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Calodenin C: a new guibourtinidol-(4alpha-->8)-afzelechin from Ochna calodendron.

Planta medica

Messanga BB, Ghogomu R, Sondengam BL, Martin MT, Blond A, Brouard JP, Bodo B.
PMID: 17253321
Planta Med. 1998 Dec;64(8):760-1. doi: 10.1055/s-2006-957577.

A new dimeric proanthocyanidin, calodenin C [guibourtinidol-(4alpha-->8)-afzelechin], was isolated from the stem bark of Ochna calodendron and its structure determined on the basis of chemical studies and spectroscopic data, including HMBC and ROESY experiments.

Cite
Messanga BB, Ghogomu R, Sondengam BL, et al. Calodenin C: a new guibourtinidol-(4alpha-->8)-afzelechin from Ochna calodendron. Planta Med. 1998;64(8):760-1doi: 10.1055/s-2006-957577.
Messanga, B. B., Ghogomu, R., Sondengam, B. L., Martin, M. T., Blond, A., Brouard, J. P., & Bodo, B. (1998). Calodenin C: a new guibourtinidol-(4alpha-->8)-afzelechin from Ochna calodendron. Planta medica, 64(8), 760-1. https://doi.org/10.1055/s-2006-957577
Messanga, B B, et al. "Calodenin C: a new guibourtinidol-(4alpha-->8)-afzelechin from Ochna calodendron." Planta medica vol. 64,8 (1998): 760-1. doi: https://doi.org/10.1055/s-2006-957577
Messanga BB, Ghogomu R, Sondengam BL, Martin MT, Blond A, Brouard JP, Bodo B. Calodenin C: a new guibourtinidol-(4alpha-->8)-afzelechin from Ochna calodendron. Planta Med. 1998 Dec;64(8):760-1. doi: 10.1055/s-2006-957577. PMID: 17253321.
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Excitation processes in H--Kr collisions.

Physical review. A, General physics

Esaulov VA, Grouard JP, Hall RI, Montmagnon JL.
PMID: 9898434
Phys Rev A Gen Phys. 1987 Mar 15;35(6):2470-2472. doi: 10.1103/physreva.35.2470.

No abstract available.

Cite
Esaulov VA, Grouard JP, Hall RI, et al. Excitation processes in H--Kr collisions. Phys Rev A Gen Phys. 1987;35(6):2470-2472doi: 10.1103/physreva.35.2470.
Esaulov, V. A., Grouard, J. P., Hall, R. I., & Montmagnon, J. L. (1987). Excitation processes in H--Kr collisions. Physical review. A, General physics, 35(6), 2470-2472. https://doi.org/10.1103/physreva.35.2470
Esaulov, et al. "Excitation processes in H--Kr collisions." Physical review. A, General physics vol. 35,6 (1987): 2470-2472. doi: https://doi.org/10.1103/physreva.35.2470
Esaulov VA, Grouard JP, Hall RI, Montmagnon JL. Excitation processes in H--Kr collisions. Phys Rev A Gen Phys. 1987 Mar 15;35(6):2470-2472. doi: 10.1103/physreva.35.2470. PMID: 9898434.
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Mechanisms of allosteric and mixed mode aromatase inhibitors.

RSC chemical biology

Souza SA, Held A, Lu WJ, Drouhard B, Avila B, Leyva-Montes R, Hu M, Miller BR, Ng HL.
PMID: 34458816
RSC Chem Biol. 2021 Mar 19;2(3):892-905. doi: 10.1039/d1cb00046b. eCollection 2021 Jun 01.

Aromatase (CYP19) catalyzes the last biosynthetic step of estrogens in mammals and is a primary drug target for hormone-related breast cancer. However, treatment with aromatase inhibitors is often associated with adverse effects and drug resistance. In this study, we...

Cite
Souza SA, Held A, Lu WJ, et al. Mechanisms of allosteric and mixed mode aromatase inhibitors. RSC Chem Biol. 2021;2(3):892-905doi: 10.1039/d1cb00046b.
Souza, S. A., Held, A., Lu, W. J., Drouhard, B., Avila, B., Leyva-Montes, R., Hu, M., Miller, B. R., & Ng, H. L. (2021). Mechanisms of allosteric and mixed mode aromatase inhibitors. RSC chemical biology, 2(3), 892-905. https://doi.org/10.1039/d1cb00046b
Souza, Samson A, et al. "Mechanisms of allosteric and mixed mode aromatase inhibitors." RSC chemical biology vol. 2,3 (2021): 892-905. doi: https://doi.org/10.1039/d1cb00046b
Souza SA, Held A, Lu WJ, Drouhard B, Avila B, Leyva-Montes R, Hu M, Miller BR, Ng HL. Mechanisms of allosteric and mixed mode aromatase inhibitors. RSC Chem Biol. 2021 Mar 19;2(3):892-905. doi: 10.1039/d1cb00046b. eCollection 2021 Jun 01. PMID: 34458816; PMCID: PMC8341375.
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