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Chemical Structure| 460746-46-7 Chemical Structure| 460746-46-7

Structure of ABT-239
CAS No.: 460746-46-7

Chemical Structure| 460746-46-7

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ABT-239 is a highly efficacious, non-imidazole class of H3R antagonist.

Synonyms: ABT-239

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Product Citations

Product Citations

Sotorilli, Giuliana Eboli ; Gravina, Humberto Doriguetto ; de Carvalho, Ana Carolina ; Shimizu, Jacqueline Farinha ; Fontoura, Marina Alves ; Melo-Hanchuk, Talita Diniz , et al.

Abstract: St. Louis encephalitis virus (SLEV) is a neglected mosquito-borne Flavivirus that may cause severe neurol. disease in humans and other animals. There are no specific treatments against SLEV infection or disease approved for human use, and drug repurposing may represent an opportunity to accelerate the development of treatments against SLEV. Here we present a scalable, medium-throughput phenotypic cell culture-based screening assay on Vero CCL81 cells to identify bioactive compounds that could be repurposed against SLEV infection. We screened eighty compounds from the Medicines for Malaria Venture (MMV) COVID Box library to identify nine (11%) compounds that protected cell cultures from SLEV-induced cytopathic effects, with low- to mid-micromolar potencies. We validated six hit compounds using viral plaque-forming assays to find that the compounds ABT-239, Amiodarone, Fluphenazine, Posaconazole, Triparanol, and Vidofludimus presented varied levels of antiviral activity and selectivity depending on the mammalian cell type used for testing. Importantly, we identified and validated the antiviral activity of the anti-flavivirus nucleoside analog 7DMA against SLEV. Triparanol and Fluphenazine reduced infectious viral loads in both Vero CCL81 and HBEC-5i cell cultures and, similar to the other validated compounds, are likely to exert antiviral activity through a mol. target in the host.

Keywords: St. Louis encephalitis virus ; cell culture-based screening ; drug repurposing ; Flavivirus ; cationic amphiphilic compounds (CAD)

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Product Details of ABT-239

CAS No. :460746-46-7
Formula : C22H22N2O
M.W : 330.42
SMILES Code : N#CC1=CC=C(C2=CC=C(OC(CCN3[C@H](C)CCC3)=C4)C4=C2)C=C1
Synonyms :
ABT-239
MDL No. :MFCD13248643
InChI Key :KFHYZKCRXNRKRC-MRXNPFEDSA-N
Pubchem ID :9818903

Safety of ABT-239

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Related Pathways of ABT-239

GPCR

Isoform Comparison

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.03mL

0.61mL

0.30mL

15.13mL

3.03mL

1.51mL

30.26mL

6.05mL

3.03mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

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