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AN-2718 - 98%, high purity , CAS No.174672-06-1

    Grade & Purity:
  • ≥98%
In stock
Item Number
A413006
Grouped product items
SKU Size
Availability
Price Qty
A413006-5mg
5mg
3
$39.90
A413006-10mg
10mg
3
$49.90
A413006-25mg
25mg
2
$93.90
A413006-50mg
50mg
2
$149.90
A413006-100mg
100mg
2
$227.90
A413006-500mg
500mg
1
$569.90

Fungal Inhibitors

View related series
Fungal (844)

Basic Description

Synonyms 5-chloro-1-hydroxy-3H-2,1-benzoxaborole | EN300-117650 | HMS3260B19 | AC-36848 | C7H6BClO2 | 810U6C2DGG | Z1198729424 | BCP16819 | MFCD18633195 | UNII-810U6C2DGG | AKOS006370225 | AS-55700 | Lopac0_000575 | 5-chloro-1,3-dihydro-2,1-benzoxaborol-1-ol | DTX
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms AN-2718 is an inhibitor of fungal growth that blocks protein synthesis via the oxaborole tRNA trapping (OBORT) mechanism.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

AN2718 is a benzoxaborole compound that displays broad antifungal effectiveness in vitro. It inhibits leucyl-tRN/A synthetase (LeuRS) from molds and yeasts (IC50s = 2 and 4.2 μM for A. fumigatus and C. albicans LeuRS, respectively), blocking protein synthesis.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organohalogen compounds
Class Aryl halides
Subclass Aryl chlorides
Intermediate Tree Nodes Not available
Direct Parent Aryl chlorides
Alternative Parents Benzenoids  Oxaborole derivatives  Boronic acid esters  Oxacyclic compounds  Organic metalloid salts  Organooxygen compounds  Organometalloid compounds  Organochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Benzenoid - Aryl chloride - 1,2-oxaborole derivative - Boronic acid ester - Boronic acid derivative - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organic metalloid moeity - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as aryl chlorides. These are organic compounds containing the acyl chloride functional group.
External Descriptors Not available

Associated Targets(Human)

HEK293 (82097 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichophyton benhamiae (1686 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Aspergillus fumigatus (16427 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichophyton rubrum (3646 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

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
Isomeric SMILES B1(C2=C(CO1)C=C(C=C2)Cl)O
Molecular Weight 168.39
Reaxy-Rn 10657792
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10657792&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number Certificate Type Date Item
B2426659 Certificate of Analysis Jan 18, 2024 A413006
B2426664 Certificate of Analysis Jan 18, 2024 A413006
B2426665 Certificate of Analysis Jan 18, 2024 A413006
B2426667 Certificate of Analysis Jan 18, 2024 A413006
B2426669 Certificate of Analysis Jan 18, 2024 A413006
B2426670 Certificate of Analysis Jan 18, 2024 A413006
B2426674 Certificate of Analysis Jan 18, 2024 A413006
B2426676 Certificate of Analysis Jan 18, 2024 A413006
B2426678 Certificate of Analysis Jan 18, 2024 A413006
B2426679 Certificate of Analysis Jan 18, 2024 A413006
B2426680 Certificate of Analysis Jan 18, 2024 A413006
B2426683 Certificate of Analysis Jan 18, 2024 A413006

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Chemical and Physical Properties

Solubility Solubility (25°C) In vitro Ethanol: mg/mL    
Sensitivity Moisture sensitive
Molecular Weight 168.390 g/mol
XLogP3
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 168.015 Da
Monoisotopic Mass 168.015 Da
Topological Polar Surface Area 29.500 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 155.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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