Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sachin B. Baravkar"'
Publikováno v:
Biomolecules, Vol 14, Iss 1, p 94 (2024)
Third-degree burn injuries pose a significant health threat. Safer, easier-to-use, and more effective techniques are urgently needed for their treatment. We hypothesized that covalently bonded conjugates of fatty acids and tripeptides can form wound-
Externí odkaz:
https://doaj.org/article/364e0047bbff43249087c11f3961086a
Autor:
Amit S. Choudhari, Sujit Bhansali, Mahendra A. Wagh, Gangadhar J. Sanjayan, Dhiman Sarkar, Laxman Nawale, Sachin B. Baravkar
Publikováno v:
ChemistrySelect. 4:2851-2857
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8774fc0060cf92f3064dd4a965b2227f
https://doi.org/10.1002/slct.201803370
https://doi.org/10.1002/slct.201803370
Autor:
Sachin B. Baravkar, Gangadhar J. Sanjayan, Manas Kumar Santra, Mahendra A. Wagh, Debasish Paul
Publikováno v:
Tetrahedron Letters. 59:3473-3476
Herein, we report synthesis and in vitro anticancer activity of conformationally constrained Smac mimetics containing reverse turn inducing motifs “Ant-Pro” and “sAnt-Pro”. The synthesis of Smac analogs with diverse hydrophobic groups at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc2f56a3a760778d9794f049b0f89e5
https://doi.org/10.1016/j.tetlet.2018.08.016
https://doi.org/10.1016/j.tetlet.2018.08.016
Autor:
Dhiman Sarkar, Rachna Borkute, Ganesh S. Jedhe, Mahendra A. Wagh, Sachin B. Baravkar, Amit S. Choudhari, Gangadhar J. Sanjayan
Publikováno v:
ChemistrySelect. 3:3122-3126
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e5bc2b56334011be136ac2bd5d2abbc
https://doi.org/10.1002/slct.201800027
https://doi.org/10.1002/slct.201800027
Autor:
Rajesh G. Gonnade, Sachin B. Baravkar, Samir R. Shaikh, Gangadhar J. Sanjayan, Amol S. Kotmale
Publikováno v:
European Journal of Organic Chemistry. 2017:2944-2949
In this paper, we provide structural insights into the hydrogen-bonding and folding pattern in Ant-Ant-Pro-Gly tetrapeptides (Ant: anthranilic acid; Pro: proline; and Gly: glycine). Comparison of the C-terminal esters and their amide analogs revealed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b718ee0457ca690ef548faf22085595
https://doi.org/10.1002/ejoc.201700181
https://doi.org/10.1002/ejoc.201700181
Publikováno v:
Chem. Commun.. 50:13874-13884
Structural mimicry of peptides has witnessed perceptible progress in the last three decades. Reverse turn and β-hairpin units are the smallest secondary structural motifs that are some of the most scrutinized functional cores of peptides and protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef9c62efd869b427f921ecd4102c941
https://doi.org/10.1039/c4cc03114h
https://doi.org/10.1039/c4cc03114h
Publikováno v:
ChemInform. 46
The formation of an unusual product (V) during the coupling reaction of benzoxazinone and amino acids, mediated by DBU is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cfec31b2914be2597b80e3d98da559b
https://doi.org/10.1002/chin.201508043
https://doi.org/10.1002/chin.201508043
This communication demonstrates the formation of an unusual nucleophilic ring opening of benzoxazinones by 1,8-diazabicycloundec-7-ene (DBU). This observation contradicts the intrinsic feature of a hindered nonnucleophilic base like DBU. Confirmation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80e2a5e0007c473e70ec43b872af1dec
