Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Archna Mathur"'
Autor:
Sergey A. Tarasov, Kamaraj Mani, Yulia O. Demidchenko, Archna Mathur, Sachin S. Sakat, Oleg I. Epstein, Evgeniy A. Gorbunov
Publikováno v:
Inflammation
The study was aimed to investigate the effect of technologically treated diclofenac (release-active dilutions of diclofenac (RAD of diclofenac)) on anti-inflammatory activity of diclofenac in carrageenan-induced rat paw edema model. Ninety male Wista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7ec65090766bf8d134508e3c7153050
https://doi.org/10.1007/s10753-020-01359-x
https://doi.org/10.1007/s10753-020-01359-x
Autor:
Sergey A. Tarasov, Oleg I. Epstein, Kamaraj Mani, Archna Mathur, Sachin S. Sakat, Yulia O. Demidchenko, Evgeniy A. Gorbunov
Publikováno v:
Inflammation. 37:1-9
The study was aimed to investigate the effect of technologically treated diclofenac (release-active dilutions of diclofenac (RAD of diclofenac)) on anti-inflammatory activity of diclofenac in carrageenan-induced rat paw edema model. Ninety male Wista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c2f38ad32e2951ea9e58b7bc23e6ba4
https://doi.org/10.1007/s10753-013-9705-0
https://doi.org/10.1007/s10753-013-9705-0
Publikováno v:
Journal of Peptide Science. 13:458-467
A large 40-residue precursor peptide (propeptide 5) was synthesized by linking together four designed anticancer peptide analogs to the neuropeptides: vasoactive intestinal peptide, somatostatin, bombesin and substance P, using enzyme cleavable lysyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adad70f812e435f24c9ae1b9b630c9f9
https://doi.org/10.1002/psc.867
https://doi.org/10.1002/psc.867
Autor:
Anu T. Singh, Neena Gupta, Archna Mathur, Rama Mukherjee, Rinku Ahuja, Rajan Sharma, Manu Jaggi, Sudhanand Prasad
Publikováno v:
International Journal of Peptide Research and Therapeutics. 12:179-185
We describe the synthesis and anticancer activities of octapeptide analogs of somatostatin incorporating α,α-dialkylated amino acids. The designed analogs of somatostatin are: d-Phe1-Cys2-Tyr3-d-Trp4-Orn5-Xxx6-Pen7-Thr8-NH2 where Xxx=α-Aminoisobut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf77017864e7e4aefdc7b323622e0e94
https://doi.org/10.1007/s10989-005-9005-0
https://doi.org/10.1007/s10989-005-9005-0
Publikováno v:
Understanding Biology Using Peptides ISBN: 9780387265698
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f3c23173cc6001bda8af7fd76b5ccb8
https://doi.org/10.1007/978-0-387-26575-9_282
https://doi.org/10.1007/978-0-387-26575-9_282
Autor:
Neena Gupta, Rama Mukherjee, Archna Mathur, Manu Jaggi, Tushar Kanti Chakraborty, Sudhanand Prasad, Ajit C. Kunwar, Rajan Sharma
Publikováno v:
Understanding Biology Using Peptides ISBN: 9780387265698
Introduction The octapeptide sequence Leu1-Met2-Tyr3-Pro4-Thr5-Tyr6-Leu7-Lys8-OH (1) is reported to be a receptor binding inhibitor of vasoactive intestinal peptide. The anticancer activity of octapeptide 1 in combination with other neuropeptide anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::678bf5613c6ccdf37aabc3718da4b1b6
https://doi.org/10.1007/978-0-387-26575-9_293
https://doi.org/10.1007/978-0-387-26575-9_293
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 13(8)
Six analogs (peptides 1–6) of the potent substance P (SP) derivative known as ‘Antagonist D’ were synthesized by substituting constrained amino acids Aib or Acp (cycloleucine, 1-amino cyclopentane carboxylic acid) at different positions in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4849a4aeccf188a058467bf4fa07d5
https://pubmed.ncbi.nlm.nih.gov/17617800
https://pubmed.ncbi.nlm.nih.gov/17617800
Autor:
Vinod K. Sanna, Neena Gupta, Anu T. Singh, Archna Mathur, Manu Jaggi, Rama Mukherjee, Sudhanand Prasad, Kakali Datta, Praveen Rajendran
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 13(1)
Six octapeptide bombesin (BN) analogs were synthesized by substituting alpha-aminoisobutyric acid (Aib), in place of Ala9 or Gly11, or both, in the [D-Phe6, desMet14]-BN (6-14) sequence: D-Phe6-Gln7-Trp8-Ala9-Val10-Gly11-His12-Leu13-NH2 (P0). Additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f78a2fdb0990beb92de3c7c6b27be725
https://pubmed.ncbi.nlm.nih.gov/17031871
https://pubmed.ncbi.nlm.nih.gov/17031871