2-Amino-6-bromopyridine

Catalog No.: A48259
PqsR Ligand
2-Amino-6-bromopyridine acts as a PqsR ligand, exhibiting a dissociation constant (Kd) of 6.8 μM as determined by surface plasmon resonance (SPR) assays. This compound demonstrates weak antagonistic activity and serves as an intermediate in the synthesis of JAK2 and MSK1 inhibitors. Furthermore, 2-Amino-6-bromopyridine is useful in research focused on Pseudomonas aeruginosa infections, contributing to studies aimed at understanding bacterial communication and virulence factors.
Grouped product items
Size Price Stock Qty
1g
$20.00
In stock
5g
$25.00
In stock
10g
$30.00
In stock
25g
$60.00
In stock
50g
$100.00
In stock
100g
$165.00
In stock
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Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
Description2-Amino-6-bromopyridine acts as a PqsR ligand, exhibiting a dissociation constant (Kd) of 6.8 μM as determined by surface plasmon resonance (SPR) assays. This compound demonstrates weak antagonistic activity and serves as an intermediate in the synthesis of JAK2 and MSK1 inhibitors. Furthermore, 2-Amino-6-bromopyridine is useful in research focused on Pseudomonas aeruginosa infections, contributing to studies aimed at understanding bacterial communication and virulence factors.
Product Information
Catalog NumA48259
FormulaC5H5BrN2
Molecular Weight173.01
CAS Number19798-81-3
SMILESNC1=NC(Br)=CC=C1
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