Total Synthesis of Biologically Potent Peptides and their In Silico Studies: A TAG Approach

The two peptides FRDEHKK and NKDRG were isolated as fine solids with 82% and 85% yield and were characterized by NMR and MASS spectroscopy. In-silico studies reveal FRDEHKK and NKDRG peptides exhibit good affinity towards EGFR and AXL kinase.

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Publication Details

Journal
Current Topics in Medicinal Chemistry
Published
2025-08-04
DOI
https://doi.org/10.2174/0115680266377804250721145504
Primary Topic
Chemical Synthesis and Analysis
Type
article
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0.00
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article

Total Synthesis of Biologically Potent Peptides and their In Silico Studies: A TAG Approach

Munagala Gayatri Ramya, G. Nagendra, Veeranjaneyulu Avula, Kiran Kumar H.B.
Current Topics in Medicinal Chemistry
Chemical Synthesis and Analysis
article

Total Synthesis of Biologically Potent Peptides and their In Silico Studies: A TAG Approach

Munagala Gayatri Ramya, G. Nagendra, Veeranjaneyulu Avula, Kiran Kumar H.B.
article en

Abstract

The two peptides FRDEHKK and NKDRG were isolated as fine solids with 82% and 85% yield and were characterized by NMR and MASS spectroscopy. In-silico studies reveal FRDEHKK and NKDRG peptides exhibit good affinity towards EGFR and AXL kinase.

Current Topics in Medicinal ChemistryVol. 25
Department of Biotechnology (IN), Department of Atomic Energy (IN), REVA University (IN)
Openalex Percentile: Top 82%
Chemical Synthesis and Analysis
DOISourceOpenAlex
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Total Synthesis of Biologically Potent Peptides and their In Silico Studies: A TAG Approach — Munagala Gayatri Ramya, G. Nagendra, et al. · Current Topics in Medicinal Chemistry (2025) | TGRS Research Map | TGRS