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A7462-1 g
Thomas Scientific
Artificial sweetener used in commercial food production. It inhibits growth of Porphyromonas and increasing latency times in pain assays. (C08-0488-547)
Price: $154.34List Price: $171.49Aspartame is a dipeptide ester that is used as an artificial sweetener in commercial food production. Aspartame exhibits antibacterial efficacy against Porphyromonas, a periodontal pathogen. -
A7462-5 g
Thomas Scientific
Artificial sweetener used in commercial food production. It inhibits growth of Porphyromonas and increasing latency times in pain assays. (C08-0489-033)
Price: $301.53List Price: $335.03Aspartame is a dipeptide ester that is used as an artificial sweetener in commercial food production. Aspartame exhibits antibacterial efficacy against Porphyromonas, a periodontal pathogen. -
A7462-25 g
Thomas Scientific
Artificial sweetener used in commercial food production. It inhibits growth of Porphyromonas and increasing latency times in pain assays. (C08-0489-741)
Price: $1,124.64List Price: $1,249.60Aspartame is a dipeptide ester that is used as an artificial sweetener in commercial food production. Aspartame exhibits antibacterial efficacy against Porphyromonas, a periodontal pathogen. -
90052-10A structural analog of capsaicin with complex interactions in the CB system inhibits the reuptake of AEA, acts as CB1 receptor agonist and is resistant to FAAH hydrolysis exhibits vasodilator, analgesic, and anti-inflammatory properties.
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90052-100A structural analog of capsaicin with complex interactions in the CB system inhibits the reuptake of AEA, acts as CB1 receptor agonist and is resistant to FAAH hydrolysis exhibits vasodilator, analgesic, and anti-inflammatory properties.
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90052-5A structural analog of capsaicin with complex interactions in the CB system inhibits the reuptake of AEA, acts as CB1 receptor agonist and is resistant to FAAH hydrolysis exhibits vasodilator, analgesic, and anti-inflammatory properties.
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90052-50A structural analog of capsaicin with complex interactions in the CB system inhibits the reuptake of AEA, acts as CB1 receptor agonist and is resistant to FAAH hydrolysis exhibits vasodilator, analgesic, and anti-inflammatory properties.
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13622-10A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&gamma (IC<sub>50</sub> = 70 nM), compared to PI3K&alpha (IC<sub>50</sub> = 240 nM), PI3K&beta (IC<sub>50</sub> = 1.45 &muM), and PI3K&delta (IC<sub>50</sub> =1.
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13622-25A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&gamma (IC<sub>50</sub> = 70 nM), compared to PI3K&alpha (IC<sub>50</sub> = 240 nM), PI3K&beta (IC<sub>50</sub> = 1.45 &muM), and PI3K&delta (IC<sub>50</sub> =1.
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13622-5A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&gamma (IC<sub>50</sub> = 70 nM), compared to PI3K&alpha (IC<sub>50</sub> = 240 nM), PI3K&beta (IC<sub>50</sub> = 1.45 &muM), and PI3K&delta (IC<sub>50</sub> =1.
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13622-50A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&gamma (IC<sub>50</sub> = 70 nM), compared to PI3K&alpha (IC<sub>50</sub> = 240 nM), PI3K&beta (IC<sub>50</sub> = 1.45 &muM), and PI3K&delta (IC<sub>50</sub> =1.
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10626-1An agonist of GPR199 that is effective both in isolated cells and in vivo increases cAMP levels in HEK293 cells transfected with human GPR119 (EC50 = 2.5 &muM) and promotes glucose-stimulated insulin secretion in mice (100 mg/kg).