SB 269970

Data Sheet For research use only. Not for human use.

Cat. No. ：BCP02382CAS No. ：201038-74-6Purity：98%

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CAS No.	201038-74-6	Cat. No.	BCP02382
Name	SB 269970
Synonyms	SB-269970;SB269970; SB 269970 hydrochloride; SB-269970 hydrochloride; SB269970 hydrochloride;
SMILES
Chemical Name
Formula	C18H28N2O3S	M. Wt	352.49
Purity	98%	Storage	Store at 4-8°C
Description	5-CT-stimulated adenylyl cyclase activity in guinea-pig hippocampal membranes (pEC(50) of 8.4+/-0.2) was inhibited by SB-269970-A (0.3 microM) with a pK(B) (8.3+/-0.1) in good agreement with its antagonist potency at the human cloned 5-HT(7(a)) receptor and its binding affinity at guinea-pig cortical membranes. 5-HT(7) receptor mRNA was highly expressed in human hypothalamus, amygdala, thalamus, hippocampus and testis [1]. Cortical slices were loaded with [(3)H]-5-HT and release was evoked by electrical stimulation. 5-CT inhibited the evoked release of [(3)H]-5-HT in a concentration-dependent manner. SB-269970 had no significant effect on [(3)H]-5-HT release while the 5-HT(1B) receptor antagonist, SB-224289 significantly potentiated [(3)H]-5-HT release. In addition, SB-269970 was unable to attenuate the 5-CT-induced inhibition of release while SB-224289 produced a rightward shift of the 5-CT response, generating estimated pK(B) values of 7.8 and 7.6 at the guinea-pig and rat terminal 5