PL90384B1 - - Google Patents

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Publication number: PL90384B1
Authority: PL; Poland
Prior art keywords: group; alkyl; formula; tetaine; aryl
Prior art date: 1973-07-26

Application number

PL1973164319A

Other languages

English (en)

Polish (pl)

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.)

1973-07-26

Filing date

1973-07-26

Publication date

1977-01-31

1973-07-26 Application filed filed Critical

1973-07-26 Priority to PL1973164319A priority Critical patent/PL90384B1/pl

1974-07-19 Priority to CA205,148A priority patent/CA1031326A/fr

1974-07-24 Priority to CH1022574A priority patent/CH605879A5/xx

1974-07-24 Priority to FR7425677A priority patent/FR2245649B1/fr

1974-07-24 Priority to HU74PO00000574A priority patent/HU172180B/hu

1974-07-24 Priority to DE2435618A priority patent/DE2435618C3/de

1974-07-25 Priority to SE7409675A priority patent/SE419216B/xx

1974-07-25 Priority to SU742049230A priority patent/SU593658A3/ru

1974-07-26 Priority to GB33017/74A priority patent/GB1481882A/en

1974-07-26 Priority to BE146999A priority patent/BE818150A/fr

1974-07-26 Priority to NL7410106.A priority patent/NL161753C/xx

1974-07-26 Priority to JP8595374A priority patent/JPS5331149B2/ja

1974-11-02 Priority to IN2403/CAL/74A priority patent/IN140677B/en

1976-11-05 Priority to US05/739,347 priority patent/US4092335A/en

1977-01-31 Publication of PL90384B1 publication Critical patent/PL90384B1/pl

Links

108700023668 bacilysin Proteins 0.000 claims description 24
125000000217 alkyl group Chemical group 0.000 claims description 20
XFOUAXMJRHNTOP-PFQXTLEHSA-N bacilysin Chemical compound C[C@H]([NH3+])C(=O)N[C@H](C([O-])=O)C[C@@H]1CCC(=O)[C@@H]2O[C@H]12 XFOUAXMJRHNTOP-PFQXTLEHSA-N 0.000 claims description 15
125000003710 aryl alkyl group Chemical group 0.000 claims description 14
125000003118 aryl group Chemical group 0.000 claims description 13
-1 tetaine oximes Chemical class 0.000 claims description 11
125000002252 acyl group Chemical group 0.000 claims description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
AVXURJPOCDRRFD-UHFFFAOYSA-N hydroxylamine group Chemical group NO AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
230000008569 process Effects 0.000 claims description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
235000019441 ethanol Nutrition 0.000 description 4
150000007857 hydrazones Chemical class 0.000 description 4
150000002923 oximes Chemical class 0.000 description 4
239000002904 solvent Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
GMPKIPWJBDOURN-UHFFFAOYSA-N Methoxyamine Chemical compound CON GMPKIPWJBDOURN-UHFFFAOYSA-N 0.000 description 2
108010013639 Peptidoglycan Proteins 0.000 description 2
125000000266 alpha-aminoacyl group Chemical group 0.000 description 2
230000003115 biocidal effect Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
241000194103 Bacillus pumilus Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
MNLRQHMNZILYPY-MDMHTWEWSA-N N-acetyl-alpha-D-muramic acid Chemical group OC(=O)[C@@H](C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O)[C@@H]1NC(C)=O MNLRQHMNZILYPY-MDMHTWEWSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
235000001014 amino acid Nutrition 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000002246 antineoplastic agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
210000002421 cell wall Anatomy 0.000 description 1
238000007385 chemical modification Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000012043 crude product Substances 0.000 description 1
229940127089 cytotoxic agent Drugs 0.000 description 1
238000003795 desorption Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
XNXVOSBNFZWHBV-UHFFFAOYSA-N hydron;o-methylhydroxylamine;chloride Chemical compound Cl.CON XNXVOSBNFZWHBV-UHFFFAOYSA-N 0.000 description 1
230000002779 inactivation Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
238000001819 mass spectrum Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
230000010534 mechanism of action Effects 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000000203 mixture Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
229940067157 phenylhydrazine Drugs 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011973 solid acid Substances 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Oncology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Communicable Diseases (AREA)
Agronomy & Crop Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Dentistry (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Epoxy Compounds (AREA)
Peptides Or Proteins (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

PL1973164319A 1973-07-26 1973-07-26 PL90384B1 (fr)

Priority Applications (14)

Application Number	Priority Date	Filing Date	Title
PL1973164319A PL90384B1 (fr)	1973-07-26	1973-07-26
CA205,148A CA1031326A (fr)	1973-07-26	1974-07-19	Derives de desalanyltetaine et mode de fabrication
CH1022574A CH605879A5 (fr)	1973-07-26	1974-07-24
FR7425677A FR2245649B1 (fr)	1973-07-26	1974-07-24
HU74PO00000574A HU172180B (hu)	1973-07-26	1974-07-24	Sposob poluchenija proizvodnykh alanina
DE2435618A DE2435618C3 (de)	1973-07-26	1974-07-24	Desalanyltetain-Derivate
SE7409675A SE419216B (sv)	1973-07-26	1974-07-25	Forfarande for framstellning av desalanyltetainetrar
SU742049230A SU593658A3 (ru)	1973-07-26	1974-07-25	Способ получени оксимов или гидразонов дезаланилотетаина или его производных
GB33017/74A GB1481882A (en)	1973-07-26	1974-07-26	Desalanyltetaine derivatives and the method for their preparation
BE146999A BE818150A (fr)	1973-07-26	1974-07-26	Derives de tetaine et leur procede de preparation
NL7410106.A NL161753C (nl)	1973-07-26	1974-07-26	Werkwijze voor het bereiden van tetaine- en desalanyltetaineverbindingen.
JP8595374A JPS5331149B2 (fr)	1973-07-26	1974-07-26
IN2403/CAL/74A IN140677B (fr)	1973-07-26	1974-11-02
US05/739,347 US4092335A (en)	1973-07-26	1976-11-05	Desalanyltetaine derivatives and the method for their preparation

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
PL1973164319A PL90384B1 (fr)	1973-07-26	1973-07-26

Publications (1)

Publication Number	Publication Date
PL90384B1 true PL90384B1 (fr)	1977-01-31

Family

ID=19963607

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL1973164319A PL90384B1 (fr)	1973-07-26	1973-07-26

Country Status (13)

Country	Link
JP (1)	JPS5331149B2 (fr)
BE (1)	BE818150A (fr)
CA (1)	CA1031326A (fr)
CH (1)	CH605879A5 (fr)
DE (1)	DE2435618C3 (fr)
FR (1)	FR2245649B1 (fr)
GB (1)	GB1481882A (fr)
HU (1)	HU172180B (fr)
IN (1)	IN140677B (fr)
NL (1)	NL161753C (fr)
PL (1)	PL90384B1 (fr)
SE (1)	SE419216B (fr)
SU (1)	SU593658A3 (fr)

1973
- 1973-07-26 PL PL1973164319A patent/PL90384B1/pl unknown
1974
- 1974-07-19 CA CA205,148A patent/CA1031326A/fr not_active Expired
- 1974-07-24 FR FR7425677A patent/FR2245649B1/fr not_active Expired
- 1974-07-24 HU HU74PO00000574A patent/HU172180B/hu unknown
- 1974-07-24 DE DE2435618A patent/DE2435618C3/de not_active Expired
- 1974-07-24 CH CH1022574A patent/CH605879A5/xx not_active IP Right Cessation
- 1974-07-25 SU SU742049230A patent/SU593658A3/ru active
- 1974-07-25 SE SE7409675A patent/SE419216B/xx unknown
- 1974-07-26 BE BE146999A patent/BE818150A/fr not_active IP Right Cessation
- 1974-07-26 GB GB33017/74A patent/GB1481882A/en not_active Expired
- 1974-07-26 JP JP8595374A patent/JPS5331149B2/ja not_active Expired
- 1974-07-26 NL NL7410106.A patent/NL161753C/xx not_active IP Right Cessation
- 1974-11-02 IN IN2403/CAL/74A patent/IN140677B/en unknown

Also Published As

Publication number	Publication date
NL161753C (nl)	1980-03-17
GB1481882A (en)	1977-08-03
SE7409675L (fr)	1975-01-27
DE2435618C3 (de)	1980-06-12
CA1031326A (fr)	1978-05-16
JPS5082036A (fr)	1975-07-03
JPS5331149B2 (fr)	1978-08-31
FR2245649A1 (fr)	1975-04-25
IN140677B (fr)	1976-12-11
BE818150A (fr)	1974-11-18
NL161753B (nl)	1979-10-15
NL7410106A (nl)	1975-01-28
DE2435618B2 (de)	1979-10-04
HU172180B (hu)	1978-06-28
CH605879A5 (fr)	1978-10-13
SE419216B (sv)	1981-07-20
DE2435618A1 (de)	1975-02-27
FR2245649B1 (fr)	1978-09-15
SU593658A3 (ru)	1978-02-15

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SU1600632A3 (ru)	1990-10-15	Способ получени производных гризеоловой кислоты
Harris et al.	1983	Synthesis of tert-butyl aminocarbonate, a new type of compound that can be used to acylate amines
EP0005614B1 (fr)	1982-02-24	Pseudomonate de lithium, procédé pour son isolation, son hydrolyse
US3502720A (en)	1970-03-24	N-(2-methyl-4-chlorophenyl)-formamidines
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US4077969A (en)	1978-03-07	Process for preparing azetidinone thiazolidine derivatives
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DK159449B (da)	1990-10-15	Fremgangsmaade til fremstilling af natrium-cefuroxim
EP0112629B1 (fr)	1987-04-29	Régulateurs de croissance végétale
SU423303A3 (ru)	1974-04-05	Способ получения производных цефалоспорина с
US4092335A (en)	1978-05-30	Desalanyltetaine derivatives and the method for their preparation
US3471523A (en)	1969-10-07	Conjugated vinyl azides and their preparation
US4229348A (en)	1980-10-21	Penicillanic acid derivatives
Fox et al.	1952	Studies on Antipodes. VIII. 1 Synthesis of a Series of Valine Derivatives2
EP0138708B1 (fr)	1988-08-03	Isoefrotomycine
SU1080744A3 (ru)	1984-03-15	Способ получени производных бензодиазепина
EP0075449A1 (fr)	1983-03-30	Dérivés de pénicilline
US3005843A (en)	1961-10-24	O-carbazyl-dl-serine
PL98154B1 (pl)	1978-04-29	Sposob otrzymywania n-acylowych pochodnych estrow i/lub oksymow oraz hydrazonow dezalanylotetainy