Claulansine F promoted the neuronal differentiation of neural stem and progenitor cells through Akt/GSK-3β/β-catenin pathway
Huang, J.Y., Ma, Y.Z., Yuan, Y.H., Zuo, W., Chu, S.F., Liu, H., Du, G.H., Zhang, D.M., Chen, N.H., Claulansine F promoted the neuronal differentiation of neural stem and progenitor cells through Akt/GSK-3β/β-catenin pathway. Eur. J. Pharmacol. 786 (2016), 72–84.
Global, regional, and national age–sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the global burden of disease study 2013
Naghavi, M., Wang, H., Lozano, R., Davis, A., Liang, X., Zhou, M., Vollset, S.E.V., Abbasoglu Ozgoren, A., Norman, R.E., Vos, T., Global, regional, and national age–sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the global burden of disease study 2013. Lancet 385 (2015), 117–171.
Synthesis of piperlongumine analogues and discovery of nuclear factor erythroid 2-related factor 2 (Nrf2) activators as potential neuroprotective agents
Peng, S., Zhang, B., Meng, X., Yao, J., Fang, J., Synthesis of piperlongumine analogues and discovery of nuclear factor erythroid 2-related factor 2 (Nrf2) activators as potential neuroprotective agents. J. Med. Chem. 58 (2015), 5242–5255.
On the structures of girinimbine, mahanimbine, isomahanimbine, koenimbidine and murrayacine
Joshi, B.S., Kamat, V.N., Gawad, D.H., On the structures of girinimbine, mahanimbine, isomahanimbine, koenimbidine and murrayacine. Tetrahedron 26 (1970), 1475–1482.
Synthesis of murrayacine. Oxidation with DDQ [2,3-dichloro-5,6-dicyanobenzoquinone] of the activated aromatic methyl group of the alkaloids of Murraya koenigii
Anwer, M.F., Masaldan, A.S., Kapil, R.S., Popli, S.P., Synthesis of murrayacine. Oxidation with DDQ [2,3-dichloro-5,6-dicyanobenzoquinone] of the activated aromatic methyl group of the alkaloids of Murraya koenigii. Indian J. Chem. 12 (1973), 1314–1315.
A multiple free-radical scavenging (MULTIS) study on the antioxidant capacity of a neuroprotective drug, edaravone as compared with uric acid, glutathione, and trolox
Kamogawa, E., Sueishi, Y., A multiple free-radical scavenging (MULTIS) study on the antioxidant capacity of a neuroprotective drug, edaravone as compared with uric acid, glutathione, and trolox. Bioorg. Med. Chem. Lett. 24 (2014), 1376–1379.
Brain distribution and bioavailability of elacridar after different routes of administration in the mouse
Sane, R., Agarwal, S., Elmquist, W.F., Brain distribution and bioavailability of elacridar after different routes of administration in the mouse. Drug Metabol. Dispos. Biol. Fate Chem., 40, 2012, 1612.
Synthesis of the pyrano[3,2-a]carbazole alkaloids koenine, koenimbine, koenigine, koenigicine, and structural reassignment of mukonicine
Schuster, C., Rönnefahrt, M., Julich-Gruner, K., Jäger, A., Schmidt, A., Knölker, H.J., Synthesis of the pyrano[3,2-a]carbazole alkaloids koenine, koenimbine, koenigine, koenigicine, and structural reassignment of mukonicine. Synthesis 48 (2015), 150–160.
Synthesis and structure–activity relationships of Lansine analogues as antileishmanial agents
Pieroni, M., Girmay, S., Sun, D., Sahu, R., Tekwani, B.L., Tan, G.T., Synthesis and structure–activity relationships of Lansine analogues as antileishmanial agents. Chemmedchem 7 (2012), 1895–1900.
Palladium(II)-catalysed total synthesis of naturally occurring pyrano[3,2-a]carbazole and pyrano[2,3-b]carbazole alkaloids
Hesse, R., Jäger, A., Schmidt, A.W., Knölker, H.J., Palladium(II)-catalysed total synthesis of naturally occurring pyrano[3,2-a]carbazole and pyrano[2,3-b]carbazole alkaloids. Org. Biomol. Chem. 12 (2014), 3866–3876.
Efficient construction of pyrano[3,2-a]carbazoles: application to a biomimetic total synthesis of cyclized monoterpenoid pyrano[3,2-a]carbazole alkaloids
Hesse, R., Gruner, K.K., Kataeva, O., Schmidt, A.W., Knölker, H.J., Efficient construction of pyrano[3,2-a]carbazoles: application to a biomimetic total synthesis of cyclized monoterpenoid pyrano[3,2-a]carbazole alkaloids. Chemistry 19 (2013), 14098–14111.
Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids–first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (-)-trans-dihydroxygirinimbine
Gruner, K.K., Hopfmann, T., Matsumoto, K., Jäger, A., Katsuki, T., Knölker, H.J., Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids–first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (-)-trans-dihydroxygirinimbine. Org. Biomol. Chem. 9 (2011), 2057–2061.
Neutralization of chemokine-like factor 1, a novel C-C chemokine, protects against focal cerebral ischemia by inhibiting neutrophil infiltration via MAPK pathways in rats
Kong, L.L., Wang, Z.Y., Han, N., Zhuang, X.M., Wang, Z.Z., Li, H., Chen, N.H., Neutralization of chemokine-like factor 1, a novel C-C chemokine, protects against focal cerebral ischemia by inhibiting neutrophil infiltration via MAPK pathways in rats. J. Neuroinflammation 11 (2014), 1–10.