SQ22536

  Cat. No.:  DC9967   Featured
Chemical Structure
17318-31-9
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More than 5000 active chemicals with high quality for research!
Field of application
SQ 22536 is a inhibitor of adenylyl cyclase (IC50 = 1.4 μM).
Cas No.: 17318-31-9
Chemical Name: 9-(Tetrahydro-2-furanyl)-9H-purin-6-amine
Synonyms: SQ 22536,SQ-22536
SMILES: N1C2C(=NC=NC=2N)N(C2CCCO2)C=1
Formula: C9H11N5O
M.Wt: 205.22
Sotrage: 4°C for 1 year, -20°C for more than 2 years
Description: SQ22536 is an effective adenylate cyclase (AC) inhibitor.
In Vitro: SQ22536 (SQ22,536) effectively inhibits the effect of forskolin with respective IC50 values of 5 μM.Preincubation with graded concentrations of SQ22536 reveals that both SQ22536 effectively inhibits PACAP-induced reporter gene activation with approximate IC50 value of 5 μM. SQ22536 more potently inhibits forskolin-induced Elk activation (IC50=10 μM) than 8-Br-cAMP-induced Elk activation (IC50=170 μM). Most notably, there are substantial differences in the reported potencies of SQ22536 to inhibit the activities of recombinant AC5 and AC6, with respective IC50 values of 2 μM and 360 μM. At a greater concentration (500 μM), SQ22536 significantly inhibits neurite elongation due to either forskolin or 8-Br-cAMP[1].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC72367 TDI-11861 TDI-11861 is second-generation soluble Adenylyl Cyclase (sAC, ADCY10) inhibitor with slow dissociation rates. TDI-11861 inhibits sAC cellular with an IC50 value of 5.5 nM.
DC10553 ST034307 ST034307 is a potent and selective adenylyl cyclase 1 (AC1) inhibitor, with IC50 of 2.3 μM.
DC9967 SQ22536 SQ 22536 is a inhibitor of adenylyl cyclase (IC50 = 1.4 μM).
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