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09/28/06 - USPTO Class 514 |  9 views | #20060217402 | Prev - Next | About this Page  514 rss/xml feed  monitor keywords

Biocidal compounds and their preparation

USPTO Application #: 20060217402
Title: Biocidal compounds and their preparation
Abstract: wherein R is H or CH3. Of particular interest are two isomers that are named malayamycin A and desmethylmalayamycin A. These isomers, which may be prepared by growing under controlled conditions a previously unknown strain of micro-organism from the species Streptomyces malaysiensis, are characterised by nmr and mass spectroscopic data. They have biocidal activity, including anti-fungal, anti-viral and anti-cancer activity, and are of special interest for use in agriculture, horticulture, animal and human health. This invention concerns new biocidal compounds of formula (I)
(end of abstract)
Agent: Syngenta Crop Protection , Inc. Patent And Trademark Department - Greensboro, NC, US
Inventors: Jill Patricia Benner, Bettina Gertrud Henriette Boehlendorf, Martin Richard Kipps, Nicolas Eugene Paul Lambert, Riet Luck, Louis-Pierre Molleyres, Snezana Neff, Traugott Christoph Schuez, Paul David Stanley
USPTO Applicaton #: 20060217402 - Class: 514269000 (USPTO)

Related Patent Categories: Drug, Bio-affecting And Body Treating Compositions, Designated Organic Active Ingredient Containing (doai), Heterocyclic Carbon Compounds Containing A Hetero Ring Having Chalcogen (i.e., O,s,se Or Te) Or Nitrogen As The Only Ring Hetero Atoms Doai, Hetero Ring Is Six-membered Consisting Of Two Nitrogens And Four Carbon Atoms (e.g., Pyridazines, Etc.), 1,4-diazine As One Of The Cyclos, Pyrimidines With Chalcogen Bonded Directly To A Ring Carbon Of Said Pyrimidine Moiety
The Patent Description & Claims data below is from USPTO Patent Application 20060217402.
Brief Patent Description - Full Patent Description - Patent Application Claims  monitor keywords



[0001] This invention relates to new biocidal compounds and to a process for their preparation. More particularly it relates to biocidal compounds which may be obtained by cultivation of Streptomyces organisms; to the use of said compounds as biocides; to compositions containing a biocidally effective amount of said compounds; a method of combating pathogens using said compounds; a new strain of Streptomyces malaysiensis and mutants thereof.

[0002] In a first aspect the invention provides a new biocidal compound of formula (I) wherein R is H or CH.sub.3.

[0003] The compound where R is H and the compound where R is CH.sub.3 are novel compounds not previously isolated. They are characterised by the nmr and mass spectroscopy data provided in the examples herein. They may be prepared by growing under controlled conditions, a previously unknown strain of micro-organism from the species Streptomyces malaysiensis. The compounds of the invention have biocidal activity and, in particular, anti-fungal, anti-viral and anti-cancer activity and are of special interest for use in agriculture, horticulture, animal and human health. The compounds may also be of use as intermediates in the preparation of further active compounds. The compounds of formula (I) may be obtained by fermentation and recovered in substantially pure form as described herein.

[0004] The compounds of formula (I) have six asymmetric centres and may exist in the form of one or more isomers. The invention includes all isomers, individually or in a mixture of one or more forms. The compounds of the invention may exist in several tautomeric forms and the invention extends to all forms.

[0005] Of particular interest are the compounds of formulae (II) and (III), which are here named malayamycin A and desmethylmalayamycin A, respectively.

[0006] The compounds of formulae (II) and (III) may exist in alternative tautomeric forms and the invention extends to said alternative forms.

[0007] The compounds of formula (I) are biocidal agents. They are active antiviral agents showing for example antiviral activity against the Human Immunodeficiency Virus associated with the disease AIDS. They have also been shown to have anti-cancer properties. For example they show an in inhibitory effect on the cell proliferation of cancer cells. As used herein the term biocidal is used to cover activity against pathogens and includes antiviral, antifungal and anticancer activity. The use of the compounds as antifungal agents, particularly against plant pathogenic fungi, is of particular interest.

[0008] The compounds of formula (I) are active fungicides and may be used to control one or more of the following plant pathogens: Pyricularia oryzae (Magnaporthe grisea) on rice and wheat and other Pyricularia spp. on other hosts; Puccinia triticina (or recondita), Puccinia striiformis and other rusts on wheat, Puccinia hordei, Puccinia striiformis and other rusts on barley, and rusts on other hosts (for example turf, rye, coffee, pears, apples, peanuts, sugar beet, vegetables and ornamental plants); Erysiphe cichoracearum on cucurbits (for example melon); Blumeria (or Erysiphe) graminis (powdery mildew) on barley, wheat, rye and turf and other powdery mildews on various hosts, such as Sphaerotheca macularis on hops, Sphaerotheca fusca (Sphaerotheca fuliginea) on cucurbits (for example cucumber), Leveillula taurica on tomatoes, aubergine and green pepper, Podosphaera leucotricha on apples and Uncinula necator on vines; Cochliobolus spp., Helminthosporium spp., Drechslera spp. (Pyrenophora spp.), Rhynchosporium spp., Mycosphaerella graminicola (Septoria tritici) and Phaeosphaeria nodorum (Stagonospora nodorum or Septoria nodorum), Pseudocercosporella herpotrichoides and Gaeumannomyces graminis on cereals (for example wheat, barley, rye), turf and other hosts; Cercospora arachidicola and Cercosporidium personatum on peanuts and other Cercospora spp. on other hosts, for example sugar beet, bananas, soya beans and rice; Botrytis cinerea (grey mould) on tomatoes, strawberries, vegetables, vines and other hosts and other Botrytis spp. on other hosts; Alternaria spp. on vegetables (for example carrots), oil-seed rape, apples, tomatoes, potatoes, cereals (for example wheat) and other hosts; Venturia spp. (including Venturia inaequalis (scab)) on apples, pears, stone fruit, tree nuts and other hosts; Cladosporium spp. on a range of hosts including cereals (for example wheat) and tomatoes; Monilinia spp. on stone fruit, tree nuts and other hosts; Didymella spp. on tomatoes, turf, wheat, cucurbits and other hosts; Phoma spp. on oil-seed rape, turf, rice, potatoes, wheat and other hosts; Aspergillus spp. and Aureobasidium spp. on wheat, lumber and other hosts; Ascochyta spp. on peas, wheat, barley and other hosts; Stemphylium spp. (Pleospora spp.) on apples, pears, onions and other hosts; summer diseases (for example bitter rot (Glomerella cingulata), black rot or frogeye leaf spot (Botryosphaeria obtusa), Brooks fruit spot (Mycosphaerella pomi), Cedar apple rust (Gymnosporangium juniperi-virginianae), sooty blotch (Gloeodes pomigena), flyspeck (Schizothyrium pomi) and white rot (Botryosphaeria dothidea)) on apples and pears; Plasmopara viticola on vines; other downy mildews, such as Bremia lactucae on lettuce, Peronospora spp. on soybeans, tobacco, onions and other hosts, Pseudoperonospora humuli on hops and Pseudoperonospora cubensis on cucurbits; Pythium spp. (including Pythium ultimum) on turf and other hosts; Phytophthora infestans on potatoes and tomatoes and other Phytophthora spp. on vegetables, strawberries, avocado, pepper, ornamentals, tobacco, cocoa and other hosts; Thanatephorus cucumeris on rice and turf and other Rhizoctonia spp. on various hosts such as wheat and barley, peanuts, vegetables, cotton and turf; Sclerotinia spp. on turf, peanuts, potatoes, oil-seed rape and other hosts; Sclerotium spp. on turf, peanuts and other hosts; Gibberella fujikuroi on rice; Colletotrichum spp. on a range of hosts including turf, coffee and vegetables; Laetisaria fuciformis on turf; Mycosphaerella spp. on bananas, peanuts, citrus, pecans, papaya and other hosts; Diaporthe spp. on citrus, soybean, melon, pears, lupin and other hosts; Elsinoe spp. on citrus, vines, olives, pecans, roses and other hosts; Verticillium spp. on a range of hosts including hops, potatoes and tomatoes; Pyrenopeziza spp. on oil-seed rape and other hosts; Oncobasidium theobromae on cocoa causing vascular streak dieback; Fusarium spp., Typhula spp., Microdochium nivale, Ustilago spp., Urocystis spp., Tilletia spp. and Claviceps purpurea on a variety of hosts but particularly wheat, barley, turf and maize; Ramularia spp. on sugar beet, barley and other hosts; post-harvest diseases particularly of fruit (for example Penicillium digitatum, Penicillium italicum and Trichoderma viride on oranges, Colletotrichum musae and Gloeosporium musarum on bananas and Botrytis cinerea on grapes); other pathogens on vines, notably Eutypa lata, Guignardia bidwellii, Phellinus igniarus, Phomopsis viticola, Pseudopeziza tracheiphila and Stereum hirsutum; other pathogens on trees (for example Lophodermium seditiosum) or lumber, notably Cephaloascus fragrans, Ceratocystis spp., Ophiostoma piceae, Penicillium spp., Trichoderma pseudokoningii, Trichoderma viride, Trichoderma harzianum, Aspergillus niger, Leptographium lindbergi and Aureobasidium pullulans; and fungal vectors of viral diseases (for example Polymyxa graminis on cereals as the vector of barley yellow mosaic virus (BYMV) and Polymyxa betae on sugar beet as the vector of rhizomania).

[0009] The compounds of formula (I) may move acropetally, basipetally or locally in plant tissue to be active against one or more fungi.

[0010] The invention therefore provides a method of combating or controlling phytopathogenic fungi which comprises applying a fungicidally effective amount of a compound of formula (I), or a composition containing a compound of formula (I), to a plant, to a seed of a plant, to the locus of the plant or seed or to soil or any other plant growth medium, e.g. nutrient solution.

[0011] The term "plant" as used herein includes seedlings, bushes and trees. Furthermore, the fungicidal method of the invention includes protectant, curative, systemic, eradicant and antisporulant treatments.

[0012] The compounds of formula (I) are preferably used for agricultural, horticultural and turfgrass purposes in the form of a composition.

[0013] In order to apply a compound of formula (I) to a plant, to a seed of a plant, to the locus of the plant or seed or to soil or any other growth medium, a compound of formula (I) is usually formulated into a composition which includes, in addition to the compound of formula (I), a suitable inert diluent or carrier and, optionally, a surface active agent (SFA). SFAs are chemicals which are able to modify the properties of an interface (for example, liquid/solid, liquid/air or liquid/liquid interfaces) by lowering the interfacial tension and thereby leading to changes in other properties (for example dispersion, emulsification and wetting). It is preferred that all compositions (both solid and liquid formulations) comprise, by weight, 0.0001 to 95%, more preferably 1 to 85%, for example 5 to 60%, of a compound of formula (I). The composition is generally used for the control of fungi such that a compound of formula (I) is applied at a rate of from 0.1 g to 10 kg per hectare, preferably from 1 g to 6 kg per hectare, more preferably from 1 g to 1 kg per hectare.

[0014] When used in a seed dressing, a compound of formula (I) is used at a rate of 0.0001 g to 10 g (for example 0.001 g or 0.05 g), preferably 0.005 g to 10 g, more preferably 0.005 g to 4 g, per kilogram of seed.

[0015] In another aspect the present invention provides a biocidal composition comprising a biocidally effective amount of a compound of formula (I) and a suitable carrier or diluent therefor.

[0016] In a preferred embodiment of this aspect the present invention provides an antiviral composition comprising an antivirally effective amount of a compound of formula (I) and a suitable carrier or diluent therefor.

[0017] In a further preferred embodiment of this aspect the present invention provides an anti-cancer composition comprising an effective amount of a compound of formula (I) which is effective in reducing the proliferation of cancer cells and a suitable carrier or diluent therefor.

[0018] In a particularly preferred embodiment of this aspect the present invention provides a fungicidal composition comprising a fungicidally effective amount of a compound of formula (I) and a suitable carrier or diluent therefor.

[0019] In a still further aspect the invention provides a method of combating and controlling viruses which comprises treating the viruses or the locus of the viruses with an antivirally effective amount of a composition comprising a compound of formula (I).

[0020] In a still further aspect the invention provides a method of combating and controlling cancer cells which comprises treating the cancer cells or the locus of the cancer cells with an effective amount of a composition comprising a compound of formula (I) said amount being effective in reducing the proliferation of said cancer cells.

[0021] In a still further preferred aspect the invention provides a method of combating and controlling fungi which comprises treating the fungi or the locus of the fungi with a fungicidally effective amount of a composition comprising a compound of formula (I).

[0022] The compositions can be chosen from a number of formulation types, including dustable powders (DP), soluble powders (SP), water soluble granules (SG), water dispersible granules (WG), wettable powders (WP), granules (GR) (slow or fast release), soluble concentrates (SL), oil miscible liquids (OL), ultra low volume liquids (UL), emulsifiable concentrates (EC), dispersible concentrates (DC), emulsions (both oil in water (EW) and water in oil (EO)), micro-emulsions (ME), suspension concentrates (SC), aerosols, fogging/smoke formulations, capsule suspensions (CS) and seed treatment formulations. The formulation type chosen in any instance will depend upon the particular purpose envisaged and the physical, chemical and biological properties of the compound of formula (I).

[0023] Dustable powders (DP) may be prepared by mixing a compound of formula (I) with one or more solid diluents (for example natural clays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite, kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium and magnesium carbonates, sulphur, lime, flours, talc and other organic and inorganic solid carriers) and mechanically grinding the mixture to a fine powder.

[0024] Soluble powders (SP) may be prepared by mixing a compound of formula (I) with one or more water-soluble inorganic salts (such as sodium bicarbonate, sodium carbonate or magnesium sulphate) or one or more water-soluble organic solids (such as a polysaccharide) and, optionally, one or more wetting agents, one or more dispersing agents or a mixture of said agents to improve water dispersibility/solubility. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water soluble granules (SG).

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