Chemical Structure : PAM_16A
货号: PC-23881Not For Human Use, Lab Use Only.
PAM_16A is a potent, selective, positive allosteric modulator of TMEM16A (Anoctamin-1, ANO1) with EC50 of 3.6 nM, activates heterologous TMEM16A channels, has no effect on the closely related TMEM16B channel.
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PAM_16A is a potent, selective, positive allosteric modulator of TMEM16A (Anoctamin-1, ANO1) with EC50 of 3.6 nM, activates heterologous TMEM16A channels, has no effect on the closely related TMEM16B channel.
PAM_16A is a potent activator that does not interfere with other measurable whole-cell currents in arterial smooth muscle cells (SMCs).
PAM_16A selectively activated TMEM16A currents in SMCs and enhanced aortic contraction caused by phenylephrine or angiotensin-II and capillary (pericyte) constriction evoked by endothelin-1 or oxygen–glucose deprivation (OGD) to simulate cerebral ischaemia.
分子量 | 371.82 | |
分子式 | C19H18ClN3O3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Patent WO2021/014168, compound 1.
2. Al-Hosni R, et al. Br J Pharmacol. 2025 Jan 19. doi: 10.1111/bph.17383.
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