Chemical Structure : P626
Catalog No.: PC-25759Not For Human Use, Lab Use Only.
P626 is a potent, selective dual adenosine A2A/A2B receptor (A2AR/A2BR) antagonist with IC50 of 5.73 nM and 34 nM at both hA2AAR and hA2BAR (cAMP assay), with no significant acitivity against hA1AR and hA3AR.
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P626 is a potent, selective dual adenosine A2A/A2B receptor (A2AR/A2BR) antagonist with IC50 of 5.73 nM and 34 nM at both hA2AAR and hA2BAR (cAMP assay), with no significant acitivity against hA1AR and hA3AR.
P626 efficiently prevented A2AR- and A2BR-dependent responses in OPCs, a mechanism consistent with its protective effects in EAE mice.
P626 treatment mitigated myelin loss and restored basal myelin levels in spinal cord samples from EAE mice.
| M.Wt | 416.47 | |
| Formula | C17H16N6O3S2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. F. Varano, et al. Bioorganic & Medicinal Chemistry Letters 30 (2020): 127067.
2. M Morozzi, et al. J Cell Mol Med. 2025 Nov;29(22):e70952.

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