EP0725563A1 - Structure marine - Google Patents

Structure marine

Info

Publication number
EP0725563A1
EP0725563A1 EP94931519A EP94931519A EP0725563A1 EP 0725563 A1 EP0725563 A1 EP 0725563A1 EP 94931519 A EP94931519 A EP 94931519A EP 94931519 A EP94931519 A EP 94931519A EP 0725563 A1 EP0725563 A1 EP 0725563A1
Authority
EP
European Patent Office
Prior art keywords
optionally substituted
alkyl
activity
amino
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP94931519A
Other languages
German (de)
English (en)
Inventor
Uffe Anthoni
Carsten Christophersen
Per Halfdan Nielsen
Eva Bie Kjaer
Gruska Folkmann Musaeus
Ann Christina Schultz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jc Hempel's Skibsfarve-Fabrik AS
Original Assignee
Jc Hempel's Skibsfarve-Fabrik AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jc Hempel's Skibsfarve-Fabrik AS filed Critical Jc Hempel's Skibsfarve-Fabrik AS
Publication of EP0725563A1 publication Critical patent/EP0725563A1/fr
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/16—Antifouling paints; Underwater paints
    • C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
    • C09D5/1612—Non-macromolecular compounds
    • C09D5/1625—Non-macromolecular compounds organic

Definitions

  • the present invention relates to marine structures, in par ⁇ ticular immersed marine structures, having an external antifouling coating on the part of the structure immersed in water, as well as antifouling paint compositions that prevent unwanted fouling organisms from attaching and growing on immersed structures that come in contact with water, espe ⁇ cially sea-water, for example vessels (including but not limited to boats, yachts, motorboats, motor launches, ocean liners, tugboats, tankers, container ships and other cargo ships, submarines, and naval vessels of all types) , pipes, shore and off-shore machinery, constructions and objects of all types such as piers, pilings, bridge substructures, underwater oil well structures, nets and other aquatic cul ⁇ ture installations, and buoys etc..
  • vessels including but not limited to boats, yachts, motorboats, motor launches, ocean liners, tugboats, tankers, container ships and other cargo ships, submarines, and naval vessels of all types
  • pipes, shore and off-shore machinery constructions and objects of all types such as
  • antifouling agents can be applied in the form of e.g. paints, solutions, dispersions, pastes, or emulsions, which on application to underwater structures and on ship hulls produce an antifouling effect.
  • antifouling effect is to be understood as a prevention or at least reduction of attachment and growth of marine organisms.
  • One of the environmental problems is related to pollution of rivers, channels, bays, harbours, lakes and other bodies of water with a low or limited water exchange with heavy metals and toxic compounds by use of such materials in e.g. pain- tings for application on underwater structures, e.g. a ship's surface.
  • certain heavy metal compounds are known to accumulate in the animal body such as fish and humans.
  • the present inventors have attempted to develop environmen ⁇ tally compatible and effective antifouling compounds. It has been found that quinoline compounds (optionally in combina ⁇ tion with other antifouling compounds) have an excellent antifouling effect.
  • the present invention provides antifouling paint compositions comprising, i.a. as an active ingredient, a quinoline compound of formula I
  • X 1 , X 2 , X 4 , X 5 , X 6 and X 7 independently designate hydro ⁇ gen; hydroxy; - ⁇ ⁇ . ⁇ -alkyl; substituted C ⁇ -alkyl; optio ⁇ nally substituted C 2 . 12 -a-lkenyl; optionally substituted C 2 . 12 -alkynyl; optionally substituted C 1 . 12 " alko ⁇ y''" optio ⁇ nally substituted heterocyclyl; optionally substituted aryl; optionally substituted aryloxy; halogen; nitro; nitroso; cyano; amino; mono(optionally substituted C 1 .
  • X 3 designates the same groups as defined for X 1 above, or X 3 is a group of the formula I'
  • Y 1 , Y 2 , Y 3 , Y 4 , Y 5 , Y 6 and Y 7 independently designate the same groups as defined for X 1 above or designate C 6 _ 12 -alkyl, and ⁇ 8 and ⁇ 9 independently designate the same groups as defined for X 1 above or designate C 6 . 12 - a l k y 1 or together form oxo, and the wavy lines signify that the substituents in question may be in either of the two possible isomeric configurations;
  • immersed in the present context relates to struc ⁇ tures intended for immersion into any kind of water, salt, brackish or fresh water.
  • C x _ 5 -alkyl is intended to mean alkyl groups with 1-5 carbon atoms which may be straight or branched or cyclic such as methyl, ethyl, propyl, iso ⁇ propyl, cyclopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, neopentyl, cyclopentyl, etc.
  • C 1 is intended to mean alkyl groups with 1-5 carbon atoms which may be straight or branched or cyclic such as methyl, ethyl, propyl, iso ⁇ propyl, cyclopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, neopentyl, cyclopentyl, etc.
  • C 1 is intended to mean alkyl groups with 1-5 carbon atoms which may be straight or branched or cyclic such as methyl
  • 12 -alkyl is intended to mean alkyl groups with 1-12 carbon atoms which may be straight or branched or cyclic such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, hexyl, octyl, dodecyl, cyclopentyl, cyclohexyl, decalinyl, etc.
  • C 6 . 12 -alkyl is intended to mean alkyl groups with 6-12 carbon atoms which may be straight or branched or cyclic, e.g. appropriate groups among those listed above.
  • substituted C 1 . 12 -alkyl is intended to mean a C 1 . 12 -alkyl group which is substituted with one or more, preferably 1-3, groups selected from carboxy; protected carboxy such as a carboxy ester, e.g. C 1 . 12 -alkoxycarbonyl; aminocarbonyl; mono- and di ( C x . 12 -alkyl)aminocarbonyl; amino- C 1 . 12 -alkyl-aminocarbonyl; mono- and di(C- L .- ⁇ -alkyl)amino- C- L .
  • Examples of such substituted ( -. 1 . x2 -alkyl groups are carboxy- c ⁇ -i 2 " alk y 1 ( e -9- carb ⁇ xymethyl and carboxyethyl) , protected carboxy-C- L .- J ⁇ -alkyl such as esterified carboxy-C 1 . 12 " alk y 1 (e.g. C 1 . 12 -alkoxycarbonyl-C 1 _ 12 _alk yl such as methoxycarbonylmethyl, ethoxycarbonylmethyl, and methoxycarbonylethyl) , aminocarbonyl- C . 12 -alkyl (e.g.
  • C 1 _ 12 -alkylaminocarbonyl-C 1 _ 12 -alkyl e.g. methylaminocarbonylmethyl and ethylaminocarbonylmethyl
  • amino-C x . 12 -alkyl-aminocarbonyl-C x . 12 -alkyl e.g. aminomethylaminocarbonylmethyl and aminoethylaminocar- bonylmethyl
  • C 2 . 12 -alkenyl is intended to mean mono-, di- or polyunsaturated alkyl groups with 2-12 carbon atoms which may be straight or branched or cyclic in which the double bond(s) may be present anywhere in the chain or the ring(s), for example vinyl, l-propenyl, 2-propenyl, hexenyl, decenyl, 1,3-heptadienyl, cyclohexenyl etc.
  • Some of the substituents exist both in a cis and a trans configura ⁇ tion. The scope of this invention comprises both the cis and trans forms.
  • C 2 . 12 -alkynyl is intended to mean a straight or branched alkyl group with 2-12 carbon atoms and incorporating one or more triple bond(s), e.g. ethynyl, 1-propynyl, 2-propynyl, 2-butynyl, 1,6-heptadiynyl, etc.
  • C 1 . 12 -alkoxy designates groups comprising an oxy function which groups optionally may be substituted one or more times with the substituents indicated for "optionally substituted alkyl” described above.
  • aryl is intended to mean phenyl, biphenyl, naphthyl, fluorenyl, tetralinyl, etc..
  • optionally substituted aryl is intended to mean aryl as defined above which may be substituted with one or more, preferably 1-3, substituents selected from the group consisting of hydrogen; hydroxy; optionally substituted G 1 . 12 -alkyl; optionally substituted C 2 . 12 -alkenyl; optionally substituted C 2 . 12 -alkynyl; optional ⁇ ly substituted C 1 . 12 -alkoxy; optionally substituted hetero- cyclyl; optionally substituted aryl; optionally substituted aryloxy; halogen; nitro; nitroso; cyano; amino; mono(C 1 .
  • the term "optionally substituted heterocyclyl” is intended to mean a 5- or 6-membered monocyclic or a 11- or 12-membered bicyclic, aromatic or partially or fully hydrogenated, heterocyclic group contai ⁇ ning one or more, preferably 1-3, heteroatoms selected from oxygen, nitrogen and sulphur, which said ring or ring system optionally being substituted with one or more substituents selected from the group consisting of hydrogen; hydroxy; optionally substituted C 1 . 12 -alkyl; optionally substituted C 2 . 12 -alkenyl; optionally substituted C 2 . 12 -alkynyl; optionally substituted C 1 .
  • heterocyclic groups are pyrrolyl, furanyl, 2,3-dihydrofuranyl, tetrahydrofuranyl, thienyl, 2,3-dihydro- thienyl, tetrahydrothienyl, imidazolyl, oxazolyl, thiazolyl, pyrazolyl, pyrrolinyl, pyrrolidinyl, pyridinyl, piperidinyl, pyrimidinyl, purinyl, quinolinyl, 1,2-dihydroquinolinyl, isoquinolinyl, indolyl, piperazinyl, pyrazinyl, dioxolanyl, dioxanyl, 1,3,5-trioxanyl, tetrahydrothiapyranyl, dithiolanyl, pyrazolidinyl, iminazolidinyl, pyridazinyl, sym- tria
  • acyl comprises C x _ x2 - alkanoyl (e.g. formyl, acetyl, propionyl, butyryl, isobuty- ryl, valeryl, isovaleryl, pivaloyl and hexanoyl) , C . ⁇ 2 - alkoxycarbonyl (e.g. methoxycarbonyl, ethoxycarbonyl, prop- oxycarbonyl, butoxycarbonyl and t-butoxycarbonyl) etc.
  • C x _ x2 - alkanoyl e.g. formyl, acetyl, propionyl, butyryl, isobuty- ryl, valeryl, isovaleryl, pivaloyl and hexanoyl
  • C . ⁇ 2 - alkoxycarbonyl e.g. methoxycarbonyl, ethoxycarbonyl, prop- oxycarbonyl, butoxycarbony
  • acyloxy designates an oxy group to which is attached a group as defined above for "acyl”.
  • Optional substituents on acyl or acyloxy groups may be the same as those described for optionally substituted alkyl above.
  • pyranosyl is intended to mean galactopyranosyl, glucopyranosyl, mannopyranosyl, allo- pyranosyl, altropyranosyl, gulopyranosyl, idopyranosyl, talopyranosyl, etc, as well as O-C- j ⁇ .- j ⁇ g-alkylated, 0-C 1 . 18 - alkanoylated or benzoylated derivatives thereof.
  • the pyrano ⁇ syl moieties can exist in both the ⁇ -anomeric and the j3-anomeric forms.
  • furanosyl is intended to mean fructofuranosyl, arabinofuranosyl, psicofuranosyl, sorbofuranosyl, xylofuranosyl, lyxofuranosyl, etc, as well as O-C- L ⁇ g-alkylated, O-C- j ⁇ .- ⁇ g-alkanoylated or benzoylated deriva ⁇ tives thereof.
  • the furanosyl moieties can exist in both the ⁇ -anomeric and the /3-anomeric forms.
  • salt is intended to comprise a salt such as an organic acid addition salt (e.g. acetate, valerate, salicylate, galacturonate, gluconate, tannate, trifluoroace- tate, maleate, tartrate, methanesulphonate, benzenesulphonate, formiate, thiocyanate and toluenesulphonate) , an inorganic acid addition salt (e.g.
  • organic acid addition salt e.g. acetate, valerate, salicylate, galacturonate, gluconate, tannate, trifluoroace- tate, maleate, tartrate, methanesulphonate, benzenesulphonate, formiate, thiocyanate and toluenesulphonate
  • an inorganic acid addition salt e.g.
  • N-oxide is intended to comprise compounds of the present invention where the ring nitrogen of the quinoline ring system is oxidized to the N-oxide.
  • the quinoline derivative of formula I is substituted in the 2-position with a substituent selected from the group consisting of H, OH, CH 3 , CH 2 C1, F, Cl, Br, COOH, and quinolinyl; in the 3-position with a substituent selected from the group consisting of H, NH 2 , CHO, COOH, F, Cl, and Br; in the 4-position with a substituent selected from the group consisting of H, OH, CH 3 , F, Cl, Br, NH 2 , N0 2 , CHO, mono- or di(C- ⁇ 6 -alkyl)amino-C- ⁇ g - alkylamino, amino-C- ⁇ g-alkylamino, a group I' as defined above, and COOH; in the 5-position with a substituent selected from the group consisting of H, OH, F, Cl, Br, and S0 3 H; in the 6-position with a substituent selected from the group consisting of H, NH 2 ,
  • the quinoline derivative of formula I is substituted in the 2- position with a substituent selected from the group consisting of H, Cl, CH 3 , and CH 2 C1; in the 3-position with a CHO; in the 4-position with a substituent selected from the group consisting of H, Cl, Br, CHO, CH 3 , NH 2 , N0 2 , a group I' as defined above, di(C- ⁇ g-alkyl)amino-C- ⁇ g-alkylamino, and amino-C 3 __ g -alkyla1rri.no; in the 5-position with a substituent selected from the group consisting of H, Cl, and OH; in the 6-position with a substituent selected from the group consisting of H, CH 3 , OCH 3 ; in the 7-position with a substituent selected from the group consisting of H, Cl, I and Br; in the 8-position with a substituent selected from the group consisting of H, OH, CH
  • the group defined by the formula I' contains several asymmetric carbon atoms and that the compounds of formula I therefore can exist as several stereoisomers.
  • the present invention comprises each of such stereoisomers as well as mixtures thereof, such as racemic mixtures.
  • the orientation of substituents on the group of formula I' correspond to the orientation in the corresponding l-azabicyclo[2,2,2]octylmethyl group in cinchona alkaloids such as quinine and quinidine.
  • quinoline compounds expressed by formula I are known compounds which can be extracted from natural sources or prepared synthetically by conventional methods known in the art. Thus, quinoline compounds of formula I can be syn- thesized by conventional methods known in the art.
  • quinine (compound no. 2 in Table 1) can be obtained by extraction from Cinchona spp. as described by N. L. Butta and C. Quassim in Indian J. Chem. 6(19) (1968), 566- 567, or by synthesis from n-benzoyl-meroquinene methyl ester and 6-methoxylepidine as described by J. Gutzwiller and M. Uskokovic, J " . Am. Chem. Soc. 92(1), (1970), 204-5.
  • the quinoline compounds, used as an active ingredient may be used alone or in combination with other antifouling agents.
  • the active ingredient may be used as a crude extract or in a purified form.
  • the antifouling agents may be used in various formulations including paints, solutions, dispersions, pastes, emulsions etc.
  • an antifouling paint is prepared by mixing one or several of the active ingredients of the formula I with one or more of the components described below.
  • a typical antifouling paint composition for use in providing a marine structure according to the invention comprises at least one antifouling agent of the formula I as well as one or more components selected among binders, fillers, pigments, dyes, solvents, and additives.
  • binders are gum rosin; wood rosin; tall oil rosin; commercial rosin derivatives; copolymers of vinyl acetate and vinyl isobutyl ether; copolymers of vinyl chlo ⁇ ride and vinyl isobutyl ether; alkyd resins or modified alkyd resins; hydrocarbon resins such as petroleum fraction conden ⁇ sates; chlorinated rubbers; styrene copolymers such as styrene/butadiene copolymers and styrene/acrylate copolymers; acrylic resins such as isobutyl methacrylate copolymers, methyl methacrylate/n-butyl methacrylate copolymers; polyamide resins such as polyamide based on dimerized tall oil fatty acids; cyclized rubbers; epoxy esters; epoxy ure- thanes; polyurethanes; epoxy polymers; silicates; silicone resins or silicone elastomers; etc., as
  • the binder may be erodible (self-polishing) or non- erodible (non-soluble) .
  • the amount of binder in a paint composition is typically in the range of 10-80 percent by weight in the wet paint, preferably 10-40 percent by weight in the wet paint.
  • fillers are calcium carbonate, dolomite, talc, mica, barium sulphate, kaolin, quartz flour, etc..
  • the amount of filler in the paint composition is typically in the range 0-20 percent by weight in the wet paint.
  • pigments are grades of titanium dioxide, zinc oxide, red iron oxide, carbon black, graphite, yellow iron oxide, phthalocyanine blue, phthalocyanine green.
  • the amount of pigment in a paint composition may typically be in the range of 1-60 percent by weight in the wet paint, preferably 5-60 percent.
  • Typical examples of dyes are 1,4-bis (butylamino)anthraquinone and other anthraquinone derivatives.
  • solvents in which the components of the antifouling paint are dissolved, dispersed or emulsified are water; alcohols such as methanol, ethanol, propanol, isopro- panol, butanol, isobutanol, and benzyl alcohol; alcohol/water mixtures such as ethanol/water mixtures; aliphatic, cycloali- phatic, and aromatic hydrocarbons such as white spirit, cyclohexane, toluene, xylene, and naphtha solvent; ketones such as methyl ethyl ketone, acetone, methyl isobutyl ketone, methyl isoamyl ketone, diacetone alcohol, and cyclohexanone; ether alcohols such as 2-butoxyethanol, propylene glycol monomethyl ether, and butyl diglycol; esters such as methoxypropyl acetate, n-butyl acetate, and 2-ethoxyeth
  • plasticizers such as chlorinated paraffin; low molecular weight polybutene; phthalates such as dibutyl phthalate, benzylbutyl phthalate, dioctyl phthalate, and diisodecyl- phthalate; phosphate esters such as tricresyl phosphate, and 2-ethylhexyl diphenyl phosphate; sulphone amides such as alkyl-p-toluene sulphone amide; and polymeric acrylic plasticizers.
  • Plasticizers may be present in amounts in the range of 0-10 percent by weight in the wet paint;
  • surfactants such as derivatives of propylene oxide or ethylene oxide such as alkylphenol-ethylene oxide conden- sates; ethoxylated monoethanolamides of unsaturated fatty acids such as ethoxylated monoethanolamides of linoleic acid; sodium dodecylsulphate; alkylphenol ethoxylates; and soya lecithin.
  • surfactants may be present in amounts in the range of 0-2 percent by weight in the wet paint;
  • defoaming agents such as silicone oils which may be present in amounts in the range of 0-1 percent by weight in the wet paint;
  • catalysts such as polymerization catalysts and initi- ators, e.g. azobisisobutyronitrile, ammonium persulphate, dilaurylperoxide, di-t-butylperoxide, cumenehydroper- oxide, and p-toluenesulphonic acid; dryers, e.g. metal octoates and metal naphthenates; and activators, e.g. salicylic acid and benzyl alcohol.
  • Catalysts may be present in amounts in the range of 0-3 percent by weight in the wet paint;
  • stabilizers such as stabilizers against light and heat, e.g. 2-hydroxy-4-methoxybenzophenone, 2- (5-chloro- (2H) - benzotriazol-2-yl) -4-methyl-6- (tert-butyl)phenol, 2,4- ditert-butyl-6- (5-chlorobenzotriazol-2-yl)phenol, which may be present in amounts in the range of 0-2 percent by weight in the wet paint; stabilizers against moisture such as molecular sieves or water scavengers, which may be present in amounts in the range of 1-3 percent by weight in the wet paint; stabilizers against oxidation such as tert-butylhydroquinone; butylated hydroxyanisole; butylated hydroxytoluene; propylgallate; tocopherols; L-ascorbyl palmitate; carotens; vitamin A, which may be present in amounts in the range of 0-2 percent by weight in the we
  • polymerization inhibitors e.g. para-benzoquinone, hydroquinone and methyl-hydroquinone, which may be pre ⁇ sent in amounts in the range of 0-3 percent by weight in the wet paint; inhibitors against corrosion such as zinc phosphate; zinc metaborate, which may be present in amounts in the range of 0-20 percent by weight in the wet paint;
  • coalescing agents such as glycols, which may be present in amounts in the range of 0-5 percent by weight in the wet paint;
  • thickeners and anti-settling agents such as colloidal silica, aluminium stearate, hydrogenated castor oil, polyethylene fibres and organo-modified clays, which may be present in amounts in the range of 2-6 percent by weight in the wet paint.
  • an antifouling paint may contain other secondary substances which enhance the antifouling activity of the quinoline compound(s) .
  • Typical examples of such enhancing substances to be used in combination with the quinoline compounds of formula I are:
  • organometals such as trialkyltin salts such as hydroxytriphenylstannane, dibutylbis (1-oxododecyloxy) - stannane, fluorotriphenylstannane, chlorotriphenyl- stannane, tributylfluorostannane, and tributyltin maleate; hexabutyldistannoxane; trialkyltin copolymers such as tributyltin resinate, tributyltin acrylate copolymer, and tributyltin methacrylate copolymer; metallo-dithiocarbamates such as bis (dimethyldi- thiocarbamato) zinc, ethylene-bis(dithiocarbamato) zinc, ethylene-bis(dithiocarbamato) anganese, and complexes between these; bis(l-hydroxy-2 (IH) -pyr
  • metal biocides such as copper, copper metal alloys such as copper-nickel alloys; metal oxides such as cuprous , oxide, and cupric oxide; metal salts such as cuprous thiocyanate, barium metaborate, and copper sulphide;
  • heterocyclic nitrogen compounds such as 3a,4,7,7a- tetrahydro-2- ( (trichloromethyl)thio) -lH-isoindole- 1,3 (2H) -dione, pyridine-triphenylborane, 1- (2,4,6- trichlorophenyl) -lH-pyrrole-2,5-dione, 2,3,5,6- tetrachloro-4- (methylsulphonyl) -pyridine, and 2- methylthio-4-tert-butylamino-6-cyclopropylamine-s- triazine;
  • heterocyclic sulphur compounds such as 2- (4-thiazolyl) - benzimidazole, 4,5-dichloro-2-octyl-3 (2H) -isothiazolone, l,2-benzisothiazolin-3-one, 4,5-dichloro-2-octyl-3 (2H) - isothiazoline, l,2-benzisothiazolin-3-one, and 2- (thiocyanatomethylthio) -benzothiazole;
  • urea derivatives such as N- (1,3-bis(hydroxymethyl) -2,5- dioxo-4-imidazolidinyl) -N,N' -bis (hydroxymethyl)urea and 3- (3,4-dichlorophenyl) -1,1-dimethyl urea;
  • amides or imides of carboxylic acids, sulphonic acids and of sulphenic acids such as l,1-dichloro-N- ( (dimethyl- amino)sulphonyl) -l-fluoro-N- (4-methylphenyl) -methanesul- phenamide, 2,2-dibromo-3-nitrilo-propionamide, N-methylol formamide, N- (dichlorofluoromethylthio) -phthalimide, and N,N-dimethyl-N' -phenyl-N' - (dichlorofluoromethylthio) - sulphamide;
  • carboxylic acids such as 2- ( (3-iodo-2- propynyl)oxy) -ethanol phenylcarbamate and N,N-didecyl-N- methyl-poly(oxyethyl)ammoniumpropionate; amines such as dehydroabiethylamines and cocodimethylamine;
  • substituted methane such as di (2-hydroxy-ethoxy)methane, 5,5' -dichloro-2,2' -dihydroxydiphenylmethane, and methylene-bisthiocyanate;
  • substituted benzene such as 2,4,5,6-tetrachloro-l,3- benzenedicarbonitrile, 1,1-dichloro-N- ( (dimethylamino) - sulphonyl) -1-fluoro-N-phenylmethanesulphenamide, and 1- ( (diiodomethyl)sulphonyl) -4-methyl-benzene;
  • tetraalkyl phosphonium halogenides such as tri-n- butyltetradecyl phosphonium chloride
  • Guanidine derivatives such as n-dodecylguanidine hydrochloride
  • disulphides such as bis- (dimethylthiocarbamoyl) - disulphide and tetramethylthiuramdisulphide;
  • the total amount of the compound(s) of formula I as well as any secondary or enhancing antifouling agent(s) may be in the range of 2-50 percent by weight in the wet paint, preferably 5-50 percent.
  • the antifouling paint composition may be prepared by any suitable technique that is commonly used within the field of paint production.
  • the various components may be mixed together using a high speed disperser, a ball mill, a pearl mill, a three-roll mill, etc..
  • the antifouling paint composition according to the invention may be applied to the marine structure to be protected by means of any of the usual techniques used within the paint field such as by means of a brush, a roller, a pad, by dip- ping, by spraying, etc..
  • the exact technique chosen depends upon the object to be protected and also upon the particular composition (such as its viscosity etc.) and upon the par ⁇ ticular situation.
  • Preferred applications techniques are spraying and by means of a brush or a roller.
  • the antifouling paint composition according to the invention may be applied to the marine structure to be protected in one or several successive layers, typically 1 to 3 layers.
  • the total dry film thickness of the coating will typically be 10-1000 ⁇ m, preferably 40-450 ⁇ m.
  • the marine structure to which the paint composition according to the invention may be applied to may be any of a wide variety of solid objects that come into contact with water, in particular sea-water, for example vessels (including but not limited to boats, yachts, motorboats, motor launches, ocean liners, tugboats, tankers, container ships and other cargo ships, submarines (both nuclear and conventional) , and naval vessels of all types) ; pipes; shore and off-shore machinery, constructions and objects of all types such as piers, pilings, bridge substructures, underwater oil well structures, etc.; nets and other mariculture installations; and buoys; and is especially applicable to the hulls of ships and boats and to pipes.
  • vessels including but not limited to boats, yachts, motorboats, motor launches, ocean liners, tugboats, tankers, container ships and other cargo ships, submarines (both nuclear and conventional) , and naval vessels of all types) ; pipes; shore and off-shore machinery, constructions and objects of all types such as piers, pilings, bridge substructures,
  • the marine structure may first be coated with a primer-system which may comprise several layers and may be any of the conventional primer systems used in connection with application of antifouling paints to marine structures.
  • the primer system may include a first layer of a tar or bitumen composition followed by a layer of an adhesion-promoting primer.
  • the primer-system is a sea-water non-erodible paint having a composition as that of the antifouling paint but which erodes at a rate of less than 1 urn per 10,000 nautical miles.
  • Suitable quinoline derivatives of the present invention are for example those which, in the Rhizoid test performed as described in Example 1 herein, gives an activity of at least 50% at a nominal concentration of the supernatant of 50 ppm, preferably an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm, more preferably an activity of at least 80% at a nominal concentration of the supernatant of 50 ppm such as an activity of at least 80% at a nominal concentration of the supernatant of 10 ppm, when the test conditions are calibrated so that the sodium dodecylsulphate reference, in a concentration of 20 ppm gives an activity of 20-60%.
  • Suitable quinoline derivatives of the present invention are for example those which, in the spore test performed as described in Example 2 herein, gives an activity of at least 50% at a nominal concentration of the supernatant of 50 ppm, preferably an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm, more preferably an activity of at least 80% at a nominal concentration of the supernatant of 50 ppm such as an activity of at least 80% at a nominal concentration of the supernatant of 10 ppm, when the test conditions are calibrated so that the TBTO reference, in a concentration of 0.007 ppm gives an activity of 50-100 %.
  • Suitable quinoline derivatives of the present invention are for example those which, in the Diatom test performed as described in Example 3 herein, gives an activity of at least 50% at a nominal concentration of the supernatant of 50 ppm, preferably an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm, more preferably an activity of at least 80% at a nominal concentration of the supernatant of 50 ppm such as an activity of at least 80% at a nominal concentration of the supernatant of 10 ppm, when the test conditions are calibrated so that the sodium dodecylsulphate reference, in a concentration of 30 ppm gives an activity of 20-60%.
  • Suitable quinoline derivatives of the present invention are for example those which, in the Ni tocra test performed as described in Example 4 herein, gives an activity of at least 50% at a nominal concentration of the supernatant of 50 ppm, preferably an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm, more preferably an activity of at least 80% at a nominal concentration of the supernatant of 50 ppm such as an activity of at least 80% at a nominal concentration of the supernatant of 10 ppm, when the test conditions are calibrated so that the TBTO reference, in a concentration of 0.007 ppm gives an activity of 5-40 %.
  • Suitable quinoline derivatives of the present invention are for example those which, in the cyprids test performed as described in Example 5 herein, gives an activity of at least 50% at a nominal concentration of the supernatant of 50 ppm, preferably an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm, more preferably an activity of at least 80% at a nominal concentration of the supernatant of 50 ppm such as an activity of at least 80% at a nominal concentration of the supernatant of 100 ppm.
  • Suitable quinoline derivatives of the present invention are those which when incorporated in a structure alone or in combination with one or more antifouling activity enhancing substances, in a paint prepared as described in Example 6 herein and tested as described in Example 7 herein, with respect to algae or animals, preferably both, result in a rating at least l rating units lower than the corresponding rating for the blank sample, when the blank sample has attained a rating in the range of 1 to 4.
  • Preferred quinoline derivatives of the present invention are those which when incorporated in a structure alone or in combination with one or more antifouling activity enhancing substances, in a paint prepared as described in Example 6 herein and tested as described in Example 7 herein, with respect to algae or animals, preferably both, result in a rating at least 2 rating units lower than the corresponding rating for the blank sample, when the blank sample has attained a rating in the range of 2 to 4.
  • More preferred quinoline derivatives of the present invention are those which when incorporated in a structure alone or in combination with one or more antifouling activity enhancing substances, in a paint prepared as described in Example 6 herein and tested as described in Example 7 herein, with respect to algae or animals, preferably both, result in a rating at least 3 rating units lower than the corresponding rating for the blank sample, when the blank sample has attained a rating in the range of 3 to 4.
  • Enteromorpha spp. is a very common fouling organism. When filaments of Enteromorpha spp. are cut into segments and exposed to normal sea-water containing no bio-active com- pounds, rhizoids which are functionally similar to small roots are produced within 3-4 days. A number of quinoline derivatives were tested for their effect on the rhizoid production of Enteromorpha intestinalis segments. Solutions of the quinoline derivative to be tested were prepared as follows: An appropriate amount (by weight) of the quinoline derivative was dissolved in 1 ml acetone and was then resuspended in an appropriate amount (by weight) of filtered natural sea-water (NSW; having a salinity of 15%o) to give the desired nominal concentration (e.g. 50 ppm) . The slurry was rotated for 24 hours and then centrifuged. The supernatant was hereafter defined as having the original nominal concentration (e.g. 50 ppm) .
  • the top and the basal part of filaments of Enteromorpha intestinalis (collected from the intertidal zone of ⁇ resund, Denmark) was first removed after which the remainder was cut into segments having an approximate length of l cm.
  • 30 ml of the prepared supernatant of the quinoline derivative to be tested was added into petri-dishes having a diameter of 9 cm. Dilutions of the prepared supernatant were also added into petri-dishes.
  • Approximately 25 segments of Enteromorpha intestinalis were placed in each petri-dish, which was then incubated for 96 hours at a temperature of about 10-15°C and with constant light (3000-4000 lux light level) .
  • the segments were placed onto microscope cover-glasses and sealed with large cover-slips.
  • the number of segments that had produced rhizoids and the number of segments that had not produced rhizoids were counted by using a light microscope, lOOx magnification.
  • the activity of each concentration of the compound tested was then calculated as the total number of segments which had not produced rhizoids divided with the total number of segments in the petri-dish.
  • N Total number of test individuals at test concentration
  • D ⁇ Total number of affected/dead individuals in control
  • N ⁇ Total number of test individuals in control
  • the reference value is calculated as a statistical average value with standard deviation based on 15 tests.
  • an Enteromorpha filament If the fertile tip of an Enteromorpha filament is given an environmental shock e.g. cold temperature or extreme light, it will release a large number of spores. These spores swim freely for about 10-15 minutes and then settle. Upon attach ⁇ ment, they will produce a small tube (called germ tube) which then develops into an Enteromorpha plant.
  • an environmental shock e.g. cold temperature or extreme light
  • cover-slips were transferred onto cover-glasses.
  • the number of spores which had produced a germ tube and the number of spores which had not produced a germ tube were counted in ten fields of view.
  • the activity was then calculated as the number of spores not producing germ tubes divided by the total number of spores in the ten fields of view.
  • Table 3 the results (corrected according to Abbott's formula above) of the spores-test are shown.
  • the compound numbering is the same as in Table 1.
  • the reference value is calculated as a statistical average value with a standard deviation based on 3 tests using TBTO (tributyl tinoxide) as the reference compound.
  • Diatoms are microalgae which function as fouling organisms and are commonly found on many marine structures such as ship's hulls.
  • One type of diatoms is the Amphora spp. .
  • Amphora coffeaeformis can be distinguished by its red fluorescence when irradiated with light (mercury lamp with a wavelength of 500-515 ⁇ m) . This property was used in the test method outlined below.
  • Slime-containing mixed populations were collected from intertidal structures (e.g. pier pilings and bridge pilings) by scraping the populations off using a scalpel blade. The slime was then transferred to petri-dishes and the popula ⁇ tions were covered with filtered natural sea-water (15%o salinity) . The samples were incubated for 24 hours at 24°C and at a photoperiod of 16 hours light (2500-3000 lux light level) and 8 hours in darkness. The content in the petri- dishes which was not attached to the bottom of the petri-dish was removed and approximately 10 ml of filtered natural sea- water (15%o salinity) was added to each petri-dish.
  • intertidal structures e.g. pier pilings and bridge pilings
  • Amphora cells were removed from the petri-dishes one by one using a rubber tube and a drawn-out glass micropipette. The cells were transferred to new petri-dishes filled with filtered natural sea-water (15%o salinity) , and the samples were incubated as described above. The removal of Amphora cells and incubation steps were repea ⁇ ted until only Amphora coffeaeformis was isolated. This culture will be referred to as the test population.
  • a sub-culture was prepared from the test population by remo- ving, with a glass micropipette, cells of Amphora coffeae ⁇ formis and adding 50-100 cells to new petri-dishes (the number of which corresponded to the number of tests) contai ⁇ ning filtered natural sea-water (15 o salinity) .
  • the samples were then incubated for 96 hours at 24°C and at a photoperiod of 16 hours in light (2500-3000 lux light level) and 8 hours in darkness.
  • the number of dead and the number of alive Amphora coffeaeformis cells in each petri-dish were counted.
  • the counting was performed as follows: The liquid content of the petri-dish was poured out and two 18x18 mm 2 coverslips were placed onto the base of the dish. An initial inspection under a light microscope (xlOO magnification) was carried out in order to obtain qualitative information of the condition of the cells (the cell-content) . After this, the petri-dishes were inspected by means of a x20 objective lens and under a fluorescent light (a mercury lamp with a wavelength of 500- 515 ⁇ m) . The number of live cells (red) and the number of dead cells (white) were counted.
  • the counting was repeated with ten fields of view.
  • the activity of the test compound was calculated as the number of dead cells divided by the number of cells counted in ten fields of view.
  • Table 4 the test results (corrected according to Abbott's formula above) of the activity of quinoline derivatives in the diatom-test is shown.
  • the compound numbers corresponds to the numbers given in Table l.
  • the reference value is calculated as a statistical average value with standard deviation based on 18 tests.
  • Ni tocra spinipes is not a fouling organism, it is a 30 very useful marine test organism as it is easy to culture. The Ni tocra test may also give an indication of how the test compound in question may influence fouling crustaceans.
  • a population of Ni tocra spinipes (including pregnant females) which was received from Vandkvalitetsinstituttet, Denmark, was used in this experiment. The population was cultured in dishes in the dark at room temperature until pregnant females had released their eggs, these immediately changing to nauplii that developed into adults. The culture was fed with Ewos 20 ® (A/S Ewos Aqua Korn- og Foderstoffer, Denmark) .
  • the glass tubes were incubated at room temperature for 96 hours in the dark. Immediately afterwards inspection/counting (numbers of dead and alive Ni tocra spinipes) was performed using a binocular microscope. The activity of the quinoline derivative was calculated as the sum of dead Ni tocra spinipes in the four test tubes divided by the total number of Ni tocra spinipes in the four test tubes.
  • a broodstock of adult Balanus amphi tri te amphi tri te was kept in an aquaria in the laboratory in 2.5-3.0% filtered (1.0 + 0.2 ⁇ m) sea-water (hereafter called filtered sea-water) at ambient temperature (22-30°C) .
  • the broodstock was kept on a diet of newly hatched Artemia salina larvae and the micro ⁇ algae Dunaliella tertiolecta . Feeding was done daily except during the weekends.
  • Substrates (glass jars or panels) with adult barnacles were transferred into a bucket with filtered sea-water and Dunaliella tertiolecta was added to the water. Within a few hours the nauplii larvae were released. They were collected with a Pasteur-pipette after being attracted to a uni ⁇ directional light source, and transferred into 50 ml of filtered sea-water.
  • a glass container with approx. 8 1 of filtered sea-water was added 8.000 to 10.000 nauplii larvae. Beforehand the water was added 1ml of a stock solution of 21.900 ppm Penicillin and 1 ml of a stock solution of 36.500 ppm Streptomycin per 1 filtered sea-water. The container with the larvae was placed in an incubator at 28°C with a light cycle of 15 h light and 9 h dark. Bacteria filtered air was bubbled through the culture. 1. 1 of the microalgae Rhodomonas sp. culture was added. On the third day b ⁇ l of Rhodomonas sp. was added to the culture.
  • the culture was checked for the appearance of cyprid larvae.
  • the culture was filtered over a 250 ⁇ m and a 125 ⁇ m filter.
  • the cyprids were collected on the 125 ⁇ m filter.
  • the cyprids were then transferred into a crystallizing dish containing approx. 120 ml of filtered sea-water and the dish was covered with the lid.
  • the cyprids were placed in a 6°C incubator. This procedure was performed on day 0. At day 5 the cyprids were used for testing.
  • each dish was viewed under the microscope in order to judge the vitality of the non-settled cyprids.
  • the test was then stopped by adding 4 drops of 4% aqueous formaldehyde to each dish.
  • the content of the dish was filtered through a 0.45 ⁇ m membrane filter.
  • the filter was placed under a dissecting microscope and a count of non- settled cyprids was made.
  • the number of settled, and settled and metamorphosed cyprid larvae in the petri-dish was counted.
  • the total number of larvae in the dish was found by adding the number of settled, the settled and metamorphosed, and the non-settled larvae on the filter.
  • the settlement% and the inhibition% could then be calculated.
  • the settling% in the control should be >50% to accept the test.
  • paints containing the compounds were prepared in the following standard manner:
  • Standard paint components 11.9 g gum rosin 3.8 g vinyl resin 22.7 g xylene
  • Biological- cally active agent(s) was/were chosen as follows:
  • Paint no. 5 49.8 g 2-methylthio-4-tert-butylamino-6- cyclopropylamine-s-triazin (Irgarol 1051 ex Ciba-Geigy, Switzerland) Paint no. 6: 2.7 g 2-methylthio-4-tert-butylamino-6-cyclo- propylamine-s-triazin (Irgarol 1051 ex Ciba- Geigy, Switzerland) + 47.1 g cuprous oxide Generally, the paints were prepared as follows:
  • Example 6 For testing, the paints produced according to Example 6 were applied to xylene-degreased acrylic test panels (10 x 20 cm 2 ) in a dry film thickness (DFT) of approximately 100 microns. The panels were dried for 24 hours at room temperature.
  • DFT dry film thickness
  • test panels were immersed in sea-water from a raft at a test site, e.g in the harbour of Villanueva y Geltr ⁇ in northeastern Spain which is situated at a latitude of ap ⁇ proximately 41.2 degrees north.
  • the sea- water temperature varies between ll-28°C throughout the year, and the salinity varies between 30-35%o.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Dentistry (AREA)
  • Health & Medical Sciences (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne une structure marine recouverte d'un revêtement constitué d'une couche contenant un composé quinoléique représenté par la formule (I), un oxyde azoté ou un sel de ce dernier présentant une activité antisalissure. On a constaté que les dérivés quinoléiques présentent une activité anti enteromorpha spp., amphora ssp., nitocra spp. et balanus spp.
EP94931519A 1993-10-29 1994-10-28 Structure marine Ceased EP0725563A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DK122693A DK122693D0 (da) 1993-10-29 1993-10-29 Marin struktur
DK1226/93 1993-10-29
PCT/DK1994/000405 WO1995011592A1 (fr) 1993-10-29 1994-10-28 Structure marine

Publications (1)

Publication Number Publication Date
EP0725563A1 true EP0725563A1 (fr) 1996-08-14

Family

ID=8102409

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94931519A Ceased EP0725563A1 (fr) 1993-10-29 1994-10-28 Structure marine

Country Status (5)

Country Link
EP (1) EP0725563A1 (fr)
AU (1) AU8057694A (fr)
DK (1) DK122693D0 (fr)
SG (1) SG49035A1 (fr)
WO (1) WO1995011592A1 (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW343227B (en) * 1994-11-14 1998-10-21 Hempels Skibsfarve Fab J C Paint composition
IL135495A (en) * 1995-09-28 2002-12-01 Hoechst Ag Intermediate compounds for the preparation of quinoline-converted amines - 2 - carboxylic acid
US6310211B1 (en) 1996-09-10 2001-10-30 Pharmacia & Upjohn Company 8-hydroxy-7-substituted quinolines as anti-viral agents
US6262269B1 (en) 1997-02-04 2001-07-17 Trega Biosciences, Inc. 4-Substituted-quinoline derivatives and 4-substituted-quinoline combinatorial libraries
BR9814323A (pt) * 1997-12-22 2004-06-29 Upjohn Co 4-hidroxiquinolina-3-carboxamidas e hidrazidas como agentes antiviróticos
JPH11209206A (ja) * 1998-01-22 1999-08-03 Takeda Chem Ind Ltd 工業用殺菌剤
ATE367379T1 (de) 2000-08-09 2007-08-15 Hoffmann La Roche Quinolin-derivate als antientzündungsmittel
MXPA04009318A (es) 2002-03-27 2005-01-25 Glaxo Group Ltd Derivados de quinolina y su uso como ligados 5-ht6.
TWI328009B (en) 2003-05-21 2010-08-01 Glaxo Group Ltd Quinoline derivatives as phosphodiesterase inhibitors
DE602004000260T2 (de) 2003-07-22 2006-08-24 Arena Pharmaceuticals, Inc., San Diego Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen
US9084742B2 (en) 2007-12-12 2015-07-21 Axovant Sciences Ltd. Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-Quinoline
WO2009123714A2 (fr) 2008-04-02 2009-10-08 Arena Pharmaceuticals, Inc. Procédés de préparation de dérivés de pyrazole utiles comme modulateurs du récepteur de la sérotonine 5-ht<sb>2a</sb>
US9126946B2 (en) 2008-10-28 2015-09-08 Arena Pharmaceuticals, Inc. Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto
MX2017016413A (es) 2015-06-12 2018-08-01 Axovant Sciences Gmbh Derivados de diaril y arilheteroaril urea como moduladores del receptor 5ht2a de serotonina útiles para la profilaxis y el tratamineto de un trastorno conductual del sueño rem.
JP2018520187A (ja) 2015-07-15 2018-07-26 アクソヴァント サイエンシーズ ゲゼルシャフト ミット ベシュレンクテル ハフツングAxovant Sciences GmbH 神経変性疾患と関連する幻覚の予防および処置のために有用な５−ｈｔ２ａセロトニン受容体のモジュレーターとしてのジアリールおよびアリールヘテロアリール尿素誘導体
KR20220087497A (ko) 2019-10-18 2022-06-24 더 리전츠 오브 더 유니버시티 오브 캘리포니아 병원성 혈관을 표적화하기 위한 화합물 및 방법

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2460981A1 (fr) * 1979-07-11 1981-01-30 Astral Peintures Vernis Nouvelles peintures a application sub-aquatique
US4426464A (en) * 1981-07-03 1984-01-17 International Paint Public Limited Company Marine paint
WO1992020747A1 (fr) * 1991-05-17 1992-11-26 Battelle Memorial Institute Compositions marines comportant de preference des domaines concentres d'agents organo anti-fouling exempts d'etain

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9511592A1 *

Also Published As

Publication number Publication date
WO1995011592A1 (fr) 1995-05-04
SG49035A1 (en) 1998-05-18
DK122693D0 (da) 1993-10-29
AU8057694A (en) 1995-05-22

Similar Documents

Publication Publication Date Title
EP0725563A1 (fr) Structure marine
DE60004248T2 (de) Selbstpolierende anwuchsverhindernde anstrichfarbe für wasserfahrzeuge - mit silizium enthaltenden copolymeren und fasern
EP1457531B1 (fr) Composition de peinture antifouling, films de peinture antifouling, et navires, structures sous marines, materiel de peche et filets de peche recouverts par ces films
JP3874486B2 (ja) 塗料組成物
JP7030116B2 (ja) 新規な炭素ベースの加水分解可能ポリマーを含む防汚塗料組成物
CN101287805B (zh) 海洋防污涂料组合物
EP2489710B1 (fr) Composition de revêtement antisalissure, film antisalissure, film composite et structure immergée dans l&#39;eau
EP1138725B1 (fr) Revêtement antisalissures
CA2617570C (fr) Utilisation d&#39;une combinaison de substances contre des organismes d&#39;encrassement biologique
JP2002526427A (ja) 防汚作用薬
EP0927230B1 (fr) Peintures antisalissure de couleur claire et lumineuse
JP4217662B2 (ja) 海洋用自己研磨型防汚ペイント組成物
EP0153885B1 (fr) Complexes de tétraarylbore-ammonium et leur utilisation
SG185477A1 (en) Antifouling paint composition, antifouling coating film, and method for controlling hydrolysis rate of antifouling coating film
JP2008248058A (ja) 水中防汚塗料及び水中構造物
JP3451786B2 (ja) 塗料組成物
EP0706758B1 (fr) Agent d&#39;antifouling marin
KR100363364B1 (ko) 수생부착성유기물의정착방지방법
JP2005060510A (ja) 塗料組成物、防汚塗膜、防汚性水中構造物、及び防汚方法
KR20000029808A (ko) 오염방지페인트의자가연마특성을개량하는방법
JPH11116857A (ja) 塗料組成物
EP2285914B1 (fr) Nouveaux agents d&#39;adhésion antimicrobiens écologiques destinés à des peintures antisalissures et peintures antisalissures contenant de tels agents
EP0659847A1 (fr) Compositions anti-selissures et contrôle de l&#39;encrassement par les organismes aquatiques muisibles
JPH08277372A (ja) 塗料組成物
JP2004307764A (ja) 塗料組成物、防汚塗膜、水中構造物、及び水中構造物の防汚塗膜形成方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19960529

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE DK ES FR GB GR IE IT NL PT

17Q First examination report despatched

Effective date: 19970618

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 19990312