Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Suresh V, Chennupati"'
Autor:
Rajiv Dahiya, Sunita Dahiya, Neeraj Kumar Fuloria, Rita Mourya, Saurabh Dahiya, Shivkanya Fuloria, Suresh Kumar, Jyoti Shrivastava, Renu Saharan, Suresh V. Chennupati, Jayvadan K. Patel
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 22:1772-1788
Abstract: Bridged peptide macrobicycles (BPMs) from natural resources belong to types of compounds that are not investigated fully in terms of their formation, pharmacological potential, and stereo- chemical properties. This division of biologically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c8f772a2e7036bc387e3f7f210a21a0
https://doi.org/10.2174/1389557522666220113122117
https://doi.org/10.2174/1389557522666220113122117
Autor:
Sunita Dahiya, Vijaya Sahadeo, Vernon Davis, Rajiv Dahiya, Suresh V. Chennupati, Jayvadan K. Patel
Publikováno v:
Current Organic Synthesis. 19:267-278
Aims: The present investigation is targeted towards the synthesis of a novel analogue of a natural peptide of marine origin. Background: Marine sponges are enriched with bioactive secondary metabolites, especially circu-lar peptides. Heterocycles are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61e6dceec6a6c5f8c7a24ace2035e41
https://doi.org/10.2174/1570179418666211005141811
https://doi.org/10.2174/1570179418666211005141811
Autor:
Rajiv Dahiya, Sunita Dahiya, Neeraj Kumar Fuloria, Suresh Kumar, Rita Mourya, Suresh V. Chennupati, Satish Jankie, Hemendra Gautam, Sunil Singh, Sanjay Kumar Karan, Sandeep Maharaj, Shivkanya Fuloria, Jyoti Shrivastava, Alka Agarwal, Shamjeet Singh, Awadh Kishor, Gunjan Jadon, Ajay Sharma
Publikováno v:
Marine Drugs, Vol 18, Iss 6, p 329 (2020)
Peptides are distinctive biomacromolecules that demonstrate potential cytotoxicity and diversified bioactivities against a variety of microorganisms including bacteria, mycobacteria, and fungi via their unique mechanisms of action. Among broad-rangin
Externí odkaz:
https://doaj.org/article/8c82a8e3a8f64d4581a2845d31ef699e
Autor:
Sunita, Dahiya, Rajiv, Dahiya, Neeraj Kumar, Fuloria, Rita, Mourya, Saurabh, Dahiya, Shivkanya, Fuloria, Suresh, Kumar, Jyoti, Shrivastava, Renu, Saharan, Suresh V, Chennupati, Jayvadan K, Patel
Publikováno v:
Mini reviews in medicinal chemistry. 22(13)
Bridged peptide macrobicycles (BPMs) from natural resources belong to types of compounds that are not investigated fully in terms of their formation, pharmacological potential, and stereo- chemical properties. This division of biologically active con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4afaeb9e305b2f02d7076009d80bc8f0
https://pubmed.ncbi.nlm.nih.gov/35049431
https://pubmed.ncbi.nlm.nih.gov/35049431
Autor:
Suresh Kumar, Rajiv Dahiya, Sukhbir Lal Khokra, Rita Mourya, Suresh V. Chennupati, Sandeep Maharaj
Publikováno v:
Molecules, Vol 22, Iss 6, p 682 (2017)
The present investigation reports the synthesis of a phenylalanine-rich N-methylated cyclopeptide, cordyheptapeptide A (8), previously isolated from the insect pathogenic fungus Cordyceps sp. BCC 1788, accomplished through the coupling of N-methylate
Externí odkaz:
https://doaj.org/article/3caca5f73c7f46fc910863692b824e72
Autor:
Rajiv, Dahiya, Stacy, Rampersad, Terry G, Ramnanansingh, Komalpreet, Kaur, Ramninder, Kaur, Rita, Mourya, Suresh V, Chennupati, Richard, Fairman, Nigel K, Jalsa, Ajay, Sharma, Shivkanya, Fuloria, Neeraj Kumar, Fuloria
Publikováno v:
Iranian Journal of Pharmaceutical Research : IJPR
Synthesis of a natural proline-rich cyclopolypeptide - rolloamide A was carried out by coupling of tri- and tetrapeptide units Boc-Phe-Pro-Val-OMe and Boc-Pro-Leu-Pro-Ile-OMe after proper deprotection at carboxyl and amino terminals using carbodiimid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a8c460e25b1e1dbb53bf6e2ec9f6211
https://pubmed.ncbi.nlm.nih.gov/33680019
https://pubmed.ncbi.nlm.nih.gov/33680019
Publikováno v:
Marine Drugs, Vol 14, Iss 12, p 228 (2016)
A natural heptacyclopeptide, stylissamide G (7), previously isolated from the Bahamian marine sponge Stylissa caribica from the Caribbean Sea, was synthesized via coupling of the tetrapeptide l-phenylalanyl-l-prolyl-l-phenylalanyl-l-proline methyl es
Externí odkaz:
https://doaj.org/article/529f5044c1eb4fcfa07babd281c40bd7
Autor:
Awadh Kishor, Rita Mourya, Jyoti Shrivastava, Ajay Sharma, Gunjan Jadon, Alka Agarwal, Hemendra Gautam, Sunil K. Singh, Satish Jankie, Shivkanya Fuloria, Neeraj Kumar Fuloria, Sunita Dahiya, Rajiv Dahiya, Sanjay Kumar Karan, Suresh Kumar, Sandeep Maharaj, Suresh V. Chennupati, Shamjeet Singh
Publikováno v:
Marine Drugs
Marine Drugs, Vol 18, Iss 329, p 329 (2020)
Marine Drugs, Vol 18, Iss 329, p 329 (2020)
Peptides are distinctive biomacromolecules that demonstrate potential cytotoxicity and diversified bioactivities against a variety of microorganisms including bacteria, mycobacteria, and fungi via their unique mechanisms of action. Among broad-rangin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32ab4ef88a546c6ecc94d60c5cda5e2e
https://doi.org/10.3390/md18060329
https://doi.org/10.3390/md18060329
Autor:
Rajiv Dahiya, Sukhbir Lal Khokra, Rita Mourya, Suresh Kumar, Sandeep Maharaj, Suresh V. Chennupati
Publikováno v:
Molecules; Volume 22; Issue 6; Pages: 682
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 6, p 682 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 6, p 682 (2017)
The present investigation reports the synthesis of a phenylalanine-rich N-methylated cyclopeptide, cordyheptapeptide A (8), previously isolated from the insect pathogenic fungus Cordyceps sp. BCC 1788, accomplished through the coupling of N-methylate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c69ed444e0928c0063c0e8f9b50bd5