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F347382-25mg(S)-(-)-5-Fluorowillardiine is an extremely potent and selective AMPA receptor agonist at hGluR1 and hGluR2. AMPA is a transmembrane glutamate receptor composed of the subunits GluR-1,2,3,4.
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F347382-50mg(S)-(-)-5-Fluorowillardiine is an extremely potent and selective AMPA receptor agonist at hGluR1 and hGluR2. AMPA is a transmembrane glutamate receptor composed of the subunits GluR-1,2,3,4.
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F347382-5mg(S)-(-)-5-Fluorowillardiine is an extremely potent and selective AMPA receptor agonist at hGluR1 and hGluR2. AMPA is a transmembrane glutamate receptor composed of the subunits GluR-1,2,3,4.
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S286600-100mgHighly potent and subtype-selective kainate agonist
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S286600-10mgHighly potent and subtype-selective kainate agonist
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S286600-50mgHighly potent and subtype-selective kainate agonist
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S288692-10mg(S)-(-)-Bay K8644, a dihydropyridine compound is a Ca2+ channel activator.It is an enantiomer of Bay K 8644. Application:(S)-(-)-Bay K8644 has been used as a L-type calcium channel (LTCC) agonist in the suprachiasmatic nucleus (SCN) slices. It has
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S288692-1mg(S)-(-)-Bay K8644, a dihydropyridine compound is a Ca2+ channel activator.It is an enantiomer of Bay K 8644. Application:(S)-(-)-Bay K8644 has been used as a L-type calcium channel (LTCC) agonist in the suprachiasmatic nucleus (SCN) slices. It has
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S288692-25mg(S)-(-)-Bay K8644, a dihydropyridine compound is a Ca2+ channel activator.It is an enantiomer of Bay K 8644. Application:(S)-(-)-Bay K8644 has been used as a L-type calcium channel (LTCC) agonist in the suprachiasmatic nucleus (SCN) slices. It has
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S288692-50mg(S)-(-)-Bay K8644, a dihydropyridine compound is a Ca2+ channel activator.It is an enantiomer of Bay K 8644. Application:(S)-(-)-Bay K8644 has been used as a L-type calcium channel (LTCC) agonist in the suprachiasmatic nucleus (SCN) slices. It has
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S288692-5mg(S)-(-)-Bay K8644, a dihydropyridine compound is a Ca2+ channel activator.It is an enantiomer of Bay K 8644. Application:(S)-(-)-Bay K8644 has been used as a L-type calcium channel (LTCC) agonist in the suprachiasmatic nucleus (SCN) slices. It has
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S287961-10mgβ3partial agonist also 5-HT1Aand 5-HT1Bantagonist more active enantiomer ofpindolol