40results about How to "Strong control activity" patented technology

The invention provides a herbicide composition consisting of 2-[(4,6-dimethoxypyrimidin-2-yl)hydroxy-methyl]-6-methoxymethyl-N-difluoromethanesulfonylanilide as the component (A) and any compound selected from more than 20 kinds of specific compounds such as orbencarb and the like as the component (B), heretofore not combined with the component (A) compound. Dispensation of the herbicide composition to paddy fields, lawns, dry fields, or non-agricultural lands gives excellent weed-controlling effects on a variety of weeds and causes no or little phytotoxicities on valuable cultivated plants.

The invention relates to a disinfectant compound with synergy function. The compound contains more than two active ingredients and acceptable agricultural inert ingredient, wherein component A is cyproconazole and component B is one of methoxyl acrylic ester disinfectant compound containing kresoxim-methyl, azoxystrobin, trifloxystrobin, SYP-1620, metominostrobin, fenazaquin, pyraclostrobin, kresoxim-methyl, etc. The disinfectant compound can be widely applied to protecting meals, vegetables, fruits, cash crops, etc. The compound is different from other agricultural disinfectant agent, promoting the preventing effect, slowing down the generation of resistance, widening the preventing range, promoting the safety, curing, preventing and increasing production of crops.

The invention relates to lung cancer preventing and treating composition extracted from selfheal and / or garden orache and application thereof in preparation of lung cancer preventing and treating medicine. The composition comprises phenolic acid component, flavone component and triterpene component and is characterized in that the weight ratio of the phenolic acid component, flavone component andtriterpene component is 5-70: 2-60: 0.5-40. In optimum proposal, the phenolic acid component takes caffeic acid and rosmarinic acid as typical ingredients; the flavone component takes rutin and quercetin as typical ingredients; the triterpene component takes ursolic acid and oleanolic acid as typical ingredients; the weight ratio of the caffeic acid, rosmarinic acid, rutin, quercetin, ursolic acid and oleanolic acid is 0-20: 5-50: 2-40: 0-20: 0.25-20: 0.25-20. The invention overcomes the defect of control is difficult in the prior art, active component is separated, purified and enriched, process is simple; preventing and treating activity on lung cancer and related diseases is strong; and mass production can be carried out.

The invention provides a new application of Eryngiolide A in medicine, in particular to an application of Eryngiolide A in preparing a drug for treating acute gout. Experimental study results prove that Eryngiolide A has a protective effect on an acute gout model with human blood vessel endothelial cell damage caused by urate, and inhibits ICAM-1 (Intercellular Cell Adhesion Molecule-1) expression, so that Eryngiolide A can be used for preparing the drug for treating an acute gout inflammation. The application of Eryngiolide A in preparing the drug for treating the acute gout is disclosed for the first time; since a matrix type is brand-new, and Eryngiolide A has unexpectedly strong activity on preventing and treating the acute gout, no probability of inspiration given by other compounds exists; and Eryngiolide A has the characteristic of prominent substantiality, and obviously has a marked progress for preventing and treating the acute gout at the same time.

The invention discloses 2-pyridine-oxyl(sulfide) benzoyloxy enoates compound with general formula(I, II); wherein X is H or S; R1 is H, halogen, or 4,6- dimethoxy pyrimidine-2- radicel or one of the following groups; methyls on N-O bonds and double bonds are in maleinoid form or anti form; R2,R3,R4,R6,R7 are selected from H or alkyl from C1-C6; R5 is alkyl from C1-C6, alcoxyl-alkyl from C2-C6, alkenyl from C3-C6 or alkynyl from C3-C6; radicals of R6 and R7 are in maleinoid form or anti form; R8 is alkyl from C1-C6, alkenyl from C3-C6 or alkynyl from C3-C6. The compound (I, II)is of activity in weeding and is safe to crops like soybean, cotton, earthnut, cole, corn, etc.

The invention provides a herbicide composition consisting of 2-[(4,6-dimethoxypyrimidin-2-yl)hydroxy-methyl]-6-methoxymethyl-N-difluoromethanesulfonylanilide as the component (A) and any compound selected from more than 20 kinds of specific compounds such as orbencarb and the like as the component (B), heretofore not combined with the component (A) compound. Dispensation of the herbicide composition to paddy fields, lawns, dry fields, or non-agricultural lands gives excellent weed-controlling effects on a variety of weeds and causes no or little phytotoxicities on valuable cultivated plants.