CN100387567C - New compound possessing insecticidal bactericidal activity - Google Patents

New compound possessing insecticidal bactericidal activity Download PDF

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Publication number
CN100387567C
CN100387567C CNB2005101129167A CN200510112916A CN100387567C CN 100387567 C CN100387567 C CN 100387567C CN B2005101129167 A CNB2005101129167 A CN B2005101129167A CN 200510112916 A CN200510112916 A CN 200510112916A CN 100387567 C CN100387567 C CN 100387567C
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China
Prior art keywords
compound
new compound
herba lycopi
bactericidal activity
compound possessing
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CN1948256A (en
Inventor
何兰
曹坳程
郭美霞
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Beijing Normal University
Institute of Plant Protection of Chinese Academy of Agricultural Sciences
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Beijing Normal University
Institute of Plant Protection of Chinese Academy of Agricultural Sciences
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Abstract

The present invention provides a new compound-eupatoria C, its chemical name is 8 alpha-hydroxy-1-isopropyl-4,7-dimethyl-1,3,4,8 alpha-tetralyl-2,6-diketone. It belongs to a hemiterpene compound. Said invention also provides its physical and chemical properties and spectral data. Said compound can be used as high-effective mycocide and pesticide or repellent of some crops.

Description

A kind of new compound with desinsection, anti-microbial activity
Technical field
The present invention relates to a kind of new compound, belong to sesquiterpenoid with desinsection, anti-microbial activity.
Background technology
Hemp Eupatorium (Eupatorium adenophorum Spreng) is the perennial subshrub plant of composite family Eupatorium, originates in Central America Mexico, therefrom remote before and after the fifties in last century, in more the border import the Yunnan Province of China south into.This kind of plant has surprising fecundity, can form intensive single kind of advantage group in blocks, repels the growth of other plant.Over nearly 30 years, Hemp Eupatorium almost with annual 30 kilometers speed northwards, rapidly spread eastwards, distribution range has reached provinces and regions such as Yunnan, Guizhou, Guangdong, Guangxi, Sichuan, Tibet, only state, the Liangshan Mountain, Sichuan hazard area just reaches more than 670,000 hectares at present, herds sideline production for the agricultural that spread the district and has brought serious harm.
For fully fully utilizing this malignant weed, it is changed harmful to treasure.This case discloses new compound Herba Lycopi C and nematicide and anti-microbial activity first, for new approaches are opened up in the Hemp Eupatorium comprehensive utilization.
Summary of the invention
The purpose of this invention is to provide a kind of desinsection, antimicrobial new compound---Herba Lycopi C that has.
Herba Lycopi C provided by the invention is a kind of new compound, its chemistry 8a-hydroxyl by name-1-sec.-propyl-4,7-dimethyl-1,3,4,8a-tetrahydrochysene how-2, and the 6-diketone belongs to sesquiterpenoids.
Physico-chemical property and the spectroscopic data of compound Herba Lycopi C are as follows:
1, colourless bulk crystals is soluble in acetone, chloroform;
2、Mp:156℃;[α] D=+64°(c=0.45,CHCl 3);EIMS(m/z):248(M+,C 15H 20O 3,35),230(65),189(43),178(100),163(86),150(97);IR(KBr)max(cm -1):3320,1719,1666,1623,1387,1160,1995;
3, the X-single crystal diffraction crystal data of Herba Lycopi C sees Table 1:
The structural formula of compound Herba Lycopi C is:
The X-single crystal diffraction crystal data of table 1. Herba Lycopi C
Figure C20051011291600041
The affirmation of compound Herba Lycopi C:
By the X-single crystal diffraction, referring to accompanying drawing 1 (CCDC 283245), can confirm this structure for [I], and provide the real structure of compound by X-single crystal diffraction spectrum: 8 Alpha-hydroxies-1-sec.-propyl-4,7-dimethyl-1,3,4,8a-tetrahydrochysene how-2,6-diketone.The methyl of this compound and sec.-propyl are in same one side, and hydroxyl is at another side.To propose especially be sec.-propyl on this sesquiterpene C-1 position and the methyl on the C-4 position in same direction, hydroxyl connects on the C-8a position, why this structure can stable existence be because hydroxyl and carbonyl have formed intermolecular hydrogen bond, referring to accompanying drawing 1.
The extraction step of compound Herba Lycopi C is as follows:
1, get exsiccant Hemp Eupatorium leaf 1Kg, with 8 times of amounts of 95% industrial methanol, soaking at room temperature 48 hours, extract 3 times, filter the back merging filtrate, concentrating under reduced pressure filtrate gets total medicinal extract.
2, (medicinal extract: dissolving methyl alcohol=10: 1) adds water (methyl alcohol: water=2: 8) to total medicinal extract then with methyl alcohol.Use sherwood oil, chloroform, ethyl acetate extraction successively, concentrated extract gets sherwood oil medicinal extract (157g), chloroform medicinal extract (24g), ethyl acetate medicinal extract (230g) and residue respectively.
3, chloroform medicinal extract (24g) is through 200~300 order silica gel column chromatographies, with sherwood oil: 20: 1~5: 1 gradient elutions of acetone, adopt TLC to follow the tracks of and detect, every 250ml connects one bottle, merge same composition after, obtain 11 B component a~Bk.Be component silica gel column chromatography, use sherwood oil: acetone (10: 1) wash-out, collect Be1, Be2, Be3, Be4 component; Be2 component acetone recrystallization obtains colourless consolidated block compound Herba Lycopi C, Herba Lycopi C through the chloroform/methanol mixed solvent cultivate the monocrystalline of the alleged Herba Lycopi C of the present invention.
Activity and the beneficial effect of compound Herba Lycopi C
This compound has certain repellent action to bollworm, beet armyworm, and peanut Cercospora bacteria, botrytis cinerea, sickle-like bacteria are had restraining effect, referring to table 2,3.And be basic framework with this new sesquiterpenoid, by the discussion of further structure activity relationship, reasonable process is designed and developed high reactivity, low toxicity sterilant, sterilant or the repellent that makes new advances.
The nematicide effect of table 2. compound Herba Lycopi C
Figure C20051011291600051
Table 3. compound Herba Lycopi C is to the inhibition determination of activity of Pyricularia oryzae
Description of drawings
Accompanying drawing 1: the X monocrystalline of Herba Lycopi C
Accompanying drawing 2: the intermolecular formation hydrogen bond of Herba Lycopi C

Claims (1)

1. one kind has desinsection, antimicrobial new compound, belongs to sesquiterpenoid, it is characterized in that the structural formula of this compound is:
Figure C2005101129160002C1
CNB2005101129167A 2005-10-14 2005-10-14 New compound possessing insecticidal bactericidal activity Expired - Fee Related CN100387567C (en)

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Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101525508B (en) * 2008-03-06 2013-07-24 中国农业科学院植物保护研究所 Application of Eupatorium adenophorum extract as anti-fouling paint antifoulant
CN101658192B (en) * 2009-09-23 2012-11-07 云南农业大学 Application of eupatorium adenophorum vinegar liquid as plant nematocide
CN101933533B (en) * 2010-07-20 2013-06-05 华南农业大学 Plant source preservative and preparation method and application thereof
CN104782676B (en) * 2015-03-19 2016-10-19 陕西乾龙高科生态农业有限公司 A kind of plant protection product and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1287786A (en) * 2000-10-08 2001-03-21 四川九章生物化工科技发展有限公司 Method for preparing biological broad spectrum insecticide

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1287786A (en) * 2000-10-08 2001-03-21 四川九章生物化工科技发展有限公司 Method for preparing biological broad spectrum insecticide

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