CS236864B2 - Fungicide agent and processing of active component - Google Patents

Fungicide agent and processing of active component Download PDF

Info

Publication number: CS236864B2
Authority: CS; Czechoslovakia
Prior art keywords: group; compound; optionally substituted; phenyl; compounds
Prior art date: 1981-12-22

Application number

CS829471A

Other languages

Czech (cs)

English (en)

Inventor

Wilfred-Hase Wells

Original Assignee

Fbc Ltd

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.)

1981-12-22

Filing date

1982-12-21

Publication date

1985-05-15

1982-12-21 Application filed by Fbc Ltd filed Critical Fbc Ltd

1985-05-15 Publication of CS236864B2 publication Critical patent/CS236864B2/cs

Links

239000000417 fungicide Substances 0.000 title description 4
150000001875 compounds Chemical class 0.000 claims abstract description 42
150000003839 salts Chemical class 0.000 claims abstract description 12
229910052751 metal Inorganic materials 0.000 claims abstract description 7
239000002184 metal Substances 0.000 claims abstract description 7
230000000855 fungicidal effect Effects 0.000 claims abstract description 6
239000002253 acid Substances 0.000 claims abstract description 5
125000002947 alkylene group Chemical group 0.000 claims abstract description 3
-1 methoxy, hydroxyl Chemical group 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 25
239000004480 active ingredient Substances 0.000 claims description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 8
239000003085 diluting agent Substances 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 3
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 2
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
125000002541 furyl group Chemical group 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 abstract description 3
125000000304 alkynyl group Chemical group 0.000 abstract description 2
125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
125000000547 substituted alkyl group Chemical group 0.000 abstract description 2
241000196324 Embryophyta Species 0.000 description 23
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 10
239000002904 solvent Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
239000013543 active substance Substances 0.000 description 8
239000002689 soil Substances 0.000 description 8
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125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical class O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
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229910052791 calcium Inorganic materials 0.000 description 1
JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
229940117949 captan Drugs 0.000 description 1
239000006013 carbendazim Substances 0.000 description 1
JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
150000001880 copper compounds Chemical class 0.000 description 1
239000006071 cream Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
229960002125 enilconazole Drugs 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
BBXXLROWFHWFQY-UHFFFAOYSA-N ethirimol Chemical compound CCCCC1=C(C)NC(NCC)=NC1=O BBXXLROWFHWFQY-UHFFFAOYSA-N 0.000 description 1
KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012458 free base Substances 0.000 description 1
ZEYJIQLVKGBLEM-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2N=C3[CH]C=CC=C3N=2)=C1 ZEYJIQLVKGBLEM-UHFFFAOYSA-N 0.000 description 1
239000002316 fumigant Substances 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000011810 insulating material Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
235000002867 manganese chloride Nutrition 0.000 description 1
239000011565 manganese chloride Substances 0.000 description 1
229940099607 manganese chloride Drugs 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
CNFDGXZLMLFIJV-UHFFFAOYSA-L manganese(II) chloride tetrahydrate Chemical compound O.O.O.O.[Cl-].[Cl-].[Mn+2] CNFDGXZLMLFIJV-UHFFFAOYSA-L 0.000 description 1
BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 1
CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
UQJQVUOTMVCFHX-UHFFFAOYSA-L nabam Chemical compound [Na+].[Na+].[S-]C(=S)NCCNC([S-])=S UQJQVUOTMVCFHX-UHFFFAOYSA-L 0.000 description 1
125000005609 naphthenate group Chemical group 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
229940049964 oleate Drugs 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
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
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000000746 purification Methods 0.000 description 1
JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229940071089 sarcosinate Drugs 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
NWZBFJYXRGSRGD-UHFFFAOYSA-M sodium;octadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCOS([O-])(=O)=O NWZBFJYXRGSRGD-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 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
DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS829471A 1981-12-22 1982-12-21 Fungicide agent and processing of active component CS236864B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB8138663		1981-12-22

Publications (1)

Publication Number	Publication Date
CS236864B2 true CS236864B2 (en)	1985-05-15

Family

ID=10526790

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS829471A CS236864B2 (en)	1981-12-22	1982-12-21	Fungicide agent and processing of active component

Country Status (17)

Country	Link
EP (1)	EP0084236A3 (da)
JP (1)	JPS58116470A (da)
KR (1)	KR840002816A (da)
AU (1)	AU538489B2 (da)
BR (1)	BR8207436A (da)
CA (1)	CA1186316A (da)
CS (1)	CS236864B2 (da)
DK (1)	DK563882A (da)
ES (1)	ES518416A0 (da)
GR (1)	GR77099B (da)
IL (1)	IL67525A0 (da)
NO (1)	NO824314L (da)
OA (1)	OA07280A (da)
PH (1)	PH18105A (da)
PL (1)	PL239683A1 (da)
PT (1)	PT76010B (da)
ZA (1)	ZA829374B (da)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0106515B1 (en) *	1982-09-30	1988-12-28	Pfizer Limited	Triazole anti-fungal agents
PH19347A (en) *	1982-09-30	1986-04-02	Pfizer	Triazole derivatives,pharmaceutical composition containing same and method of use thereof
DE3682711D1 (de) *	1985-06-18	1992-01-16	Ici Plc	Als fungizide verwendbare heterocyclische verbindungen.
ATE133408T1 (de) *	1986-12-16	1996-02-15	Zeneca Ltd	Pyrrol-derivate und ihre verwendung in der landwirtschaft
NZ229783A (en) *	1988-07-22	1990-12-21	Cl Pharma	Allylaminoethylazoles; fungicidal and antimycotic compositions, methods for preparation and combating fungi
DE4041173A1 (de) *	1990-12-21	1992-06-25	Henkel Kgaa	1-mono- bzw. 1,3-bis-substituierte imidazoliumsalze und deren benzoanaloga, verfahren zur herstellung und ihre verwendung
PT1611088E (pt) *	2003-04-07	2009-09-24	Pharmacyclics Inc	Hidroxamatos como agentes terapêuticos
PT2099442E (pt)	2006-12-26	2015-02-10	Pharmacyclics Inc	Métodos de utilização de inibidores de histona desacetilase e monitorização de biomarcadores em terapia de combinação
US7838234B2 (en)	2007-01-30	2010-11-23	Pharmacyclics, Inc.	Methods for determining cancer resistance to histone deacetylase inhibitors
US8603521B2 (en)	2009-04-17	2013-12-10	Pharmacyclics, Inc.	Formulations of histone deacetylase inhibitor and uses thereof
UA110853C2 (uk)	2011-09-13	2016-02-25	Фармасайклікс, Інк.	Лікарські форми інгібітора гістондеацетилази у комбінації з бендамустином та їхнє застосування
JP6800750B2 (ja)	2013-08-02	2020-12-16	ファーマサイクリックスエルエルシー	固形腫瘍の処置方法
CN111574385B (zh) *	2020-05-27	2022-10-04	石家庄万业化工科技有限公司	一种2-(2,4,6-三氯苯氧基)乙基丙胺的合成方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1535777A (en) *	1975-08-26	1978-12-13	Ici Ltd	Imidazole and 1,2,4-triazole compounds and their use as pesticides
DE2845293A1 (de) *	1978-10-18	1980-05-08	Basf Ag	Alpha -azolyl- alpha -phenylessigsaeurederivate

1982
- 1982-12-14 EP EP82306664A patent/EP0084236A3/en not_active Ceased
- 1982-12-20 OA OA57874A patent/OA07280A/xx unknown
- 1982-12-20 IL IL67525A patent/IL67525A0/xx unknown
- 1982-12-20 PH PH28299A patent/PH18105A/en unknown
- 1982-12-20 DK DK563882A patent/DK563882A/da not_active Application Discontinuation
- 1982-12-21 AU AU91733/82A patent/AU538489B2/en not_active Ceased
- 1982-12-21 JP JP57223144A patent/JPS58116470A/ja active Pending
- 1982-12-21 NO NO824314A patent/NO824314L/no unknown
- 1982-12-21 ZA ZA829374A patent/ZA829374B/xx unknown
- 1982-12-21 CA CA000418220A patent/CA1186316A/en not_active Expired
- 1982-12-21 CS CS829471A patent/CS236864B2/cs unknown
- 1982-12-21 KR KR1019820005719A patent/KR840002816A/ko not_active Withdrawn
- 1982-12-21 ES ES82518416A patent/ES518416A0/es active Granted
- 1982-12-21 PT PT76010A patent/PT76010B/pt unknown
- 1982-12-21 GR GR70136A patent/GR77099B/el unknown
- 1982-12-22 PL PL23968382A patent/PL239683A1/xx unknown
- 1982-12-22 BR BR8207436A patent/BR8207436A/pt unknown

Also Published As

Publication number	Publication date
OA07280A (en)	1984-08-31
IL67525A0 (en)	1983-05-15
PT76010B (en)	1985-10-04
KR840002816A (ko)	1984-07-21
EP0084236A3 (en)	1983-08-03
CA1186316A (en)	1985-04-30
DK563882A (da)	1983-06-23
AU9173382A (en)	1983-08-04
ES8402581A1 (es)	1984-02-01
EP0084236A2 (en)	1983-07-27
NO824314L (no)	1983-06-23
GR77099B (da)	1984-09-06
JPS58116470A (ja)	1983-07-11
ZA829374B (en)	1983-10-26
BR8207436A (pt)	1983-10-18
PL239683A1 (en)	1984-02-27
PT76010A (en)	1983-01-01
PH18105A (en)	1985-03-20
ES518416A0 (es)	1984-02-01
AU538489B2 (en)	1984-08-16

Publication	Publication Date	Title
JP2530590B2 (ja)	1996-09-04	殺菌・殺カビ剤
GB2279252A (en)	1995-01-04	Fungicidal seed treatment using phosphorous acid or its salts
JPS6097962A (ja)	1985-05-31	１−置換イミダゾ−ル−５−カルボン酸誘導体，それらの製造方法ならびにそれらを含有する殺菌剤，除草剤および植物生長調整剤
US4933358A (en)	1990-06-12	Fungicidal compositions
GB2124208A (en)	1984-02-15	Triazole derivatives of use as fungicides
CA1186316A (en)	1985-04-30	Triazolyl- and imidazolyl-acetamides
US4250179A (en)	1981-02-10	Metal complex imidazole fungicides, and methods of controlling fungi with them
JPS58172372A (ja)	1983-10-11	３−アゾリル−１，２−ジアリ−ル−１−ハロゲン−１−プロペン、その製造方法ならびにそれを含有する植物保護剤
EP0088545B1 (en)	1985-12-11	Fungicidal cyanopropenoates and compositions containing them
JPH058161B2 (da)	1993-02-01
US4549027A (en)	1985-10-22	Fungicidal and plant growth regulant triazole and imidazole sulfide compounds
CS227695B2 (en)	1984-05-14	Fungicide
CS208456B2 (en)	1981-09-15	Fungicide means and method of making the active substances
PL153804B1 (en)	1991-06-28	Fungicide
EP0445656B1 (en)	1994-12-21	Novel fungicidal imidazole complexes
US5292743A (en)	1994-03-08	Fungicidal compositions, fungicidal compounds, their production and use
EP0140571A1 (en)	1985-05-08	Diazole and triazole compounds
IE56044B1 (en)	1991-03-27	Fungicidal mixtures
JPS61221180A (ja)	1986-10-01	トリアゾール誘導体
JPS60255775A (ja)	1985-12-17	イミダゾ−ル誘導体及び非医療用殺菌剤
AU6507590A (en)	1991-05-16	Guanidines as fungicides
JP2002145708A (ja)	2002-05-22	植物病害防除剤
PL112528B1 (en)	1980-10-31	Fungicide
GB2128605A (en)	1984-05-02	Fungicidal alpha -aryl 1 H-1,2,4-triazole-1-ethanols
JPS6310151B2 (da)	1988-03-04