DK169624B1 - Fremgangsmåde til bekæmpelse af mikroorganismer, heterocycliske pentalenderivater og fremgangsmåde til fremstilling af derivaterne - Google Patents

Fremgangsmåde til bekæmpelse af mikroorganismer, heterocycliske pentalenderivater og fremgangsmåde til fremstilling af derivaterne Download PDF

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Publication number: DK169624B1
Authority: DK; Denmark
Prior art keywords: general formula; sulfur; compound; derivatives; together represent
Prior art date: 1985-07-19

Application number

DK340786A

Other languages

Danish (da)

English (en)

Other versions

DK340786A (da

DK340786D0 (da

Inventor

Susan Jayne Turner

Michael Thomas Clark

Original Assignee

Shell Int Research

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.)

1985-07-19

Filing date

1986-07-17

Publication date

1994-12-27

1986-07-17 Application filed by Shell Int Research filed Critical Shell Int Research

1986-07-17 Publication of DK340786D0 publication Critical patent/DK340786D0/da

1987-01-20 Publication of DK340786A publication Critical patent/DK340786A/da

1994-12-27 Application granted granted Critical

1994-12-27 Publication of DK169624B1 publication Critical patent/DK169624B1/da

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-1 heterocyclic pentane derivatives Chemical class 0.000 title description 18
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ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000007884 disintegrant Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000008157 edible vegetable oil Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
ZIUSEGSNTOUIPT-UHFFFAOYSA-N ethyl 2-cyanoacetate Chemical compound CCOC(=O)CC#N ZIUSEGSNTOUIPT-UHFFFAOYSA-N 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000003925 fat Substances 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
210000005095 gastrointestinal system Anatomy 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000001727 glucose Nutrition 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
229940093915 gynecological organic acid Drugs 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
229940035429 isobutyl alcohol Drugs 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
229910001629 magnesium chloride Inorganic materials 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
244000000010 microbial pathogen Species 0.000 description 1
230000003158 microbiostatic effect Effects 0.000 description 1
JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003973 paint Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
229920001592 potato starch Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical class CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
238000005057 refrigeration Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000013535 sea water Substances 0.000 description 1
235000020374 simple syrup Nutrition 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000001540 sodium lactate Substances 0.000 description 1
229940005581 sodium lactate Drugs 0.000 description 1
235000011088 sodium lactate Nutrition 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
230000019086 sulfide ion homeostasis Effects 0.000 description 1
125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
239000000829 suppository Substances 0.000 description 1
239000002511 suppository base Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
230000009182 swimming Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
229940116362 tragacanth Drugs 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
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D515/04—Ortho-condensed 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
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D515/06—Peri-condensed systems
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Zoology (AREA)
Pest Control & Pesticides (AREA)
Environmental Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Oncology (AREA)
Communicable Diseases (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Steroid Compounds (AREA)
Pyridine Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DK340786A 1985-07-19 1986-07-17 Fremgangsmåde til bekæmpelse af mikroorganismer, heterocycliske pentalenderivater og fremgangsmåde til fremstilling af derivaterne DK169624B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB858518213A GB8518213D0 (en)	1985-07-19	1985-07-19	Heterocyclic pentalenes
GB8518213		1985-07-19

Publications (3)

Publication Number	Publication Date
DK340786D0 DK340786D0 (da)	1986-07-17
DK340786A DK340786A (da)	1987-01-20
DK169624B1 true DK169624B1 (da)	1994-12-27

Family

ID=10582507

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK340786A DK169624B1 (da)	1985-07-19	1986-07-17	Fremgangsmåde til bekæmpelse af mikroorganismer, heterocycliske pentalenderivater og fremgangsmåde til fremstilling af derivaterne

Country Status (23)

Country	Link
US (1)	US4737507A (de)
EP (1)	EP0219141B1 (de)
JP (1)	JPS6236388A (de)
CN (1)	CN1014062B (de)
AR (1)	AR242583A1 (de)
AT (1)	ATE57704T1 (de)
AU (1)	AU589432B2 (de)
BR (1)	BR8603374A (de)
CA (1)	CA1274833A (de)
DE (1)	DE3675142D1 (de)
DK (1)	DK169624B1 (de)
EG (1)	EG18258A (de)
GB (1)	GB8518213D0 (de)
GR (1)	GR861871B (de)
HU (1)	HU204171B (de)
MA (1)	MA20738A1 (de)
NO (1)	NO168504C (de)
NZ (1)	NZ216886A (de)
OA (1)	OA08366A (de)
PT (1)	PT83003B (de)
TN (1)	TNSN86108A1 (de)
TR (1)	TR22911A (de)
ZA (1)	ZA865329B (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU6637494A (en) *	1993-04-22	1994-11-08	Fmc Corporation	Method for treating water using an organic sanitizer and a persulfate
US20250059144A1 (en) *	2021-12-06	2025-02-20	Kaohsiung Medical University	Tellurium-containing compounds and the use of treating bacterial infections thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0068557B1 (de) *	1981-06-24	1987-12-09	Shell Internationale Researchmaatschappij B.V.	Herbizidmittel, heterocyclische Pentaleneenthaltend

1985
- 1985-07-19 GB GB858518213A patent/GB8518213D0/en active Pending
1986
- 1986-06-27 CA CA000512627A patent/CA1274833A/en not_active Expired - Lifetime
- 1986-06-30 EP EP86201145A patent/EP0219141B1/de not_active Expired - Lifetime
- 1986-06-30 AT AT86201145T patent/ATE57704T1/de not_active IP Right Cessation
- 1986-06-30 DE DE8686201145T patent/DE3675142D1/de not_active Expired - Lifetime
- 1986-07-09 US US06/883,663 patent/US4737507A/en not_active Expired - Lifetime
- 1986-07-17 DK DK340786A patent/DK169624B1/da not_active IP Right Cessation
- 1986-07-17 CN CN86104745A patent/CN1014062B/zh not_active Expired
- 1986-07-17 JP JP61166882A patent/JPS6236388A/ja active Pending
- 1986-07-17 NO NO862887A patent/NO168504C/no unknown
- 1986-07-17 NZ NZ216886A patent/NZ216886A/xx unknown
- 1986-07-17 GR GR861871A patent/GR861871B/el unknown
- 1986-07-17 AU AU60265/86A patent/AU589432B2/en not_active Ceased
- 1986-07-17 ZA ZA865329A patent/ZA865329B/xx unknown
- 1986-07-17 PT PT83003A patent/PT83003B/pt not_active IP Right Cessation
- 1986-07-17 HU HU862947A patent/HU204171B/hu not_active IP Right Cessation
- 1986-07-17 BR BR8603374A patent/BR8603374A/pt active Search and Examination
- 1986-07-17 TR TR31637A patent/TR22911A/xx unknown
- 1986-07-17 MA MA20966A patent/MA20738A1/fr unknown
- 1986-07-18 OA OA58907A patent/OA08366A/xx unknown
- 1986-07-18 TN TNTNSN86108A patent/TNSN86108A1/fr unknown
- 1986-07-20 EG EG442/86A patent/EG18258A/xx active
- 1986-07-21 AR AR86304568A patent/AR242583A1/es active

Also Published As

Publication number	Publication date
DK340786A (da)	1987-01-20
ZA865329B (en)	1987-02-25
US4737507A (en)	1988-04-12
PT83003A (en)	1986-08-01
DE3675142D1 (de)	1990-11-29
HUT42919A (en)	1987-09-28
HU204171B (en)	1991-12-30
NO168504B (no)	1991-11-25
MA20738A1 (fr)	1987-04-01
TNSN86108A1 (fr)	1990-01-01
OA08366A (en)	1988-02-29
CN86104745A (zh)	1987-01-28
EP0219141A1 (de)	1987-04-22
ATE57704T1 (de)	1990-11-15
NO862887L (no)	1987-01-20
CA1274833A (en)	1990-10-02
PT83003B (pt)	1988-07-01
AR242583A1 (es)	1993-04-30
EP0219141B1 (de)	1990-10-24
AU6026586A (en)	1987-01-22
CN1014062B (zh)	1991-09-25
NO168504C (no)	1992-03-04
TR22911A (tr)	1988-11-15
EG18258A (en)	1992-12-30
DK340786D0 (da)	1986-07-17
GB8518213D0 (en)	1985-08-29
NZ216886A (en)	1989-05-29
GR861871B (en)	1986-11-24
JPS6236388A (ja)	1987-02-17
BR8603374A (pt)	1987-02-24
NO862887D0 (no)	1986-07-17
AU589432B2 (en)	1989-10-12

Legal Events

Date	Code	Title	Description
1994-12-27	B1	Patent granted (law 1993)
1997-03-24	PBP	Patent lapsed

Publication	Publication Date	Title
EP0001312B1 (de)	1981-12-30	Neue 1,2-Dichlorcyanvinyl Sulfide, Sulfoxide und Sulfone, diese enthaltende biozide Präparate und Methode zur Hemmung von Mikroorganismen unter Verwendung dieser Verbindungen oder Präparate
EP0105548B1 (de)	1987-05-13	Propinylaminoisoxazol-Derivate
US4649154A (en)	1987-03-10	Fungicidal and/or bactericidal compositions containing nitrothiophenes, and use thereof
EP0371560B1 (de)	1993-05-05	Biozide aromatische Azocarbonsäure-Derivate
JPS5913516B2 (ja)	1984-03-30	新規２−アミノ−１，３−チアジン類の製造方法
EP0111904A2 (de)	1984-06-27	Propynylaminothiazol-Derivate
US5157051A (en)	1992-10-20	Composition and use of 3-thiocyano-2-halo-2-propenenitriles as antimicrobial agents
US4737507A (en)	1988-04-12	Heterocyclic pentalene derivatives for use in combating microorganisms
AU752376B2 (en)	2002-09-19	Xenorxides with antibacterial and antimycotic properties
US3186905A (en)	1965-06-01	Bactericidal and fungicidal dichloronitro-quinoxalines
NO166433B (no)	1991-04-15	Antimikrobielt preparat, samt anvendelse av det for aa inhibere vekst av bakterier, sopp og alger.
US5334603A (en)	1994-08-02	Composition and use of 3-phenyl-5-thiocyano-methylthio-1,3,4-thiadiazole-2(3h)thione
DK144658B (da)	1982-05-03	Fremgangsmaade til fremstilling af antibiotikum c-15003 p-4
Rollas et al.	1991	N‐[4‐(3H‐1, 3, 4‐Oxadiazoline‐2‐thion‐5‐yl) phenyl]‐N′‐substituted Thioureas: Synthesis and Antimicrobiological Activities
EP0411720A1 (de)	1991-02-06	Biozide Verbindungen
US5206227A (en)	1993-04-27	Composition and use of phosphonic acid, (2-halo-2-cyanoethenyl)-dialkyl esters as antimicrobials
US5118534A (en)	1992-06-02	Alkylthioethanamine carbamic acid derivatives and their use in biocidal compositions
US5114970A (en)	1992-05-19	Use of 3-iodo-2-chloro-2-propenenitrile as an antimicrobial
US5155119A (en)	1992-10-13	3-(2-pyridinylthio)-N-oxide, 2-halo-2-propenenitrile compounds useful as antimicrobials
US3988357A (en)	1976-10-26	Certain oxime carbonates
US5155131A (en)	1992-10-13	Alkylthioethanamine carbamic acid derivatives and their use in biocidal compositions
US5126349A (en)	1992-06-30	Composition and use of substituted 3-thio-2-propynenitriles as an industrial antimicrobial
US5270307A (en)	1993-12-14	Pyrrolo(1,2-b)-(1,2)-benzothiazin-10-one and its use as an antimicrobial
US3711605A (en)	1973-01-16	Antibiotic a150a
US4956294A (en)	1990-09-11	Culture of Streptoverticillium synroense for producing an antibacterial