Chemical Structure : ADS1017
Catalog No.: PC-23592Not For Human Use, Lab Use Only.
ADS1017 is a potent, selective histamine H3 receptor antagonist with pKi of 7.9/6.8 for rH3R/hH3R in radioligand binding assays respectively, 20-fold selective over H4R.
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ADS1017 is a potent, selective histamine H3 receptor antagonist with pKi of 7.9/6.8 for rH3R/hH3R in radioligand binding assays respectively, 20-fold selective over H4R.
ADS1017 demonstrates marked H3 receptor antagonist activity in the guinea pig jejunum functional assay (gpH3R pA2 = 8.21) and weak but competitive antagonism toward H1R with pA2 = 6.70.
ADS1017 shows a broad spectrum of analgesic activity in both nociceptive and neuropathic pain models.
M.Wt | 479.71 | |
Formula | C29H45N5O | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Karcz T, et al. ACS Chem Neurosci. 2024 Dec 9. doi: 10.1021/acschemneuro.4c00480.
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