ligands acting on targets

ApplicationAn antioxidant derived from water-soluble vitamin E.

(±)-AC 7954 hydrochloride.

(±)-AC 7954 hydrochloride.

The longer side-chain precursor of α-CEHC and a minor metabolite of α-tocopherol. Pretreatment of Hep-G2 cells with rifampicin, an inducer of the CYP3A family of cytochrome P450s, results in a 5-fold increase in α-CEHC. This shows that metabolism of

The longer side-chain precursor of α-CEHC and a minor metabolite of α-tocopherol. Pretreatment of Hep-G2 cells with rifampicin, an inducer of the CYP3A family of cytochrome P450s, results in a 5-fold increase in α-CEHC. This shows that metabolism of

CXCR3 antagonist: inhibits cell migration and metastasis.

CXCR3 antagonist: inhibits cell migration and metastasis.

Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.

(±)-Anatoxin A is a racemic preparation of the cyanotoxin alkaloid Anatoxin A, a potent AChR agonist. Potent modulation of the AChR-ion channel is reported at nanomolar concentrations with the (+)-Anatoxin and at low micromolar concentrations with

Product Describtion:Bay K 8644, a dihydropyridine compound, is a specific L-type Ca2+ channel agonist. Bay K 8644 increases Ca2+ influx through sarcolemmal Ca2+ channels by increasing the open time of the channel.

Product Describtion:Bay K 8644, a dihydropyridine compound, is a specific L-type Ca2+ channel agonist. Bay K 8644 increases Ca2+ influx through sarcolemmal Ca2+ channels by increasing the open time of the channel.

Product Describtion:Bay K 8644, a dihydropyridine compound, is a specific L-type Ca2+ channel agonist. Bay K 8644 increases Ca2+ influx through sarcolemmal Ca2+ channels by increasing the open time of the channel.