OA13292A - The use of N-arylhydrazine derivatives for combating pests. - Google Patents

The use of N-arylhydrazine derivatives for combating pests. Download PDF

Info

Publication number: OA13292A
Authority: OA; OAPI
Prior art keywords: formula; pests; diptera; compounds; orders
Prior art date: 2003-12-04

Application number

OA1200600173A

Other languages

English (en)

Inventor

Nigel Armes

Christopher Koradin

David G Kuhn

Hassan Oloumi-Sadeghi

Wolfgang Von Deyn

Original Assignee

Basf Ag

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.)

2003-12-04

Filing date

2004-12-02

Publication date

2007-01-31

2004-12-02 Application filed by Basf Ag filed Critical Basf Ag

2007-01-31 Publication of OA13292A publication Critical patent/OA13292A/en

Links

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WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
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GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
229910052794 bromium Inorganic materials 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 3
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GEPDYQSQVLXLEU-AATRIKPKSA-N methyl (e)-3-dimethoxyphosphoryloxybut-2-enoate Chemical compound COC(=O)\C=C(/C)OP(=O)(OC)OC GEPDYQSQVLXLEU-AATRIKPKSA-N 0.000 description 1
VLGWYKOEXANHJT-UHFFFAOYSA-N methylsulfanol Chemical compound CSO VLGWYKOEXANHJT-UHFFFAOYSA-N 0.000 description 1
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CMYVGTJJWKDGRX-UHFFFAOYSA-N n-[2,6-dichloro-4-(trifluoromethyl)anilino]-n'-ethyl-2,2-dimethylpropanimidamide Chemical compound CCN=C(C(C)(C)C)NNC1=C(Cl)C=C(C(F)(F)F)C=C1Cl CMYVGTJJWKDGRX-UHFFFAOYSA-N 0.000 description 1
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231100000252 nontoxic Toxicity 0.000 description 1
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238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 1
PMCVMORKVPSKHZ-UHFFFAOYSA-N oxydemeton-methyl Chemical compound CCS(=O)CCSP(=O)(OC)OC PMCVMORKVPSKHZ-UHFFFAOYSA-N 0.000 description 1
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229940044654 phenolsulfonic acid Drugs 0.000 description 1
XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 1
BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 1
IOUNQDKNJZEDEP-UHFFFAOYSA-N phosalone Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=S)(OCC)OCC)C2=C1 IOUNQDKNJZEDEP-UHFFFAOYSA-N 0.000 description 1
RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
229950001664 phoxim Drugs 0.000 description 1
QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 1
235000021118 plant-derived protein Nutrition 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000011120 plywood Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
150000004804 polysaccharides Polymers 0.000 description 1
244000144977 poultry Species 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 1
230000005180 public health Effects 0.000 description 1
QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
208000005687 scabies Diseases 0.000 description 1
125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
229960003885 sodium benzoate Drugs 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
229940014213 spinosad Drugs 0.000 description 1
DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
239000005936 tau-Fluvalinate Substances 0.000 description 1
INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 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
DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000006200 vaporizer Substances 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1
239000003021 water soluble solvent Substances 0.000 description 1
239000005943 zeta-Cypermethrin Substances 0.000 description 1

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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Tropical Medicine & Parasitology (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Organic Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Public Health (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)
Pretreatment Of Seeds And Plants (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Pyridine Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Catching Or Destruction (AREA)

OA1200600173A 2003-12-04 2004-12-02 The use of N-arylhydrazine derivatives for combating pests. OA13292A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US52660903P	2003-12-04	2003-12-04

Publications (1)

Publication Number	Publication Date
OA13292A true OA13292A (en)	2007-01-31

Family

ID=34652460

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200600173A OA13292A (en)	2003-12-04	2004-12-02	The use of N-arylhydrazine derivatives for combating pests.

Country Status (34)

Country	Link
US (2)	US20070259962A1 (es)
EP (3)	EP1691607B1 (es)
JP (3)	JP2007513116A (es)
KR (3)	KR20060123420A (es)
CN (3)	CN1889832A (es)
AP (1)	AP1959A (es)
AR (2)	AR046745A1 (es)
AT (3)	ATE372674T1 (es)
AU (3)	AU2004294299A1 (es)
BR (3)	BRPI0417060A (es)
CA (3)	CA2547420A1 (es)
CO (2)	CO5680375A2 (es)
CR (1)	CR8451A (es)
DE (3)	DE602004006020T2 (es)
DK (2)	DK1691607T3 (es)
EA (3)	EA200601078A1 (es)
EC (2)	ECSP066609A (es)
ES (2)	ES2290785T3 (es)
IL (3)	IL175544A0 (es)
MA (2)	MA28280A1 (es)
MX (1)	MXPA06005988A (es)
MY (1)	MY137761A (es)
NO (1)	NO20062632L (es)
NZ (1)	NZ547362A (es)
OA (1)	OA13292A (es)
PE (1)	PE20050702A1 (es)
PL (2)	PL1691607T3 (es)
PT (1)	PT1691607E (es)
SI (2)	SI1691607T1 (es)
TW (3)	TW200529836A (es)
UA (2)	UA79571C2 (es)
UY (2)	UY28655A1 (es)
WO (3)	WO2005053402A2 (es)
ZA (3)	ZA200605459B (es)

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EP1895839A1 (en) *	2005-06-03	2008-03-12	Basf Se	Method of combating bugs
KR20080018934A (ko) *	2005-06-03	2008-02-28	바스프 악티엔게젤샤프트	해충에 대한 보호 활성을 제공하는 섬유, 직물 및 네팅함침용 조성물
US20080249182A1 (en) *	2005-11-04	2008-10-09	Basf Se	Crystalline Modification of N-Ethyl-2,2-Dichloro-1-Methylcyclopropane-Carboxamide-2-(2,6-Dichloro-Alpha, Alpha, Alpha-Trifluoro-P-Tolyl)Hydrazone
JP5239148B2 (ja) *	2005-12-01	2013-07-17	住友化学株式会社	３−イミノプロペン化合物、それを含有する有害生物防除剤、およびその有害生物防除用途
BRPI0619187A2 (pt) *	2005-12-01	2011-09-13	Sumitomo Chemical Co	composto de iminopropeno e uso do mesmo
AP2008004548A0 (en) *	2006-01-04	2008-08-31	Basf Se	Method of combating root weevils
AR058921A1 (es) *	2006-01-05	2008-03-05	Basf Ag	Mezcla de disolventes para preparar una formulacion de concentrado de liquido hidrosoluble de compuestos plaguicidas organicos
DE102006011403A1 (de) *	2006-03-11	2007-09-13	Bayer Cropscience Ag	Köder auf Zuckerbasis
US20100010220A1 (en) *	2006-08-03	2010-01-14	Basf Se	Process for Preparing Amidrazones
DE102006061537A1 (de) *	2006-12-27	2008-07-03	Bayer Healthcare Ag	Mittel zur Bekämpfung von Parasiten an Tieren
WO2008092851A2 (en) *	2007-01-30	2008-08-07	Basf Se	Pesticidal compositions comprising 3 -acetyl-i- phenylpyrazole compounds
US20100099774A1 (en) *	2007-02-01	2010-04-22	Basf Se	Method for Controlling Harmful Fungi
WO2008092818A2 (en) *	2007-02-01	2008-08-07	Basf Se	Pesticidal mixtures
WO2009055044A1 (en)	2007-10-25	2009-04-30	Valent Biosciences Corporation	Enhancement of plant growth
WO2009059603A1 (en)	2007-11-05	2009-05-14	Vestergaard Frandsen Sa	Room with two counter-resistant insecticidal objects
CN101747320B (zh) *	2008-12-19	2013-10-16	华东理工大学	二醛构建的具有杀虫活性的含氮或氧杂环化合物及其制备方法
ES2587232T3 (es)	2010-07-20	2016-10-21	Vestaron Corporation	Triazinas y pirimidinas insecticidas
CN108685894B (zh) *	2012-04-04	2022-04-26	英特维特国际股份有限公司	软咀嚼药用产品
WO2014163933A1 (en) *	2013-03-13	2014-10-09	Dow Agrosciences Llc	Process for preparation of triaryl pesticide intermediate
WO2014163932A1 (en) *	2013-03-13	2014-10-09	Dow Agrosciences Llc	Preparation of haloalkoxyarylhydrazines and intermediates therefrom
WO2015058024A1 (en)	2013-10-17	2015-04-23	Dow Agrosciences Llc	Processes for the preparation of pesticidal compounds
WO2018125817A1 (en)	2016-12-29	2018-07-05	Dow Agrosciences Llc	Processes for the preparation of pesticidal compounds
CN115251086A (zh) *	2022-08-03	2022-11-01	广州毅田生物技术有限公司	一种含绿僵菌的红火蚁防治药剂及其防治方法

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JPS5576804A (en) *	1978-12-06	1980-06-10	Sankyo Co Ltd	Agricultural and horticultural microbicide
MY131441A (en) *	1992-12-29	2007-08-30	American Cyanamid Co	Amidrazones and their use as insecticidal and acaricidal agents
US5420165A (en) *	1992-12-29	1995-05-30	American Cyanamid Company	Amidrazones and their use as insecticidal and acaricidal agents

2004
- 2004-02-12 UA UAA200607447A patent/UA79571C2/uk unknown
- 2004-11-30 PE PE2004001178A patent/PE20050702A1/es not_active Application Discontinuation
- 2004-12-02 EA EA200601078A patent/EA200601078A1/ru unknown
- 2004-12-02 AU AU2004294299A patent/AU2004294299A1/en not_active Abandoned
- 2004-12-02 PT PT04803437T patent/PT1691607E/pt unknown
- 2004-12-02 EP EP04803437A patent/EP1691607B1/en not_active Expired - Lifetime
- 2004-12-02 PL PL04803437T patent/PL1691607T3/pl unknown
- 2004-12-02 PL PL04819647T patent/PL1694122T3/pl unknown
- 2004-12-02 UA UAA200607448A patent/UA81561C2/xx unknown
- 2004-12-02 AU AU2004294298A patent/AU2004294298A1/en not_active Abandoned
- 2004-12-02 AT AT04819647T patent/ATE372674T1/de not_active IP Right Cessation
- 2004-12-02 KR KR1020067013330A patent/KR20060123420A/ko not_active Withdrawn
- 2004-12-02 EA EA200601076A patent/EA010019B1/ru not_active IP Right Cessation
- 2004-12-02 KR KR1020067010774A patent/KR20060123241A/ko not_active Withdrawn
- 2004-12-02 CN CNA2004800361659A patent/CN1889832A/zh active Pending
- 2004-12-02 WO PCT/EP2004/013685 patent/WO2005053402A2/en not_active Ceased
- 2004-12-02 JP JP2006541894A patent/JP2007513116A/ja not_active Withdrawn
- 2004-12-02 DE DE602004006020T patent/DE602004006020T2/de not_active Expired - Lifetime
- 2004-12-02 EP EP04819647A patent/EP1694122B1/en not_active Expired - Lifetime
- 2004-12-02 WO PCT/EP2004/013687 patent/WO2005053403A2/en not_active Ceased
- 2004-12-02 AT AT04803436T patent/ATE424724T1/de not_active IP Right Cessation
- 2004-12-02 DK DK04803437T patent/DK1691607T3/da active
- 2004-12-02 WO PCT/EP2004/013686 patent/WO2005053401A2/en not_active Ceased
- 2004-12-02 DE DE602004008966T patent/DE602004008966T2/de not_active Expired - Fee Related
- 2004-12-02 CA CA002547420A patent/CA2547420A1/en not_active Abandoned
- 2004-12-02 AU AU2004294712A patent/AU2004294712B2/en not_active Ceased
- 2004-12-02 ES ES04819647T patent/ES2290785T3/es not_active Expired - Lifetime
- 2004-12-02 US US10/580,700 patent/US20070259962A1/en not_active Abandoned
- 2004-12-02 AT AT04803437T patent/ATE359707T1/de not_active IP Right Cessation
- 2004-12-02 EA EA200601077A patent/EA200601077A1/ru unknown
- 2004-12-02 CN CNB2004800361682A patent/CN100438760C/zh not_active Expired - Fee Related
- 2004-12-02 BR BRPI0417060-1A patent/BRPI0417060A/pt not_active IP Right Cessation
- 2004-12-02 AP AP2006003647A patent/AP1959A/xx active
- 2004-12-02 NZ NZ547362A patent/NZ547362A/en unknown
- 2004-12-02 AR ARP040104495A patent/AR046745A1/es not_active Application Discontinuation
- 2004-12-02 SI SI200430336T patent/SI1691607T1/sl unknown
- 2004-12-02 CA CA002547412A patent/CA2547412A1/en not_active Abandoned
- 2004-12-02 MX MXPA06005988A patent/MXPA06005988A/es not_active Application Discontinuation
- 2004-12-02 DK DK04819647T patent/DK1694122T3/da active
- 2004-12-02 BR BRPI0417247-7A patent/BRPI0417247A/pt not_active IP Right Cessation
- 2004-12-02 CN CNA2004800361663A patent/CN1889833A/zh active Pending
- 2004-12-02 US US10/580,595 patent/US20070129442A1/en not_active Abandoned
- 2004-12-02 OA OA1200600173A patent/OA13292A/en unknown
- 2004-12-02 BR BRPI0417181-0A patent/BRPI0417181A/pt not_active IP Right Cessation
- 2004-12-02 SI SI200430463T patent/SI1694122T1/sl unknown
- 2004-12-02 DE DE602004019995T patent/DE602004019995D1/de not_active Expired - Fee Related
- 2004-12-02 CA CA002546110A patent/CA2546110A1/en not_active Abandoned
- 2004-12-02 JP JP2006541893A patent/JP2007513115A/ja not_active Withdrawn
- 2004-12-02 EP EP04803436A patent/EP1841317B1/en not_active Expired - Lifetime
- 2004-12-02 AR ARP040104496A patent/AR046746A1/es unknown
- 2004-12-02 KR KR1020067010797A patent/KR20060115889A/ko not_active Withdrawn
- 2004-12-02 ES ES04803437T patent/ES2285550T3/es not_active Expired - Lifetime
- 2004-12-02 JP JP2006541895A patent/JP2007513117A/ja active Pending
- 2004-12-03 TW TW093137506A patent/TW200529836A/zh unknown
- 2004-12-03 MY MYPI20045034A patent/MY137761A/en unknown
- 2004-12-03 TW TW093137470A patent/TWI304724B/zh active
- 2004-12-03 TW TW093137564A patent/TW200528022A/zh unknown
- 2004-12-03 UY UY28655A patent/UY28655A1/es unknown
- 2004-12-03 UY UY28654A patent/UY28654A1/es unknown
2006
- 2006-05-10 IL IL175544A patent/IL175544A0/en unknown
- 2006-05-17 IL IL175712A patent/IL175712A0/en unknown
- 2006-05-23 CO CO06049472A patent/CO5680375A2/es not_active Application Discontinuation
- 2006-05-23 IL IL175852A patent/IL175852A0/en unknown
- 2006-06-02 CO CO06053415A patent/CO5670341A2/es not_active Application Discontinuation
- 2006-06-05 EC EC2006006609A patent/ECSP066609A/es unknown
- 2006-06-08 NO NO20062632A patent/NO20062632L/no not_active Application Discontinuation
- 2006-06-12 EC EC2006006632A patent/ECSP066632A/es unknown
- 2006-06-13 CR CR8451A patent/CR8451A/es unknown
- 2006-07-03 ZA ZA200605459A patent/ZA200605459B/en unknown
- 2006-07-03 ZA ZA200605458A patent/ZA200605458B/en unknown
- 2006-07-03 MA MA29155A patent/MA28280A1/fr unknown
- 2006-07-03 ZA ZA200605460A patent/ZA200605460B/en unknown
- 2006-07-04 MA MA29163A patent/MA28282A1/fr unknown

Also Published As

Publication number	Publication date
TW200528022A (en)	2005-09-01
JP2007513115A (ja)	2007-05-24
EP1694122B1 (en)	2007-09-12
MA28282A1 (fr)	2006-11-01
UY28654A1 (es)	2005-06-30
JP2007513117A (ja)	2007-05-24
US20070129442A1 (en)	2007-06-07
ZA200605459B (en)	2007-11-28
BRPI0417247A (pt)	2007-03-06
IL175712A0 (en)	2006-09-05
AP2006003647A0 (en)	2006-06-30
CA2546110A1 (en)	2005-06-16
KR20060123420A (ko)	2006-12-01
EP1691607A2 (en)	2006-08-23
UA81561C2 (en)	2008-01-10
MXPA06005988A (es)	2006-08-23
JP2007513116A (ja)	2007-05-24
DE602004008966T2 (de)	2008-01-17
CA2547420A1 (en)	2005-06-16
EA200601077A1 (ru)	2006-10-27
MY137761A (en)	2009-03-31
CN100438760C (zh)	2008-12-03
EP1841317A2 (en)	2007-10-10
TW200529836A (en)	2005-09-16
DK1691607T3 (da)	2007-07-30
AU2004294299A1 (en)	2005-06-16
WO2005053403A3 (en)	2005-07-28
ATE372674T1 (de)	2007-09-15
CR8451A (es)	2006-12-07
KR20060123241A (ko)	2006-12-01
BRPI0417181A (pt)	2007-03-06
EA200601078A1 (ru)	2006-10-27
NO20062632L (no)	2006-06-27
CO5670341A2 (es)	2006-08-31
IL175544A0 (en)	2006-09-05
WO2005053401A3 (en)	2005-07-28
CN1889832A (zh)	2007-01-03
PE20050702A1 (es)	2005-10-24
ECSP066609A (es)	2006-10-25
TW200529750A (en)	2005-09-16
DE602004008966D1 (de)	2007-10-25
AR046745A1 (es)	2005-12-21
WO2005053402A3 (en)	2005-08-04
DE602004006020T2 (de)	2007-08-23
EA010019B1 (ru)	2008-06-30
CN1889834A (zh)	2007-01-03
BRPI0417060A (pt)	2007-03-27
CA2547412A1 (en)	2005-06-16
ATE424724T1 (de)	2009-03-15
PT1691607E (pt)	2007-05-31
UA79571C2 (en)	2007-06-25
AU2004294712B2 (en)	2010-04-22
EP1694122A2 (en)	2006-08-30
DE602004006020D1 (de)	2007-05-31
ATE359707T1 (de)	2007-05-15
EP1841317B1 (en)	2009-03-11
AR046746A1 (es)	2005-12-21
ZA200605460B (en)	2007-12-27
NZ547362A (en)	2008-12-24
SI1691607T1 (sl)	2007-10-31
WO2005053401A2 (en)	2005-06-16
ECSP066632A (es)	2006-10-25
AP1959A (en)	2009-02-20
US20070259962A1 (en)	2007-11-08
SI1694122T1 (sl)	2007-12-31
ES2290785T3 (es)	2008-02-16
EA200601076A1 (ru)	2006-10-27
PL1691607T3 (pl)	2007-09-28
ES2285550T3 (es)	2007-11-16
EP1691607B1 (en)	2007-04-18
PL1694122T3 (pl)	2008-01-31
DK1694122T3 (da)	2007-12-03
ZA200605458B (en)	2007-11-28
CN1889833A (zh)	2007-01-03
AU2004294712A1 (en)	2005-06-16
DE602004019995D1 (de)	2009-04-23
CO5680375A2 (es)	2006-09-29
TWI304724B (en)	2009-01-01
WO2005053403A2 (en)	2005-06-16
MA28280A1 (fr)	2006-11-01
WO2005053402A2 (en)	2005-06-16
IL175852A0 (en)	2006-10-05
KR20060115889A (ko)	2006-11-10
UY28655A1 (es)	2005-06-30
AU2004294298A1 (en)	2005-06-16

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