CS239936B2 - Agent for improving effectiveness of growing plants in vitro - Google Patents
Agent for improving effectiveness of growing plants in vitro Download PDFInfo
- Publication number
- CS239936B2 CS239936B2 CS829321A CS932182A CS239936B2 CS 239936 B2 CS239936 B2 CS 239936B2 CS 829321 A CS829321 A CS 829321A CS 932182 A CS932182 A CS 932182A CS 239936 B2 CS239936 B2 CS 239936B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- plants
- align
- formula
- vitro
- grown
- Prior art date
Links
- 238000000338 in vitro Methods 0.000 title claims abstract description 32
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 239000007864 aqueous solution Substances 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims description 43
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 3
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims description 2
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 25
- 230000008569 process Effects 0.000 abstract description 4
- 150000001408 amides Chemical class 0.000 abstract description 2
- 150000001470 diamides Chemical class 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 99
- 240000006497 Dianthus caryophyllus Species 0.000 description 17
- 235000009355 Dianthus caryophyllus Nutrition 0.000 description 17
- 235000010633 broth Nutrition 0.000 description 16
- 239000001993 wax Substances 0.000 description 16
- 230000000644 propagated effect Effects 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 12
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 11
- 238000001727 in vivo Methods 0.000 description 11
- 239000002689 soil Substances 0.000 description 11
- -1 alkyl radical Chemical class 0.000 description 10
- LPVPNRSVMLNXGQ-UHFFFAOYSA-N 1-(azepan-1-yl)-2,2-dichloroethanone Chemical compound ClC(Cl)C(=O)N1CCCCCC1 LPVPNRSVMLNXGQ-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 150000002632 lipids Chemical class 0.000 description 7
- 241000735332 Gerbera Species 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 210000000170 cell membrane Anatomy 0.000 description 5
- 239000001963 growth medium Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 4
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 4
- 229960004488 linolenic acid Drugs 0.000 description 4
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- 230000001902 propagating effect Effects 0.000 description 4
- 230000001850 reproductive effect Effects 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 230000004083 survival effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OUYNYRUBFQVLEE-UHFFFAOYSA-N 1-(azepan-1-yl)-2-chloroethanone Chemical compound ClCC(=O)N1CCCCCC1 OUYNYRUBFQVLEE-UHFFFAOYSA-N 0.000 description 3
- VNEWJRXBYULGIA-UHFFFAOYSA-N 1-(azepan-1-yl)ethanone Chemical compound CC(=O)N1CCCCCC1 VNEWJRXBYULGIA-UHFFFAOYSA-N 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 3
- 244000172730 Rubus fruticosus Species 0.000 description 3
- 235000010419 agar Nutrition 0.000 description 3
- 235000021029 blackberry Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 244000038559 crop plants Species 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 235000011194 food seasoning agent Nutrition 0.000 description 3
- 235000020778 linoleic acid Nutrition 0.000 description 3
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000003138 primary alcohols Chemical class 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- KJSVAEGLTPBKAA-UHFFFAOYSA-N 2,2-dichloro-n-phenylacetamide Chemical compound ClC(Cl)C(=O)NC1=CC=CC=C1 KJSVAEGLTPBKAA-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 241000219094 Vitaceae Species 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 2
- 238000009395 breeding Methods 0.000 description 2
- 230000001488 breeding effect Effects 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 235000021021 grapes Nutrition 0.000 description 2
- 239000003617 indole-3-acetic acid Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- FVSBKXQDYFGZIC-UHFFFAOYSA-N n-benzyl-2,2-dichloroacetamide Chemical compound ClC(Cl)C(=O)NCC1=CC=CC=C1 FVSBKXQDYFGZIC-UHFFFAOYSA-N 0.000 description 2
- KFVGMOVXFIJZCM-UHFFFAOYSA-N n-tert-butyl-2,2-dichloroacetamide Chemical compound CC(C)(C)NC(=O)C(Cl)Cl KFVGMOVXFIJZCM-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 238000012090 tissue culture technique Methods 0.000 description 2
- BBRWUVXMQWSGEM-QQVIJGCNSA-N (Z)-hexadec-9-enoic acid octadecanoic acid (Z)-octadec-9-enoic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O BBRWUVXMQWSGEM-QQVIJGCNSA-N 0.000 description 1
- CNGCYJGUZSCNER-UULNMNGPSA-N (z)-hexadec-9-enoic acid;octadecanoic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O CNGCYJGUZSCNER-UULNMNGPSA-N 0.000 description 1
- XAEHXXXXLOJOST-UHFFFAOYSA-N 2,2-dichloro-n-cyclohexylacetamide Chemical compound ClC(Cl)C(=O)NC1CCCCC1 XAEHXXXXLOJOST-UHFFFAOYSA-N 0.000 description 1
- NUMDJEKBRCXWKQ-UHFFFAOYSA-N 2,2-dichloro-n-propan-2-ylacetamide Chemical compound CC(C)NC(=O)C(Cl)Cl NUMDJEKBRCXWKQ-UHFFFAOYSA-N 0.000 description 1
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
- MKPCNMXYTMQZBE-UHFFFAOYSA-N 7h-purin-6-amine;sulfuric acid;dihydrate Chemical compound O.O.OS(O)(=O)=O.NC1=NC=NC2=C1NC=N2.NC1=NC=NC2=C1NC=N2 MKPCNMXYTMQZBE-UHFFFAOYSA-N 0.000 description 1
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical group F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- FAIXYKHYOGVFKA-UHFFFAOYSA-N Kinetin Natural products N=1C=NC=2N=CNC=2C=1N(C)C1=CC=CO1 FAIXYKHYOGVFKA-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- RUOFIIKCANAEBW-UHFFFAOYSA-N N-Ethyl-hexahydro-1H-azepine Chemical compound CCN1CCCCCC1 RUOFIIKCANAEBW-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 241000985694 Polypodiopsida Species 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 229960001669 kinetin Drugs 0.000 description 1
- JBYXKEJXXFUJKU-UHFFFAOYSA-N n-butyl-2,2-dichloroacetamide Chemical compound CCCCNC(=O)C(Cl)Cl JBYXKEJXXFUJKU-UHFFFAOYSA-N 0.000 description 1
- XBTFKFOPYRYZDH-UHFFFAOYSA-N n-butyl-2-chloroacetamide Chemical compound CCCCNC(=O)CCl XBTFKFOPYRYZDH-UHFFFAOYSA-N 0.000 description 1
- RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000003976 plant breeding Methods 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000021749 root development Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/0018—Culture media for cell or tissue culture
- C12N5/0025—Culture media for plant cell or plant tissue culture
Landscapes
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Cell Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Cultivation Of Plants (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU813840A HU187396B (en) | 1981-12-18 | 1981-12-18 | Process for the improvement of the multiplication efficiency of cultural plants in in vitro tissue cultures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS239936B2 true CS239936B2 (en) | 1986-01-16 |
Family
ID=10965724
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS829321A CS239936B2 (en) | 1981-12-18 | 1982-12-17 | Agent for improving effectiveness of growing plants in vitro |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4554252A (xx) |
| JP (1) | JPS58165714A (xx) |
| AU (1) | AU555018B2 (xx) |
| BE (1) | BE895365A (xx) |
| BG (1) | BG37679A3 (xx) |
| BR (1) | BR8207370A (xx) |
| CA (1) | CA1179858A (xx) |
| CS (1) | CS239936B2 (xx) |
| DD (1) | DD208795A5 (xx) |
| DE (1) | DE3246864A1 (xx) |
| FR (1) | FR2518531A1 (xx) |
| GB (1) | GB2112413B (xx) |
| HU (1) | HU187396B (xx) |
| IL (1) | IL67506A (xx) |
| NL (1) | NL8204874A (xx) |
| PH (1) | PH20018A (xx) |
| PL (1) | PL132926B1 (xx) |
| SU (1) | SU1417787A3 (xx) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU182177B (en) * | 1980-08-13 | 1983-12-28 | Eszakmagyar Vegyimuevek | Composition for influencing plant growth |
| GB8616685D0 (en) * | 1986-07-09 | 1986-08-13 | Ici Plc | Micropropagation process |
| US4813997B1 (en) * | 1987-04-06 | 1995-07-18 | Cpc International Inc | Method for regulating plant growth |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4021224A (en) * | 1971-12-09 | 1977-05-03 | Stauffer Chemical Company | Herbicide compositions |
| GB2097375A (en) * | 1981-03-30 | 1982-11-03 | Murphy Chemical Ltd | Agricultural treatment using guanidated aliphatic polyamines |
-
1981
- 1981-12-18 HU HU813840A patent/HU187396B/hu not_active IP Right Cessation
-
1982
- 1982-12-12 AU AU91708/82A patent/AU555018B2/en not_active Ceased
- 1982-12-13 US US06/449,071 patent/US4554252A/en not_active Expired - Fee Related
- 1982-12-16 BG BG058926A patent/BG37679A3/xx unknown
- 1982-12-16 BE BE1/10664A patent/BE895365A/fr not_active IP Right Cessation
- 1982-12-17 CS CS829321A patent/CS239936B2/cs unknown
- 1982-12-17 FR FR8221176A patent/FR2518531A1/fr active Pending
- 1982-12-17 CA CA000418014A patent/CA1179858A/en not_active Expired
- 1982-12-17 JP JP57221755A patent/JPS58165714A/ja active Pending
- 1982-12-17 DE DE19823246864 patent/DE3246864A1/de not_active Withdrawn
- 1982-12-17 DD DD82246174A patent/DD208795A5/de unknown
- 1982-12-17 GB GB08235949A patent/GB2112413B/en not_active Expired
- 1982-12-17 PH PH28293A patent/PH20018A/en unknown
- 1982-12-17 PL PL1982239589A patent/PL132926B1/pl unknown
- 1982-12-17 NL NL8204874A patent/NL8204874A/nl not_active Application Discontinuation
- 1982-12-17 IL IL67506A patent/IL67506A/xx unknown
- 1982-12-17 BR BR8207370A patent/BR8207370A/pt unknown
- 1982-12-18 SU SU823526204A patent/SU1417787A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| GB2112413A (en) | 1983-07-20 |
| JPS58165714A (ja) | 1983-09-30 |
| FR2518531A1 (fr) | 1983-06-24 |
| SU1417787A3 (ru) | 1988-08-15 |
| GB2112413B (en) | 1985-07-24 |
| DD208795A5 (de) | 1984-04-11 |
| AU555018B2 (en) | 1986-09-11 |
| AU9170882A (en) | 1983-06-23 |
| IL67506A (en) | 1986-02-28 |
| CA1179858A (en) | 1984-12-27 |
| BR8207370A (pt) | 1983-10-18 |
| PL239589A1 (en) | 1983-06-20 |
| US4554252A (en) | 1985-11-19 |
| DE3246864A1 (de) | 1983-06-30 |
| NL8204874A (nl) | 1983-07-18 |
| BE895365A (fr) | 1983-06-16 |
| IL67506A0 (en) | 1983-05-15 |
| PL132926B1 (en) | 1985-04-30 |
| PH20018A (en) | 1986-09-01 |
| HU187396B (en) | 1985-12-28 |
| BG37679A3 (en) | 1985-07-16 |
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