Chemical Structure : IHCH-2330
Catalog No.: PC-28264Not For Human Use, Lab Use Only.
IHCH-2330 is a potent, selective 5-HT2AR agonist with Ki of 7.24 nM and 45.71 nM for 5-HT2AR and 5-HT2BR respectively, simultaneously antagonizing 5-HT2BR.
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IHCH-2330 is a potent, selective 5-HT2AR agonist with Ki of 7.24 nM and 45.71 nM for 5-HT2AR and 5-HT2BR respectively, simultaneously antagonizing 5-HT2BR.
IHCH-2330 displays 9-, 19-, 24-, 40- and 62-fold selectivity over 5-HT1DR, 5-HT1BR, 5-HT6R, β2-AR and 5-HT1FR, respectively. IHCH-2330 also exhibits negligible agonist activity at the remaining 5-HT receptors, only weak antagonist activity at α1A-AR, α1B-AR, α2C-AR, and M1R.
IHCH-2330 exhibits potent 5-HT2AR agonism in both Gαq and β-arrestin signals with EC50 of 7.08 nM and 44.61 nM respectively.
| M.Wt | 449.47 | |
| Formula | C23H26F3N3O3 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Tang L, et al. Nat Commun. 2026 Sep 17;17(1):9873.

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