To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

From Wikipedia, the free encyclopedia

Chemical structure of diflubenzuron, a commonly used benzoylurea insecticide

Benzoylureas are chemical derivatives of N-benzoyl-N-phenylurea (benzoylurea). They are best known for their use as insecticides.[1] They act as insect growth regulators by inhibiting synthesis of chitin in the insect's body.

One of the more commonly used benzoylurea pesticides is diflubenzuron. Others include chlorfluazuron, flufenoxuron, hexaflumuron, and triflumuron. Lufenuron is the active compound in flea control medication for pet dogs and cats.

3-(Iodoacetamido)-benzoylurea (3-IAABU) is one of several benzoylurea compounds which have been investigated as potential anticancer agents. [2]

YouTube Encyclopedic

  • 1/3
    Views:
    1 454
    8 946
    4 650
  • Diflubenzuron 25% WP | INDO BIOCHEM
  • Lufenuron Insecticide / IGR (Insect Growth Regulator) || Uses & Mode Of Action ( Urdu/Hindi)
  • Mod-06 Lec-27 Chemical Control - History and classification

Transcription

Environmental toxicity

When applied in a dispersed way, for example through fumigation or spraying, these chemicals have an effect against a wide range of insect species, some of which may be beneficial to human activities, including crop-pollinators such as bees. In addition, as with many insecticides, application may result in the killing of natural predators or controls along with the pest,[citation needed] risking the possibility of a 'rebound effect' or pest resurgence, where the original target for the treatment returns with equal or even greater voracity.

Flufenoxuron was banned in the European Union in 2011[3] due to its high potential for bioaccumulation in the food chain and high risk to aquatic organisms. Flufenoxuron is marketed as having 'high persistence' in the environment and the product data-sheet states that it does not biodegrade easily.[4]

References

  1. ^ Junquera, Pablo; Hosking, Barry; Gameiro, Marta; Macdonald, Alicia (2019). "Benzoylphenyl ureas as veterinary antiparasitics. An overview and outlook with emphasis on efficacy, usage and resistance". Parasite. 26: 26. doi:10.1051/parasite/2019026. ISSN 1776-1042. PMC 6492539. PMID 31041897. open access
  2. ^ Jiang, J. D.; Davis, A. S.; Middleton, K.; Ling, Y. H.; Perez-Soler, R.; Holland, J. F.; Bekesi, J. G. (1998-12-01). "3-(Iodoacetamido)-benzoylurea: a novel cancericidal tubulin ligand that inhibits microtubule polymerization, phosphorylates bcl-2, and induces apoptosis in tumor cells". Cancer Research. 58 (23): 5389–5395. PMID 9850070.
  3. ^ Commission Implementing Regulation (EU) No 942/2011 of 22 September 2011 concerning the non-approval of the active substance flufenoxuron
  4. ^ BASF Cascade Product Details

Further reading

  • Lewis, W.H. and M.P.F. Elvin-Lewis. (2003). Medical Botany. Hoboken: Wiley. pg. 590
This page was last edited on 6 August 2023, at 08:00
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.