JP2020523386A - アルカロイド含有組成物及びその使用 - Google Patents
アルカロイド含有組成物及びその使用 Download PDFInfo
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- JP2020523386A JP2020523386A JP2019569387A JP2019569387A JP2020523386A JP 2020523386 A JP2020523386 A JP 2020523386A JP 2019569387 A JP2019569387 A JP 2019569387A JP 2019569387 A JP2019569387 A JP 2019569387A JP 2020523386 A JP2020523386 A JP 2020523386A
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- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- ILVGAIQLOCKNQA-UHFFFAOYSA-N propyl 2-hydroxypropanoate Chemical compound CCCOC(=O)C(C)O ILVGAIQLOCKNQA-UHFFFAOYSA-N 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 244000000040 protozoan parasite Species 0.000 description 1
- 238000013138 pruning Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000012521 purified sample Substances 0.000 description 1
- 229960000996 pyrantel pamoate Drugs 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- 125000001422 pyrrolinyl group Chemical group 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000007560 sedimentation technique Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- NTWXWSVUSTYPJH-UHFFFAOYSA-M sodium;1,4-bis(2-methylpropoxy)-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CC(C)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(C)C NTWXWSVUSTYPJH-UHFFFAOYSA-M 0.000 description 1
- UELAIMNOXLAYRW-UHFFFAOYSA-M sodium;1,4-dicyclohexyloxy-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].C1CCCCC1OC(=O)C(S(=O)(=O)[O-])CC(=O)OC1CCCCC1 UELAIMNOXLAYRW-UHFFFAOYSA-M 0.000 description 1
- ZEVCJZRMCOYJSP-UHFFFAOYSA-N sodium;2-(dithiocarboxyamino)ethylcarbamodithioic acid Chemical compound [Na+].SC(=S)NCCNC(S)=S ZEVCJZRMCOYJSP-UHFFFAOYSA-N 0.000 description 1
- NFTPETPDJZUWPQ-UHFFFAOYSA-M sodium;4-cyclohexyloxy-4-oxo-3-sulfobutanoate Chemical compound [Na+].[O-]C(=O)CC(S(=O)(=O)O)C(=O)OC1CCCCC1 NFTPETPDJZUWPQ-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000012430 stability testing Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000007103 stamina Effects 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 210000004233 talus Anatomy 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 125000005304 thiadiazolidinyl group Chemical group 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 229960005053 tinidazole Drugs 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 229930003802 tocotrienol Natural products 0.000 description 1
- 239000011731 tocotrienol Substances 0.000 description 1
- 229940068778 tocotrienols Drugs 0.000 description 1
- 235000019148 tocotrienols Nutrition 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 description 1
- 230000005945 translocation Effects 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 125000006168 tricyclic group Chemical group 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- 125000005455 trithianyl group Chemical group 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 235000010930 zeaxanthin Nutrition 0.000 description 1
- 239000001775 zeaxanthin Substances 0.000 description 1
- 229940043269 zeaxanthin Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/18—Bridged systems
-
- 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
- A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
- A01G13/00—Protecting plants
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Catching Or Destruction (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
a)組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は約20未満であるか、又は
b)組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は約20超であり、並びに、ここで、組成物のヒドロキシル基又は窒素含有基の求核係数は約0.6eV未満であり;
ここで、窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される。
a)組成物におけるN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は約20以下であるか;又は
b)組成物におけるN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は、約10又は約20超、好ましくは約40、約35又は約30未満であり、並びに、組成物におけるヒドロキシル基及び窒素含有基の求核係数は、約0.6eV未満、好ましくは0.55eV、より好ましくは約0.5eV未満であり、
ここで、窒素含有基は、アンモニア、第一級アミン基、第二級アミン基、又は、これらのいずれか2種以上の組み合わせから選択される。
ここで、組成物中に存在するN−ホルミルロリンの濃度は、54℃(1atm)で少なくとも2週間保管された場合に、約10%未満低減する。
a)組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は約20未満であるか、又は
b)組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は20超であり、並びに、ここで、組成物のヒドロキシル基又は窒素含有基の求核係数は0.55eV未満であり;
ここで、窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される。
を含む。
1)ロリン(ここで、R=CH3であり、及び、R’=Hである);
2)ノルロリン(ここで、R=Hであり、及び、R’=Hである);
3)N−メチルロリン(ここで、R=CH3であり、及び、R’=CH3である);
4)N−ホルミルロリン(ここで、R=CH3であり、及び、R’=CHOである);
5)N−ホルミルノルロリン(ここで、R=Hであり、及び、R’=CHOである);
6)N−アセチルロリン(ここで、R=CH3であり、及び、R’=COCH3である);並びに
7)N−アセチルノルロリン(ここで、R=Hであり、及び、R’=COCH3である)
を含む。
a)ポリアルキレングリコール、又は、そのエーテル若しくはエステル、例えば、式R10O−[(C1−6アルキレン)O]x−R1のポリアルキレングリコール、又は、そのエーテル若しくはエステル、
b)モノアルキレングリコール、又は、そのエーテル若しくはエステル、例えば、式R20O−(C1−6アルキレン)O−R2のモノアルキレングリコール、又は、そのエーテル若しくはエステル、
c)式R25R26R27Nのアミン、
d)モノアルキレンジアミン、例えば、式R31NH−(C1−6アルキレン)NR30−R32のモノアルキレンジアミン、
e)式CH3CH(OH)C(=O)NR3R4のアミド
f)ケトン、例えば、式R7C(=O)R8のケトン、
g)脂肪族アルコール、例えば、式R40OR41の脂肪族アルコール、
h)脂環式アルコール、
i)芳香族アルコール、
j)トリオール、又は、そのエーテル、エステル若しくは炭酸塩、例えば、式R70OCH2CH(OR71)CH2OR72のトリオール、又は、そのエーテル、エステル若しくは炭酸塩、
k)モノエステル、例えば、式R77C(O)OR17のモノエステル、
l)ジエステル、例えば、式R19OC(O)C1−6アルキルC(O)OR18のジエステル、
m)トリエステル、例えば、式
n)ニトリル、例えば、式R12−CNのニトリル、
o)スルホキシド、例えば、式R13S(O)R14のスルホキシド、
p)スルホン、例えば、式R15SO2R16のスルホン、又は
q)上記のa)〜p)のいずれか2つ以上、
を含む群から選択され、
ここで、上記の式における可変要素の各々は、本明細書において定義されている実施形態のいずれかにおいて定義されているとおり用いられている。
a)N−ホルミルロリン(NFL)、及び、任意選択により、1種以上のさらなる式(I)のロリンアルカロイドを提供するステップ、並びに
b)ロリンアルカロイドと1種以上の溶剤とを組み合わせて組成物を形成するステップ
を含み、ここで、組成物に係るN−ホルミルロリンに対するヒドロキシル及び窒素含有基の全量のモル比は、約20以下である。
a)本発明に係る組成物を提供するステップ、
b)組成物を植物に局部的に適用するステップ
を含み、これにより、1種以上のロリンアルカロイドを植物に摂取させて浸透移行性有害生物耐性を付与する方法を提供する。
1種以上のロリンアルカロイドを含む本明細書に記載の組成物を提供するステップ、
組成物を植物に局部的に適用して、植物の全身循環に1種以上のロリンアルカロイドを摂取させるステップ
を含む方法に関する。
例えば非合成原料に由来する1種以上の実質的に純粋なロリンアルカロイドといった、1種以上のロリンアルカロイドを含む本明細書に記載の組成物を提供するステップ、
組成物を植物に局部的に適用するステップ
を含み、これにより、1種以上のロリンアルカロイドを植物に摂取させて浸透移行性病害虫耐性を付与する方法に関する。
「及び/又は」という用語は、「及び」又は「又は」を意味することが可能である。
ロリンアルカロイドは、イネ科植物の感染に際して、内部寄生菌、特にエピクロエ属(Epichlooe)の内部寄生菌(これは、命名法の再編成に従って、現在では、以前は別分類とされていた無性世代ネオティホディウム属(Neotyphodium)を含む)によって共生的に生成される。これらの内部寄生菌は生体保護的であり、有害生物に対する保護、並びに、場合により干ばつ及び病害に対する保護を、これらが一部を形成する共生生物に与えると考えられている。
一態様において、本発明は、上記に記載されている、式[II]の構造を有するN−ホルミルロリン:
昆虫などの有害生物に対して有効であると共に本発明による使用に好適である本発明の組成物は、本発明の組成物と比較される対照処理剤と比して、標的有害生物種の個体群を統計的に有意な量で低減させる効果を有するものとして同定される。このような組成物は、有害生物防除効力を有するものとしてみなすことが可能である。本明細書に記載されているとおり、標的有害生物の個体群の低減は種々の拮抗メカニズムによるものであり得る。例えば、組成物は、有害生物の成長又は発達を無能力化し、不妊化し、阻害し得、及び/又は、好ましくは有害生物を死滅させ得、又は、成長と、本発明のロリンアルカロイドと一緒に組成物中に存在する(個別、同時又は順次にのいずれかで)有害生物防除性真菌などの同様に存在する1種以上の他の有害生物防除剤の有害生物防除効力とを支持若しくは促進し得る。このように、本発明の組成物は、有害生物を、無能力化し、不妊化し、及び/又は、好ましくは死滅させる有害生物防除剤の能力を実現可能とし、又は、支持し得る。本発明の組成物はまた、例えば組成物が適用される植物又はその周囲といった環境を、有害生物にとって好ましくないものとすることによって、標的有害生物の個体群を低減し得る。本実施形態において、組成物は、忌避剤として作用し、植物若しくはその周囲などの生息地の近傍における標的有害生物の有効個体群を低減させるとみなされ得る。
本発明では、例えば、米国、ニュージーランド及び欧州の国々のものを含む多くの国の農業及び園芸部門で植物有害生物における有害生物防除剤耐性の増大に関する問題に直面していることが認識されている。この問題は、いくつかの規制制度下において、規制上の障壁による新規の化学殺虫剤の入手可能性の低減、及び、市場からの既存の化学殺虫剤の排除によって、複雑化している。
他の実施形態において、本発明の組成物は水分散性顆粒を含む。この顆粒は、1種以上の本発明の組成物を、任意選択により、1種以上の他の薬剤と共に含む。
他の実施形態において、本発明の組成物は、水和剤、粉剤、乾燥配合物、ペレット又はコロイド状濃縮物を含む。この粉末は、1種以上の本発明の組成物を、任意選択により、1種以上の他の薬剤と共に含む。本発明の組成物のこのような乾燥形態は、湿らせた場合にすぐに溶解するよう、又は、代替的に、徐放性、持効性又は他の時間依存の様式で溶解するよう配合され得る。このような組成物は、標的有害生物に適用されるか、又は、標的有害生物により摂取され得、これにより、所与の環境における有害生物の数又はこのような有害生物の拡散の制御に用いられ得る。
他の実施形態において、本発明の組成物は、1種以上のロリンアルカロイドの水性懸濁液を、任意選択により、1種以上の溶解されているか、又は、そうでなければ死んでいる、又は、非生存内部寄生菌細胞(ロリンアルカロイドの生成に用いられる1種以上の内部寄生菌細胞を含む)と一緒に含み、これは、例えば培養ろ液、培養上澄、培養媒体、又は、これらから得られる抽出物若しくは画分を含む。このような水性懸濁液は、適用に先立って希釈される濃縮ストック溶液、又は、代替的に、すぐに適用可能な希釈液として提供され得る。
例えば複数の有害生物種の防除が所望される場合などといった一定の実施形態において、本明細書に記載の配合物はまた、1種以上の化学的有害生物防除剤(化学的有害生物防除剤、抗線虫薬、殺菌・殺カビ剤、抗ウイルス薬、殺微生物剤、殺アメーバ薬、殺虫剤等など)などの1種以上の他の薬剤、及び/又は、本明細書において同定されている殺虫性ロリンアルカロイドと同一又は異なる殺虫活性若しくは殺虫特異性を有する1種以上のロリンアルカロイドをさらに含み得る。本発明の組成物はまた、配合物を一回投薬した後における標的領域への長期の投薬を可能とする、肥料、除草剤、抗凍結剤、界面活性剤、洗剤、モノフルオロトリン、ドーマントオイル(dormant oil)、ポリマー、及び/又は、持続放出性若しくは生分解性キャリア配合物などの他の処理剤と併せて用いられ得る。同様に、配合物は、可食性の「餌」に調製され得、又は、標的有害生物による組成物の給餌若しくは摂食が可能である有害生物「トラップ」とされ得る。
本発明は、ヒト又は対象動物における有害生物、寄生生物又は昆虫感染の処置又は予防方法を提供するものであり、治療的に有効な量の本発明の組成物を投薬するステップを含む。
本明細書に記載の組成物中のロリンアルカロイドの含水量及び濃度を識別し判定する方法は、技術分野において周知である。
含水量は、カールフィッシャー(KF)電量滴定とオーブンサンプラで計測した。
本方法において用いた好適な器具は以下である:801 Stirrer(Metrohm)、874 Oven Sampler Processor(Metrohm)、852 Titrando+ダイアフラムレス滴定セル(Metrohm)、Software Tiamo(Metrohm)、6mlバイアル+セプタム(Metrohm)、及び、Analytical balance A T261 DeltaRange(Mettler)。
以下の詳細が好適な試薬の例であり、代替的な同等の試薬を用いることが可能である。オーブンサンプラと組み合わされるダイアフラムを有さない電量セルは、HYDRANAL Coulomat AG Ovenを必要とし、陰極液溶液は不要である。KFオーブンシステムのSSTには、34693 HYDRANAL Water Standard KF Oven(140℃〜160℃)及びキャリーガス(乾燥空気又は不活性ガス)を用いることが可能である。
カールフィッシャーオーブンを用いる推奨パラメータを表1に示す。
滴定セルをコンディショニングした後、サンプル容器の盲検消費を測定する。空のサンプル容器の含水量を三重に測定する。サンプルに関する盲検消費に同一の方法条件を適用する必要がある。
以下の注入シーケンスが提案される:
C B1 B2 B3 S1 S1 S2 S2 SST
C=滴定セルのコンディショニング
B=盲検消費(1、2、3)
S=サンプル(1、2、.....n)
SST=システム適合性テスト
機器は、滴定の終点に達するために必要な時間及び電流を計測する。乗法の積(経時的な電流の積分である電荷)は、生成されたヨウ素の量、従って、サンプル中に存在する水の量と正比例する。
NANL、NFL、NAL及びロリン含有量を、ガスクロマトグラフィ−水素炎イオン化検出器(GC−FID)により計測した。
ガスクロマトグラフィによるロリンの分析のための好適な器具及び条件を表2に示す。
標準物質は、ロリンの技術的混合物、又は、各ロリンの標準材料である。用いた内標準(IS)はコハク酸ジブチルであり、溶剤は、アセトニトリル中の2% v/v NH3(水中の濃縮物)である。標準溶液は、およそ70μg/mlのロリン(NANL、NFL、NAL及びロリンの和)及び300μg/mlのISを含有している。
単純な化学系中における局所的求核性特徴は、十分に確立された求核性指数技法[Journal of Molecular Structure:THEOCHEM,2009,895,86−91;Computational and Theoretical Chemistry,2012,980,49−55]に基づいてシミュレートすることが可能である。得られる係数は、付加環化反応における試薬及び他の有機分子に導入されたグローバル求核性ディスクリプタNの拡大を構成する[Journal of Organic Chemistry 2008,73,4615−4624;Journal of Molecular Structure(THEOCHEM),2008,865,68−72]。
すべての分子の幾何学的配置を、Gaussian09プログラム[Gaussian Inc.,2013,Wallingford,CT]を用いて、理論のDFT−B3LYP/6−31G(d,p)[Journal of Chemical Physics,1993,98,5648−5652;Physical Review B, 1988,37,785−789]レベルで最適化(分析)した。N−1電子種に対する非制限開殻法を用いるエネルギー計算を、既に得られている最適化された幾何学的配置N−電子で理論の同一レベルで行った。縮合福井関数を、Gaussian09プログラムに実装されている自然密度分析(NPA)[Chemical Review,1988,88,899−926]を用いて算出した。
この実施例は、異なる溶剤系におけるロリンアルカロイドの化学安定性を実証する。
この実施例は、ジメチルラクトアミド(DMLA)中におけるNFLの安定性を調べる。
この実施例は、固体配合物中におけるA2の安定性を調べる。
この実施例は、水の存在下におけるロリンへのNFLの分解、及び、分解速度論におけるpH及び温度の役割を調べる。
この実施例は、保管後における、異なる溶剤系中にNFLを含む配合物の効力を調べる。
本発明の組成物及び方法は、植物の有害生物を防除するための有用な手段を園芸家にもたらす、及び、ヒト又は非ヒト動物における昆虫の感染又は外寄生を処置又は予防するための治療をもたらすなど、農業、園芸、医学及び獣医学に係る広い範囲の用途における実用性を有する。
Claims (30)
- 少なくとも約10g/Lの式[I]の構造を有する1種以上のロリンアルカロイド:
a)前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量のモル比は約20未満であるか、又は
b)前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量の前記モル比は約20超であり、並びに、ここで、前記組成物の前記ヒドロキシル基又は窒素含有基の求核係数は約0.6eV未満であり;
ここで、前記窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される、組成物。 - 前記式[II]の構造を有するN−ホルミルロリンが、少なくとも部分的に精製されているか、又は、単離されている、請求項1に記載の組成物。
- 前記組成物中に存在するN−ホルミルロリンの濃度が、54℃(1atm)で少なくとも2週間保管された場合に、約10%未満低減する、請求項1又は2に記載の組成物。
- 少なくとも約10g/Lの式[I]の構造を有する1種以上のロリンアルカロイド:
ここで、前記組成物中に存在するN−ホルミルロリンの濃度は、54℃(1atm)で少なくとも2週間保管された場合に、約10%未満低減する、組成物。 - a)前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量の前記モル比が約20未満であるか、又は
b)前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量の前記モル比が20超であり、並びに、ここで、前記組成物の前記ヒドロキシル基又は窒素含有基の求核係数が0.6eV未満であり;
前記窒素含有基が、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される、請求項4に記載の組成物。 - 前記1種以上の溶剤に係る前記ヒドロキシル又は窒素含有基の前記求核係数が、0.5eV未満である、請求項1〜5のいずれか一項に記載の組成物。
- 前記1種以上のロリンアルカロイドが、ロリン、ノルロリン、N−アセチルロリン(NAL)、N−アセチルノルロリン(NANL)及びN−メチルロリン(NML)、N−ホルミルノルロリン、又は、これらのいずれか2種以上の組み合わせを含む群から選択される、請求項1〜6のいずれか一項に記載の組成物。
- 前記組成物が、N−ホルミルロリン(NFL)、N−アセチルロリン(NAL)及びN−アセチルノルロリン(NANL)を含む、請求項1〜7のいずれか一項に記載の組成物。
- [NANL]:[NFL]:[NAL]の重量比が、約1:12:1〜約2:5:3である、請求項1〜8のいずれか一項に記載の組成物。
- 少なくとも約5g/Lの前記式[II]の構造を有するN−ホルミルロリンを含む、請求項1〜9のいずれか一項に記載の組成物。
- 前記組成物が、少なくとも約50g/Lの前記式[I]の構造を有するロリンアルカロイドを含む、請求項1〜10のいずれか一項に記載の組成物。
- 前記式[II]の構造を有するN−ホルミルロリン、及び/又は、前記式[I]の構造を有する1種以上のロリンアルカロイドが実質的に純粋である、請求項1〜11のいずれか一項に記載の組成物。
- 前記組成物が、非ロリン植物由来アルカロイド又は物質を実質的に含まない、請求項1〜12のいずれか一項に記載の組成物。
- 任意選択により式[I]の1種以上のロリンアルカロイドを伴うN−ホルミルロリンと、1種以上の溶剤とから実質的に構成される、請求項1〜13のいずれか一項に記載の組成物。
- 前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量の前記モル比が約10未満であり;ここで、前記窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される、請求項1〜14のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が前記組成物の少なくとも約10%w/wを構成する、請求項1〜15のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が、アルコール、ケトン、エステル、エーテル、炭酸塩、アミン、アミド、ニトリル、スルホキシド及びスルホンを含む群から選択される、請求項1〜16のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が、
a)ポリアルキレングリコール、又は、そのエーテル若しくはエステル、好ましくは、式R10O−[(C1−6アルキレン)O]x−R1(式中、R1及びR10は各々、水素、脂肪族、脂環式、アシル、アリール又はアリール脂肪族から独立して選択され、及び、xは2〜140の整数である)のポリアルキレングリコール、又は、そのエーテル若しくはエステル;
b)モノアルキレングリコール、又は、そのエーテル若しくはエステル、好ましくは、式R20O−(C1−6アルキレン)O−R2(式中、R20及びR2は各々、水素、脂肪族、脂環式、アシル、アリール、又はアリール脂肪族から独立して選択される)のモノアルキレングリコール、又は、そのエーテル若しくはエステル;
c)式R25R26R27N(式中、R25、R26及びR27は各々、水素若しくは脂肪族から独立して選択され、又は、R26及びR27は、これらが結合している窒素原子と一緒になって、任意選択により追加のヘテロ原子を含む5〜8員ヘテロシクリル環を形成する)のアミン;
d)モノアルキレンジアミン、好ましくは式R31NH−(C1−6アルキレン)NR30−R32(式中、R31及びR32は各々、水素、脂肪族、脂環式、アシル、アリール又はアリール脂肪族から独立して選択され、及び、R30は、水素又は脂肪族から選択される)のモノアルキレンジアミン;
e)式CH3CH(OH)C(=O)NR3R4(式中、R3及びR4は各々、水素、C1−6アルキル、C2−6アルケニル又はC3−6シクロアルキルから独立して選択され、これらの各々は、フェニル、ヒドロキシル、C1−5アルコキシ、モルホリニル及びNR5R6(式中、R5及びR6は各々、C1−3アルキル、又は、C1−3アルキルから独立して選択される3個以下の置換基によって任意選択により置換されているフェニルから独立して選択される)から独立して選択される3個以下の置換基によって任意選択により置換され;又は、R3及びR4は、これらが結合している窒素原子と一緒になって、モルホリニル、ピロリジニル、ピペリジニル若しくはアゼパニル環を形成し、これらの各々は、C1−3アルキルから各々独立して選択される3個以下の置換基によって任意選択により置換される)のアミド;
f)ケトン、好ましくは、式R7C(=O)R8(式中、R7及びR8は各々、脂肪族、脂環式、アリール、又はアリール脂肪族から独立して選択される)のケトン;
g)脂肪族アルコール、好ましくは、式R40OR41(式中、R40は脂肪族、好ましくはC1−6アルキルであり、及び、R41は、水素、脂肪族、好ましくはC1−6アルキル又はアシルである)の脂肪族アルコール;
h)脂環式アルコール、好ましくは、C5−8シクロアルキルアルコール;
i)芳香族アルコール、好ましくは、アリール脂肪族−OH;
j)トリオール、又は、そのエーテル、エステル若しくは炭酸塩、好ましくは、式R70OCH2CH(OR71)CH2OR72(式中、R70、R71、及びR72は各々、水素、脂肪族、脂環式、アリール、アリール脂肪族、アシルから独立して選択され、又は、R71及びR72は、これらが結合している酸素と一緒になって、5員環を形成する)のトリオール、又は、そのエーテル、エステル若しくは炭酸塩;
k)モノエステル、好ましくは、式R77C(O)OR17(式中、R77及びR17は各々、脂肪族、脂環式、アリール又はアリール脂肪族基から独立して選択され、これらの各々は、1個以上のヒドロキシル基で任意選択により置換されている)のモノエステル;
l)ジエステル、好ましくは、式R19OC(O)C1−6アルキルC(O)OR18(式中、R19及びR18は各々、脂肪族、脂環式、アリール又はアリール脂肪族基から独立して選択される)のジエステル;
m)トリエステル、好ましくは、式
n)ニトリル、好ましくは、式R12−CN(式中、R12は、脂肪族、脂環式、アリール又はアリール脂肪族基である)のニトリル;
o)スルホキシド、好ましくは、式R13S(O)R14(式中、R13及びR14は各々、脂肪族、脂環式、アリール、アリール脂肪族から独立して選択される)のスルホキシド;並びに
p)スルホン、好ましくは、式R15SO2R16(式中、R15及びR16は各々、脂肪族、脂環式、アリール、アリール脂肪族から独立して選択される)のスルホン
を含む群から選択される、請求項1〜17のいずれか一項に記載の組成物。 - 前記1種以上の溶剤が、ジメチルラクトアミド、ジプロピレングリコールメチルエーテル、エチレングリコールフェニルエーテル、アセトフェノン、シクロヘキサノール、ポリエチレングリコール、ポリエチレングリコールメチルエーテル、ジメチルスクシネート、ジメチルグルタレート、アジピン酸ジメチル(dimethyl adapate)、安息香酸ブチル、トリエチルシトレート、グリセリンカーボネート、エチレングリコール、プロピレングリコール、乳酸2−エチルヘキシル及びベンジルアルコールを含む群から選択される、請求項1〜18のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が、ジメチルラクトアミド、エチレングリコールフェニルエーテル、100〜6000の分子量を有するポリエチレングリコール、100〜1000の分子量を有するポリエチレングリコールメチルエーテル、ジメチルスクシネート、ジメチルグルタレート、アジピン酸ジメチル(dimethyl adapate)、安息香酸ブチル、トリエチルシトレート、グリセリンカーボネート、乳酸2−エチルヘキシル及びベンジルアルコールを含む群から選択される、請求項1〜18のいずれか一項に記載の組成物。
- 前記1種以上の溶剤の1種がジメチルラクトアミドである、請求項19又は20に記載の組成物。
- 前記1種以上の溶剤に係る前記ヒドロキシル基又は窒素含有基の前記求核係数が0.3eV未満であり;ここで、前記窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される、請求項1〜21のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が、実質的に非水性である溶剤系を含む、請求項1〜22のいずれか一項に記載の組成物。
- 前記1種以上の溶剤が、5%w/w未満の水を含む溶剤系を含む、請求項1〜23のいずれか一項に記載の組成物。
- 前記組成物に係るN−ホルミルロリンに対するヒドロキシル基及び窒素含有基の全量の前記モル比が約10未満であり、前記組成物に係る前記ヒドロキシル又は窒素含有基の前記求核係数が、0.6eV未満、好ましくは0.5eV未満であり、並びに、前記窒素含有基は、アンモニア、第一級アミン基、第二級アミン基又はこれらの混合物から選択される、請求項1〜24のいずれか一項に記載の組成物。
- 1種以上のロリンアルカロイドと1種以上の溶剤とを混合して組成物を形成するステップを含み、前記組成物がヒドロキシル基を含む溶剤を実質的に含まない、請求項1〜25のいずれか一項に記載の組成物を生成する方法。
- 植物に浸透移行性病害虫耐性を付与する方法であって、請求項1〜25のいずれか一項に記載の組成物を提供するステップ、及び、前記組成物を前記植物に局部的に適用するステップを含み、これにより、前記1種以上のロリンアルカロイドを前記植物に摂取させて浸透移行性病害虫耐性を付与する方法。
- 植物又はその周囲に、請求項1〜25のいずれか一項に記載の組成物を適用するステップを含む、1種以上の病害虫を防除する方法。
- 1種以上の昆虫を防除する方法であって、前記1種以上の昆虫に有効量の請求項1〜25のいずれか一項に記載の組成物を接触させるステップを含む方法。
- 1種以上の病害虫を防除するための配合物の生産における、請求項1〜25のいずれか一項に記載の組成物の使用。
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