S 32212 HCl 25mg 25mg | Purity Not Available
Adooq Bioscience
S 32212 hydrochloride is an inverse agonist of 5-HT2C receptors (pKi = 8.18 at human 5-HT2C INI receptors).
More Information Supplier PageS 32212 hydrochloride is an inverse agonist of 5-HT2C receptors (pKi = 8.18 at human 5-HT2C INI receptors).
More Information Supplier PageS 32212 hydrochloride is an inverse agonist of 5-HT2C receptors (pKi = 8.18 at human 5-HT2C INI receptors).
More Information Supplier PageCloprostenol is a synthetic analog of prostaglandin F2?? (PGF2??). It is 200 times and 100 times more potent than PGF2?? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2??.
More Information Supplier PageCloprostenol is a synthetic analog of prostaglandin F2?? (PGF2??). It is 200 times and 100 times more potent than PGF2?? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2??.
More Information Supplier PageCloprostenol is a synthetic analog of prostaglandin F2?? (PGF2??). It is 200 times and 100 times more potent than PGF2?? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2??.
More Information Supplier PageCloprostenol is a synthetic analog of prostaglandin F2?? (PGF2??). It is 200 times and 100 times more potent than PGF2?? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2??.
More Information Supplier PageA-889425 is a selective TRPV1 receptor antagonist. A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (human).
More Information Supplier PageA-889425 is a selective TRPV1 receptor antagonist. A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (human).
More Information Supplier Page