Abstract: An improved ointment for the topical administration of steroids is comprised of a therapeutically effective amount of a 17-mono or 17,21-diester of betamethasone in a non-aqueous base comprised of 5-15% of a glycol solvent, 1-3% of a principle emulsifying agent; 0-7% of a secondary emulsifying agent; and 70-90% of a petrolatum base.
Abstract: Disclosed herein is the novel compound, 2-aminomethyl-5-chloro-3-(2,4-dichlorophenyl)indole, useful by virtue of its antimicrobial, sanitizing, disinfectant, preservative, viricidal and herbicidal properties.
Abstract: This invention relates to the preparation of novel 1-desamino-1-oxo-aminoglycosides and their use as intermediates in the preparation of novel 1-desamino-1-hydroxy and 1-desamino-1-epi-hydroxyaminoglycoside antibacterial agents.
Abstract: The present 2-substituted imidazolines possess valuable hypoglycemic activity. The compounds are prepared by the condensation of an appropriately substituted aryl nitrile with a diamine.
Abstract: This disclosure relates to the preparation of garamine, its use as an antibacterial, and its use as an intermediate in the novel processes for preparing novel pseudotrisaccharides containing a garamine moiety, and to the use of the novel pseudotrisaccharides as antimicrobial, anthelmintic, antiprotozoal and antiviral agents.
Abstract: Novel 6-(polyhaloisopropyl)quinazoline-2,4-diones, preparable from polyhaloisopropylarylureas, are disclosed herein. These compounds display potent hypotensive activity and are thus useful in the treatment of mammalian hypertension.
Abstract: Rosamicin is an antibiotic elaborated by Micromonospora rosaria. The compounds described herein are antibacterial derivatives of rosamicin. Also described are processes for the preparation of these antibacterial derivatives from rosamicin.
Type:
Grant
Filed:
March 5, 1976
Date of Patent:
November 1, 1977
Assignee:
Schering Corporation
Inventors:
Hans Reimann, Robert S. Jaret, Mohammad Mehdi Nafissi-Varchei
Abstract: Amides having aromatic substituents of the formula: ##STR1## wherein R is an acyl radical derived from a carboxylic acid having from 3 to 20 carbon atoms, X and Y are members selected from the group consisting of hydrogen, fluoro, trifluoromethyl and hydroxy, and n is an integer selected from the group consisting of 0, 1 and 2, exhibit an effect upon the central nervous system.
Abstract: Novel N-diphenylalkyl-2-benzyl azacyclic compounds are disclosed which can be used as antiobesity agents. Some of these compounds also exhibit useful antimicrobial properties. Additionally, novel chemical intermediates for the synthesis of this series are provided.
Abstract: A cosmetically elegant and stable oil in water emulsion for use as a topical anesthetic containing 0.5-15% benzocaine solubilized in water with a dialkyl ester of an alkanedioic acid having the formula ROOC--C.sub.n H.sub.2n --C00R' where R and R' are alkyl groups of from 1 to 4 carbon atoms and n is an integer from 1 to 8.
Abstract: An in vitro test method for the diagnosis of systemic candidiasis in mammals is carried out with an antigen solution containing a specified concentration and ratio of protein antigen and mannan antigen whereby false readings are reduced.
Abstract: Micromonospora inyoensis strain 155OF-1G NRRL 5742 is incapable of producing antibiotics unless an aminocyclitol is added to the fermentation medium. When such a compound is added, antibiotics are produced, said antibiotics being analogs of known aminoglycoside antibiotics differing therefrom with respect to the aminocyclitol subunit.
Type:
Grant
Filed:
December 15, 1976
Date of Patent:
September 20, 1977
Assignee:
Schering Corporation
Inventors:
Marvin Joseph Weinstein, Peter John Lovell Daniels, Gerald Howard Wagman, Raymond Thomas Testa
Abstract: In the fermentation production of gentamicin C a plurality of additional antibiotic compounds are obtained. Four of these compounds, gentamicin A, gentamicin B, gentamicin B.sub.1 and gentamicin X exhibit significant anti-protozoal and anthelmintic activity while gentamicin B and B.sub.1 have significant antibacterial properties with markedly reduced side effects.
Type:
Grant
Filed:
October 1, 1975
Date of Patent:
September 20, 1977
Assignee:
Schering Corporation
Inventors:
David J. Cooper, Jay Allan Waitz, Mae Counelis, Jay Weinstein
Abstract: A method for the treatment of canine seborrhea comprising oral administration of a daily dosage of 5-25 mg/kg of either 4-nitro-3-trifluoromethylisobutyranilide or its metabolite 4'-nitro-3'-trifluoromethyl-2-hydroxyisobutyranilide.
Abstract: This invention relates to compositions of matter useful as anti-diarrheal agents and to the method of controlling and treating diarrhea in warm blooded animals. The active anti-diarrheal agents are substituted N-aryl-anthranilic acids, and salts thereof and ester and hydrazine derivatives of said acids.
Abstract: Everninomicin derivatives devoid of a nitro group and having antibacterial activity are prepared by electrochemically reducing the corresponding everninomicin having a nitro function or salts thereof in an aprotic anhydrous solvent in the absence of carbon dioxide. A preferred starting compound is everninomicin D whereby is produced a product mixture of antibacterial agents identified as desevernitrose everninomicin D, everninomicin D-3, and everninomicin D-7, respectively.
Type:
Grant
Filed:
January 19, 1976
Date of Patent:
May 31, 1977
Assignee:
Schering Corporation
Inventors:
Peter Kabasakalian, Sami Y. Kalliney, Ashit K. Ganguly, Anita Westcott
Abstract: A novel compound, N-carbomethoxy-N'-methyl-N'-(2-nitro-4-N-propyloxyphenyl)thiourea, is highly effective in the treatment of pinworm infections.
Abstract: 21-Halogeno-17.alpha.-acyloxy-20-keto-4-pregnenes having physiological properties are prepared by the reaction of a 17.alpha.,21-dihydroxy-20-keto-4-pregnene 17.alpha.,21-orthoester with a triphenylmethyl halide in an organic solvent, said halide being chloride or bromide.