Abstract: Antibiotic A16886I and antibiotic A16886II and their salts, having antibacterial and anthelmintic activity, prepared by fermentation of Streptomyces clavuligerus NRRL 3585.
Type:
Grant
Filed:
May 20, 1976
Date of Patent:
March 4, 1980
Assignee:
Eli Lilly and Company
Inventors:
Marvin Gorman, Calvin E. Higgens, Ramakrishnan Nagarajan
Abstract: 5,6-Diaryl-1,2,4-triazines, topically-active anti-inflammatory agents, having the formula, ##STR1## wherein R is hydrogen or -(X).sub.n R.sub.1, in which X is either O or S, n is an integer which is either 0 or 1, and R.sub.1 is C.sub.1 -C.sub.8 alkyl, C.sub.7 -C.sub.8 aralkyl, C.sub.3 -C.sub.8 cycloalkyl, or C.sub.4 -C.sub.8 (cycloalkyl)alkyl; and R.sub.2 and R.sub.3 independently are C.sub.1 -C.sub.3 alkoxy or di(C.sub.1 -C.sub.3 alkyl)amino; with the proviso that when R.sub.2 and R.sub.3 both are methoxy, R cannot be H or methylthio; and the pharmaceutically-acceptable acid addition salts of basic members thereof.
Abstract: A series of new diphenylamines have small alkyl substituents on the amino nitrogen. One phenyl ring bears dinitro-trifluoromethyl substitution, and the other is preferably substituted with halogen or pseudo-halogen groups. The new diphenylamines are useful as rodenticides.
Abstract: The present invention is directed to a process for reducing the concentration of nitrosamines in dinitroanilines, which comprises treating a nitrosamine-containing dinitroaniline with PCl.sub.3, PCl.sub.5, PBr.sub.3, POCl.sub.3, SCl.sub.2, SOCl.sub.2, SO.sub.2 Cl.sub.2, SOBr.sub.2, or TiCl.sub.4.
Type:
Grant
Filed:
February 17, 1978
Date of Patent:
January 22, 1980
Assignee:
Eli Lilly and Company
Inventors:
Richard F. Eizember, Kathleen R. Vogler
Abstract: Antibiotic A16886I and antibiotic A16886II and their salts, having antibacterial and anthelmintic activity, prepared by fermentation of Streptomyces clavuligerus NRRL 3585.
Type:
Grant
Filed:
August 10, 1970
Date of Patent:
November 6, 1979
Assignee:
Eli Lilly and Company
Inventors:
Marvin Gorman, Calvin E. Higgens, Ramakrishnan Nagarajan
Abstract: Thieno[1,5]benzodiazepines having useful CNS activity containing the novel tricyclic ring system: ##STR1## the 10-position being substituted by an amino, preferably a piperazino, group.
Abstract: A class of 2,6-dinitroanilines having a broad range of substituent groups on the anilino nitrogen and in the 3- and 4-positions of the phenyl ring are used for the protection of plants against soil-borne phytopathogens of the genus Phytophthora.
Abstract: Propanoic acid derivatives of the formula: ##STR1## where R.sup.1 is a C.sub.1-8 alkyl group optionally substituted by hydroxyl or --COOH and R.sup.2 is hydrogen or a protecting group, are useful as anti-thrombotic agents.
Type:
Grant
Filed:
December 4, 1975
Date of Patent:
April 24, 1979
Assignee:
Lilly Industries Limited
Inventors:
William Dawson, Michael J. Foulis, Norman J. A. Gutteridge, Colin W. Smith
Abstract: Novel 1,4-disubstituted-3-nitropyrazoles having antimicrobial, parasiticidal, and herbicidal activity are prepared by a reaction sequence of which the individual steps are conventional. The new 3-nitropyrazoles are characterized by a 1-substituent and a usually carbonyl-containing 4-substituent. The novel 3(5)-nitro-4-pyrazolecarbonitrile is obtained as an intermediate in the preparation of the biologically-active compounds. Preferred compounds are 1-alkyl or -alkenyl-4-pyrazolecarboxamides and carbonitriles. The new compounds are particularly useful for the control of bacterial animal diseases.
Abstract: The present invention is directed to 7-amino-3-carbamoyloxymethyl-3-cephem-4-carboxylic acid: ##STR1## and to precursors and derivatives. The compound, its precursors, and its derivatives exhibit antibacterial activity, which, in the instance of certain of the derivatives, is of an enhanced degree.
Abstract: Novel 3-phenoxyphenylalkyl amines and the amides, alcohols, tetrazoles, and carbamates related thereto as well as novel intermediates useful in the preparation of such compounds. The compounds of this invention are useful as anti-inflammatory, analgesic, and antipyretic agents.
Abstract: The present invention is directed to a process for the displacement of the acetoxy group of a cephalosporanic acid by a sulfur nucleophile, in an organic solvent and under essentially anhydrous conditions.
Abstract: A novel process for the preparation of s-triazolo[3,4-b]benzothiazole compounds comprises reacting a molar equivalent of base in an amide solvent at a temperature from 60.degree. C. to 200.degree. C. with (a) a 1-acyl-4-(o-halophenyl)thiosemicarbazide compound or (b) a 4-(o-halophenyl)-1,2,4-triazole-3-thiol compound and recovering the product. The s-triazolo[3,4-b]benzothiazole compounds are useful for the control of plant pathogens.
Abstract: Novel benzophenone derivatives having anti-allergy activity, and pharmaceutical formulations and methods of treatment utilizing benzophenone derivatives.
Type:
Grant
Filed:
October 11, 1977
Date of Patent:
January 16, 1979
Assignee:
Eli Lilly and Company
Inventors:
Delme Evans, John C. Saunders, William R. N. Williamson
Abstract: Antibiotic A16886I and antibiotic A16886II and their salts, having antibacterial and anthelmintic activity, prepared by fermentation of Streptomyces clavuligerus NRRL 3585.
Type:
Grant
Filed:
May 20, 1976
Date of Patent:
January 2, 1979
Assignee:
Eli Lilly and Company
Inventors:
Marvin Gorman, Calvin E. Higgens, Ramakrishnan Nagarajan