AN2718


CAS No. : 174672-06-1

AN2718,174672-06-1
Product Details
For research use only. Not Intended for Therapeutic Use!
Cat No:I002322
Synonyms:AN2718; AN-2718; AN 2718;5-chlorobenzo[c][1,2]oxaborol-1(3H)-ol
Molecular Formula:C7H6BClO2
Molecular Weight:168.383
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Inventory Status:In stock
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Appearance:Solid powder
Purity: > 98%
Cat No:I002322
Cas No:174672-06-1
Product-Name:AN2718
IUPAC Name:5-chloro-1-hydroxy-3H-2,1-benzoxaborole
InChI:InChI=1S/C7H6BClO2/c9-6-1-2-7-5(3-6)4-11-8(7)10/h1-3,10H,4H2
InChIKey:HMAFTPZYFJFEHK-UHFFFAOYSA-N
SMILES:B1(C2=C(CO1)C=C(C=C2)Cl)O
AN2718(cas 174672-06-1) is a novel boron-containing small molecule that inhibits an essential protein synthesis enzyme, leucyl-transfer RNA synthetase, or LeuRS. This enzyme plays an essential role in fungal protein synthesis by attaching the leucine amino acid to transfer RNA, or tRNA. AN2718, an investigational topical anti-fungal product candidate for the potential treatment of skin and nail infections. At various concentrations, AN2718 gel showed low irritation potential, leading investigators to conclude that application site reactions in future efficacy trials would be unlikely.
1. Expert Opin Investig Drugs. 2014 Jan;23(1):97-106. doi: 10.1517/13543784.2013.840289. Epub 2013 Sep 26.
Investigational drugs for onychomycosis.
Gupta AK(1), Simpson FC.
Author information:
(1)Department of Medicine, University of Toronto , Toronto, Ontario , Canada +1 519 657 4222 ext. 277 ; +1 519 657 4233 ; agupta@execulink.com.
INTRODUCTION: Onychomycosis is the fungal infection of the nail plate by dermatophytes, yeasts and nondermatophyte molds. The treatment of onychomycosis poses many challenges due to low initial cure rates and a high rate of relapse and recurrence. Oral therapy is limited by adverse events and drug-drug interactions, whereas topical therapy has limited penetrance through the nail plate.
AREAS COVERED: New and reformulated drugs are in development for the treatment of onychomycosis. Experimental molecules include both oral and topical azole molecules, topical reformulations of terbinafine, the benzoxaboroles tavaborole and AN2718, the aganocide NVC-422 and the photosensitizer Sylsens B. These drugs are in varying stages of development so results from in vitro studies to Phase III clinical trials are discussed to present a complete picture of the current development pipeline for onychomycosis.
EXPERT OPINION: The development of new molecules from familiar and novel classes for both oral and topical administration is encouraging. It is clear that there is currently more emphasis on the development of topical drugs than orals, due to their lower potential for adverse events and drug-drug interactions. The emergence of novel molecular targets is encouraging for the possibility of combination therapy and any future drug-resistant strains of fungi.
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