Chemical Structure : SB-710411
Catalog No.: PC-28270Not For Human Use, Lab Use Only.
SB-710411 is a selective peptidic urotensin-II receptor (UTR, U-II receptor, GPR14) antagonist, inhibits [(125)I]urotensin-II rat and monkey UT receptor binding with pKi of 7.50 and 6.85 respectively.
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SB-710411 is a selective peptidic urotensin-II receptor (UTR, U-II receptor, GPR14) antagonist, inhibits [(125)I]urotensin-II rat and monkey UT receptor binding with pKi of 7.50 and 6.85 respectively.
SB-710411 inhibits hU-II-induced contraction in rat isolated aorta causing a significant, parallel shift in the agonist concentration-response curve (pK(b) 6.28.
SB-710411 antagonizes urotensin-II-induced inositol phosphate formation at the rat UT receptor (pK(b) 6.54).
SB-710411 functions as an agonist at the monkey UT receptor (pEC(50) 6.56).
| M.Wt | 1146.22 | |
| Formula | C54H66Cl2N12O8S2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Behm DJ, et al. Br J Pharmacol. 2002 Oct;137(4):449-58.

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