Abstract: Hydroxymethyl-substituted-2(1H)-quinazolinones, e.g., 7-hydroxymethyl-1-isopropyl-4-phenyl-2(1H)-quinazolinone, are useful as anti-inflammatory agents.
Abstract: This disclosure describes novel compounds of the formula: ##STR1## where R is ##STR2## and R.sub.1 is straight chain lower alkyl, or ##STR3## where R.sub.3 is hydrogen or halo having an atomic weight of about 19 to 36,Which are useful as minor tranquilizers, sleep inducers and muscle relaxants.
Abstract: The present invention concerns novel 2-(1-piperazinyl)-thiazole derivatives of the formula, ##STR1## wherein R.sub.1 is alkyl or cycloalkly,R.sub.2 is hydrogen or alkyl, andR.sub.3 is benzyl, alkoxyalkyl or alkoxycarbonyl, or alkyl, alkenyl, alkanoyl or hydroxyalkyl, or acyloxyalkyl,Useful as vigilance increasing agents, anorexigenic agents and anti-migraine agents.
Abstract: Flameproofed cellulose includes as a flameproofing agent a compound selected from esters, ester-amides and amides of pyrophosphoric, of mono-, di- and trithiopyrophosphoric, of triphosphoric, and of mono-, di-, tri- and pentathiotriphosphoric acids. Preferred flameproofed cellulose, and other polymeric organic materials include as a flameproofing agent a compound selected from a smaller class of the above compounds.
Abstract: This invention provides a single needle dialysis blood tubing occluder, comprising in a preferred aspect, a pair of pivotly mounted clamping arms having a leaf spring affixed to the non-pivot end of each occluder with the spring in slidable engagement with a symmetrical cam. Means are provided for actuating the cam, whereby the cam moves the tubing occluder to alternately occlude and non-occlude a pair of blood tubings.
Abstract: Substituted-iminodimethylene-di-tert-alkylophenones, e.g., 4",4"'-methyliminodimethylene-dipivalophenone, are prepared by treating a corresponding .alpha.-halo-p-tert-alkanoyl toluene with a substituted amine. The phenols are prepared from the corresponding phenones and both the phenones and the phenols are useful as hypolipidemic agents.
Abstract: This invention provides new compounds of formula I, ##STR1## wherein R.sub.1 is hydrogen, alkyl of 1 to 4 carbon atoms,Or hydroxyalkyl of 1 to 4 carbon atoms, andR.sub.2 is hydrogen or halogen,Useful as anti-psychotics and sleep-inducing agents.
Abstract: The invention provides structurally modified interferons, processes for producing such and a method of purification of interferons and structurally modified interferons. The modified interferons are useful as anti-viral agents.
Type:
Grant
Filed:
February 6, 1975
Date of Patent:
December 6, 1977
Assignee:
Sandoz Ltd.
Inventors:
Friedrich Dorner, Marianne Scriba, Rudolf Weil
Abstract: Pyranone carboxamides, e.g., 2,6-diphenyl-N-methyl-4-oxo-4H-pyran-3-carboxamide, are prepared by cyclizing and dehydrogenating 2-aminomethylene-5-hydroxy-N-methyl-3-oxo-alkylamides and are useful as anti-allergic agents.
Abstract: Derivatives of trifluoromethyl-substituted anthranilic acid amides, e.g., N-methyl-o-amino-.alpha.,.alpha.,.alpha.-trifluoromethyl-p-toluamide, are useful as minor tranquilizers and muscle relaxants.
Abstract: The present invention relates to methods of dyeing and printing of textile materials and specifically to the use of fixing agents in such methods. In particular, the present invention relates to the use of aromatic carboxylic acid esters and amides as fixing agents in the dyeing and printing of textile materials.
Abstract: The present invention concerns a novel method of antistatically treating synthetic, semi-synthetic or natural porous material, particularly fibrous material, which comprises applying thereto a polychlorohydrin ether of tris-(hydroxymethyl)-aminomethane and a polyglycol bis-epichlorohydrin in admixture and/or in partially condensed form, and curing the compound(s) on the material.
Abstract: Asymmetric 1:2 chromium complexes of the formula ##STR1## in which R.sub.1 signifies a hydrogen or halogen atom or a nitro group,R.sub.2 signifies a hydrogen or halogen atom, a nitro or sulpho group,R.sub.3 signifies a hydrogen or halogen atom, or a lower alkyl radical,R.sub.4 signifies a hydrogen or halogen atom, a lower alkyl radical or a sulpho group,Each of R.sub.5, R.sub.6 and R.sub.7, independently, signifies a hydrogen or halogen atom or a lower alkyl radical,R signifies a hydrogen atom or a lower alkyl radical, andM.sup.+ signifies a cation,With the provisosI. the radicals R.sub.1 and R.sub.2 occupy the 4- and 6-positions,Ii. where R.sub.4 signifies a sulpho group one of the radicals R.sub.1 and R.sub.2 signifies a halogen atom or a nitro group in the 4-position, andIii.
Abstract: Dyes of the formula ##STR1## AND SUBSTITUTED DERIVATIVES THEREOF, WHEREIN R is a coupling component radical,R.sub.1 is a coupling component radical, with the proviso that R and R.sub.1 are different, andN is 1 to 8,Are disclosed. They are useful for dyeing and printing natural and synthetic polyamides, cotton and other cellulosic fibers, polypropylene fibers modified by basic groups, synthetic polyamides and polyesters modified by acid groups, paper and leather. They exhibit good fastness to light, wet treatments and abrasion.
Abstract: The present invention concerns novel compounds of formula I, ##STR1## wherein R.sub.1 is hydroxy, or ##STR2## wherein N IS AN INTEGER FROM 1 TO 5, ANDR.sub.3 and R.sub.4 are independently alkyl of 1 to 4 carbon atoms, orR.sub.3 and R.sub.4 together form an alkylene chain of 2 or 3 carbon atoms,R.sub.2 is hydrogen, alkyl of 1 to 4 carbon atoms, phenylalkyl of 7 to 9 carbon atoms, or phenylalkyl of 7 to 9 carbon atoms mono- or disubstituted on the phenyl radical by halogen, alkyl of 1 to 4 carbon atoms or alkoxy of 1 to 4 carbon atoms, andEitherX is hydrogen, andY is methyl,OrX is methylthio or dialkylamino, wherein the alkyl chains are independently of 1 to 4 carbon atoms, andY is hydrogen,OrX is chlorine or bromine, andY is chlorine,Or, when R.sub.1 is the above acetal group, X also signifies hydrogen, chlorine, bromine or methyl, and Y signifies hydrogen,Useful as salidiuretics.
Abstract: 5,5,7,7-tetramethyl-3-substituted or unsubstituted-phenylfuro[3,4-e]-as-triazines and corresponding 4-oxides, e.g., 5,7-dihydro-5,5,7,7-tetramethyl-3-phenylfuro[3,4-e]-as-triazine and 5,7-dihydro-5,5,7,7-tetramethyl-3-phenylfuro[3,4-e]-as-triazine-4-oxide, are prepared from 2,2,5,5-tetramethyl-3,4(2H,5H)-furandione-3-hydrazone-4-oximes and are useful as sleep inducers and minor tranquilizers.
Abstract: Hydroxyalkyl and aryl or heterocyclic substituted-4,5-dihydropyridazin(2H)-3-ones and diazobicyclo-ene-ones, e.g., 6-(p-chlorophenyl)-2-(2-hydroxybutyl)-4,5-dihydropyridazin(2H)-3-one are prepared by condensing 1-hydrazino-2-alkanols with aryl or heterocyclic-.gamma.-keto acids and are useful as central nervous system depressants.
Abstract: Basically substituted imidazolyl-2-quinazolines of the formula ##STR1## where R.sub.1 is hydrogen, lower alkyl or halogen;R.sub.2 is lower alkyl, lower alkenyl or lower hydroxalkyl; andR.sub.3 is a basic organic substituent,Are useful as anti-parasitic agents and as mycoplasma growth inhibiting agents.