CN107950546A - Application of the Isoquinolinium Alkaloid in terms of as herbicide - Google Patents

Application of the Isoquinolinium Alkaloid in terms of as herbicide Download PDF

Info

Publication number
CN107950546A
CN107950546A CN201711158169.XA CN201711158169A CN107950546A CN 107950546 A CN107950546 A CN 107950546A CN 201711158169 A CN201711158169 A CN 201711158169A CN 107950546 A CN107950546 A CN 107950546A
Authority
CN
China
Prior art keywords
herbicide
coptisine
grass
sanguinarine
tetrahydropalmatine
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
CN201711158169.XA
Other languages
Chinese (zh)
Other versions
CN107950546B (en
Inventor
周利娟
黄继光
田延琴
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
South China Agricultural University
Original Assignee
South China Agricultural University
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.)
Filing date
Publication date
Application filed by South China Agricultural University filed Critical South China Agricultural University
Priority to CN202010382978.4A priority Critical patent/CN111642508B/en
Priority to CN202010389612.XA priority patent/CN111480654B/en
Priority to CN202010383789.9A priority patent/CN111557303B/en
Priority to CN202010390208.4A priority patent/CN111493080B/en
Priority to CN201711158169.XA priority patent/CN107950546B/en
Publication of CN107950546A publication Critical patent/CN107950546A/en
Application granted granted Critical
Publication of CN107950546B publication Critical patent/CN107950546B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, 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

Abstract

The invention discloses application of the Isoquinolinium Alkaloid in terms of as herbicide.Present invention research is found, Isoquinolinium Alkaloid, specifically hydrochloric acid coptisine, dehydrocorydaline, palmatine, dihydroberberine, Corydalis Saxicolae, coptisine, epiberberine, N-1, worenine, Tetrahydrocoptisine, Corydaline, rotundin, dextrorotation tetrahydropalmatine, berberrubine, jateorrhizine, Sanguinarine hydrochloride, allocryptopine, tetrahydropalmatine, oxyberberine, remove methylene jamaicin and sanguinarine, to arabidopsis, Mikania micrantha, eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, a variety of common weeds such as duckweed are respectively provided with significant herbicidal effect, it is and environmentally safe, to people and animals' low toxicity, herbicide use can be prepared into, for carrying out preventing and kill off for weeds in actual production, environmental protection, safety.In addition, the exploitation of such material herbicide effect, can promote the comprehensive utilization of its resource plant, development prospect is wide.

Description

Application of the Isoquinolinium Alkaloid in terms of as herbicide
Technical field
The invention belongs to agricultural chemicals research and development technical field.More particularly, to Isoquinolinium Alkaloid as weeding Application in terms of agent.
Background technology
Herbicide(herbicide)Refer to make weeds that withered medicament thoroughly or selectively occur, eliminating or Suppress a kind of material of plant growth.Currently, efficient, low toxicity, the herbicide kind of wide spectrum, play increasingly in agricultural production Important effect.
Alkaloid is to be present in nature(Predominantly plant, but some exists in animal)In a kind of nitrogenous alkalescence Organic compound.Lot of documents reports the medical and agricultural effect of alkaloid compound, and alkaloids substance is vdiverse in function, Tool has been widely used in daily life, and plays huge effect in terms of medicine and agricultural.
Further research and development alkaloids substance has broad application prospects and significant social effect.It is this to grind Study carefully and develop including two aspects, when to having determined that the alkaloids substance of structure further develops its new application, second, Study and find new alkaloids substance, and its clear and definite physiological function, develop as social production and people's service for life Good product.
The content of the invention
The technical problem to be solved in the present invention is the defects of overcoming the above-mentioned prior art and deficiency, there is provided one kind has weeding Activity isoquinoline alkaloid, be specifically hydrochloric acid coptisine, dehydrocorydaline, palmatine, dihydroberberine, Corydalis Saxicolae, Coptisine, epiberberine, N-1, worenine, Tetrahydrocoptisine, Corydaline, rotundin, dextrorotation tetrahydrochysene bar Ma Ting, berberrubine, jateorrhizine, Sanguinarine hydrochloride, allocryptopine, tetrahydropalmatine, oxyberberine, go methylene small Bark of a cork tree alkali, sanguinarine;These alkaloids substances are for arabidopsis, Mikania micrantha, eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, floating Duckweed etc. has good activity of weeding, environmentally safe, to people and animals' low toxicity, can be prepared into herbicide use.
The object of the present invention is to provide application of the Isoquinolinium Alkaloid in terms of as herbicide.
Another object of the present invention is to provide a kind of herbicide.
Above-mentioned purpose of the present invention is achieved through the following technical solutions:
Isoquinolinium Alkaloid as or application in terms of preparing herbicide.
The isoquinoline alkaloid for hydrochloric acid coptisine, dehydrocorydaline, palmatine, dihydroberberine, Corydalis Saxicolae, Coptisine, epiberberine, N-1, worenine, Tetrahydrocoptisine, Corydaline, rotundin, dextrorotation tetrahydrochysene bar Ma Ting, berberrubine, jateorrhizine, Sanguinarine hydrochloride, allocryptopine, tetrahydropalmatine, oxyberberine, go methylene small Bark of a cork tree alkali or sanguinarine.
Preferably, the effective object of herbicide described in above application is arabidopsis, Mikania micrantha, eleusine indica, lady's-grass, three leaves Beggar-ticks, feather cockscomb, duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, Bermuda grass, the rhizome of nutgrass flatsedge, cyperus iria, Ageratum conyzoides, dent The common the worst weeds such as amaranth, Amaranthus retroflexus, concave head amaranth and/or Hairy Bittercress.
Particularly preferably:To Mikania micrantha activity of weeding most preferably:Worenine, hydrochloric acid coptisine, N-1, Dehydrocorydaline, dextrorotation tetrahydropalmatine, Corydalis Saxicolae, rotundin, Tetrahydrocoptisine, dihydroberberine, palmatine, corydalis tuber A prime.
To bidens pilosa activity of weeding most preferably:Hydrochloric acid coptisine, Tetrahydrocoptisine, dehydrocorydaline, palmatine, N-1, epiberberine, coptisine.
To eleusine indica activity of weeding most preferably:Epiberberine, Tetrahydrocoptisine, dehydrocorydaline, hydrochloric acid coptisine, bar Ma Ting, tetrahydropalmatine, rotundin, berberrubine, coptisine, dihydroberberine, allocryptopine, Corydaline, methyl yellow Even alkali, jateorrhizine.
To lady's-grass activity of weeding most preferably:Coptisine, worenine, dextrorotation tetrahydropalmatine, Corydaline, salt Sour coptisine, palmatine, epiberberine, Corydalis Saxicolae, dehydrocorydaline, dihydroberberine, jateorrhizine, rotundin, salt Sour sanguinarine, N-1, berberrubine.
To feather cockscomb activity of weeding most preferably:Remove methylene jamaicin, hydrochloric acid coptisine, oxyberberine, hydrochloric acid red root Alkali, epiberberine, dihydroberberine, coptisine, palmatine, berberrubine, dehydrocorydaline, Corydalis Saxicolae.
To arabidopsis activity of weeding most preferably:Hydrochloric acid coptisine, worenine, dihydroberberine.
To duckweed activity of weeding most preferably:Hydrochloric acid coptisine, worenine, dehydrocorydaline, dihydroberberine, Huang Even alkali, Corydalis Saxicolae, Sanguinarine hydrochloride, sanguinarine.
It is highly preferred that to Mikania micrantha activity of weeding most preferably:It is worenine, hydrochloric acid coptisine, N-1, de- Hydrogen corydaline, dextrorotation tetrahydropalmatine, Corydalis Saxicolae.
To bidens pilosa activity of weeding most preferably:Coptisine, hydrochloric acid coptisine, Tetrahydrocoptisine.
To eleusine indica activity of weeding most preferably:Epiberberine, Tetrahydrocoptisine, dehydrocorydaline, hydrochloric acid coptisine, bar Ma Ting, tetrahydropalmatine, rotundin, berberrubine, coptisine, dihydroberberine, allocryptopine, Corydaline, methyl yellow Even alkali, jateorrhizine, obvious to the root long inhibiting rate of eleusine indica, more than 75%, effect exceedes jamaicin.
To lady's-grass activity of weeding most preferably:Coptisine, worenine, Corydaline, hydrochloric acid coptisine, bar horse Spit of fland, epiberberine, rotundin, Sanguinarine hydrochloride.
To feather cockscomb activity of weeding most preferably:Go methylene jamaicin, hydrochloric acid coptisine, oxyberberine, epiberberine, Coptisine, palmatine.
To arabidopsis activity of weeding most preferably:Hydrochloric acid coptisine, worenine.
To duckweed activity of weeding most preferably:Hydrochloric acid coptisine, worenine, coptisine, sanguinarine.
A kind of herbicide containing above-mentioned isoquinoline alkaloid is also within protection scope of the present invention.
Preferably, the herbicide is for arabidopsis, Mikania micrantha, eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, floating Duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, Bermuda grass, the rhizome of nutgrass flatsedge, cyperus iria, Ageratum conyzoides, purslane, Amaranthus retroflexus, concave head The herbicide of the common the worst weeds such as amaranth and/or Hairy Bittercress.
The following achievement in research of above-mentioned aspect content and application based on the present inventor seminar:Seminar is in research process In, found by test of many times, a variety of isoquinoline alkaloid class materials are to a variety of weeds(Including a variety of invasive weeds)Have There is significant herbicidal effect.Specific isoquinoline alkaloid class includes above-mentioned hydrochloric acid coptisine, dehydrocorydaline, bar horse Spit of fland, dihydroberberine, Corydalis Saxicolae, coptisine, epiberberine, N-1, worenine, Tetrahydrocoptisine, prolong recklessly Suo Jiasu, rotundin, dextrorotation tetrahydropalmatine, berberrubine, jateorrhizine, Sanguinarine hydrochloride, allocryptopine, corydalis tuber second Element, oxyberberine, remove methylene jamaicin and sanguinarine.By experiment, find this kind of material to arabidopsis(Wild type), common vetch Camomile, eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, Bermuda grass, rhizoma cyperi The weeds such as son, cyperus iria, Ageratum conyzoides, purslane, Amaranthus retroflexus, concave head amaranth and/or Hairy Bittercress have significant activity of weeding.
The invention has the advantages that:
The invention discloses new application of the Isoquinolinium Alkaloids material as herbicide, this kind of material can significantly press down Arabidopsis processed, Mikania micrantha, eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, dog The root growth of the weeds such as root of the tooth, the rhizome of nutgrass flatsedge, cyperus iria, Ageratum conyzoides, purslane, Amaranthus retroflexus, concave head amaranth and/or Hairy Bittercress or plant Strain growth, herbicidal effect are notable.
In addition, such material derives from a wealth of sources, raw material is easy to get, and comes from naturally, there is smoothly degraded way in nature Footpath, pollution-free, noresidue will not generation environment pollution.
Furthermore isoquinoline alkaloid class material mostly there is certain insecticidal and antibacterial to act on, while management of weeds, Also there is control action to crop pests and disease, produce the effect that a medicine uses.
4th, the research and development of such material herbicide effect, can promote the comprehensive exploitation containing such material plant resources Utilize.
Embodiment
Further illustrate the present invention below in conjunction with specific embodiment, but embodiment the present invention is not done it is any type of Limit.Unless stated otherwise, the reagent of the invention used, method and apparatus is the art conventional reagent, methods and apparatus.
Unless stated otherwise, following embodiments agents useful for same and material are purchased in market.
Following embodiments list the weeding experiment of several frequently seen weeds, and it is more significant that data only give effect.
Embodiment 1 tests the activity of weeding of Mikania micrantha
1st, nearly 40 kinds of isoquinoline alkaloid materials are configured to certain density mother liquor respectively, then with Huo Gelan nutrient solutions It is diluted to 10 mg/L concentration.
2nd, using jamaicin as reference, activity of weeding of these materials to Mikania micrantha is determined using small-radius curve track, is grown 7 days Plant strain growth situation is investigated afterwards.
3rd, the results show that 11 kinds of isoquinoline alkaloid class materials as shown in table 1, i.e. worenine, hydrochloric acid Huang Even alkali, N-1, dehydrocorydaline, dextrorotation tetrahydropalmatine, Corydalis Saxicolae, rotundin, Tetrahydrocoptisine, dihydro barberry Alkali, palmatine, Corydaline, all show Mikania micrantha good inhibitory action, under 10 mg/L concentration, to Mikania micrantha Root long inhibiting rate more than 65%, to the fresh weight inhibition of Mikania micrantha more than 70%.
Wherein, hydrochloric acid coptisine, worenine, dehydrocorydaline, N-1 are to the root long inhibiting rate of Mikania micrantha Exceed 80% with fresh weight inhibition.
Inhibitory action of the table 1 to Mikania micrantha
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Worenine 89.19±0.87a 87.93±0.90a
Hydrochloric acid coptisine 88.27±1.65ab 85.92±3.82ab
N-1 88.65±17.84ab 84.00±15.66ab
Dehydrocorydaline 84.36±16.30ab 84.38±15.93ab
Dextrorotation tetrahydropalmatine 76.21±8.60abc 75.78±11.47ab
Corydalis Saxicolae 75.38±6.23abc 78.01±3.47ab
Rotundin 71.24±1.48bc 70.97±1.09ab
Tetrahydrocoptisine 71.07±5.03bc 77.41±5.43ab
Dihydroberberine 67.20±4.58bc 78.16±7.06ab
Palmatine 66.15±2.83bc 74.48±2.53ab
Corydaline 65.02±5.44bc 70.52±7.02ab
Jamaicin 70.20±6.69abc 74.90±8.72ab
Note:The measured concentration of all medicaments is 10 mg/L;Represented in table after same column numerical value with the identical person of lowercase 0.05 Difference is not notable in level.
Embodiment 2 tests the activity of weeding of bidens pilosa
1st, with embodiment 1, subjects are changed to bidens pilosa, these materials are determined using small-radius curve track for test method and setting To the activity of weeding of bidens pilosa, growth investigates plant strain growth situation after 7 days.
2nd, the results show that bidens pilosa seminal root cannot normally be grown, some root rots;As shown in table 27 kinds are different Quinoline alkaloid class material, i.e. hydrochloric acid coptisine, Tetrahydrocoptisine, dehydrocorydaline, palmatine, N-1, table are small Bark of a cork tree alkali, coptisine, show bidens pilosa preferable activity of weeding.
Wherein, hydrochloric acid coptisine, Tetrahydrocoptisine, dehydrocorydaline to the root long inhibiting rate of bidens pilosa 80% More than;Tetrahydrocoptisine and coptisine show bidens pilosa good fresh weight inhibitory activity, its activity is substantially better than small Bark of a cork tree alkali.
Inhibitory action of the table 2 to bidens pilosa
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Hydrochloric acid coptisine 89.28±0.81a 6.46±0.64ef
Tetrahydrocoptisine 82.82±0.22bc 42.56±0.49b
Dehydrocorydaline 81.33±1.05bc 11.54±0.77d
Palmatine 79.82±0.92c 14.26±0.57d
N-1 66.07±3.35d 9.82±0.45de
Epiberberine 60.84±1.87e -3.90±1.51f
Coptisine 53.47±2.50f 48.56±2.40a
Jamaicin 85.18±0.44ab 24.37±1.81c
Note:The measured concentration of all medicaments is 10 mg/L;Represented in table after same column numerical value with the identical person of lowercase 0.05 Difference is not notable in level.
Embodiment 3 tests the activity of weeding of eleusine indica
1st, with embodiment 1, subjects are changed to eleusine indica, these materials are determined to ox using small-radius curve track for test method and setting The activity of weeding of muscle grass, growth investigate plant strain growth situation after 7 days.
2nd, the results show that 18 kinds of isoquinoline alkaloid class materials as shown in table 3, i.e. epiberberine, the tetrahydrochysene coptis Alkali, dehydrocorydaline, hydrochloric acid coptisine, palmatine, tetrahydropalmatine, rotundin, berberrubine, coptisine, dihydroberberine, Allocryptopine, Corydaline, worenine, jateorrhizine, it is obvious to the root long inhibiting rate of eleusine indica, more than 70%, absolutely Major part is more than 80%, even more than 90%.
Inhibitory action of the table 3 to eleusine indica
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Epiberberine 94.66±0.08a 40.83±2.05ef
Tetrahydrocoptisine 92.53±0.26ab 71.69±1.49a
Dehydrocorydaline 91.11±0.28bc 28.86±0.84k
Hydrochloric acid coptisine 90.02±0.91bcd 32.54±1.44hijk
Palmatine 88.54±0.92cde 31.08±1.89ijk
Tetrahydropalmatine 87.18±0.49def 37.41±0.47fg
Rotundin 85.41±0.25efg 29.47±1.29jk
Berberrubine 85.92±0.70efg 33.48±0.60ghij
Coptisine 84.03±0.34fg 53.93±0.23c
Dihydroberberine 82.84±1.12gh 55.42±0.86c
Allocryptopine 80.59±0.33hi 40.83±2.04ef
Corydaline 79.53±0.32i 54.45±0.45c
Worenine 77.60±1.46i 48.89±0.20d
Jateorrhizine 72.70±0.46j 31.19±0.81ijk
Sanguinarine 70.17±1.06jk 42.81±0.34e
Dextrorotation tetrahydropalmatine 67.10±0.15k 29.09±0.75k
N-1 63.54±1.33l 56.87±1.97c
Corydalis Saxicolae 61.49±1.07l 47.70±0.46d
Jamaicin 72.62±1.33j 64.57±2.46b
Note:The measured concentration of all medicaments is 10 mg/L.Represented in table after same column numerical value with the identical person of lowercase 0.05 Difference is not notable in level.
Embodiment 4 tests the activity of weeding of lady's-grass
1st, with embodiment 1, subjects are changed to lady's-grass, these materials are determined to lady's-grass using small-radius curve track for test method and setting Activity of weeding, growth 7 days after investigate plant strain growth situation.
2nd, the results show that 15 kinds of isoquinoline alkaloid class materials as shown in table 4, i.e. coptisine, worenine, Dextrorotation tetrahydropalmatine, Corydaline, hydrochloric acid coptisine, palmatine, epiberberine, Corydalis Saxicolae, dehydrocorydaline, dihydro Jamaicin, jateorrhizine, rotundin, Sanguinarine hydrochloride, N-1, berberrubine, show lady's-grass root long suppression System and fresh weight inhibitory action, under the processing of 10 mg/L concentration, root long inhibiting rate is more than 50%, and most of more than 80%, explanation can Suppress the root growth of monocotyledon weed lady's-grass.Totally show that these materials have significant control potentiality to lady's-grass.
Inhibitory action of the table 4 to lady's-grass
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Coptisine 93.09±0.27a 54.34±0.44a
Worenine 90.29±0.09bc 49.65±1.37b
Dextrorotation tetrahydropalmatine 88.50±0.23bc 31.12±0.51g
Corydaline 87.56±0.91c 40.21±1.36c
Hydrochloric acid coptisine 84.77±0.23d 38.32±0.22cd
Palmatine 79.00±0.77e 38.92±1.47cd
Epiberberine 78.94±0.32e 37.83±0.45cd
Corydalis Saxicolae 76.62±0.76e 20.45±1.14i
Dehydrocorydaline 73.98±0.85f 33.58±0.38fg
Dihydroberberine 72.42±0.36f 31.15±0.84g
Jateorrhizine 65.97±1.88g 31.08±0.69g
Rotundin 65.41±1.19gh 36.49±0.76de
Sanguinarine hydrochloride 62.80±0.98h 35.09±0.93ef
N-1 54.15±1.17i 24.23±0.74h
Berberrubine 53.97±1.26i 25.34±1.17h
Jamaicin 90.84±0.26ab 34.68±1.17ef
Note:The measured concentration of all medicaments is 10mg/L;Represented in table after same column numerical value with the identical person of lowercase in 0.05 water Flat upper difference is not notable.
Embodiment 5 tests the activity of weeding of feather cockscomb
1st, with embodiment 1, subjects are changed to feather cockscomb, these materials are determined to feather cockscomb using small-radius curve track for test method and setting Activity of weeding, growth 7 days after investigate plant strain growth situation.
2nd, the results show that 11 kinds of isoquinoline alkaloid class materials as shown in table 5, that is, remove methylene jamaicin, salt It is sour coptisine, oxyberberine, Sanguinarine hydrochloride, epiberberine, dihydroberberine, coptisine, palmatine, berberrubine, de- Hydrogen corydaline, Corydalis Saxicolae, show feather cockscomb root long suppression and fresh weight inhibitory action, under the processing of 10mg/L concentration, root long Inhibiting rate, wherein going methylene jamaicin, the inhibiting rate of hydrochloric acid coptisine to be up to more than 90%, is shown excellent more than 50% Root growth inhibitory action.
Wherein, methylene jamaicin, hydrochloric acid coptisine, oxyberberine, coptisine etc. is gone to suppress notable to feather cockscomb fresh weight, Illustrate that the growth to feather cockscomb has inhibition.
Inhibitory action of the table 5 to feather cockscomb
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Remove methylene jamaicin 96.53±0.29a 75.68±0.86a
Hydrochloric acid coptisine 94.71±0.29a 58.18±1.65c
Oxyberberine 77.71±3.03b 69.31±1.62b
Sanguinarine hydrochloride 75.93±1.58b 15.64±1.40gh
Epiberberine 65.01±1.09c 25.49±1.68e
Dihydroberberine 61.30±1.33cd 12.88±0.40gh
Coptisine 56.01±3.58de 35.09±1.80d
Palmatine 54.68±1.02edf 26.37±1.64e
Berberrubine 55.74±2.25de 10.98±0.94h
Dehydrocorydaline 52.87±3.44efg 14.64±1.90gh
Corydalis Saxicolae 51.86±2.73efg 13.84±0.57gh
Jamaicin 77.31±0.89b 23.32±3.14ef
Note:The measured concentration of all medicaments is 10mg/L;Represented in table after same column numerical value with the identical person of lowercase in 0.05 water Flat upper difference is not notable.
Embodiment 6 tests the activity of weeding of arabidopsis
1st, with embodiment 1, subjects are changed to arabidopsis, these materials are determined to intending using small-radius curve track for test method and setting The activity of weeding of southern mustard, growth investigate plant strain growth situation after 7 days.
2nd, the results show that 3 kinds of isoquinoline alkaloid class materials as shown in table 6, i.e. hydrochloric acid coptisine, the methyl coptis Alkali, dihydroberberine, show arabidopsis significant inhibitory action, and arabidopsis growth is extremely slow, and root is unable to normal growth, Root long inhibiting rate shows preferable activity of weeding more than 80%.
Inhibitory action of the table 6 to arabidopsis
Medicament Root long inhibiting rate(%±SE) Fresh weight inhibition(%±SE)
Hydrochloric acid coptisine 85.26±0.75a 64.43±0.89a
Worenine 87.66±0.57a 65.46±1.36a
Dihydroberberine 80.39±1.30a 27.84±0.52c
Jamaicin 84.73±0.77a 60.71±1.35a
Note:The measured concentration of all medicaments is 10mg/L;Represented in table after same column numerical value with the identical person of lowercase in 0.05 water Flat upper difference is not notable.
Embodiment 7 tests the activity of weeding of duckweed
1st, with embodiment 1, subjects are changed to duckweed, these materials are determined to duckweed using water culture for test method and setting Activity of weeding, growth 7 days after investigate its chlorophyll content.
2nd, the results show that 8 kinds of isoquinoline alkaloid class materials as shown in table 7, i.e. hydrochloric acid coptisine, the methyl coptis Alkali, dehydrocorydaline, dihydroberberine, coptisine, Corydalis Saxicolae, Sanguinarine hydrochloride, sanguinarine, chlorophyll a, leaf to duckweed The synthesis of green element b and chlorophyll have obvious inhibitory action, illustrate that it can inhibit the growth of aquatic weed duckweed.
Wherein in addition to Corydalis Saxicolae, other several materials have exceeded duckweed chlorophyll inhibiting rate 70%, and major part exists More than 80% even more than 90%, the symptoms such as withered and yellow, wilting are shown for the duckweed of examination, illustrate that these compounds have good suppress The effect of duckweed growth.
Inhibitory action of the table 7 to duckweed
Note:The measured concentration of all medicaments is 10mg/L;Represented in table after same column numerical value with the identical person of lowercase in 0.05 water Flat upper difference is not notable.
Above-described embodiment is the preferable embodiment of the present invention, but embodiments of the present invention and from above-described embodiment Limitation, other any Spirit Essences without departing from the present invention with made under principle change, modification, replacement, combine, simplification, Equivalent substitute mode is should be, is included within protection scope of the present invention.

Claims (4)

1. Isoquinolinium Alkaloid as or application in terms of preparing herbicide, it is characterised in that the iloquinoline derivative Alkaloid is hydrochloric acid coptisine, dehydrocorydaline, palmatine, dihydroberberine, Corydalis Saxicolae, coptisine, epiberberine, tetrahydrochysene Jamaicin, worenine, Tetrahydrocoptisine, Corydaline, rotundin, dextrorotation tetrahydropalmatine, berberrubine, Africa are anti- Own alkali, Sanguinarine hydrochloride, allocryptopine, tetrahydropalmatine, oxyberberine, remove methylene jamaicin or sanguinarine.
2. application according to claim 1, it is characterised in that the effective object of the herbicide for arabidopsis, Mikania micrantha, Eleusine indica, lady's-grass, bidens pilosa, feather cockscomb, duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, Bermuda grass, the rhizome of nutgrass flatsedge, crack rice Nutgrass flatsedge, Ageratum conyzoides, purslane, Amaranthus retroflexus, concave head amaranth and/or Hairy Bittercress.
3. a kind of herbicide, it is characterised in that yellow containing hydrochloric acid coptisine, dehydrocorydaline, palmatine, dihydroberberine, rock Even alkali, coptisine, epiberberine, N-1, worenine, Tetrahydrocoptisine, Corydaline, rotundin, dextrorotation Tetrahydropalmatine, berberrubine, jateorrhizine, Sanguinarine hydrochloride, allocryptopine, tetrahydropalmatine, oxyberberine, go to Asia One or more in methyl jamaicin, sanguinarine.
4. herbicide according to claim 3, it is characterised in that the herbicide is for arabidopsis, Mikania micrantha, Cowhells Grass, lady's-grass, bidens pilosa, feather cockscomb, duckweed, barnyard grass, green bristlegrass, amur foxtail, annual bluegrass, Bermuda grass, the rhizome of nutgrass flatsedge, crack rice Sha Grass, Ageratum conyzoides, purslane, Amaranthus retroflexus, the herbicide of concave head amaranth and/or Hairy Bittercress.
CN201711158169.XA 2017-11-20 2017-11-20 Application of isoquinoline alkaloids as herbicide Active CN107950546B (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CN202010382978.4A CN111642508B (en) 2017-11-20 2017-11-20 Application of corydaline substances as herbicide
CN202010389612.XA CN111480654B (en) 2017-11-20 2017-11-20 Application of coptisine substances as herbicide
CN202010383789.9A CN111557303B (en) 2017-11-20 2017-11-20 Use of allocryptopine as herbicide
CN202010390208.4A CN111493080B (en) 2017-11-20 2017-11-20 Application of berberine compounds as herbicide
CN201711158169.XA CN107950546B (en) 2017-11-20 2017-11-20 Application of isoquinoline alkaloids as herbicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711158169.XA CN107950546B (en) 2017-11-20 2017-11-20 Application of isoquinoline alkaloids as herbicide

Related Child Applications (4)

Application Number Title Priority Date Filing Date
CN202010382978.4A Division CN111642508B (en) 2017-11-20 2017-11-20 Application of corydaline substances as herbicide
CN202010390208.4A Division CN111493080B (en) 2017-11-20 2017-11-20 Application of berberine compounds as herbicide
CN202010383789.9A Division CN111557303B (en) 2017-11-20 2017-11-20 Use of allocryptopine as herbicide
CN202010389612.XA Division CN111480654B (en) 2017-11-20 2017-11-20 Application of coptisine substances as herbicide

Publications (2)

Publication Number Publication Date
CN107950546A true CN107950546A (en) 2018-04-24
CN107950546B CN107950546B (en) 2021-01-26

Family

ID=61965114

Family Applications (5)

Application Number Title Priority Date Filing Date
CN202010383789.9A Active CN111557303B (en) 2017-11-20 2017-11-20 Use of allocryptopine as herbicide
CN202010382978.4A Active CN111642508B (en) 2017-11-20 2017-11-20 Application of corydaline substances as herbicide
CN201711158169.XA Active CN107950546B (en) 2017-11-20 2017-11-20 Application of isoquinoline alkaloids as herbicide
CN202010390208.4A Active CN111493080B (en) 2017-11-20 2017-11-20 Application of berberine compounds as herbicide
CN202010389612.XA Active CN111480654B (en) 2017-11-20 2017-11-20 Application of coptisine substances as herbicide

Family Applications Before (2)

Application Number Title Priority Date Filing Date
CN202010383789.9A Active CN111557303B (en) 2017-11-20 2017-11-20 Use of allocryptopine as herbicide
CN202010382978.4A Active CN111642508B (en) 2017-11-20 2017-11-20 Application of corydaline substances as herbicide

Family Applications After (2)

Application Number Title Priority Date Filing Date
CN202010390208.4A Active CN111493080B (en) 2017-11-20 2017-11-20 Application of berberine compounds as herbicide
CN202010389612.XA Active CN111480654B (en) 2017-11-20 2017-11-20 Application of coptisine substances as herbicide

Country Status (1)

Country Link
CN (5) CN111557303B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108849942A (en) * 2018-09-05 2018-11-23 西南大学 A kind of jamaicin soluble granula and preparation method thereof
CN110787162A (en) * 2019-12-09 2020-02-14 朱峰 Use of methylprednisolone coptisine as JNK2 kinase inhibitor and for treating psoriasis

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1687061A (en) * 2005-03-29 2005-10-26 沈阳化工研究院 Compound of isobioquin group and application thereof
CN101044883A (en) * 2006-03-28 2007-10-03 北京资源亚太饲料科技有限公司 Feed additive for enhancing domestic animals or birds eating food and then accelerating their growth
CN101874830A (en) * 2009-04-30 2010-11-03 成都中医药大学 New application of golden thread processed product
CN102100694A (en) * 2011-02-18 2011-06-22 浙江大学 Application of tetrahydropalmatine enantiomers in preparation of P-glycoprotein inhibitor
CN102349520A (en) * 2011-08-25 2012-02-15 华南农业大学 Application of berberine as herbicide
CN105075630A (en) * 2015-08-31 2015-11-25 莫玲 Safflower planting method
CN105726539A (en) * 2016-02-25 2016-07-06 吉林大学 Application of sanguinarine hydrochloride to preparation of medicine for treating salmonella infection
CN105766977A (en) * 2016-05-13 2016-07-20 创新美兰(合肥)股份有限公司 Dicamba, nicosulfuron and mesotrione compound dispersible oil suspension concentrate and preparation method thereof
CN105941431A (en) * 2016-05-13 2016-09-21 创新美兰(合肥)股份有限公司 Pretilachlor, cyhalofop-butyl and penoxsulam compounded dispersible oil suspension agent and preparation method thereof
CN106818831A (en) * 2017-01-24 2017-06-13 贵州省武陵山药用植物白芨开发有限公司 A kind of special herbicide of bletilla striata and its application

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1316994B1 (en) * 2000-02-25 2003-05-26 Michelangelo Leis USE OF PIPERIDINE BENZODERIVATES AS FUNGICIDES.
CN1827618A (en) * 2005-03-04 2006-09-06 周桂华 Isoquinoline derivatives and their preparation process and application
CN1857421A (en) * 2006-03-07 2006-11-08 邹广 Preparing method of total corydaline extract and corydalis preparation
CN101401579A (en) * 2008-11-14 2009-04-08 曾建国 Uses of allocryptopine in agricultural pesticide
CN102067847B (en) * 2010-11-19 2015-07-22 浙江农林大学 Preservative combination containing Chinese herbal medicine extract components and application thereof
MX2011010032A (en) * 2011-09-23 2013-03-25 Promotora Tecnica Ind S A De C V Pesticide made of isoquinoline alkaloids, flavonoids and vegetable and/or essential oils.
CN103284998A (en) * 2012-02-28 2013-09-11 中国医学科学院药用植物研究所 Protoberberine quaternary ammonium base composition and use thereof
CN103830235A (en) * 2012-11-23 2014-06-04 青岛百草汇中草药研究所 Drug rehabilitation medicine with corydaline as effective component
CN104027332A (en) * 2013-03-04 2014-09-10 北京以岭药业有限公司 Application of tetrahydroberberine in preparation of drugs used for treating senile dementia
CN103919773A (en) * 2013-12-20 2014-07-16 中国药科大学 Application of 9-demethylberberine in preparation of hypolipidemic drug
CN103919774A (en) * 2013-12-20 2014-07-16 中国药科大学 Application of demethyleneberberine in preparation of hypolipidemic drug
CN106309442A (en) * 2015-06-19 2017-01-11 南京大学医学院附属鼓楼医院 Application of dehydrocorydaline in preparation of anti-inflammatory and analgesic drugs
CN105434435B (en) * 2015-12-07 2018-07-17 西安交通大学 It is a kind of to have effects that the pharmaceutical composition of synergistic antitumor and its application
CN106290674A (en) * 2016-10-12 2017-01-04 广西河丰药业有限责任公司 The quality determining method of Corydalis saxicola Bunting injection
CN106577697A (en) * 2016-11-16 2017-04-26 徐州得铸生物科技有限公司 Pesticide composition for prevention and treatment of tomato late blight
CN106942286B (en) * 2017-04-25 2019-07-19 华南农业大学 A kind of plant extracts and its application with activity of weeding
CN107223513A (en) * 2017-06-23 2017-10-03 安徽德昌苗木有限公司 A kind of Chinese chestnut tree implantation methods

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1687061A (en) * 2005-03-29 2005-10-26 沈阳化工研究院 Compound of isobioquin group and application thereof
CN101044883A (en) * 2006-03-28 2007-10-03 北京资源亚太饲料科技有限公司 Feed additive for enhancing domestic animals or birds eating food and then accelerating their growth
CN101874830A (en) * 2009-04-30 2010-11-03 成都中医药大学 New application of golden thread processed product
CN102100694A (en) * 2011-02-18 2011-06-22 浙江大学 Application of tetrahydropalmatine enantiomers in preparation of P-glycoprotein inhibitor
CN102349520A (en) * 2011-08-25 2012-02-15 华南农业大学 Application of berberine as herbicide
CN105075630A (en) * 2015-08-31 2015-11-25 莫玲 Safflower planting method
CN105726539A (en) * 2016-02-25 2016-07-06 吉林大学 Application of sanguinarine hydrochloride to preparation of medicine for treating salmonella infection
CN105766977A (en) * 2016-05-13 2016-07-20 创新美兰(合肥)股份有限公司 Dicamba, nicosulfuron and mesotrione compound dispersible oil suspension concentrate and preparation method thereof
CN105941431A (en) * 2016-05-13 2016-09-21 创新美兰(合肥)股份有限公司 Pretilachlor, cyhalofop-butyl and penoxsulam compounded dispersible oil suspension agent and preparation method thereof
CN106818831A (en) * 2017-01-24 2017-06-13 贵州省武陵山药用植物白芨开发有限公司 A kind of special herbicide of bletilla striata and its application

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
KINUKO IWASA等: "Fungicidal and Herbicidal Activities of Berberine Related Alkaloids", 《BIOSCIENCE,BIOTECHNOLOGY,AND BIOCHEMISTRY》 *
周利娟等: "毛茛科植物的农药活性及成分", 《江西农业大学学报》 *
邝芷琪等: "小檗碱的农用活性研究进展", 《农药》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108849942A (en) * 2018-09-05 2018-11-23 西南大学 A kind of jamaicin soluble granula and preparation method thereof
CN110787162A (en) * 2019-12-09 2020-02-14 朱峰 Use of methylprednisolone coptisine as JNK2 kinase inhibitor and for treating psoriasis

Also Published As

Publication number Publication date
CN111480654B (en) 2021-06-15
CN111493080B (en) 2021-07-09
CN111642508B (en) 2021-09-24
CN111557303B (en) 2021-02-19
CN107950546B (en) 2021-01-26
CN111480654A (en) 2020-08-04
CN111557303A (en) 2020-08-21
CN111493080A (en) 2020-08-07
CN111642508A (en) 2020-09-11

Similar Documents

Publication Publication Date Title
Ferreira et al. Land‐use type effects on soil organic carbon and microbial properties in a semi‐arid region of northeast Brazil
Thompson et al. Energy availability, spatial heterogeneity and ecosystem size predict food‐web structure in streams
Smit et al. Nurse plants, tree saplings and grazing pressure: changes in facilitation along a biotic environmental gradient
de Oliveira et al. Organic carbon and nitrogen stocks in soils of northeastern Brazil converted to irrigated agriculture
Rahman et al. Impact of organic soil amendments, including poultry-litter biochar, on nematodes in a Riverina, New South Wales, vineyard
Tälle et al. The conservation benefit of mowing vs grazing for management of species‐rich grasslands: a multi‐site, multi‐year field experiment
Earl et al. Effects of leachate from tree leaves and grass litter on tadpoles
DeLonge et al. Managing grazing lands to improve soils and promote climate change adaptation and mitigation: a global synthesis
Yang et al. Defoliation and arbuscular mycorrhizal fungi shape plant communities in overgrazed semiarid grasslands
Udawatta et al. Agroforestry for biodiversity conservation
Dingaan et al. Influence of grazing on plant diversity-productivity relationship in semi-arid grassland of South Africa
CN107950546A (en) Application of the Isoquinolinium Alkaloid in terms of as herbicide
Gundale et al. Variation in protein complexation capacity among and within six plant species across a boreal forest chronosequence
Islam Status of forest genetic resources conservation and management in Bangladesh.
Lucas et al. Needle chlorosis in Sitka spruce following a three‐year exposure to low concentrations of ozone: changes in mineral content, pigmentation and ascorbic acid
Riggs et al. Contrasting effects of plant species traits and moisture on the decomposition of multiple litter fractions
Taleshi et al. Leaf morphological variation of Quercus brantii Lindl. along an altitudinal gradient in Zagros forests of Fars Province, Iran
Adams et al. On the controls of root lifespan: assessing the role of soluble phenolics
Zarekia et al. Changes of vegetation structure and biomass in response to the livestock grazing in steppe rangelands of Iran.
Zong et al. Nitrogen addition stimulated compensatory growth responses to clipping defoliation in a Northern Tibetan alpine meadow
Idol et al. Changes in Microbial Nitrogen Across a 100‐Year Chronosequence of Upland Hardwood Forests
Munevar et al. Soil and plant silicon status in oil palm crops in Colombia
Arosa et al. Temporal effects dominate land use as factors affecting soil nematode communities in Mediterranean oak woodlands
McGee et al. Relationships among forest age, composition and elemental dynamics of Adirondack northern hardwood forests1
Shrivastava et al. Effect of leaf extract of Lantana camara on growth of seedlings of Cicer aeritinum

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant