/32 , C07C323/48 , C07D211/06 , C07D215/22 , C07D215/227 , C07D241/04 , C07D295/18 , C07D295/192 , C07D295/22 , C07D295/26 , C07D311/58 , C07D317/32 , C07F9/11 , C07F9/40
Abstract: Phenylhydrazones of formula I I in which R1 to R6 and m and n have the meanings stated above, and the manufacture thereof. The substances are suitable for combating disease and for cosmetic use.
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公开(公告)号:DE4117371A1
公开(公告)日:1992-12-03
申请号:DE4117371
申请日:1991-05-28
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , LORENZ GISELA DR , STEINER GERD DR , JANSSEN BERND DR , ANKE TIMM PROF DR , STEGLICH WOLFGANG PROF DR
IPC: A61K31/165 , A61K31/215 , A61K31/415 , A61K31/42 , A61K31/44 , A61K31/505
Abstract: Antimycotic compositions containing a compound of the formula in which = Y is =CH-OCH3, =CH-CH3, =CH-CH2-CH3, =CH-SCH3 or =N-OCH3 and X is oxygen, or in which X can also be NH when Y is =N-OCH3, Z is halogen, nitro, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroarylalkyl, optionally substituted heretoaryloxyalkyl, optionally substituted heteroarylthioalkyl, optionally substituted alkenyl, optionally substituted aralkenyl, optionally substituted aryloxyalkenyl, optionally substituted arylthioalkenyl, optionally substituted heteroarylalkenyl, optionally substituted heteroaryloxyalkenyl, optionally substituted heteroarylthioalkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted amino, optionally substituted arylazo, optionally substituted acylamino, OR , SR , SOR , SO2R , -COOR , -CONR R , -COR , -CR =NR , -N=CR R , -CR =N-OR , -CR R -O-N=CR R , and U, V, W are hydrogen or can have one of the meanings stated for Z, or in which two of the groups Z, U, V or W in adjacent positions on the phenyl ring optionally form together an optionally substituted 5- or 6-membered, aromatic or aliphatic ring which is fused onto the phenyl ring and which can optionally contain 1 to 3 hetero atoms (N, S, O), where the groups R to R are optionally identical or different hydrogen, optionally substituted C1-C8-alkyl, optionally substituted C2-C8-alkenyl, optionally substituted C2-C8-alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroaryloxyalkyl or optionally substituted heteroarylthioalkyl, and their use for controlling mycoses.
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公开(公告)号:CS9003897A2
公开(公告)日:1991-08-13
申请号:CS389790
申请日:1990-08-07
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR
IPC: A61K31/095 , A61K8/46 , A61K31/10 , A61K31/255 , A61K31/35 , A61K31/352 , A61P17/00 , A61P35/00 , A61P37/00 , A61Q19/00 , C07C315/04 , C07C317/14 , C07C317/22 , C07C319/00 , C07C319/20 , C07C321/24 , C07C321/28 , C07C323/18 , C07D311/04 , C07D311/58
Abstract: Diarylacetylenes of the formula I I where R1 is hydrogen or C1-C4-alkyl, R2 and R3 are each hydrogen or, when R1 is hydrogen, together form a -C(CH3)2-B-C(CH3)2- group (where B is -CH2Ch2- or -CH(CH3)-) or -OC(Ch3) (Z)CH2CH2- group (where Z is C1-C2-alkyl) or R2 is C1-C3-alkoxy and R3 is C1-C10-alkyl or, when R2 is hydrogen, R1 and R3 are each alkyl as defined above, R4 is C1-C6-alkyl and n is 0, 1 or 2, are prepared as described and used as active compounds in drugs and cosmetics.
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公开(公告)号:DE3903991A1
公开(公告)日:1990-08-30
申请号:DE3903991
申请日:1989-02-10
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR
IPC: A61K31/15 , A61K20060101 , A61K8/00 , A61K8/30 , A61K31/165 , A61K31/19 , A61K31/195 , A61K31/235 , A61K31/255 , A61K31/275 , A61P17/00 , A61P27/02 , A61P29/00 , A61P31/04 , A61P35/00 , A61Q17/00 , C07C20060101 , C07C229/60 , C07C233/65 , C07C249/16 , C07C251/80 , C07C255/66 , C07C259/10 , C07C309/46 , C07C317/32 , C07C317/34 , C07C403/18
Abstract: Phenylhydrazones of beta -ionone, of the formula I … … in which R assumes the meaning given in the description, and their preparation are described. The substances are suitable for controlling diseases and as cosmetic agents.
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公开(公告)号:DE3903988A1
公开(公告)日:1990-08-30
申请号:DE3903988
申请日:1989-02-10
Applicant: BASF AG
Inventor: JANSSEN BERND DR , WUEST HANS-HEINER DR
IPC: A61K31/075 , A61K31/10 , A61K31/11 , A61K31/12 , A61K31/135 , A61K31/165 , A61K31/19 , A61K31/235 , A61K31/255 , A61K31/41 , A61P17/00 , A61P27/02 , A61P29/00 , A61P31/04 , A61P35/00 , C07C39/18 , C07C43/23 , C07C45/46 , C07C49/697 , C07C59/90 , C07C65/21 , C07C65/26 , C07C65/32 , C07C65/40 , C07C69/76 , C07C69/773 , C07C205/45 , C07C211/42 , C07C217/48 , C07C225/18 , C07C229/60 , C07C233/25 , C07C255/53 , C07C255/54 , C07C309/42 , C07C317/22 , C07C317/44 , C07C323/00 , C07C323/16 , C07C323/19 , C07C323/22 , C07C323/41 , C07C323/56 , C07C323/62 , C07D257/04 , C07D317/22 , C07D405/12
Abstract: Oxidised diphenylheteroalkanes of the formula I in which R to R and A have the meanings given in the description, and their preparation are described. The substances are suitable for combating diseases and as cosmetic agents.
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公开(公告)号:DE3737888A1
公开(公告)日:1989-05-18
申请号:DE3737888
申请日:1987-11-07
Applicant: BASF AG
Inventor: KURBACH STEFAN DR , JANSSEN BERND DR , RECKER HANS-GERT DR , SMUDA HUBERT DR , MEYER NORBERT DR , JUNG JOHANN PROF DR , RADEMACHER WILHELM DR
IPC: A01N43/50 , A01N43/653 , C07D405/06 , C07D521/00
Abstract: Method of influencing plant growth, characterised in that the soil, the seed and/or the plants are treated with an azolyl methyl oxirane of the formula in which the substituents A and B represent C1-C4-alkyl, phenyl, naphthyl, diphenyl or phenyl which is substituted by one to three radicals from amongst the group comprising halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, nitro or phenoxy and Z represents the CH group or nitrogen, or their metal salts or acid addition salts, and compositions for influencing plant growth which contain at least one azolyl methyl oxirane.
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公开(公告)号:DE3511409A1
公开(公告)日:1986-10-02
申请号:DE3511409
申请日:1985-03-29
Applicant: BASF AG
Inventor: JANSSEN BERND DR , KOENIG HORST PROF DR , SCHARWAECHTER PETER DR
IPC: C07D249/08 , A61K31/41 , A61P31/12 , A61P31/22
Abstract: Viral diseases are treated by a method in which an effective amount of 1-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)ethan- 1-ol (formula I) (I) is administered enterally, parenterally or topically to a patient suffering therefrom.
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公开(公告)号:DE3307479A1
公开(公告)日:1984-09-13
申请号:DE3307479
申请日:1983-03-03
Applicant: BASF AG
Inventor: JANSSEN BERND DR , MEYER NORBERT DR , KOHLMANN FRIEDRICH-WILHELM DR , WESENBERG WALTER , HEBERLE WOLFGANG DR
IPC: A01N43/50 , A01N43/653 , A61K31/41 , A61K31/415 , B27K3/34 , C07C29/14 , C07C33/24 , C07C45/44 , C07C47/457 , C07D233/56 , C07D249/08 , C07D521/00
Abstract: Azolylmethylcycloalkanes of the formula I in which A and B are identical or different and denote hydrogen, alkyl having 1 to 4 C atoms, which can optionally be substituted by halogen, naphthyl, heteroaryl, biphenyl or phenyl, where the phenyl radical can be substituted by halogen, nitro, alkyl, alkoxy or haloalkyl each having 1 to 4 C atoms, phenoxy or the phenylsulphenyl radical, D and E are identical or different and denote hydrogen or halogen, Z denotes CH or N, m can be 1, 2, 3 or 4 and n can be 0, 1 or 2, and their physiologically tolerable acid addition salts and their preparation are described. The compounds are suitable for combating diseases.
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