Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T64830 | ||||
Target Name | Somatostatin receptor type 5 (SSTR5) | ||||
Type of Target |
Successful |
||||
Drug Potency against Target | Drug Info | IC50 = 10.8 nM | [4] | ||
Cytotoxin Peptide Conjugate | Drug Info | IC50 = 2.79 nM | [1] | ||
D-Phe-c[Cys-Tyr-D-Trp-Lys-Val-Cys]-Asp-NH2 | Drug Info | IC50 = 5.6 nM | [5] | ||
Des-AA1,2,4,12,13-[D-Trp8]SRIF | Drug Info | IC50 = 31 nM | [3] | ||
Des-AA1,2,4,13-[D-Trp8]SRIF | Drug Info | IC50 = 9.5 nM | [3] | ||
Des-AA1,2,4,5,13-[D-Trp8]-SRIF | Drug Info | IC50 = 43 nM | [3] | ||
Des-AA1,2,4,5-[D-Trp8]SRIF | Drug Info | IC50 = 8.6 nM | [3] | ||
Des-AA1,2,5,12,13-[D-Trp8]SRIF | Drug Info | IC50 = 13 nM | [3] | ||
Des-AA1,2,5-[D-Trp8,Tyr11]SRIF | Drug Info | IC50 = 4.8 nM | [2] | ||
Des-AA5-[D-Trp8]SRIF | Drug Info | IC50 = 5 nM | [2] | ||
Edotreotide | Drug Info | IC50 = 393 nM | [4] | ||
H-D-Phe-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2 | Drug Info | Ki = 13.1 nM | [5] | ||
H-D-Phe-c[Cys-Ala-D-Trp-Lys-Thr-Cys]-Thr-NH2 | Drug Info | IC50 = 158 nM | [6] | ||
H-DPhe-c[Cys-Phe-DTrp-Lys-Thr-Cys]-Thr-NH2 | Drug Info | IC50 = 2.7 nM | [6] | ||
ODT-8 | Drug Info | IC50 = 46 nM | [3] | ||
PTR-3046 | Drug Info | IC50 = 67 nM | [7] | ||
SOMATOSTATIN | Drug Info | IC50 = 0.2 nM | [5] | ||
SRIF-28 | Drug Info | IC50 = 2.4 nM | [8] | ||
References | |||||
REF 1 | An adjustable release rate linking strategy for cytotoxin-peptide conjugates. Bioorg Med Chem Lett. 2003 Mar 10;13(5):799-803. | ||||
REF 2 | Somatostatin receptor 1 selective analogues: 2. N(alpha)-Methylated scan. J Med Chem. 2005 Jan 27;48(2):507-14. | ||||
REF 3 | Somatostatin receptor 1 selective analogues: 3. Dicyclic peptides. J Med Chem. 2005 Jan 27;48(2):515-22. | ||||
REF 4 | N-terminal sugar conjugation and C-terminal Thr-for-Thr(ol) exchange in radioiodinated Tyr3-octreotide: effect on cellular ligand trafficking in vi... J Med Chem. 2005 Apr 21;48(8):2778-89. | ||||
REF 5 | Discovery of iodinated somatostatin analogues selective for hsst2 and hsst5 with excellent inhibition of growth hormone and prolactin release from ... J Med Chem. 2005 Oct 20;48(21):6643-52. | ||||
REF 6 | Novel sst2-selective somatostatin agonists. Three-dimensional consensus structure by NMR. J Med Chem. 2006 Jul 27;49(15):4487-96. | ||||
REF 7 | Highly potent 4-amino-indolo[2,3-c]azepin-3-one-containing somatostatin mimetics with a range of sst receptor selectivities. J Med Chem. 2009 Jan 8;52(1):95-104. | ||||
REF 8 | Novel octreotide dicarba-analogues with high affinity and different selectivity for somatostatin receptors. J Med Chem. 2010 Aug 26;53(16):6188-97. | ||||
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