Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Liva Harinantenaina Rakotondraibe"'
Autor:
Susumu Kawakami, Chieko Kanagawa, Liva Harinantenaina Rakotondraibe, Masanori Inagaki, Motohiro Nishimura, Hideaki Otsuka, Toshio Seyama, Katsuyoshi Matsunami, Falitiana Marrino Rakotoarisoa, Stéphan Richard Rakotonandrasana, Alain Michel Ratsimbason
Publikováno v:
Chemical and Pharmaceutical Bulletin. 70:901-906
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f29b3d116c398dbec547926d1a5c08f0
https://doi.org/10.1248/cpb.c22-00648
https://doi.org/10.1248/cpb.c22-00648
Autor:
Leslie N. Aldrich, Joanna E. Burdette, Esperanza Carcache de Blanco, Christopher C. Coss, Alessandra S. Eustaquio, James R. Fuchs, A. Douglas Kinghorn, Amanda MacFarlane, Brittney K. Mize, Nicholas H. Oberlies, Jimmy Orjala, Cedric J. Pearce, Mitch A. Phelps, Liva Harinantenaina Rakotondraibe, Yulin Ren, Djaja Doel Soejarto, Brent R. Stockwell, Jack C. Yalowich, Xiaoli Zhang
Publikováno v:
J Nat Prod
Research progress from mainly over the last five years is described for a multidisciplinary collaborative program project directed toward the discovery of potential anticancer agents from a broad range of taxonomically defined organisms. Selected lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::863674aa9c1ff16c3ad9cc483f37b26e
https://pubmed.ncbi.nlm.nih.gov/35213158
https://pubmed.ncbi.nlm.nih.gov/35213158
Autor:
Susumu, Kawakami, Chieko, Kanagawa, Liva Harinantenaina, Rakotondraibe, Masanori, Inagaki, Motohiro, Nishimura, Hideaki, Otsuka, Toshio, Seyama, Katsuyoshi, Matsunami, Falitiana Marrino, Rakotoarisoa, Stéphan Richard, Rakotonandrasana, Alain Michel, Ratsimbason
Publikováno v:
Chemicalpharmaceutical bulletin. 70(12)
From the less polar fraction of the MeOH extract of the leaves and twigs of Omphalea oppositifolia, five new ent-rosane-type diterpenoids, named omphalines A-E (1-5), were isolated together with one known compound, 7-keto-ent-kaurane-16β,17-diol (6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef688c2ad0ba9d651769f1477dfd6fc6
https://pubmed.ncbi.nlm.nih.gov/36450588
https://pubmed.ncbi.nlm.nih.gov/36450588
Autor:
Petr Bartunek, Alena Špičáková, Christopher C. Coss, Tyler A. Wilson, Jayaprakash Narayana Kolla, Tehane Ali, Keisuke Ishita, Chad Bennett, Hongyan Wang, Zbigniew J. Leśnikowski, Werner Tjarks, Pavel Anzenbacher, Hanna S. Radomska, David Sedlák, Dasheng Wang, Liva Harinantenaina Rakotondraibe, Sandip Vibhute
Publikováno v:
Journal of Medicinal Chemistry. 64:9330-9353
Selective agonism of the estrogen receptor (ER) subtypes, ERα and ERβ, has historically been difficult to achieve due to the high degree of ligand-binding domain structural similarity. Multiple efforts have focused on the use of classical organic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00aeffb2cbe2dead4c22b0b814f33e5b
https://doi.org/10.1021/acs.jmedchem.1c00555
https://doi.org/10.1021/acs.jmedchem.1c00555
Autor:
David, Sedlák, Tyler A, Wilson, Werner, Tjarks, Hanna S, Radomska, Hongyan, Wang, Jayaprakash Narayana, Kolla, Zbigniew J, Leśnikowski, Alena, Špičáková, Tehane, Ali, Keisuke, Ishita, Liva Harinantenaina, Rakotondraibe, Sandip, Vibhute, Dasheng, Wang, Pavel, Anzenbacher, Chad, Bennett, Petr, Bartunek, Christopher C, Coss
Publikováno v:
Journal of medicinal chemistry. 64(13)
Selective agonism of the estrogen receptor (ER) subtypes, ERα and ERβ, has historically been difficult to achieve due to the high degree of ligand-binding domain structural similarity. Multiple efforts have focused on the use of classical organic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::19ca42c75bf9fd8c71369d33b3caf2ff
https://pubmed.ncbi.nlm.nih.gov/34181409
https://pubmed.ncbi.nlm.nih.gov/34181409
Autor:
Peter M. Piermarini, Katharina Happel, Beenhwa Lee, Preston K. Manwill, Andrew DeLaat, Anton Walter, Liva Harinantenaina Rakotondraibe, Megha Kalsi, Bao Nguyen, Rose Sepesy, Renata Rusconi Trigueros
Publikováno v:
Pestic Biochem Physiol
Cinnamodial (CDIAL) is a drimane sesquiterpene dialdehyde found in the bark of Malagasy medicinal plants (Cinnamosmaspecies; family Canellaceae). We previously demonstrated that CDIAL was insecticidal, antifeedant, and repellent againstAedes aegyptim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee05b7082333c92ed80dec25e9c64b9b
https://europepmc.org/articles/PMC7770332/
https://europepmc.org/articles/PMC7770332/
Autor:
Carla Slebodnick, Tran Ngoc Ninh, DD Soejarto, Liva Harinantenaina Rakotondraibe, PA Benatrehina, AD Kinghorn
Publikováno v:
Planta Medica. 81:S1-S381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14aca7330961771c5a1622f50ac6da26
https://doi.org/10.1055/s-0036-1596515
https://doi.org/10.1055/s-0036-1596515
Autor:
Benjamin, Métoyer, Nicolas, Lebouvier, Edouard, Hnawia, Louis, Thouvenot, Fengrui, Wang, Liva, Harinantenaina Rakotondraibe, Phila, Raharivelomanana, Yoshinori, Asakawa, Mohammed, Nour
Publikováno v:
Natural product research. 35(12)
The first chemotaxonomic study based on volatile components of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e81d66e5e1f59554cd6e019ffd94f2f
https://pubmed.ncbi.nlm.nih.gov/31441670
https://pubmed.ncbi.nlm.nih.gov/31441670
Autor:
Esperanza J. Carcache de Blanco, Gerardo D. Anaya-Eugenio, Liva Harinantenaina Rakotondraibe, Tehane Ali
Publikováno v:
Anti-cancer drugs. 30(4)
In our continuing effort to identify bioactive secondary metabolites from natural sources, the antiproliferative activity of 23 compounds, previously isolated from Penicillium concentricum, was assessed using the sulforhodamine B assay. The cytotoxic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5191f40703d71cf5d2e53874d94a9fc8
https://pubmed.ncbi.nlm.nih.gov/30688672
https://pubmed.ncbi.nlm.nih.gov/30688672
Autor:
Yan Zhang, Choon Yong Tan, Liva Harinantenaina Rakotondraibe, A. Douglas Kinghorn, James R. Fuchs, Richard W. Spjut
Publikováno v:
Phytochemistry
Three undescribed stictanes, nieblastictanes A−C, two flavicanes, nieblaflavicanes A and B, together with three already reported stictanes, along with the known compounds (+)-usnic acid, sekikaic acid, divaricatic acid, and divaricatinic acid methy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::526e3f3cbee3d29ad061d0877a072b81
https://doi.org/10.1016/j.phytochem.2020.112521
https://doi.org/10.1016/j.phytochem.2020.112521