Results 81 to 90 of about 494 (132)

Nitidine chloride inhibits the progression of hepatocellular carcinoma by suppressing IGF2BP3 and modulates metabolic pathways in an m⁶A-dependent manner. [PDF]

Mol Med
Xiong DD, Chen ZD, Li JD, Deng YL, He RQ, Huang ZG, An SQ, Dang YW, Chen G.   +8 more
europepmc   +1 more source

A Yellow Flower With Jaundice Power: Liver Injury Attributed to Greater Celandine. [PDF]

ACG Case Rep J
Power S, Barritt AS.
europepmc   +1 more source

Metabolic engineering of Saccharomyces cerevisiae for chelerythrine biosynthesis. [PDF]

Microb Cell Fact
Zhu J, Zhang K, He Y, Zhang Q, Ran Y, Tan Z, Cui L, Feng Y.   +7 more
europepmc   +1 more source

Protopine and Allocryptopine Interactions with Plasma Proteins. [PDF]

Int J Mol Sci
Marciniak A, Kotynia A, Krzyżak E, Czyżnikowska Ż, Zielińska S, Kozłowska W, Białas M, Matkowski A, Jezierska-Domaradzka A.   +8 more
europepmc   +1 more source

Multi-enzymatic biomimetic cerium-based MOFs mediated precision chemodynamic synergistic antibacteria and tissue repair for MRSA-infected wounds. [PDF]

J Nanobiotechnology
Chen S, Li Y, Ma Q, Liang J, Feng Z, Wang S, Zhang S, Han K, Sun B, Wang H, Jiang H.   +10 more
europepmc   +1 more source

Integrating bioinformatics and experimental models to investigate the mechanism of the chelidonine-induced mitotic catastrophe via the AKT/FOXO3/FOXM1 axis in breast cancer cells. [PDF]

Biomol Biomed
Li H, Tang X, Sun Z, Qu Z, Zou X.
europepmc   +1 more source

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A new intermolecular benzyne cycloaddition approach to benzophenanthridines

Tetrahedron Letters, 1990
Abstract The Intermolecular Benzyne Cycloaddition (IBC) approach was used for the synthesis of benzophenanthridines by constructing ring C in the key cycloaddition ...
Enrique Guitian
exaly   +2 more sources

Structural insights into the benzophenanthridines binding to human glycine transporter GlyT1

European Journal of Pharmacology, 2015
We previously identified cysteine 475 as a key residue for the inhibitory action of sanguinarine on the human glycine transporter GlyT1c. To define potential benzophenanthridine binding pocket more closely, we created a structural homology model of GlyT1 and also mutated several amino acids in the vicinity of cysteine 475.
František Jursky, Martina Baliova
exaly   +3 more sources

The Benzophenanthridines

1978
Jérôme L Moniot, Maurice Shamma
exaly   +2 more sources

The Benzophenanthridines

Organic Chemistry, 1972
exaly   +2 more sources