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10008370-10AL 8810 methyl ester is a lipid soluble, esterified prodrug form of AL 8810 analogous to the commonly used therapeutic intraocular PG compounds such as latanoprost and travoprost. The pharmacology of AL 8810 methyl ester has not been published.
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10008370-5AL 8810 methyl ester is a lipid soluble, esterified prodrug form of AL 8810 analogous to the commonly used therapeutic intraocular PG compounds such as latanoprost and travoprost. The pharmacology of AL 8810 methyl ester has not been published.
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16735-1AL 8810 is an 11&beta-fluoro analog of PGF2&alpha which acts as a potent and selective antagonist at the FP receptor. AL 8810 has weak intrinsic agonist activity on FP receptor preparations in the 200-300 nM range, yet it fully antagonizes the
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16735-10AL 8810 is an 11&beta-fluoro analog of PGF2&alpha which acts as a potent and selective antagonist at the FP receptor. AL 8810 has weak intrinsic agonist activity on FP receptor preparations in the 200-300 nM range, yet it fully antagonizes the
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16735-25AL 8810 is an 11&beta-fluoro analog of PGF2&alpha which acts as a potent and selective antagonist at the FP receptor. AL 8810 has weak intrinsic agonist activity on FP receptor preparations in the 200-300 nM range, yet it fully antagonizes the
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16735-5AL 8810 is an 11&beta-fluoro analog of PGF2&alpha which acts as a potent and selective antagonist at the FP receptor. AL 8810 has weak intrinsic agonist activity on FP receptor preparations in the 200-300 nM range, yet it fully antagonizes the
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11425-1A membrane active peptide antibiotic of the peptaibol class that strongly induces helical peptide structures and forms voltage-gated ion channels in the lipid bilayers of cell membranes often used to study ion channel assembly, voltage gating, and
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11425-10A membrane active peptide antibiotic of the peptaibol class that strongly induces helical peptide structures and forms voltage-gated ion channels in the lipid bilayers of cell membranes often used to study ion channel assembly, voltage gating, and
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11425-5A membrane active peptide antibiotic of the peptaibol class that strongly induces helical peptide structures and forms voltage-gated ion channels in the lipid bilayers of cell membranes often used to study ion channel assembly, voltage gating, and
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17577-1A process impurity associated with salbutamol sulfate.
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17577-5A process impurity associated with salbutamol sulfate.
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17577-500A process impurity associated with salbutamol sulfate.