Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Chandrashekhar, Madasu"'
Autor:
Ya-ming Xu, Chandrashekhar Madasu, Manping X. Liu, E. M. Kithsiri Wijeratne, David Dierig, Bob White, István Molnár, A. A. Leslie Gunatilaka
Publikováno v:
ACS Omega, Vol 6, Iss 23, Pp 15486-15498 (2021)
Externí odkaz:
https://doaj.org/article/e9660fa750f44859b1b8b1fd673aff1a
Publikováno v:
In Bioorganic Chemistry February 2019 82:306-323
Autor:
Marielle C. Inacio, Weimao Zhong, Ya-Ming Xu, E.M. Kithsiri Wijeratne, Chandrashekhar Madasu, István Molnár, A.A. Leslie Gunatilaka
Publikováno v:
Phytochemistry Letters. 55:124-130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3eed21f772d8066afe91781de6ea5e4b
https://doi.org/10.1016/j.phytol.2023.05.001
https://doi.org/10.1016/j.phytol.2023.05.001
Autor:
Ram K. Modukuri, Diana Monsivais, Feng Li, Murugesan Palaniappan, Kurt M. Bohren, Zhi Tan, Angela F. Ku, Yong Wang, Chandrashekhar Madasu, Jian-Yuan Li, Suni Tang, Gabriella Miklossy, Stephen S. Palmer, Damian W. Young, Martin M. Matzuk
Publikováno v:
Journal of Medicinal Chemistry. 66:2143-2160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::899e0b4e19580a2aa29d02840b07db86
https://doi.org/10.1021/acs.jmedchem.2c01886
https://doi.org/10.1021/acs.jmedchem.2c01886
Autor:
Chandrashekhar, Madasu, Nayak, Vadithe Lakshma, Ramakrishna, Sistla, Mallavadhani, Uppuluri Venkata
Publikováno v:
In European Journal of Medicinal Chemistry 23 May 2016 114:293-307
Autor:
Leslie Gunatilaka, Manping X. Liu, Chandrashekhar Madasu, E. M. Kithsiri Wijeratne, Ya-Ming Xu, István Molnár
Publikováno v:
Madasu, C, Xu, Y M, Wijeratne, E M K, Liu, M X, Molnár, I & Gunatilaka, A A L 2022, ' Semi-synthesis and cytotoxicity evaluation of pyrimidine, thiazole, and indole analogues of argentatins A–C from guayule (Parthenium argentatum) resin ', Medicinal Chemistry Research, vol. 31, no. 7, pp. 1088-1098 . https://doi.org/10.1007/s00044-021-02835-1
Argentatins A–C (1–3), the major cycloartane-type triterpenoids of guayule resin, a byproduct of commercial rubber production, were converted into their pyrimidine (7–12), thiazole (13–15), and indole (16–18) analogues by a molecular hybrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc1dce10dcc68ea03fff4124256a04f4
https://doi.org/10.21203/rs.3.rs-975607/v1
https://doi.org/10.21203/rs.3.rs-975607/v1
Autor:
Bob White, Ya Ming Xu, István Molnár, A. A. Leslie Gunatilaka, Chandrashekhar Madasu, E. M. Kithsiri Wijeratne, Manping X. Liu, David Dierig
Publikováno v:
Xu, Y M, Madasu, C, Liu, M X, Wijeratne, E M K, Dierig, D, White, B, Molnár, I & Gunatilaka, A A L 2021, ' Cycloartane-And Lanostane-Type Triterpenoids from the Resin of Parthenium argentatum AZ-2, a Byproduct of Guayule Rubber Production ', ACS Omega, vol. 6, no. 23, pp. 15486-15498 . https://doi.org/10.1021/acsomega.1c01714
ACS Omega, Vol 6, Iss 23, Pp 15486-15498 (2021)
ACS Omega, Vol 6, Iss 23, Pp 15486-15498 (2021)
A total of 12 new cycloartane- and lanostane-type triterpenoids including 16-deoxyargentatin A (1), 16-deoxyisoargentatin A (2), 7-oxoisoargentatin A (3), 24-epi-argentatin H (4), 24-O-p-anisoylargentatin C (5), 24-O-trans-cinnamoylargentatin C (6),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8068b65d883e0f45e655d64e12be4a89
https://cris.vtt.fi/en/publications/d0f66bb8-470d-4ca8-931a-75ff8557f668
https://cris.vtt.fi/en/publications/d0f66bb8-470d-4ca8-931a-75ff8557f668
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 148:2183-2193
Myrrhanone A (5S,8R,9R,10R)-3-oxo-8,30-dihydroxypolypoda-13E,17E,21E-triene), a bicyclic triterpene isolated from guggul (Commiphora mukul Hook) gum resin, was found to be a very useful bioactive natural scaffold. The aim of this work is to carry out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe6aad7e16fcea277b8b40fdd735ece5
https://doi.org/10.1007/s00706-017-2024-7
https://doi.org/10.1007/s00706-017-2024-7
Autor:
Shailaja Karri, Ramakrishna Sistla, Mallavadhani Venkata Uppuluri, Rajendra Sangaraju, Chandrashekhar Madasu
Publikováno v:
European Journal of Medicinal Chemistry. 188:111974
A series of 28 novel 1,2,3-triazole hybrids of myrrhanone B have been designed and synthesized by employing regioselective Cu catalyzed Huisgen 1,3-dipolar cycloaddition reaction in highly efficient manner. All the synthesized analogues were assessed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b2789954bff7408c08e524b0ec52149
https://doi.org/10.1016/j.ejmech.2019.111974
https://doi.org/10.1016/j.ejmech.2019.111974
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