(+) -JNJ-A07

CAT: 0804-HY-139602-01Size: 5 mgDry Ice: NoHazardous: No
CAT#:0804-HY-139602-01Size:5 mg
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AVAILABILITY: InStock
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
(+) -JNJ-A07 is a highly potent, orally active pan-serotype dengue virus inhibitor targeting the NS3-NS4B interaction. (+) -JNJ-A07 exerts nanomolar to picomolar activity against a panel of 21 clinical isolates. (+) -JNJ-A07 has a favourable pharmacokinetic profile that results in outstanding efficacy against dengue virus infection in mouse infection models[1].
CAS Number
[2135640-93-4]
UNSPSC
12352005
Target
Dengue Virus; Flavivirus; Virus Protease
Type
Reference compound
Related Pathways
Anti-infection
Applications
COVID-19-anti-virus
Field of Research
Infection
Assay Protocol
https://www.medchemexpress.com/plus-jnj-a07.html
Concentration
10mM
Purity
98.46
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
OC(CCCOC1=CC(OC)=CC(NC(C2=CC=C(C=C2)Cl)C(N3C4=CC(OC(F)(F)F)=CC=C4CC3)=O)=C1)=O.[Rotation(+)]
Molecular Formula
C28H26ClF3N2O6
Molecular Weight
578.96
References & Citations
[1]Kaptein SJF, et al. A pan-serotype dengue virus inhibitor targeting the NS3-NS4B interaction [published correction appears in Nature. 2021 Nov;599 (7883) :E2]. Nature. 2021;598 (7881) :504-509.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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