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G610600-25mgglycopyrrolate.
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G610600-5mgglycopyrrolate.
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G610602-25mgglycyl-[¹³C₃]-sarcosine.
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G610602-5mgglycyl-[¹³C₃]-sarcosine.
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G288753-100mgA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G288753-10mgA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G288753-25mgA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G288753-50mgA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G288753-5mgA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G423352-1mlA cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (<:1 min: 95% inhibition at 50 µM: Ki = 4.3 µM in CFTR-expressing FRT cells for apical membrane Cl-
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G610603-25mgGlyT1 inhibitor 27a.