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Chemical Structure : SW-106
Catalog No.: PC-70262Not For Human Use, Lab Use Only.
A potent, selective, competitive PTH/PTH-related peptide receptor (PPR) antagonist with IC50 of 0.99 uM.
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A potent, selective, competitive PTH/PTH-related peptide receptor (PPR) antagonist with IC50 of 0.99 uM; displays higher affinity for the PPR relative to the other GPCRs; specificly blocks PTH-initiated cAMP accumulation.
| M.Wt | 361.312 | |
| Formula | C17H16F5NO2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Carter PH, et al. Proc Natl Acad Sci U S A. 2007 Apr 17;104(16):6846-51.
2. Carter PH, et al. Mol Endocrinol. 2015 Feb;29(2):307-21.
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