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Chemical Structure : BAY 2686013
Catalog No.: PC-20945Not For Human Use, Lab Use Only.
BAY 2686013 is a selective, allosteric antagonist of human pituitary adenylate cyclase activating polypeptide receptor (hPAC1-R) with IC50 of 0.92 and 0.4 uM in cAMP HTRF and Ca2+ release assays, respectively.
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BAY 2686013 is a selective, allosteric antagonist of human pituitary adenylate cyclase activating polypeptide receptor (hPAC1-R) with IC50 of 0.92 and 0.4 uM in cAMP HTRF and Ca2+ release assays, respectively.
BAY 2686013 is a valuable tool compound for better understanding the signalling and function of hPAC1-R.
| M.Wt | 392.30 | |
| Formula | C17H14F6N2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Gernot Langer, et al. Mol Pharmacol. 2023 Jun 22;MOLPHARM-AR-2022-000662.
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