CH 275 (acetate)
目录号 : GC91848CH 275 is a cyclic peptide agonist of somatostatin receptor 1 (SST1; IC50 = 30.9 nM for the human receptor).
Sample solution is provided at 25 µL, 10mM.
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- Purity: >95.00%
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CH 275 is a cyclic peptide agonist of somatostatin receptor 1 (SST1; IC50 = 30.9 nM for the human receptor).[1] It is selective for SST1 over SST2, SST3, SST4, and SST5 (IC50s = >10,000, 345, >1,000, and >10,000 nM, respectively, for the human receptors). CH 275 (500 nM) inhibits basal growth hormone secretion from primary mouse pituitary cells.[2] It inhibits glucose-induced increases in electrical activity without inducing membrane hyperpolarization in a whole-cell patch-clamp assay using MIN6 pancreatic β-cells when used at a concentration of 100 nM.[3]
References:
[1].Rivier, J.E., Hoeger, C., Erchegyi, J., et al.Potent somatostatin undecapeptide agonists selective for somatostatin receptor 1 (sst1)J. Med. Chem.44(13)2238-2246(2001).
[2].Kreienkamp, H.J., Akgün, E., Baumeister, H., et al.Somatostatin receptor subtype 1 modulates basal inhibition of growth hormone release in somatotrophsFEBS Lett.462(3)464-466(1999).
[3].Smith, P.A., Sellers, L.A., and Humphrey, P.P.Somatostatin activates two types of inwardly rectifying K+ channels in MIN-6 cellsJ. Physiol.532(Pt 1)127-142(2001).
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 0.673 mL | 3.3652 mL | 6.7304 mL |
5 mM | 0.1346 mL | 0.673 mL | 1.3461 mL |
10 mM | 0.0673 mL | 0.3365 mL | 0.673 mL |
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% DMSO % % Tween 80 % saline | ||||||||||
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2.
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