Synthesis, Antiproliferative Effect and In Silico LogP Prediction of BIM-23052 Analogs Containing Tyr Instead of Phe

(1) Background: Hydrophobicity (or lipophilicity) is a limiting factor in the ability of molecules to pass through cell membranes and to perform their function. The ability to efficiently access cytosol is especially important when a synthetic compound has the potential to become a drug substance. D...

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Main Authors: Dancho Danalev (Author), Ivan Iliev (Author), Stefan Dobrev (Author), Silvia Angelova (Author), Stoiko Petrin (Author), Tatyana Dzimbova (Author), Elena Ivanova (Author), Dessislava Borisova (Author), Emilia Naydenova (Author)
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Published: MDPI AG, 2023-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Dancho Danalev  |e author 
700 1 0 |a Ivan Iliev  |e author 
700 1 0 |a Stefan Dobrev  |e author 
700 1 0 |a Silvia Angelova  |e author 
700 1 0 |a Stoiko Petrin  |e author 
700 1 0 |a Tatyana Dzimbova  |e author 
700 1 0 |a Elena Ivanova  |e author 
700 1 0 |a Dessislava Borisova  |e author 
700 1 0 |a Emilia Naydenova  |e author 
245 0 0 |a Synthesis, Antiproliferative Effect and In Silico LogP Prediction of BIM-23052 Analogs Containing Tyr Instead of Phe 
260 |b MDPI AG,   |c 2023-03-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15041123 
500 |a 1999-4923 
520 |a (1) Background: Hydrophobicity (or lipophilicity) is a limiting factor in the ability of molecules to pass through cell membranes and to perform their function. The ability to efficiently access cytosol is especially important when a synthetic compound has the potential to become a drug substance. D-Phe-Phe-Phe-D-Trp-Lys-Thr-Phe-Thr-NH<sub>2</sub> (BIM-23052) is a linear analog of somatostatin with established in vitro GH-inhibitory activity in nanomolar (nm) concentrations and high affinity to different somatostatin receptors. (2) Methods: Series of analogs of BIM-23052 were synthesized where Phe residue(s) in the BIM-23052 molecule were replaced with Tyr using standard SPPS, Fmoc/t-Bu strategy. Analyses of target compounds were performed using HPLC/MS technique. Toxicity and antiproliferative activity were studied using in vitro NRU and MTT assays. The values of logP (partition coefficient in octanol/water) for BIM-23052 and its analogs were calculated. (3) Results: The obtained data show the best antiproliferative effect against studied cancer cells for compound D-Phe-Phe-Phe-D-Trp-Lys-Thr-Tyr<sup>7</sup>-Thr-NH<sub>2</sub> (DD8), the most lipophilic compound according to the predicted logP values. (4) Conclusions: Multiple analyses of the obtained data reveal that compound D-Phe-Phe-Phe-D-Trp-Lys-Thr-Tyr<sup>7</sup>-Thr-NH<sub>2</sub> (DD8) where one Phe is replaced by Tyr has the best combination of cytotoxicity, antiproliferative effect and hydrolytic stability. 
546 |a EN 
690 |a BIM-23052 analogs 
690 |a somatostatin 
690 |a lipophilicity 
690 |a antiproliferative effect 
690 |a cytotoxicity 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 4, p 1123 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/4/1123 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/d82a6f044e184e70acf75b75b677df3e  |z Connect to this object online.