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408397-25MGSynonyms: Phenyl (E)-(3S)-3-amino-5-phenylpent-1-enyl sulfone hydrochloride Purity Limit: &ge 99% (HPLC) Molecular Formula: C17H19NO2S·HCl Molecular Weight: 337.86 MDL No.
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16793-1An enantiomer of ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form also inhibits activation of NF-&kappaB more effectively than (R)-ibuprofen (IC<sub>50</sub>s = 62 and 122
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16793-10An enantiomer of ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form also inhibits activation of NF-&kappaB more effectively than (R)-ibuprofen (IC<sub>50</sub>s = 62 and 122
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16793-5An enantiomer of ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form also inhibits activation of NF-&kappaB more effectively than (R)-ibuprofen (IC<sub>50</sub>s = 62 and 122
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16793-500An enantiomer of ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form also inhibits activation of NF-&kappaB more effectively than (R)-ibuprofen (IC<sub>50</sub>s = 62 and 122
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16407-1A potent inhibitor of COX-1 and COX-2 (IC<sub>50</sub>s = 1.9 and 27 nM, respectively), whereas the (R)-enantiomer is 100 to 1,000 times less potent.
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16407-100A potent inhibitor of COX-1 and COX-2 (IC<sub>50</sub>s = 1.9 and 27 nM, respectively), whereas the (R)-enantiomer is 100 to 1,000 times less potent.
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16407-5A potent inhibitor of COX-1 and COX-2 (IC<sub>50</sub>s = 1.9 and 27 nM, respectively), whereas the (R)-enantiomer is 100 to 1,000 times less potent.
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16407-500A potent inhibitor of COX-1 and COX-2 (IC<sub>50</sub>s = 1.9 and 27 nM, respectively), whereas the (R)-enantiomer is 100 to 1,000 times less potent.
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13617-1The pharmacologically inactive optical enentiomer of (R)-LSF.
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13617-10The pharmacologically inactive optical enentiomer of (R)-LSF.
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13617-5The pharmacologically inactive optical enentiomer of (R)-LSF.