Abstract: .omega.-NOR-CYCLOALKYL-13,14-DEHYDRO-PROSTAGLANDIN COMPOUNDS, SPECIFICALLY 13,14-DEHYDRO-17-CYCLOHEXYL-20,19,18-TRINOR-PGF.sub.2.alpha. having antiulcer and luteolytic activity, are disclosed.
Type:
Grant
Filed:
September 21, 1977
Date of Patent:
September 25, 1979
Assignee:
Carlo Erba S.p.A.
Inventors:
Carmelo Gandolfi, Renato Pellegata, Roberto Ceserani, Maria M. Usardi
Abstract: Pyridazinyl-ergoline compounds having neuroleptic activity are obtained by reacting an 8.beta.-tosylmethyl ergoline with the sodium derivative of an amino-pyridazine or a mercaptopyridazine in a dipolar aprotic solvent.
Type:
Grant
Filed:
January 17, 1978
Date of Patent:
September 4, 1979
Assignee:
Farmitalia Carlo Erba S.p.A.
Inventors:
Luigi Bernardi, Carlo Elli, Giovanni Falconi, Alberto Bonsignori
Abstract: 3,4-Dihydro-4-oxo-quinazoline derivatives substituted in the 2-position by a substituted phenyl group are disclosed. The derivatives possess anti-allergy properties and can be used for the treatment of allergic conditions.
Type:
Grant
Filed:
December 2, 1977
Date of Patent:
June 26, 1979
Assignee:
Carlo Erba S.p.A.
Inventors:
Gianfederico Doria, Ciriaco Romeo, Piernicola Giraldi, Francesco Lauria, Maria L. Corno, Piero Sberze, Marcello Tibolla
Abstract: Improved apparatus for providing skin cuts to a predetermined measure in order to determine blood bleeding time, comprising a casing having a cutting blade accommodated therein and restrained to the casing through a pin coupling within an elongate groove. The blade is moved by a rotating spring member to cause its cutting end to project from a casing slit to a degree and travel that are exactly predetermined and repeatable.
Type:
Grant
Filed:
December 29, 1977
Date of Patent:
June 5, 1979
Assignee:
Farmitalia Carlo Erba S.p.A.
Inventors:
Michele Maiorano, Luigi Valentini, Claudio Praga
Abstract: A new process is disclosed for the preparation of compounds of structure: ##STR1## and are as defined herein characterized in that a compound of structure ##STR2## where R and R.sup.1 have the meanings given herein, is reacted in a suitable solvent with a haloamide in the presence of a metal oxide or a haloamide in the presence of a free radical initiator under the influence of light or heat or alternatively with a halogen in the presence of a metal oxide, to give a compound of structure: ##STR3## where R and R.sup.
Type:
Grant
Filed:
August 1, 1977
Date of Patent:
May 22, 1979
Assignee:
Farmitalia Carlo Erba S.p.A.
Inventors:
Maurizio Foglio, Antonino Suarato, Paolo Masi, Giovanni Franceschi, Giorgio Palamidessi, Luigi Bernardi
Abstract: Unsaturated derivatives of 7-acylamido-3-cephem-4-carboxylic acid are disclosed which exhibit antibacterial activity against Gram-positive and Gram-negative microorganisms and can be used to treat infections caused by such microorganisms.
Type:
Grant
Filed:
August 8, 1977
Date of Patent:
May 15, 1979
Assignee:
Carlo Erba S.p.A.
Inventors:
Giuliano Nannini, Ettore Perrone, Dino Severino, Giuseppe Meinardi, Gisella Monti, Alberta Bianchi, Angelo Forgione, Carlo Confalonieri
Abstract: Chromone compounds carrying a pyridyl substituent at the 2-position are disclosed, such as, for instance, 6-carboxy-2-(2'-pyridyl)-chromone. The disclosed compounds are useful in the treatment of allergies.
Type:
Grant
Filed:
September 16, 1977
Date of Patent:
April 10, 1979
Assignee:
Carlo Erba S.p.A.
Inventors:
Gianfederico Doria, Piernicola Giraldi, Francesco Lauria, Maria L. Corno, Piero Sberze, Marcello Tibolla
Abstract: Novel N-tricyclic derivatives of azetidine are disclosed of the general formula ##STR1## where A is a C.sub.1 -C.sub.3 alkylene group, a C.sub.2 -C.sub.3 alkenylene group or a cyclopropylene group, the remaining substituents being defined in the specification. Such compounds are useful for their anti-depressant, anti-convulsant and anxiolytic activities. The compound 1-[5-(10, 11-dihydro-5H-dibenzo [a,d]cyclopheptenyl)]-3-methyl-amino-azetidine is illustrative.
Type:
Grant
Filed:
January 9, 1976
Date of Patent:
October 31, 1978
Assignee:
Carlo Erba, S.p.A.
Inventors:
Piero Melloni, Arturo Della Torre, Francesco Lauria, Norina Passerini, Alessandro Rossi, Raffaele Tommasini
Abstract: Optically active 8,12-diisoprostanoic acids and derivatives, processes for making same, pharmaceutical compositions containing same, and intermediates for producing same are disclosed. The acids include, for instance, 5c,13t-11.alpha.,15S-dihydroxy-9-oxo-8,12-diisoprostadienoic acid. The compounds of the present invention can be used in the same uses as the natural prostaglandins, including the treatment of asthma, parturition to facilitate child bearing labor and as abortion agents.
Type:
Grant
Filed:
December 15, 1972
Date of Patent:
May 16, 1978
Assignee:
Carlo Erba S.p.A.
Inventors:
Carmelo Gandolfi, Gianfederico Doria, Pietro Gaio
Abstract: A pharmaceutical composition, and method of treating allergic conditions therewith, is disclosed, wherein said composition contains a 5:6-benzo-.gamma.-pyrone derivative, such as, for instance, 6-carboxy-2'-isopropoxy-flavone.The composition may be used to treat various allergic conditions, including bronchial asthma, allergic rhinitis, hay fever, urticaria and dermatosis.
Type:
Grant
Filed:
October 27, 1976
Date of Patent:
April 11, 1978
Assignee:
Carlo Erba, S.p.A.
Inventors:
Gianfederico Doria, Pier Nicola Giraldi, Francesco Lauria, Maria Luisa Corno, Piero Sberze, Marcello Tibolla
Abstract: Novel N-tricyclic derivatives of azetidine are disclosed of the general formula: ##STR1## WHERE A is a --CH.sub.2 --S-- or --S--CH.sub.2 -- group, the remaining substituents being defined in the specification. Illustrative is the compound 1-[11-(6,11-dihydro-dibenzo [b,e] thiopinyl)]-3-methylamino-azetidine. The compounds are useful for their anti-depressant, anti-convulsant and anxiolytic activities.
Type:
Grant
Filed:
November 2, 1976
Date of Patent:
March 7, 1978
Assignee:
Carlo Erba S.p.A.
Inventors:
Piero Melloni, Arturo Della Torre, Francesco Lauria, Norina Passerini, Alessandro Rossi, Raffaele Tommasini
Abstract: Novel N-tricyclic derivatives of azetidine of the formula: ##STR1## wherein A is a --CH.sub.2 --O-- or an --O--CH.sub.2 group, and the remaining substituents being defined in the specification are disclosed. An illustrative compound is 1-[11-(6,11-dihydro-dibenzo [b,e] oxepinyl)]-3-methylamino-azetidine. The compounds are useful for their anti-depressant, anti-convulsant and anxiolytic activities.
Type:
Grant
Filed:
November 2, 1976
Date of Patent:
March 7, 1978
Assignee:
Carlo Erba S.p.A.
Inventors:
Piero Melloni, Arturo Della Torre, Francesco Lauria, Norina Passerini, Alessandro Rossi, Raffaele Tommasini
Abstract: Compounds of the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3 are hydrogen, C.sub.1-6 alkyl or alkoxy, at least one of R.sup.1, R.sup.2 and R.sup.3 is other than hydrogen, R.sup.4 is carboxy, carbalkoxy or a carboxamide group, or a pharmaceutically acceptable salt when R.sup.4 is carboxy are disclosed.
Abstract: Omega-nor-cycloalkyl-13,14-dehydro-prostaglandin compounds, specifically 13,14-dehydro-17-cyclohexyl-20,19,18-trinor-PGF.sub.2.sub..alpha., having selective luteolytic, abortifacient and labor-inducing activity and extremely low untoward gastrointestinal effects are disclosed.
Type:
Grant
Filed:
August 8, 1975
Date of Patent:
July 12, 1977
Assignee:
Carlo Erba, S.p.A.
Inventors:
Carmelo Gandolfi, Renato Pellegata, Roberto Ceserani, Maria M. Usardi