CS276186B6 - Algicidal composition based on 1- (2- / alkoxycarbaniloyloxycycloheptyl) / methyl / piperidinium chloride - Google Patents
Algicidal composition based on 1- (2- / alkoxycarbaniloyloxycycloheptyl) / methyl / piperidinium chloride Download PDFInfo
- Publication number
- CS276186B6 CS276186B6 CS902340A CS234090A CS276186B6 CS 276186 B6 CS276186 B6 CS 276186B6 CS 902340 A CS902340 A CS 902340A CS 234090 A CS234090 A CS 234090A CS 276186 B6 CS276186 B6 CS 276186B6
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- methyl
- piperidinium chloride
- compounds
- algal
- alkoxycarbaniloyloxycycloheptyl
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Algicídny prostriedok, ktorý ako účinnú látku obsahuje zlúčeninu obecného vzorca I, kde R je priamy alkyl s 1 až 4 atómami uhlíka. Syntéza zlúčenín podía obecného vzorca I je predmetom čs. autorského Osvedčenia č. 269023 autorov: Gregáň F., Tůmová I., Šiška J. (1989). Zlúčeniny podía vynálezu pogobia algicídne pri koncentráciách 1,74.10 mól.dm a vyš ších (tj. 7,4 mg.dm a vyšších). Zlúčeniny možno využit, samostatné alebo v zmesi s iný mi látkami ako účinnú zložku antialgálnych prípravkov.Algicidal agent, which contains as an active substance a compound of the general formula I, where R is a straight alkyl with 1 to 4 carbon atoms. The synthesis of compounds according to the general formula I is the subject of Czechoslovak Author's Certificate No. 269023 of the authors: Gregáň F., Tůmová I., Šiška J. (1989). The compounds according to the invention have an algicidal effect at concentrations of 1.74.10 mol.dm and higher (i.e. 7.4 mg.dm and higher). The compounds can be used, alone or in a mixture with other substances, as an active component of anti-algal preparations.
Description
Vynález sa týká algicídneho prostriedku, ktorý ako účinnú látku obsahuje zlúčeninu obecného vzorea IThe invention relates to an algicidal composition which contains a compound of the formula I as active ingredient
Cl /1/ kde R je priamy alkyl s 1 až 4 atómami uhlíka.Cl (1) wherein R is direct alkyl of 1 to 4 carbon atoms.
Syntéza zlúčenín obecného vzorea I je predmetom ěs. autorského osvedčenia č. 269023 autorov: Gregáň F., Tůmová I., šiška J. (1989). Tieto zlúčeniny vykazujú lokálně anestetickú účinnost.The synthesis of compounds of formula I is the subject of ees. author's certificate no. 269023 authors: Gregáň F., Tůmová I., šiška J. (1989). These compounds show local anesthetic activity.
Pri úaíšom štúdiu biologickej účinnosti zlúčenín obecného vzorea I sme zistili, že tieto výrazné inhibujú rast a syntézu chlorofylu rias.In a further study of the biological activity of the compounds of formula I, we found that these significantly inhibited the growth and synthesis of algal chlorophyll.
Inhibičná účinnost zlúčenín obecného vzorea I na riasy sa testovala stacionárnou kultiváciou synchronněj kultúry rias Chlorella vulgaris. Hodnotil sa nárast buniek rias, ako aj obsah syntetizovaného chlorofylu. Podrobný popis metody hodnotenia je uvedený v příklade 1. Miera antialgálnej účinnosti zlúčenín obecného vzorea I je vyjádřená údajmi v tab. 1.The inhibitory activity of the compounds of the formula I on algae was tested by stationary cultivation of a synchronous algal culture of Chlorella vulgaris. The growth of algal cells as well as the content of synthesized chlorophyll were evaluated. A detailed description of the evaluation method is given in Example 1. The degree of antialgal activity of the compounds of general formula I is expressed by the data in tab. 1.
Inhibičný vplyv na riasy sa sledoval u nasledujúcich zlúčenín obecného vzorea I:The inhibitory effect on algae was monitored for the following compounds of formula I:
1. 1-[ 2-(metoxykarbaniloyloxycykloheptyl)metylj piperidíniumchlorid1. 1- [2- (methoxycarbaniloyloxycycloheptyl) methyl] piperidinium chloride
2. 1- [2-(etoxykarbaniloyloxycykloheptyl)metyl] piperidíniumchlorid2. 1- [2- (ethoxycarbaniloyloxycycloheptyl) methyl] piperidinium chloride
3. 1- {2-(propoxykarbaniloyloxycykloheptyl)metyljpiperidíniumchlorid3. 1- {2- (propoxycarbaniloyloxycycloheptyl) methyl] piperidinium chloride
4. 1- £2-(butoxykarbaniloyloxycykloheptyl)metylj piperidíniumchlorid4. 1- [2- (butoxycarbaniloyloxycycloheptyl) methyl] piperidinium chloride
TABULKA 1TABLE 1
Inhibičná účinnost látok obecného vzorea I na riasy Chlorella vulgarisInhibitory activity of substances of general formula I on algae Chlorella vulgaris
IC^q značí koncentráciu študovanej látky, pri ktorej dochádza k 50 %nej inhibícii hodnoteného parametra rias vzhladom na kontrolné vzorky;IC 50 denotes the concentration of the test substance at which 50% inhibition of the evaluated algal parameter occurs relative to control samples;
MIC značí minimálnu koncentráciu študovanej látky, pri ktorej dochádza k úplnéj inhibícii hodnoteného parametra rias.MIC indicates the minimum concentration of the test substance at which complete inhibition of the evaluated algal parameter occurs.
CS 276186 B6 2CS 276186 B6 2
Nasledujúci příklad bližšie osvětluje inhibičnú účinnosE zlúčenín podlá vynálezu na zelené riasy.The following example further illustrates the inhibitory activity of the compounds of the invention on green algae.
Příklad 1Example 1
Očinok zlúčenín podía vynálezu na rast rias Chlorella vulgaris a obsah syntetizovaného chlorofyluEffect of the compounds according to the invention on the growth of the algae Chlorella vulgaris and the content of synthesized chlorophyll
Riasy Chlorella vulgaris sa pěstovali stacionárnou kultiváciou pri teplotě 25 + 1 'c, pri svetelnom režime 16 hodin světlo / 8 hodin tma, v kultivačnom médiu podlá Šetlika (šetlik I.: Annual Report of Algolog Lab. for 1967, 71 až 140, Třeboň, 1968). K živnému médiu sa přidával roztok študovanéj zlúčeniny v destilovanéj vodě takej koncentrácie, aby sa získala séria kultivačných baniek s odstupňovanou koncentráciou látky a odstupňovaným biologickým účinkom. Banky sa inokulovali přesným objemem homogénnej suspenzie rias. Po 7-dennej kultivácii sa objem kultivačného média doplnil destilovanou vodou na povodný objem (vyrovnanie odparu vody) a v suspenzii buniek sa merala absorbancia pri 660 nm (úměrná množstvu buniek rias) a obsah chlorofylu po jeho extrakcii dimetylformamidom z odcentrifugovaných buniek rias. Celkový obsah chlorofylu rias v kultivačnom médiu sa vyhodnotil -3 z podía rovnice: Chl /mg.dm /= 17,9 Ag^? + 8,08 A gg^ g, kde A je absorbancia vzorky pri ' 647, resp. 664,5 nm v 1 cm kývete (Inskeep W. P., Bloom P. R.: Plant Physiol. 77/2/, 483 až 485, 1985).Algae Chlorella vulgaris were grown by stationary cultivation at a temperature of 25 + 1 'c, in a light regime of 16 hours light / 8 hours dark, in the culture medium according to Šetlik (file I .: Annual Report of Algolog Lab. For 1967, 71 to 140, Třeboň , 1968). A solution of the study compound in distilled water of such concentration was added to the nutrient medium to obtain a series of culture flasks with a graded concentration of substance and a graded biological effect. The flasks were inoculated with the exact volume of a homogeneous algal suspension. After culturing for 7 days, the volume of the culture medium was supplemented with distilled water to the flood volume (water evaporation compensation), and the absorbance at 660 nm (proportional to the number of algal cells) and chlorophyll content after extraction with dimethylformamide from centrifuged algal cells were measured in the cell suspension. The total chlorophyll content of algae in the culture medium was evaluated -3 from the equation: Chl /mg.dm / = 17.9 Ag ^? + 8.08 A gg ^ g, where A is the absorbance of the sample at '647, resp. Swing 664.5 nm in 1 cm (Inskeep W. P., Bloom P. R .: Plant Physiol. 77/2 /, 483-485, 1985).
Získané hodnoty týchto parametrov sa porovnávali s hodnotami parametrov kontrolných vzoriek (vyhodnotené ako % kontroly). Na základe týchto hodnot sa extrapoláciou vyčíslili koncentrácie študovaných zlúčenín, pri ktorých sa dosiahla 50 %ná inhibícia (ICgg) a v případe hodnot chlorofylu aj úplná inhibícia (MIC). Z hodnot absorbancie sa MIC nevyhodnocovala, nakolko touto metodou sa stanovujú tiež odfarbené mrtvé buňky rias, a teda aj pri úplnéj inhibícii sa namerajú určité hodnoty absorbancie.The obtained values of these parameters were compared with the values of the parameters of the control samples (evaluated as% of the control). Based on these values, the concentrations of the studied compounds at which 50% inhibition (ICgg) was achieved and, in the case of chlorophyll values, also complete inhibition (MIC) were calculated by extrapolation. The MIC was not evaluated from the absorbance values, as this method also determines discolored dead algal cells, and thus certain absorbance values are measured even with complete inhibition.
Například v případe testovania účinku l-[2-(etoxykarbaniloyloxycykloheptyl)metylj piperidíniumchloridu (látka č. 2) sa k 12 ml kultivačného· média s ino kulom rias přidalo -3 -3 -3For example, in the case of testing the effect of 1- [2- (ethoxycarbaniloyloxycycloheptyl) methyl] piperidinium chloride (Compound No. 2), -3 -3 -3 was added to 12 ml of algal inoculum culture medium.
0,12 ml vodného roztoku látky č. 2 nasledovných koncentrácii: 5.10 , 2,5.10 , 1.10 , -4 -4 - -3 .0.12 ml of an aqueous solution of substance no. 2 of the following concentrations: 5.10, 2.5.10, 1.10, -4 -4 - -3.
5. 10 a 1.10 mol.dm . Skutečné koncentrácie zlúčeniny č. 2 v kultivačnom médiu a pří- slušné hodnoty inhibície rastu rias a syntézy chlorofylu, vyjádřené v % kontrolných vzoriek sú uvedené v tab. 2.5. 10 and 1.10 mol.dm. Actual concentrations of compound no. 2 in the culture medium and the respective values of inhibition of algal growth and chlorophyll synthesis, expressed in% of control samples, are given in Tab. 2.
' Hodnoty koncentrácie študovanej zlúčeniny, pri ktorých dochádza k 50 %nej, resp. úplnéj inhibícii študovaného parametra rias sa zisEuje extrapoláciou zo závislosti vyššie uvedených hodnot % zistenej inhibície sledovaného parametra od logaritmu aplikovanej koncentrácie študovanej zlúčeniny.The values of the concentration of the studied compound at which 50% or more of The complete inhibition of the algal parameter under study is obtained by extrapolation from the dependence of the above values of the% inhibition of the observed parameter on the logarithm of the applied concentration of the study compound.
TABULKA 2TABLE 2
Inhibícia rastu rias a syntézy chlorofylu v přítomnosti l-£2-(etoxykarbaniloyl-oxycykloheptyl)metylJ piperidíniumchloriduInhibition of algal growth and chlorophyll synthesis in the presence of 1- [2- (ethoxycarbanilolyloxycycloheptyl) methyl] piperidinium chloride
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS902340A CS234090A3 (en) | 1990-05-14 | 1990-05-14 | Algicide based on 1-/2-/alkoxycarbaniloyloxy) cycloheptyl/ methyl/ piperidinium chlorides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS902340A CS234090A3 (en) | 1990-05-14 | 1990-05-14 | Algicide based on 1-/2-/alkoxycarbaniloyloxy) cycloheptyl/ methyl/ piperidinium chlorides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS276186B6 true CS276186B6 (en) | 1992-04-15 |
| CS234090A3 CS234090A3 (en) | 1992-04-15 |
Family
ID=5360232
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS902340A CS234090A3 (en) | 1990-05-14 | 1990-05-14 | Algicide based on 1-/2-/alkoxycarbaniloyloxy) cycloheptyl/ methyl/ piperidinium chlorides |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS234090A3 (en) |
-
1990
- 1990-05-14 CS CS902340A patent/CS234090A3/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CS234090A3 (en) | 1992-04-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69624701T2 (en) | FREEZER PRESERVATION OF DIFFERENT PLANT CELLS | |
| US20070020384A1 (en) | Environmentally benign crop protection agents | |
| CN103145700A (en) | 2-(2-benzyl hydrazono)-4-(benzofuran-5-yl) thiazole and preparation method and application thereof | |
| KR20120071350A (en) | Synergistic combination of a glyphosate compound and ipbc | |
| CS276186B6 (en) | Algicidal composition based on 1- (2- / alkoxycarbaniloyloxycycloheptyl) / methyl / piperidinium chloride | |
| DD150841A5 (en) | INSECTICIDAL AGENTS CONTAINING SALTS OF THIAZOLYLIDENOXO-PROPIONITRILENE | |
| CS276185B6 (en) | Algicide based on 1- (2-alkoxycarbaniloyloxy) cyclohexylmethyl / dimethylammonium chloride | |
| CN109956904B (en) | Pyrazole amide compounds and their applications and fungicides | |
| CS276178B6 (en) | Algicidal composition of the type N-alkyl-4-piperidyl esters of alkoxycarbanilic acids | |
| CS276061B6 (en) | Alkoxyphenylcarbamic acid pyrrolidinoethyl esters | |
| JPS61291591A (en) | Zinc and copper complexes of methyl ester of ethylenebisdithiocarbamic acid and n-(benzimidazoyl-2)-carbamic acid and its production | |
| SK277815B6 (en) | Algicidal agent of 2-alkylthio-6-amino-benzothiazole type | |
| CS276062B6 (en) | Alkoxyphenylcarbamic acid dimethylaminoethyl ether aliphatic agent | |
| CS276184B6 (en) | Algicidal composition of the N-ethyl-2-pyrrolidinylmethyl ester type of alkoxycarbanilic acids | |
| CS275634B6 (en) | A regulating effect on algal growth and chlorophyll synthesis | |
| SK277957B6 (en) | Algicidal agent | |
| SK277958B6 (en) | Algicidal aget | |
| CS276060B6 (en) | Algicidal composition not based on piperidinoethyl esters of substituted alkoxyphenylcarbamates | |
| EP0256789B1 (en) | Substituted benzimidazole fungicide | |
| SK205592A3 (en) | Algicide agent of morpholineethylesters of substituted alcoxyphenylecarbame acids type | |
| US3245874A (en) | Cyanine dyes as an agricultural bactericide | |
| CN101020678B (en) | Trisubstituted dihydro agarofuran compound and its pesticidal activity | |
| SK278130B6 (en) | 1-methyl-2-(2-diethylaminoetoxy)-ethylesters of alkoxyphenylcarbames acids | |
| SK278131B6 (en) | 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzoxazolinthiones and method of their preparation | |
| SK278266B6 (en) | 1-methyl-2-(n-piperidinyletoxy)ethylesters alcoxyphenylalcarbame acids and method of their production |