Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ranganathan Balasubramanian"'
Autor:
Ranganathan Balasubramanian
Publikováno v:
Hinduism and Tribal Religions ISBN: 9789402410365
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc199909451998dbece643ae13cfef3e
https://doi.org/10.1007/978-94-024-1188-1_325
https://doi.org/10.1007/978-94-024-1188-1_325
Autor:
Ranganathan Balasubramanian
Publikováno v:
Hinduism and Tribal Religions ISBN: 9789402410365
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f0bd9adb7919630d9d53a599e74b82
https://doi.org/10.1007/978-94-024-1036-5_565-1
https://doi.org/10.1007/978-94-024-1036-5_565-1
Autor:
Amrutha B. Chittethu, Asha Asokan Manakadan, Ranganathan Balasubramanian, Sathianarayanan, T.S. Saranya, Asha Jose
Publikováno v:
Journal of Young Pharmacists. 9:218-223
Objective: The present study was aimed to determine cytotoxic and apoptotic activity of isatin semicarbazones against mammary carcinoma. Methodology: The preparation of these target compounds involved substitution at the third position of the isatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23d859b34b5c32f2ef1ba1c604d6f0c4
https://doi.org/10.5530/jyp.2017.9.43
https://doi.org/10.5530/jyp.2017.9.43
Autor:
Ranganathan Balasubramanian, Sathianarayanan, Ashitha Balakrishnan, Asha Jose, Diana Thomas, Rajasekaran Aiyalu
Publikováno v:
Journal of Young Pharmacists. 8:398-405
Objective: The current study investigates the potential of alcoholic extract of Wrightia tinctoria leaves and its isolates in repairing the DNA damage induced by gamma radiation. Methodology: The ethanolic extract of Wrightia tinctoria ( EEWT ) the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eea4ccca3ab6fa05c76397ff92e1b1b6
https://doi.org/10.5530/jyp.2016.4.16
https://doi.org/10.5530/jyp.2016.4.16
Publikováno v:
Indian Journal Of Pharmaceutical Education And Research. 47:31-38
A series of monosubstituted chalcones with potential anti-inflammatory activity have been rationally designed leading to a focused library of ligands 4a-jwith ring-A substitution. Subsequent to drug-likeness and druggability assessments, the library
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61ac6006c50dc0904422525c4e6b450f
https://doi.org/10.5530/ijper.47.4.5
https://doi.org/10.5530/ijper.47.4.5
Publikováno v:
Pakistan journal of pharmaceutical sciences. 29(1)
An over production of reactive oxygen species beyond basal levels generated continuously in the body as part of natural metabolic processes often results in serious and diverse disease conditions including cancer. Chalcones are known to possess good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45ada7d0b732703b2edd97435a820274
https://pubmed.ncbi.nlm.nih.gov/26826830
https://pubmed.ncbi.nlm.nih.gov/26826830
Synthesis, anti-inflammatory and antioxidant activity of ring-A-monosubstituted chalcone derivatives
Publikováno v:
IndraStra Global.
A library of ring-A-monosubstituted chalcone derivatives (4a-4i, 5a and 5b) was designed and synthesised. The structures as well as the identities of these compounds were established on the basis of spectral (1H NMR, 13C NMR, FT-IR and Mass) and elem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fb7cb6d795a0ddafda3aad74bb96410
https://igi.indrastra.com/items/show/82273
https://igi.indrastra.com/items/show/82273
A stereoselective total synthesis of the cytotoxic natural products tubulysin U, tubulysin V, and its unnatural epimer epi-tubulysin V, is reported. A series of simplified analogs containing N,N-dimethyl-D-alanine as a replacement for the N-terminal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4548917114cf88b2f0929b8f1f9bb726
https://europepmc.org/articles/PMC4183140/
https://europepmc.org/articles/PMC4183140/
Autor:
Ranganathan Balasubramanian, Dan L. Sackett, Jaeson C. Steele, Bhooma Raghavan, Robert A. Fecik
Publikováno v:
Journal of medicinal chemistry. 51(6)
An efficient route for the synthesis of the tubulysin family of antimitotic peptides was developed. Simplified tubulysin analogues were synthesized to define the minimum pharmacophore required for cytotoxicity. Simplified tubulysin analogues retain s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85ada6991cd40e59168ff1fd9482aaa0
https://pubmed.ncbi.nlm.nih.gov/18314944
https://pubmed.ncbi.nlm.nih.gov/18314944